Y-27632 dihydrochloride
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![]() Y-27632 dihydrochloride |
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A3008-10 | ApexBio | 10 mg | EUR 142 |
Description: Y-27632 dihydrochloride is a small-molecule inhibitor of Rho-associated protein kinase p160ROCK with the IC50 of 140 nM. Y-27632 suppresses the kinase activity of both ROCK-1 and ROCK-2 in vitro, and this compound inhibits the kinases by binding to the catalytic site of ROCK-1 and ROCK-2. |
![]() Y-27632 dihydrochloride |
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A3008-200 | ApexBio | 200 mg | EUR 1070 |
Description: Y-27632 dihydrochloride is a small-molecule inhibitor of Rho-associated protein kinase p160ROCK with the IC50 of 140 nM. Y-27632 suppresses the kinase activity of both ROCK-1 and ROCK-2 in vitro, and this compound inhibits the kinases by binding to the catalytic site of ROCK-1 and ROCK-2. |
![]() Y-27632 dihydrochloride |
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A3008-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 148 |
Description: Y-27632 dihydrochloride is a small-molecule inhibitor of Rho-associated protein kinase p160ROCK with the IC50 of 140 nM. Y-27632 suppresses the kinase activity of both ROCK-1 and ROCK-2 in vitro, and this compound inhibits the kinases by binding to the catalytic site of ROCK-1 and ROCK-2. |
![]() Y-27632 dihydrochloride |
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A3008-50 | ApexBio | 50 mg | EUR 421 |
Description: Y-27632 dihydrochloride is a small-molecule inhibitor of Rho-associated protein kinase p160ROCK with the IC50 of 140 nM. Y-27632 suppresses the kinase activity of both ROCK-1 and ROCK-2 in vitro, and this compound inhibits the kinases by binding to the catalytic site of ROCK-1 and ROCK-2. |
![]() Y-27632, dihydrochloride |
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1596-1 | Biovision | EUR 175 |
![]() Y-27632, dihydrochloride |
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1596-5 | Biovision | EUR 463 |
![]() Y-27632, dihydrochloride |
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1596-50 | Biovision | EUR 2469 |
![]() Y-27632 |
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B1293-10 | ApexBio | 10 mg | EUR 142 |
Description: Y-27632 is a specific inhibitor of Rho-associated kinases(ROCK) family with Ki values of 0.22?M and 0.30?M for ROCK1 and ROCK2, respectively.Y-27632 has shown selectivity of inhibition by comparing their Ki values for other Rho effector kinases, citron kinase and PKN, as well as PKC?. |
![]() Y-27632 |
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B1293-200 | ApexBio | 200 mg | EUR 1070 |
Description: Y-27632 is a specific inhibitor of Rho-associated kinases(ROCK) family with Ki values of 0.22?M and 0.30?M for ROCK1 and ROCK2, respectively.Y-27632 has shown selectivity of inhibition by comparing their Ki values for other Rho effector kinases, citron kinase and PKN, as well as PKC?. |
![]() Y-27632 |
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B1293-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 108 |
Description: Y-27632 is a specific inhibitor of Rho-associated kinases(ROCK) family with Ki values of 0.22?M and 0.30?M for ROCK1 and ROCK2, respectively.Y-27632 has shown selectivity of inhibition by comparing their Ki values for other Rho effector kinases, citron kinase and PKN, as well as PKC?. |
![]() Y-27632 |
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B1293-50 | ApexBio | 50 mg | EUR 421 |
Description: Y-27632 is a specific inhibitor of Rho-associated kinases(ROCK) family with Ki values of 0.22?M and 0.30?M for ROCK1 and ROCK2, respectively.Y-27632 has shown selectivity of inhibition by comparing their Ki values for other Rho effector kinases, citron kinase and PKN, as well as PKC?. |
![]() Y-27632 |
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E1KS1049 | EnoGene | 2 mg | EUR 325 |
![]() Y-27632 |
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HY-10071 | MedChemExpress | 100mg | EUR 1234 |
![]() Y 27632 |
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20-abx076548 | Abbexa |
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![]() EZSolution? Y-27632 |
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1784-5 | Biovision | EUR 446 |
![]() EZSolution? Y-27632, Sterile-Filtered |
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1994-1 | Biovision | EUR 359 |
![]() Y 27632 (ROCK kinase inhibitor) |
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SIH-486-1MG | Stressmarq | 1 mg | EUR 149 |
