MK-5 with vented cover (polycarbonate
To Order Now: info@anbioq.org
![]() MK-8745 |
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B1942-5 | Biovision | EUR 153 |
![]() MK-0752 |
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B1980-5 | Biovision | EUR 457 |
![]() MK-5172 |
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B2118-5 | Biovision | EUR 185 |
![]() MK-7655 |
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B2289-5 | Biovision | EUR 196 |
![]() MK-0557 |
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B2317-5 | Biovision | EUR 196 |
![]() MK-3903 |
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B2431-5 | Biovision | EUR 414 |
![]() MK-886 |
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B2517-5 | Biovision | EUR 175 |
![]() MK-0941 |
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B1207-5 | Biovision | EUR 185 |
![]() MK-8931 |
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B1315-5 | Biovision | EUR 512 |
![]() MK-5108 |
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B1344-5 | Biovision | EUR 262 |
![]() MK-3102 |
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9599-5 | Biovision | EUR 457 |
![]() MK-4827 |
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9462-5 | Biovision | EUR 305 |
![]() MK 886 |
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B6684-5 | ApexBio | 5 mg | EUR 137 |
![]() MK 571 |
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B7023-5 | ApexBio | 5 mg | EUR 128 |
Description: MK 571 (L-660,711) is a novel potent and selective antagonist of leukotriene D4 receptor with Ki values of 0.22 nM and 2.1 nM in guinea pig and human lung membranes, respectively [1]. |
![]() MK-4101 |
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B7803-5 | ApexBio | 5 mg | EUR 261 |
Description: IC50: 1.5 ?mol/L for in mouse Light II cells by Gli_luc assayMK-4101 is a Hedgehog (Hh) signaling pathway inhibitor.Abnormal activation of the Hedgehog (Hh) signaling pathway is reported in the pathogenesis of various cancers, such as medulloblastoma and basal cell carcinoma. |
![]() MK-0752 |
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A4006-5 | ApexBio | 5 mg | EUR 247 |
Description: MK-0752 is a potent gamma secretase inhibitor in clinical development (IC50 ~50 nM). |
![]() MK-2048 |
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A4072-5 | ApexBio | 5 mg | EUR 270 |
Description: MK-2048 is a second generation inhibitor of HIV-1 integrase with IC50 values of 0.075 ?M and 0.08 ?M for subtype B and subtype C integrase, respectively.Integration of viral cDNA into the host genome is one of the definitive features of retrovirus replication. |
![]() MK-8245 |
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A4345-5 | ApexBio | 5 mg | EUR 268 |
Description: MK-8245 is a potent and liver-selective inhibitor of stearoyl-CoA desaturase (SCD) with IC50 value of 1nM [1].SCD1 represents a therapeutic target for the treatment of type II diabetes, dyslipidemia, obesity, and metabolic diseases. |
![]() MK-1775 |
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A5755-5 | ApexBio | 5 mg | EUR 148 |
Description: MK-1775 is a potent and selective Wee1 inhibitor with an IC50 of 5.2 nM in a cell-free assay. MK-1775 abolishes cyclin-dependent kinase 1 (CDC2) activity by phosphorylation of the Tyr15 residue [1]. |
![]() MK-2461 |
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A8476-5 | ApexBio | 5 mg | EUR 268 |
Description: MK-2461 is a potent inhibitor of Met, Flt1, Flt 3, Ron, PDGFR?, and Mer with IC50 of 2.5 nM, 10 nM, 22 nM, 7 nM, and 24 nM, respectively. |
![]() MK 6096 |
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A8953-5 | ApexBio | 5 mg | EUR 321 |
Description: MK 6096 |
![]() MK 0893 |
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A3608-5 | ApexBio | 5 mg | EUR 415 |
Description: MK 0893 is an inhibitor of both glucagon receptor and IGF-1R with IC50 values of 6.6nM and 6nM, respectively [1, 2]. |
![]() MK-0591 |
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A3609-5 | ApexBio | 5 mg | EUR 284 |
Description: MK-0591, an analog of MK-886 is a potent and orally active leukotriene biosynthesis inhibitor with an IC50 value of 600 ng/ml. |
![]() MK-0812 |
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A3611-5 | ApexBio | 5 mg | EUR 379 |
Description: MK-0812 is an antagonist of chemokine receptor CCR-2 [1].C-C chemokine receptor type 2 (CCR-2) is a chemokine receptor expressing on monocytes and macrophages and plays a critical and apparently non-redundant role in orchestrating the trafficking of monocytes to tissues [1]. |
![]() MK-0974 |
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A3612-5 | ApexBio | 5 mg | EUR 395 |
Description: MK-0974 (Telcagepant) is a highly potent, selective, and orally bioavailable antagonist of CGRP receptor with IC50 value of 0.77 nM [1]. |
![]() MK-2894 |
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A3613-5 | ApexBio | 5 mg | EUR 357 |
Description: MK-2894 is a highly potent and selective inhibitor of EP4 receptor with IC50 value of 2.5 nM [1]. |
![]() MK-3207 |
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A3615-5 | ApexBio | 5 mg | EUR 340 |
Description: MK-3207 is a new, highly selective CGRP receptor antagonist that is approximately 40- to 65-fold more potent than telcagepant for the human CGRP receptor. The IC50 is 0.12 nM and The Ki value is 0.024 nM. It is highly selective versus human AM1, AM2, CTR, and AMY3. |
![]() MK-4827 |
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A3617-5 | ApexBio | 5 mg | EUR 209 |
Description: MK-4827 is a novel, selective and orally bioavailable PARP1/PARP2 inhibitor with IC50 of 3.8 nM and 2.1 nM, respevctively.MK-4827 has shown great activity against cancer cells with mutant BRCA-1 and BRCA-2; >330-fold selective against PARP3, V-PARP and Tank1 [1]. |
