PD-0325901
To Order Now: info@anbioq.org
![]() PD-1/PD-L1 Inhibitor 1 |
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B1213-25 | Biovision | EUR 566 |
![]() PD-1/PD-L1 inhibitor 2 |
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B6023-25 | ApexBio | 25 mg | EUR 438 |
Description: PD-1/PD-L1 inhibitor 2 is a PD-1/PD-L1 interaction inhibitor. |
![]() PD-1/PD-L1 inhibitor 2 |
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B6023-5 | ApexBio | 5 mg | EUR 171 |
Description: PD-1/PD-L1 inhibitor 2 is a PD-1/PD-L1 interaction inhibitor. |
![]() PD-1/PD-L1 inhibitor 1 |
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B6172-25 | ApexBio | 25 mg | EUR 453 |
Description: IC50: 0.006-0.10 ?MPD-1/PD-L1 inhibitor 1 is a PD-1/PD-L1 interaction inhibitor.Plenty of studies show that blocking the PD-1/PD-Ll interactions can lead to the restorage and augment of T cell activation in many systems. |
![]() PD-1/PD-L1 inhibitor 1 |
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B6172-5 | ApexBio | 5 mg | EUR 168 |
Description: IC50: 0.006-0.10 ?MPD-1/PD-L1 inhibitor 1 is a PD-1/PD-L1 interaction inhibitor.Plenty of studies show that blocking the PD-1/PD-Ll interactions can lead to the restorage and augment of T cell activation in many systems. |
![]() PD 98059 |
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1666-5 | Biovision | EUR 158 |
![]() PD 173074 |
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1675-1 | Biovision | EUR 137 |
![]() PD 173074 |
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1675-100 | Biovision | Ask for price |
![]() PD 150,606 |
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1906-25 | Biovision | EUR 370 |
![]() PD 150,606 |
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1906-5 | Biovision | EUR 137 |
![]() PD 169316 |
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B1703-25 | Biovision | EUR 544 |
![]() PD 169316 |
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B1703-5 | Biovision | EUR 175 |
![]() PD-166866 |
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B2223-25 | Biovision | EUR 675 |
![]() PD-166866 |
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B2223-5 | Biovision | EUR 207 |
![]() PD-146176 |
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B2313-25 | Biovision | EUR 675 |
![]() PD-146176 |
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B2313-5 | Biovision | EUR 207 |
![]() PD-168393 |
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B2352-25 | Biovision | EUR 414 |
![]() PD-168393 |
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B2352-5 | Biovision | EUR 142 |
![]() PD-ECGF |
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PR15044 | Neuromics | 10 ug | EUR 487 |
![]() PD 98,059 |
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GK2140-10MG | Glentham Life Sciences | 10 mg | EUR 172 |
![]() PD 98,059 |
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GK2140-1MG | Glentham Life Sciences | 1 mg | EUR 91 |
![]() PD 98,059 |
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GK2140-50MG | Glentham Life Sciences | 50 mg | EUR 378 |
![]() PD 98,059 |
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GK2140-5MG | Glentham Life Sciences | 5 mg | EUR 137 |
![]() PD 150,606 |
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GL2543-25MG | Glentham Life Sciences | 25 mg | EUR 413 |
![]() PD 150,606 |
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GL2543-5MG | Glentham Life Sciences | 5 mg | EUR 154 |
![]() PD-ECGF |
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GT15181 | Neuromics | 100 ug | EUR 526 |
![]() PD 407824 |
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HY-18961 | MedChemExpress | 100mg | EUR 1542 |
![]() PD 151746 |
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HY-19749 | MedChemExpress | 50mg | EUR 491 |
![]() PD 169316 |
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HY-10578 | MedChemExpress | 10mM/1mL | EUR 255 |
![]() PD 90780 |
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HY-110166 | MedChemExpress | 5mg | EUR 326 |
![]() PD 117519 |
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HY-100032 | MedChemExpress | 5mg | EUR 119 |
![]() PD-166866 |