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Description: The substance Y 27632 is a rock kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to pale yellow powder which is soluble in DMSO (25 mg/ml), methanol (25 mg/ml), acetonitrile (<1 mg/ml), dioxan (<1 mg/ml), water (very soluble. |
![]() Y 27632 (ROCK kinase inhibitor) |
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SIH-486-5MG | Stressmarq | 5 mg | EUR 328 |
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Description: The substance Y 27632 is a rock kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to pale yellow powder which is soluble in DMSO (25 mg/ml), methanol (25 mg/ml), acetonitrile (<1 mg/ml), dioxan (<1 mg/ml), water (very soluble. |
![]() Y-39983 dihydrochloride |
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B1176-10 | ApexBio | 10 mg | EUR 412 |
Description: Y-39983 dihydrochloride is a novel and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK [1]. |
![]() Y-39983 dihydrochloride |
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B1176-100 | ApexBio | 100 mg | EUR 2401 |
Description: Y-39983 dihydrochloride is a novel and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK [1]. |
![]() Y-39983 dihydrochloride |
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B1176-5 | ApexBio | 5 mg | EUR 267 |
Description: Y-39983 dihydrochloride is a novel and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK [1]. |
![]() Y-39983 dihydrochloride |
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B1176-50 | ApexBio | 50 mg | EUR 1497 |
Description: Y-39983 dihydrochloride is a novel and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK [1]. |
![]() Y-33075 (dihydrochloride) |
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HY-10069 | MedChemExpress | 5mg | EUR 215 |
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27632-100ul | SAB | 100ul | EUR 252 |
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B3248-10 | ApexBio | 10 mg | EUR 118 |
Description: Vanoxerine is an antagonist of dopamine transporter (DAT1) with Ki value of 16.9nM [1].As an antagonist of DAT, vanoxerine is developed for treatment of Parkinson's disease and depression but has no effect on these diseases. |
![]() Vanoxerine dihydrochloride |
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B3248-25 | ApexBio | 25 mg | EUR 210 |
Description: Vanoxerine is an antagonist of dopamine transporter (DAT1) with Ki value of 16.9nM [1].As an antagonist of DAT, vanoxerine is developed for treatment of Parkinson's disease and depression but has no effect on these diseases. |
![]() Vanoxerine dihydrochloride |
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B3248-50 | ApexBio | 50 mg | EUR 332 |
Description: Vanoxerine is an antagonist of dopamine transporter (DAT1) with Ki value of 16.9nM [1].As an antagonist of DAT, vanoxerine is developed for treatment of Parkinson's disease and depression but has no effect on these diseases. |
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B3342-1000 | ApexBio | 1 g | EUR 150 |
Description: Spectinomycin Dihydrochloride is a new parenteral antibiotic prepared from Streptomyces spectabilis. |
![]() Spectinomycin dihydrochloride |
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B3342-5.1 | ApexBio | 10 mM (in 1mL H2O) | EUR 168 |
Description: Spectinomycin Dihydrochloride is a new parenteral antibiotic prepared from Streptomyces spectabilis. |
![]() Spectinomycin dihydrochloride |
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B3342-5000 | ApexBio | 5 g | EUR 283 |
Description: Spectinomycin Dihydrochloride is a new parenteral antibiotic prepared from Streptomyces spectabilis. |
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B3416-50 | ApexBio | 50 mg | EUR 128 |
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B5650-10 | ApexBio | 10 mg | EUR 321 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
![]() IT1t dihydrochloride |
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B5650-100 | ApexBio | 100 mg | EUR 1750 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
![]() IT1t dihydrochloride |
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B5650-25 | ApexBio | 25 mg | EUR 592 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
![]() IT1t dihydrochloride |
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B5650-5 | ApexBio | 5 mg | EUR 203 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
![]() IT1t dihydrochloride |