![]() MK-5172 |
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A3618-5 | ApexBio | 5 mg | EUR 154 |
Description: MK-5172 is a selective inhibitor of Hepatitis C Virus NS3/4a Protease [1].Hepatitis C (HCV) virus is a member of the Flaviviridae family of viruses in the Hepacivirus genus and encoded by a 9.6-kb positive strand RNA genome [2]. |
![]() MK-6892 |
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A3623-5 | ApexBio | 5 mg | EUR 502 |
Description: Description:IC50 Value: 4.0 nM (Ki for Human GPR109A) [1]MK-6892 is a highly potential GPR109A agonists.in vitro: . Despite the increased serum shift of these compounds, the representative 1e was highly potent |
![]() MK-8033 |
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A3624-5 | ApexBio | 5 mg | EUR 466 |
Description: MK-8033 is a c-MET inhibitor in clinical trials. MK8033 is a selective small-molecule inhibitor, ATP competitive. Phase I investigation of the cMet inhibitor MK-8033 is ongoing. |
![]() Human Midkine (MK) ELISA Kit |
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DLR-MK-Hu-48T | DL Develop | 48T | EUR 479 |
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Description: A sandwich quantitative ELISA assay kit for detection of Human Midkine (MK) in samples from tissue homogenates, cell lysates, cell culture supernates or other biological fluids. |
![]() Human Midkine (MK) ELISA Kit |
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DLR-MK-Hu-96T | DL Develop | 96T | EUR 621 |
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Description: A sandwich quantitative ELISA assay kit for detection of Human Midkine (MK) in samples from tissue homogenates, cell lysates, cell culture supernates or other biological fluids. |
![]() Mouse Midkine (MK) ELISA Kit |
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DLR-MK-Mu-48T | DL Develop | 48T | EUR 489 |
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Description: A sandwich quantitative ELISA assay kit for detection of Mouse Midkine (MK) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids. |
![]() Mouse Midkine (MK) ELISA Kit |
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DLR-MK-Mu-96T | DL Develop | 96T | EUR 635 |
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Description: A sandwich quantitative ELISA assay kit for detection of Mouse Midkine (MK) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids. |
![]() Rat Midkine (MK) ELISA Kit |
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DLR-MK-Ra-48T | DL Develop | 48T | EUR 508 |
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Description: A sandwich quantitative ELISA assay kit for detection of Rat Midkine (MK) in samples from serum, plasma or other biological fluids. |
![]() Rat Midkine (MK) ELISA Kit |
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DLR-MK-Ra-96T | DL Develop | 96T | EUR 661 |
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Description: A sandwich quantitative ELISA assay kit for detection of Rat Midkine (MK) in samples from serum, plasma or other biological fluids. |
![]() Human Midkine (MK) ELISA Kit |
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RDR-MK-Hu-48Tests | Reddot Biotech | 48 Tests | EUR 500 |
![]() Human Midkine (MK) ELISA Kit |
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RDR-MK-Hu-96Tests | Reddot Biotech | 96 Tests | EUR 692 |
![]() Mouse Midkine (MK) ELISA Kit |
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RDR-MK-Mu-48Tests | Reddot Biotech | 48 Tests | EUR 511 |
![]() Mouse Midkine (MK) ELISA Kit |
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RDR-MK-Mu-96Tests | Reddot Biotech | 96 Tests | EUR 709 |
![]() Rat Midkine (MK) ELISA Kit |
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RDR-MK-Ra-48Tests | Reddot Biotech | 48 Tests | EUR 534 |
![]() Rat Midkine (MK) ELISA Kit |
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RDR-MK-Ra-96Tests | Reddot Biotech | 96 Tests | EUR 742 |
![]() Human Midkine (MK) ELISA Kit |
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RD-MK-Hu-48Tests | Reddot Biotech | 48 Tests | EUR 478 |
![]() Human Midkine (MK) ELISA Kit |
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RD-MK-Hu-96Tests | Reddot Biotech | 96 Tests | EUR 662 |
![]() Mouse Midkine (MK) ELISA Kit |
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RD-MK-Mu-48Tests | Reddot Biotech | 48 Tests | EUR 489 |
![]() Mouse Midkine (MK) ELISA Kit |
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RD-MK-Mu-96Tests | Reddot Biotech | 96 Tests | EUR 677 |
![]() Rat Midkine (MK) ELISA Kit |
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RD-MK-Ra-48Tests | Reddot Biotech | 48 Tests | EUR 511 |
![]() Rat Midkine (MK) ELISA Kit |
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RD-MK-Ra-96Tests | Reddot Biotech | 96 Tests | EUR 709 |
![]() CORNING® 100X10MM PETRI DISH WITH COVER |
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70165-100 | CORNING | 12/pk | EUR 105 |
Description: Vista Petri Dishes; PYREX VISTA Petri Dishes |
![]() CORNING® 100X15MM PETRI DISH WITH COVER |
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70165-101 | CORNING | 12/pk | EUR 104 |
Description: Vista Petri Dishes; PYREX VISTA Petri Dishes |
![]() CORNING® 100X20MM PETRI DISH WITH COVER |
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70165-102 | CORNING | 12/pk | EUR 104 |
Description: Vista Petri Dishes; PYREX VISTA Petri Dishes |
![]() MK-571 sodium |
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2692-5 | Biovision | EUR 185 |
![]() MK-4827 (Tosylate) |