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HY-101296 | MedChemExpress | 10mM/1mL | EUR 138 |
![]() PD-159020 |
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HY-101598 | MedChemExpress | 1mg | EUR 1125 |
![]() PD 123319 |
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HY-10259 | MedChemExpress | 5mg | EUR 182 |
![]() PD 0332991 |
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E1KS1116 | EnoGene | 5mg | EUR 677 |
![]() PD 150606 |
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A4413-25 | ApexBio | 25 mg | EUR 428 |
Description: PD 150606 is a specific inhibitor of calpain with Ki value of 0.21 ?M and 0.37 ?M for mu- and m- calpains, respectively [1]. |
![]() PD 150606 |
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A4413-5 | ApexBio | 5 mg | EUR 144 |
Description: PD 150606 is a specific inhibitor of calpain with Ki value of 0.21 ?M and 0.37 ?M for mu- and m- calpains, respectively [1]. |
![]() PD 166793 |
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A4438-10 | ApexBio | 10 mg | EUR 242 |
Description: Broad spectrum MMP inhibitor. Displays high affinity for MMP-2, -3 and -13 (IC50 values are 4, 7 and 8 nM respectively) and exhibits > 750-fold selectivity over MMP-1, -7 and -9. Attenuates left ventricular remodelling and dysfunction in rat model of heart failure. |
![]() PD 166793 |
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A4438-25 | ApexBio | 25 mg | EUR 498 |
Description: Broad spectrum MMP inhibitor. Displays high affinity for MMP-2, -3 and -13 (IC50 values are 4, 7 and 8 nM respectively) and exhibits > 750-fold selectivity over MMP-1, -7 and -9. Attenuates left ventricular remodelling and dysfunction in rat model of heart failure. |
![]() PD 166793 |
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A4438-5 | ApexBio | 5 mg | EUR 187 |
Description: Broad spectrum MMP inhibitor. Displays high affinity for MMP-2, -3 and -13 (IC50 values are 4, 7 and 8 nM respectively) and exhibits > 750-fold selectivity over MMP-1, -7 and -9. Attenuates left ventricular remodelling and dysfunction in rat model of heart failure. |
![]() PD 173074 |
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A8253-10 | ApexBio | 10 mg | EUR 108 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
![]() PD 173074 |
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A8253-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 119 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
![]() PD 173074 |
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A8253-50 | ApexBio | 50 mg | EUR 212 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
![]() PD 173074 |
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A8253-S | ApexBio | Evaluation Sample | EUR 81 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
![]() PD 180970 |
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A8606-10 | ApexBio | 10 mg | EUR 431 |
Description: ATP-competitive inhibitor of p210bcr/abl tyrosine kinase; selectively induces apoptosis in chronic myeloid leukemia (CML) K562 cells. Inhibits in vivo tyrosine phosphorylation of Gab2, CrkL and p210bcr/abl (IC50 values are 80, 80 and 170 nM respectively). |
![]() PD 145305 |
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C5830-10 | ApexBio | 10 mg | EUR 428 |
Description: PD 145305 is an inactive analog of PD 150606, a potent and selective calpains inhibitor [1]. Calpain is a class of cytosolic cysteine protease that is activated by elevated intracellular calcium. |
![]() PD 145305 |
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C5830-5 | ApexBio | 5 mg | EUR 263 |
Description: PD 145305 is an inactive analog of PD 150606, a potent and selective calpains inhibitor [1]. Calpain is a class of cytosolic cysteine protease that is activated by elevated intracellular calcium. |
![]() PD 169316 |
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A8689-10 | ApexBio | 10 mg | EUR 163 |
Description: IC50: A potent, selective and cell-permeable suppressor of p38 MAP kinase, with the IC50 value of 89 nM.PD169316, a specific p38 MAPK inhibitor, blocks signal transduction mediated by both TGF-? and Activin A, but not bone morphogenetic protein (BMP) 4. |