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B5650-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 218 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
![]() IT1t dihydrochloride |
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B5650-50 | ApexBio | 50 mg | EUR 1027 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
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B5785-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 108 |
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B5785-50 | ApexBio | 50 mg | EUR 112 |
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B6132-100 | ApexBio | 100 mg | EUR 150 |
Description: EC50: 1.24 ?MFluphenazine is a dopamine D1 and D2 receptor inhibitor.Dopamine D1 and D2 receptor immunohistochemistry has been used to study the structure of the adult rat arcuate-median eminence complex, particularly in relation to the tubero-infundibular dopamine neurons. |
![]() Fluphenazine dihydrochloride |
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B6132-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 168 |
Description: EC50: 1.24 ?MFluphenazine is a dopamine D1 and D2 receptor inhibitor.Dopamine D1 and D2 receptor immunohistochemistry has been used to study the structure of the adult rat arcuate-median eminence complex, particularly in relation to the tubero-infundibular dopamine neurons. |
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B6366-10 | ApexBio | 10 mg | EUR 221 |
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B6557-10 | ApexBio | 10 mg | EUR 139 |
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B6557-100 | ApexBio | 100 mg | EUR 215 |
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B6557-200 | ApexBio | 200 mg | EUR 337 |
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B6557-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 150 |
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B6557-50 | ApexBio | 50 mg | EUR 186 |
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B6582-100 | ApexBio | 100 mg | EUR 134 |
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B6582-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 150 |
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B6669-50 | ApexBio | 50 mg | EUR 1455 |
![]() 1400W dihydrochloride |
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B6730-10 | ApexBio | 10 mg | EUR 142 |
Description: 1400W dihydrochloride is a potent and selective inhibitor of inducible nitric oxide synthase with Kd value of 7 nM [1]. Inducible nitric oxide synthase (iNOS) is an enzyme catalyzing the production of nitric oxide (NO) and is involved in immune response. |
![]() 1400W dihydrochloride |
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B6730-100 | ApexBio | 100 mg | EUR 728 |
Description: 1400W dihydrochloride is a potent and selective inhibitor of inducible nitric oxide synthase with Kd value of 7 nM [1]. Inducible nitric oxide synthase (iNOS) is an enzyme catalyzing the production of nitric oxide (NO) and is involved in immune response. |
![]() 1400W dihydrochloride |
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B6730-50 | ApexBio | 50 mg | EUR 438 |
Description: 1400W dihydrochloride is a potent and selective inhibitor of inducible nitric oxide synthase with Kd value of 7 nM [1]. Inducible nitric oxide synthase (iNOS) is an enzyme catalyzing the production of nitric oxide (NO) and is involved in immune response. |
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B1116-100 | ApexBio | 100 mg | EUR 238 |
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B1116-200 | ApexBio | 200 mg | EUR 390 |
Description: Mizolastine dihydrochloride is a histamine H1-receptor antagonist with IC50 of 47 nM used in the treatment of hay fever (seasonal allergic rhinitis), hives and other allergic reactions. |
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B1116-500 | ApexBio | 500 mg | EUR 653 |
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B7587-5.1 | ApexBio | 10 mM (in 1mL H2O) | EUR 119 |
Description: Puromycin dihydrochloride [1] is an analog of aminoacyl-tRNA. |
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![]() Latrepirdine (dihydrochloride) |
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HY-14537 | MedChemExpress | 10mM/1mL | EUR 113 |
![]() Inolitazone (dihydrochloride) |
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HY-14792B | MedChemExpress | 5mg | EUR 544 |
![]() Bavisant (dihydrochloride) |
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HY-14880A | MedChemExpress | 5mg | EUR 326 |
![]() Mirodenafil (dihydrochloride) |