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B2003-5 | Biovision | EUR 240 |
![]() Grazoprevir (MK-5172) |
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B2337-5 | Biovision | EUR 185 |
![]() MK-4827 Racemate |
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B3393-5 | ApexBio | 5 mg | EUR 209 |
Description: MK-4827 racemate (Niraparib racemate) is a selective inhibitor of PARP1/2 with IC50 of 3.8 nM/2.1 nM; >330-fold selective against PARP3, V-PARP and Tank1. |
![]() MK-4827 hydrochloride |
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B1163-5 | ApexBio | 5 mg | EUR 212 |
Description: MK-4827(Niraparib) Hcl is a selective inhibitor of PARP1/PARP2 with IC50 of 3.8 nM/2.1 nM; with great activity in cancer cells with mutant BRCA-1 and BRCA-2; >330-fold selective against PARP3, V-PARP and Tank1. |
![]() MK-4827 tosylate |
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B1164-5 | ApexBio | 5 mg | EUR 232 |
Description: MK-4827(Niraparib) tosylate is a selective inhibitor of PARP1/PARP2 with IC50 of 3.8 nM/2.1 nM; with great activity in cancer cells with mutant BRCA-1 and BRCA-2; >330-fold selective against PARP3, V-PARP and Tank1. |
![]() MK-3207 HCl |
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B1436-5 | ApexBio | 5 mg | EUR 303 |
Description: MK-3207 is a potent and orally bioavailable CGRP receptor antagonist (IC50= 0.12 nM; Ki value= 0.024 nM); highly selective versus human AM1, AM2, CTR, and AMY3. |
![]() Verubecestat (MK-8931) |
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B6195-5 | ApexBio | 5 mg | EUR 160 |
Description: Ki: 2.2 and 3.4 nM for human and mouse Bace1, respectivelyVerubecestat (MK-8931) is a BACE1 inhibitor.?-Amyloid (A?) peptides are regarded to be involved in the etiology of AD. |
![]() Raltegravir (MK-0518) |
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A4073-5 | ApexBio | 5 mg | EUR 148 |
Description: Raltegravir, formerly named MK-0518, is an HIV-1 integrase strand transfer inhibitor which has been shown to have activity against multidrug-resistant HIV-1 and both CCR5-trophic and CXCR4-trophic HIV-1 in vitro. |
![]() Anacetrapib (MK-0859) |
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A4375-5 | ApexBio | 5 mg | EUR 189 |
Description: Anacetrapib, also known as MK-0859, is a potent and selective inhibitor of cholesteryl ester transfer protein (CETP) that exhibits strong inhibition against CETP-mediated transfer of cholesteryl esters and triglycerides with values of inhibition constant IC50 of 16 nM and 29 nM respectively. |
![]() MK-5172 hydrate |
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A3619-5 | ApexBio | 5 mg | EUR 212 |
Description: IC50 Value: 7.4nM and 7nM for genotype1b and 1a respectively, in replicon system [1]MK-5172 is a novel P2-P4 quinoxaline macrocyclic HCV NS3/4a protease inhibitor currently in clinical development. |
![]() Odanacatib (MK-0822) |
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A2487-5 | ApexBio | 5 mg | EUR 166 |
Description: Odanacatib (MK-0822) is a potent, orally active and selective inhibitor of Cathepsin K with IC50 value of 0.20 nM [1],Cathepsin K is expressed predominantly in osteoclasts and degrades the collagen matrix componentsofbone. |
![]() CORNING®150X20 MM PETRI DISH WITH COVER |
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70165-152 | CORNING | 12/pk | EUR 243 |
Description: Vista Petri Dishes; PYREX VISTA Petri Dishes |
![]() Cover Plate |
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1292235 | Atto | 5unit | EUR 251 |
![]() (+)-MK 801 Hydrogen Maleate |
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B2326-5 | Biovision | EUR 131 |
![]() (-)-MK 801 Hydrogen Maleate |
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B2327-5 | Biovision | EUR 131 |
![]() MK-591 sodium salt |
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B2519-5 | Biovision | EUR 349 |
![]() MK-591, Free acid |
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B2520-5 | Biovision | EUR 349 |
![]() MK-5108 (VX-689) |
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A4120-5 | ApexBio | 5 mg | EUR 189 |
Description: MK-5108, also known as VX-689, is a novel, potent and selective inhibitor of Aurora A kinase (AAK) that competitively binds to the ATP binding site of AAK and hence potently inhibits the activity of AAK with 50% inhibition concentration IC50 value of 0.064 nM |
![]() MK-8776 (SCH-900776) |
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A8477-5 | ApexBio | 5 mg | EUR 177 |
Description: SCH 900776 is a potent and selective inhibitor of cell cycle checkpoint kinase 1 (Chk1), Chk2 and Cdk3 with IC50 value of 3 nM, 1.5µM and 0.16 µM, respectively. |
![]() MK-5172 potassium salt |
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A3620-5 | ApexBio | 5 mg | EUR 212 |
Description: IC50 Value: 7.4nM and 7nM for genotype1b and 1a respectively, in replicon system [1]MK-5172 is a novel P2-P4 quinoxaline macrocyclic HCV NS3/4a protease inhibitor currently in clinical development. |
![]() MK-5172 sodium salt |
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A3621-5 | ApexBio | 5 mg | EUR 212 |
Description: IC50 Value: 7.4nM and 7nM for genotype1b and 1a respectively, in replicon system [1]MK-5172 is a novel P2-P4 quinoxaline macrocyclic HCV NS3/4a protease inhibitor currently in clinical development. |
![]() Stainless Steel Dish with Cover (for 30 Slide Holder) |
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IMS004 | ScyTek Laboratories | 1 ea. | EUR 96 |
![]() MK-571 sodium salt hydrate |
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B8031-5 | ApexBio | 5 mg | EUR 115 |
Description: MK571 sodium salt is a specific CysLT1 (Cysteinyl-Leukotriene Type 1 Receptor) antagonist [1].Cysteinyl leukotriene receptor 1, also termed as CYSLTR1, is a receptor for cysteinyl leukotrienes (LT)which mediates a large variety of allergic and hypersensitivity reactions in humans [2]. |
![]() Orange viewing cover |
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E5001-OC | BenchMark | 1 PC | EUR 87.62 |
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![]() FALCON® 875CM² RECTANGULAR STRAIGHT NECK CELL CULTURE MULTI-FLASK, 5-LAYER WITH VENTED CAP |
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353144 | CORNING | 8/pk | EUR 167 |
Description: Lab Cell Culture - DL; High Density Flasks |
![]() CORNING®60 X 15 MM PETRI DISH WITH COVER |
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70165-60 | CORNING | 12/pk | EUR 119 |
Description: Vista Petri Dishes; PYREX VISTA Petri Dishes |
![]() BATTERY COVER WITH WINGS FOR CORNING® STRIPETTOR™ ULTRA |
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4995 | CORNING | 3/pk | EUR 44 |
Description: Handheld Pipettor Repairs; Liquid Handling Device Repairs |
![]() TubeRoller with 5 rollers |
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R3005-E | BenchMark | 1 PC | EUR 1065.86 |
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Description: TubeRoller ensures gentle rolling motion, Smooth +/-5° tilt action, available for tubes/bottles from 8mm to 200mm diameter |
![]() FALCON® 25CM² RECTANGULAR CANTED NECK CELL CULTURE FLASK WITH VENTED CAP |
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353108 | CORNING | 20/pk | EUR 82 |
Description: Lab Cell Culture - DL; TC Flasks - DL |
![]() FALCON® 25CM² RECTANGULAR CANTED NECK CELL CULTURE FLASK WITH VENTED CAP |
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353109 | CORNING | 20/pk | EUR 85 |
Description: Lab Cell Culture - DL; TC Flasks - DL |
![]() FALCON® 75CM² RECTANGULAR STRAIGHT NECK CELL CULTURE FLASK WITH VENTED CAP |
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353110 | CORNING | 5/pk | EUR 118 |
Description: Lab Cell Culture - DL; TC Flasks - DL |
![]() FALCON® 175CM² RECTANGULAR STRAIGHT NECK CELL CULTURE FLASK WITH VENTED CAP |
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353112 | CORNING | 5/pk | EUR 101 |
Description: Lab Cell Culture - DL; TC Flasks - DL |
![]() FALCON® 75CM² RECTANGULAR CANTED NECK CELL CULTURE FLASK WITH VENTED CAP |
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353136 | CORNING | 5/pk | EUR 83 |
Description: Lab Cell Culture - DL; TC Flasks - DL |
![]() FALCON® 225CM² RECTANGULAR CANTED NECK CELL CULTURE FLASK WITH VENTED CAP |
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353138 | CORNING | 5/pk | EUR 139 |
Description: Lab Cell Culture - DL; TC Flasks - DL |
![]() FALCON® 150CM² RECTANGULAR CANTED NECK CELL CULTURE FLASK WITH VENTED CAP |
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355001 | CORNING | 5/pk | EUR 112 |
Description: Lab Cell Culture - DL; TC Flasks - DL |
![]() CORNING® BIOCOAT™ POLY-D-LYSINE 175CM² FLASK WITH VENTED CAP |
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356539 | CORNING | 5/pk | EUR 552 |
Description: Advanced Cells - DL; Flasks BCT |
![]() MK-1775 |
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2373-25 | Biovision | EUR 430 |
![]() MK-571 |
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2691-25 | Biovision | EUR 544 |
![]() MK-2206 |
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1888-1000 | Biovision | EUR 240 |
![]() MK-2206 |
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1888-500 | Biovision | EUR 156 |
![]() (-)-MK 801 |
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B1627-10 | ApexBio | 10 mg | EUR 102 |
Description: (+)-MK 801 Maleate is a potent antagonist of NMDA with Ki value of 30.5nM [1].MK 801 is a potent anticonvulsant exhibits both anxiolytic and sympathomimetic properties. It is found to be a noncompetitive antagonist of NMDA. MK 801 can penetrate into the central nervous system. |
![]() (-)-MK 801 |
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B1627-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 113 |
Description: (+)-MK 801 Maleate is a potent antagonist of NMDA with Ki value of 30.5nM [1].MK 801 is a potent anticonvulsant exhibits both anxiolytic and sympathomimetic properties. It is found to be a noncompetitive antagonist of NMDA. MK 801 can penetrate into the central nervous system. |
![]() (-)-MK 801 |
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B1627-50 | ApexBio | 50 mg | EUR 224 |
Description: (+)-MK 801 Maleate is a potent antagonist of NMDA with Ki value of 30.5nM [1].MK 801 is a potent anticonvulsant exhibits both anxiolytic and sympathomimetic properties. It is found to be a noncompetitive antagonist of NMDA. MK 801 can penetrate into the central nervous system. |
![]() MK-1064 |
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B1641-25 | Biovision | EUR 865 |
![]() MK-8745 |
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B1942-25 | Biovision | EUR 457 |
![]() MK-0752 |
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B1980-1 | Biovision | EUR 153 |
![]() MK-5172 |
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B2118-25 | Biovision | EUR 588 |
![]() MK-7655 |
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B2289-25 | Biovision | EUR 631 |
![]() MK-0557 |
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B2317-25 | Biovision | EUR 631 |
![]() MK-3903 |
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B2431-1 | Biovision | EUR 142 |
![]() MK-886 |
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B2517-25 | Biovision | EUR 544 |
![]() MK 0343 |
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B5585-10 | ApexBio | 10 mg | EUR 438 |
![]() MK 0343 |