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HY-14930A | MedChemExpress | 50mg | EUR 2116 |
![]() SCH79797 (dihydrochloride) |
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HY-14994 | MedChemExpress | 10mg | EUR 1175 |
![]() Ipatasertib dihydrochloride |
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HY-15186A | MedChemExpress | 50mg | EUR 383 |
![]() GW791343 (dihydrochloride) |
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HY-15469 | MedChemExpress | 5mg | EUR 147 |
![]() Merestinib dihydrochloride |
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HY-15514A | MedChemExpress | 10mg | EUR 354 |
![]() Mibefradil (dihydrochloride) |
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HY-15553A | MedChemExpress | 10mg | EUR 259 |
![]() Ceritinib dihydrochloride |
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HY-15656A | MedChemExpress | 5mg | EUR 108 |
![]() CRT0066101 dihydrochloride |
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HY-15698A | MedChemExpress | 25mg | EUR 463 |
![]() Pyridoxamine dihydrochloride |
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GP8560-1G | Glentham Life Sciences | 1 g | EUR 58 |
![]() Putrescine dihydrochloride |
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GP9873-100G | Glentham Life Sciences | 100 g | EUR 94 |
![]() Putrescine dihydrochloride |
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GP9873-10G | Glentham Life Sciences | 10 g | EUR 52 |
![]() Putrescine dihydrochloride |
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GP9873-1G | Glentham Life Sciences | 1 g | EUR 44 |
![]() Putrescine dihydrochloride |
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GP9873-25G | Glentham Life Sciences | 25 g | EUR 61 |
![]() Ethylenediamine dihydrochloride |
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GK6724-100G | Glentham Life Sciences | 100 g | EUR 54 |
![]() Ethylenediamine dihydrochloride |
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GK6724-250G | Glentham Life Sciences | 250 g | EUR 86 |
![]() Ethylenediamine dihydrochloride |
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GK6724-500G | Glentham Life Sciences | 500 g | EUR 118 |
![]() 1400W dihydrochloride |
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GK6799-100MG | Glentham Life Sciences | 100 mg | EUR 551 |
![]() 1400W dihydrochloride |
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GK6799-25MG | Glentham Life Sciences | 25 mg | EUR 229 |
![]() 1400W dihydrochloride |
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GK6799-5MG | Glentham Life Sciences | 5 mg | EUR 114 |
![]() Hydroxyzine dihydrochloride |
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GK7844-10G | Glentham Life Sciences | 10 g | EUR 126 |
![]() Cystamine dihydrochloride |
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GK9885-100G | Glentham Life Sciences | 100 g | EUR 82 |
![]() Cystamine dihydrochloride |
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GK9885-250G | Glentham Life Sciences | 250 g | EUR 142 |
![]() Cystamine dihydrochloride |
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GK9885-25G | Glentham Life Sciences | 25 g | EUR 50 |
![]() SAG dihydrochloride |
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GL1175-1MG | Glentham Life Sciences | 1 mg | EUR 195 |
![]() SAG dihydrochloride |
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GL1175-5MG | Glentham Life Sciences | 5 mg | EUR 574 |
![]() Opipramol dihydrochloride |
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GL4485-100MG | Glentham Life Sciences | 100 mg | EUR 174 |
![]() Opipramol dihydrochloride |
|||
GL4485-1G | Glentham Life Sciences | 1 g | EUR 628 |
![]() Trifluoperazine dihydrochloride |
|||
GL5164-10G | Glentham Life Sciences | 10 g | EUR 110 |
![]() Trifluoperazine dihydrochloride |
|||
GL5164-25G | Glentham Life Sciences | 25 g | EUR 186 |
![]() Trifluoperazine dihydrochloride |
|||
GL5164-5G | Glentham Life Sciences | 5 g | EUR 78 |
![]() Antipain dihydrochloride |
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GL6582-25MG | Glentham Life Sciences | 25 mg | EUR 235 |
![]() Antipain dihydrochloride |
|||
GL6582-5MG | Glentham Life Sciences | 5 mg | EUR 114 |
![]() Retigabine dihydrochloride |
|||
GP0386-100MG | Glentham Life Sciences | 100 mg | EUR 95 |
![]() Retigabine dihydrochloride |
|||
GP0386-250MG | Glentham Life Sciences | 250 mg | EUR 139 |
![]() Pirenzepine dihydrochloride |
|||
GP0823-1G | Glentham Life Sciences | 1 g | EUR 174 |
![]() Pirenzepine dihydrochloride |
|||
GP0823-250MG | Glentham Life Sciences | 250 mg | EUR 78 |