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B5585-50 | ApexBio | 50 mg | EUR 1639 |
![]() MK-0941 |
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B1207-25 | Biovision | EUR 588 |
![]() MK-8931 |
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B1315-1 | Biovision | EUR 175 |
![]() MK-5108 |
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B1344-25 | Biovision | EUR 756 |
![]() MK 1903 |
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B5658-10 | ApexBio | 10 mg | EUR 389 |
![]() MK 1903 |
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B5658-50 | ApexBio | 50 mg | EUR 1476 |
![]() MK-3102 |
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9599-1 | Biovision | EUR 153 |
![]() MK-4827 |
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9462-25 | Biovision | EUR 1023 |
![]() MK-677 |
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abx188791-10g | Abbexa | 10 g | EUR 606 |
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![]() Mk-0822 |
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20-abx182578 | Abbexa |
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![]() Mk-2206 |
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20-abx182579 | Abbexa |
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![]() MK-2206 |
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E1KS1078 | EnoGene | 5 mg | EUR 443 |
![]() MK 3207 |
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E1KS1542 | EnoGene | 10mg | EUR 1504 |
![]() MK-0752 |
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E1KS2660 | EnoGene | 5mg | EUR 1111 |
![]() MK 886 |
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B6684-10 | ApexBio | 10 mg | EUR 206 |
![]() MK 886 |
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B6684-25 | ApexBio | 25 mg | EUR 398 |
![]() MK 571 |
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B7023-10 | ApexBio | 10 mg | EUR 186 |
Description: MK 571 (L-660,711) is a novel potent and selective antagonist of leukotriene D4 receptor with Ki values of 0.22 nM and 2.1 nM in guinea pig and human lung membranes, respectively [1]. |
![]() MK 571 |
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B7023-50 | ApexBio | 50 mg | EUR 659 |
Description: MK 571 (L-660,711) is a novel potent and selective antagonist of leukotriene D4 receptor with Ki values of 0.22 nM and 2.1 nM in guinea pig and human lung membranes, respectively [1]. |
![]() MK-4101 |
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B7803-10 | ApexBio | 10 mg | EUR 366 |
Description: IC50: 1.5 ?mol/L for in mouse Light II cells by Gli_luc assayMK-4101 is a Hedgehog (Hh) signaling pathway inhibitor.Abnormal activation of the Hedgehog (Hh) signaling pathway is reported in the pathogenesis of various cancers, such as medulloblastoma and basal cell carcinoma. |
![]() MK-4101 |
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B7803-100 | ApexBio | 100 mg | EUR 2312 |
Description: IC50: 1.5 ?mol/L for in mouse Light II cells by Gli_luc assayMK-4101 is a Hedgehog (Hh) signaling pathway inhibitor.Abnormal activation of the Hedgehog (Hh) signaling pathway is reported in the pathogenesis of various cancers, such as medulloblastoma and basal cell carcinoma. |
![]() MK-4101 |
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B7803-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 279 |
Description: IC50: 1.5 ?mol/L for in mouse Light II cells by Gli_luc assayMK-4101 is a Hedgehog (Hh) signaling pathway inhibitor.Abnormal activation of the Hedgehog (Hh) signaling pathway is reported in the pathogenesis of various cancers, such as medulloblastoma and basal cell carcinoma. |
![]() MK-4101 |
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B7803-50 | ApexBio | 50 mg | EUR 1286 |
Description: IC50: 1.5 ?mol/L for in mouse Light II cells by Gli_luc assayMK-4101 is a Hedgehog (Hh) signaling pathway inhibitor.Abnormal activation of the Hedgehog (Hh) signaling pathway is reported in the pathogenesis of various cancers, such as medulloblastoma and basal cell carcinoma. |
![]() MK-0752 |
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A4006-10 | ApexBio | 10 mg | EUR 316 |
Description: MK-0752 is a potent gamma secretase inhibitor in clinical development (IC50 ~50 nM). |
![]() MK-0752 |
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A4006-100 | ApexBio | 100 mg | EUR 1302 |
Description: MK-0752 is a potent gamma secretase inhibitor in clinical development (IC50 ~50 nM). |
![]() MK-0752 |
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A4006-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 305 |
Description: MK-0752 is a potent gamma secretase inhibitor in clinical development (IC50 ~50 nM). |
![]() MK-0752 |
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A4006-50 | ApexBio | 50 mg | EUR 734 |
Description: MK-0752 is a potent gamma secretase inhibitor in clinical development (IC50 ~50 nM). |
![]() MK-0752 |
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A4006-S | ApexBio | Evaluation Sample | EUR 81 |
Description: MK-0752 is a potent gamma secretase inhibitor in clinical development (IC50 ~50 nM). |
![]() MK-2048 |
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A4072-10 | ApexBio | 10 mg | EUR 351 |
Description: MK-2048 is a second generation inhibitor of HIV-1 integrase with IC50 values of 0.075 ?M and 0.08 ?M for subtype B and subtype C integrase, respectively.Integration of viral cDNA into the host genome is one of the definitive features of retrovirus replication. |
![]() MK-2048 |
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A4072-100 | ApexBio | 100 mg | EUR 1186 |
Description: MK-2048 is a second generation inhibitor of HIV-1 integrase with IC50 values of 0.075 ?M and 0.08 ?M for subtype B and subtype C integrase, respectively.Integration of viral cDNA into the host genome is one of the definitive features of retrovirus replication. |
![]() MK-2048 |
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A4072-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 456 |
Description: MK-2048 is a second generation inhibitor of HIV-1 integrase with IC50 values of 0.075 ?M and 0.08 ?M for subtype B and subtype C integrase, respectively.Integration of viral cDNA into the host genome is one of the definitive features of retrovirus replication. |
![]() MK-2048 |
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A4072-50 | ApexBio | 50 mg | EUR 838 |
Description: MK-2048 is a second generation inhibitor of HIV-1 integrase with IC50 values of 0.075 ?M and 0.08 ?M for subtype B and subtype C integrase, respectively.Integration of viral cDNA into the host genome is one of the definitive features of retrovirus replication. |
![]() MK-8245 |
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A4345-10 | ApexBio | 10 mg | EUR 350 |
Description: MK-8245 is a potent and liver-selective inhibitor of stearoyl-CoA desaturase (SCD) with IC50 value of 1nM [1].SCD1 represents a therapeutic target for the treatment of type II diabetes, dyslipidemia, obesity, and metabolic diseases. |
![]() MK-8245 |
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A4345-200 | ApexBio | 200 mg | EUR 2055 |
Description: MK-8245 is a potent and liver-selective inhibitor of stearoyl-CoA desaturase (SCD) with IC50 value of 1nM [1].SCD1 represents a therapeutic target for the treatment of type II diabetes, dyslipidemia, obesity, and metabolic diseases. |
![]() MK-8245 |
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A4345-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 282 |
Description: MK-8245 is a potent and liver-selective inhibitor of stearoyl-CoA desaturase (SCD) with IC50 value of 1nM [1].SCD1 represents a therapeutic target for the treatment of type II diabetes, dyslipidemia, obesity, and metabolic diseases. |
![]() MK-8245 |
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A4345-50 | ApexBio | 50 mg | EUR 918 |
Description: MK-8245 is a potent and liver-selective inhibitor of stearoyl-CoA desaturase (SCD) with IC50 value of 1nM [1].SCD1 represents a therapeutic target for the treatment of type II diabetes, dyslipidemia, obesity, and metabolic diseases. |
![]() MK-1775 |
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A5755-10 | ApexBio | 10 mg | EUR 200 |
Description: MK-1775 is a potent and selective Wee1 inhibitor with an IC50 of 5.2 nM in a cell-free assay. MK-1775 abolishes cyclin-dependent kinase 1 (CDC2) activity by phosphorylation of the Tyr15 residue [1]. |
![]() MK-1775 |
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A5755-100 | ApexBio | 100 mg | EUR 815 |
Description: MK-1775 is a potent and selective Wee1 inhibitor with an IC50 of 5.2 nM in a cell-free assay. MK-1775 abolishes cyclin-dependent kinase 1 (CDC2) activity by phosphorylation of the Tyr15 residue [1]. |
![]() MK-1775 |
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A5755-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 166 |
Description: MK-1775 is a potent and selective Wee1 inhibitor with an IC50 of 5.2 nM in a cell-free assay. MK-1775 abolishes cyclin-dependent kinase 1 (CDC2) activity by phosphorylation of the Tyr15 residue [1]. |
![]() MK-1775 |
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A5755-50 | ApexBio | 50 mg | EUR 508 |
Description: MK-1775 is a potent and selective Wee1 inhibitor with an IC50 of 5.2 nM in a cell-free assay. MK-1775 abolishes cyclin-dependent kinase 1 (CDC2) activity by phosphorylation of the Tyr15 residue [1]. |
![]() MK-1775 |
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A5755-S | ApexBio | Evaluation Sample | EUR 81 |
Description: MK-1775 is a potent and selective Wee1 inhibitor with an IC50 of 5.2 nM in a cell-free assay. MK-1775 abolishes cyclin-dependent kinase 1 (CDC2) activity by phosphorylation of the Tyr15 residue [1]. |
![]() MK-2461 |
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A8476-10 | ApexBio | 10 mg | EUR 432 |
Description: MK-2461 is a potent inhibitor of Met, Flt1, Flt 3, Ron, PDGFR?, and Mer with IC50 of 2.5 nM, 10 nM, 22 nM, 7 nM, and 24 nM, respectively. |
![]() MK-2461 |
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A8476-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 287 |
Description: MK-2461 is a potent inhibitor of Met, Flt1, Flt 3, Ron, PDGFR?, and Mer with IC50 of 2.5 nM, 10 nM, 22 nM, 7 nM, and 24 nM, respectively. |
![]() MK-8745 |
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A8807-10 | ApexBio | 10 mg | EUR 128 |
Description: MK-8745 is a novel and selective inhibitor of Aurora A with IC50 value of 0.6 nM [1].Aurora A kinase is a member of mitotic serine/threonine kinases and plays an important role in cellular division by controlling chromatid segregation. |
![]() MK-8745 |
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A8807-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 119 |
Description: MK-8745 is a novel and selective inhibitor of Aurora A with IC50 value of 0.6 nM [1].Aurora A kinase is a member of mitotic serine/threonine kinases and plays an important role in cellular division by controlling chromatid segregation. |
![]() MK-8745 |
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A8807-50 | ApexBio | 50 mg | EUR 268 |
Description: MK-8745 is a novel and selective inhibitor of Aurora A with IC50 value of 0.6 nM [1].Aurora A kinase is a member of mitotic serine/threonine kinases and plays an important role in cellular division by controlling chromatid segregation. |
![]() MK 6096 |
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A8953-10 | ApexBio | 10 mg | EUR 502 |
Description: MK 6096 |
![]() MK 6096 |
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A8953-100 | ApexBio | 100 mg | EUR 1823 |
Description: MK 6096 |
![]() MK 6096 |
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A8953-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 348 |
Description: MK 6096 |
![]() MK 6096 |
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A8953-50 | ApexBio | 50 mg | EUR 1225 |
Description: MK 6096 |
![]() (+)-MK 801 |
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A3100-10 | ApexBio | 10 mg | EUR 105 |
Description: (+)-MK 801 is a potent antagonist of NMDA with Ki value of 30.5nM [1].MK 801 is a potent anticonvulsant exhibits both anxiolytic and sympathomimetic properties. |
![]() (+)-MK 801 |
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A3100-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 108 |
Description: (+)-MK 801 is a potent antagonist of NMDA with Ki value of 30.5nM [1].MK 801 is a potent anticonvulsant exhibits both anxiolytic and sympathomimetic properties. |
![]() (+)-MK 801 |
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A3100-50 | ApexBio | 50 mg | EUR 266 |
Description: (+)-MK 801 is a potent antagonist of NMDA with Ki value of 30.5nM [1].MK 801 is a potent anticonvulsant exhibits both anxiolytic and sympathomimetic properties. |
![]() MK 0893 |
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A3608-10 | ApexBio | 10 mg | EUR 711 |
Description: MK 0893 is an inhibitor of both glucagon receptor and IGF-1R with IC50 values of 6.6nM and 6nM, respectively [1, 2]. |
![]() MK 0893 |
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A3608-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 525 |
Description: MK 0893 is an inhibitor of both glucagon receptor and IGF-1R with IC50 values of 6.6nM and 6nM, respectively [1, 2]. |
![]() MK 0893 |
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A3608-50 | ApexBio | 50 mg | EUR 1703 |
Description: MK 0893 is an inhibitor of both glucagon receptor and IGF-1R with IC50 values of 6.6nM and 6nM, respectively [1, 2]. |
![]() MK-0591 |
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A3609-10 | ApexBio | 10 mg | EUR 366 |
Description: MK-0591, an analog of MK-886 is a potent and orally active leukotriene biosynthesis inhibitor with an IC50 value of 600 ng/ml. |
![]() MK-0591 |
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A3609-100 | ApexBio | 100 mg | EUR 2222 |
Description: MK-0591, an analog of MK-886 is a potent and orally active leukotriene biosynthesis inhibitor with an IC50 value of 600 ng/ml. |
![]() MK-0591 |
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A3609-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 354 |
Description: MK-0591, an analog of MK-886 is a potent and orally active leukotriene biosynthesis inhibitor with an IC50 value of 600 ng/ml. |
![]() MK-0591 |
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A3609-50 | ApexBio | 50 mg | EUR 1453 |
Description: MK-0591, an analog of MK-886 is a potent and orally active leukotriene biosynthesis inhibitor with an IC50 value of 600 ng/ml. |
![]() MK-0812 |
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A3611-1 | ApexBio | 1 mg | EUR 132 |
Description: MK-0812 is an antagonist of chemokine receptor CCR-2 [1].C-C chemokine receptor type 2 (CCR-2) is a chemokine receptor expressing on monocytes and macrophages and plays a critical and apparently non-redundant role in orchestrating the trafficking of monocytes to tissues [1]. |
![]() MK-0812 |
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A3611-10 | ApexBio | 10 mg | EUR 666 |
Description: MK-0812 is an antagonist of chemokine receptor CCR-2 [1].C-C chemokine receptor type 2 (CCR-2) is a chemokine receptor expressing on monocytes and macrophages and plays a critical and apparently non-redundant role in orchestrating the trafficking of monocytes to tissues [1]. |
![]() MK-0974 |
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A3612-1 | ApexBio | 1 mg | EUR 126 |
Description: MK-0974 (Telcagepant) is a highly potent, selective, and orally bioavailable antagonist of CGRP receptor with IC50 value of 0.77 nM [1]. |
![]() MK-0974 |
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A3612-10 | ApexBio | 10 mg | EUR 661 |
Description: MK-0974 (Telcagepant) is a highly potent, selective, and orally bioavailable antagonist of CGRP receptor with IC50 value of 0.77 nM [1]. |
![]() MK-2894 |
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A3613-10 | ApexBio | 10 mg | EUR 567 |
Description: MK-2894 is a highly potent and selective inhibitor of EP4 receptor with IC50 value of 2.5 nM [1]. |
![]() MK-2894 |
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A3613-50 | ApexBio | 50 mg | EUR 2004 |
Description: MK-2894 is a highly potent and selective inhibitor of EP4 receptor with IC50 value of 2.5 nM [1]. |
![]() MK-3207 |
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A3615-10 | ApexBio | 10 mg | EUR 547 |
Description: MK-3207 is a new, highly selective CGRP receptor antagonist that is approximately 40- to 65-fold more potent than telcagepant for the human CGRP receptor. The IC50 is 0.12 nM and The Ki value is 0.024 nM. It is highly selective versus human AM1, AM2, CTR, and AMY3. |
![]() MK-4827 |
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A3617-10 | ApexBio | 10 mg | EUR 318 |
Description: MK-4827 is a novel, selective and orally bioavailable PARP1/PARP2 inhibitor with IC50 of 3.8 nM and 2.1 nM, respevctively.MK-4827 has shown great activity against cancer cells with mutant BRCA-1 and BRCA-2; >330-fold selective against PARP3, V-PARP and Tank1 [1]. |
![]() MK-4827 |
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A3617-100 | ApexBio | 100 mg | EUR 1636 |
Description: MK-4827 is a novel, selective and orally bioavailable PARP1/PARP2 inhibitor with IC50 of 3.8 nM and 2.1 nM, respevctively.MK-4827 has shown great activity against cancer cells with mutant BRCA-1 and BRCA-2; >330-fold selective against PARP3, V-PARP and Tank1 [1]. |
![]() MK-4827 |
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A3617-50 | ApexBio | 50 mg | EUR 951 |
Description: MK-4827 is a novel, selective and orally bioavailable PARP1/PARP2 inhibitor with IC50 of 3.8 nM and 2.1 nM, respevctively.MK-4827 has shown great activity against cancer cells with mutant BRCA-1 and BRCA-2; >330-fold selective against PARP3, V-PARP and Tank1 [1]. |
![]() MK-5172 |
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A3618-10 | ApexBio | 10 mg | EUR 212 |
Description: MK-5172 is a selective inhibitor of Hepatitis C Virus NS3/4a Protease [1].Hepatitis C (HCV) virus is a member of the Flaviviridae family of viruses in the Hepacivirus genus and encoded by a 9.6-kb positive strand RNA genome [2]. |
![]() MK-5172 |
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A3618-100 | ApexBio | 100 mg | EUR 804 |
Description: MK-5172 is a selective inhibitor of Hepatitis C Virus NS3/4a Protease [1].Hepatitis C (HCV) virus is a member of the Flaviviridae family of viruses in the Hepacivirus genus and encoded by a 9.6-kb positive strand RNA genome [2]. |
![]() MK-5172 |
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A3618-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 186 |
Description: MK-5172 is a selective inhibitor of Hepatitis C Virus NS3/4a Protease [1].Hepatitis C (HCV) virus is a member of the Flaviviridae family of viruses in the Hepacivirus genus and encoded by a 9.6-kb positive strand RNA genome [2]. |
![]() MK-5172 |
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A3618-50 | ApexBio | 50 mg | EUR 572 |
Description: MK-5172 is a selective inhibitor of Hepatitis C Virus NS3/4a Protease [1].Hepatitis C (HCV) virus is a member of the Flaviviridae family of viruses in the Hepacivirus genus and encoded by a 9.6-kb positive strand RNA genome [2]. |
![]() MK-6892 |
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A3623-10 | ApexBio | 10 mg | EUR 737 |
Description: Description:IC50 Value: 4.0 nM (Ki for Human GPR109A) [1]MK-6892 is a highly potential GPR109A agonists.in vitro: . Despite the increased serum shift of these compounds, the representative 1e was highly potent |
![]() MK-6892 |
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A3623-100 | ApexBio | 100 mg | EUR 2583 |
Description: Description:IC50 Value: 4.0 nM (Ki for Human GPR109A) [1]MK-6892 is a highly potential GPR109A agonists.in vitro: . Despite the increased serum shift of these compounds, the representative 1e was highly potent |
![]() MK-6892 |
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A3623-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 547 |
Description: Description:IC50 Value: 4.0 nM (Ki for Human GPR109A) [1]MK-6892 is a highly potential GPR109A agonists.in vitro: . Despite the increased serum shift of these compounds, the representative 1e was highly potent |
![]() MK-6892 |
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A3623-50 | ApexBio | 50 mg | EUR 1678 |
Description: Description:IC50 Value: 4.0 nM (Ki for Human GPR109A) [1]MK-6892 is a highly potential GPR109A agonists.in vitro: . Despite the increased serum shift of these compounds, the representative 1e was highly potent |
![]() MK-4101 |
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HY-100036 | MedChemExpress | 100mg | EUR 854 |
![]() MK-3328 |
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HY-100275 | MedChemExpress | 1mg | EUR 912 |
![]() MK-447 |
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HY-100297 | MedChemExpress | 10mg | EUR 1706 |
![]() MK-6913 |
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HY-100327 | MedChemExpress | 10mg | EUR 6122 |
![]() MK-3697 |
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HY-12301 | MedChemExpress | 50mg | EUR 1076 |
![]() MK-0354 |
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HY-13008 | MedChemExpress | 10mM/1mL | EUR 277 |
![]() MK-8245 |
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HY-13070 | MedChemExpress | 10mM/1mL | EUR 191 |
![]() MK-5108 |
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HY-13252 | MedChemExpress | 100mg | EUR 1083 |
![]() MK-8033 |
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HY-13299 | MedChemExpress | 5mg | EUR 573 |
![]() MK-2048 |
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HY-13305 | MedChemExpress | 1mg | EUR 257 |
![]() MK-4256 |
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HY-13466 | MedChemExpress | 100mg | EUR 4596 |
![]() MK-8745 |
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HY-13819 | MedChemExpress | 10mM/1mL | EUR 141 |
![]() MK-886 |
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HY-14166 | MedChemExpress | 5mg | EUR 147 |
![]() MK-5046 |
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HY-14342 | MedChemExpress | 100mg | EUR 2736 |
![]() MK-0429 |
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HY-15102 | MedChemExpress | 100mg | EUR 3896 |
![]() MK-0557 |
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HY-15411 | MedChemExpress | 10mM/1mL | EUR 263 |
![]() MK-7622 |
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HY-15618 | MedChemExpress | 5mg | EUR 176 |
![]() MK-7246 |
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HY-15853 | MedChemExpress | 50mg | EUR 2116 |
![]() MK-1064 |
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HY-19914 | MedChemExpress | 100mg | EUR 1413 |