Y-27632 dihydrochloride
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![]() Y-27632, dihydrochloride |
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1596-50 | Biovision | EUR 2469 |
![]() 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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HY-10583 | MedChemExpress | 50mg | EUR 291 |
![]() Y-27632 dihydrochloride |
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GK8578-1MG | Glentham Life Sciences | 1 mg | EUR 142 |
![]() Y-27632 dihydrochloride |
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GK8578-25MG | Glentham Life Sciences | 25 mg | EUR 788 |
![]() Y-27632 dihydrochloride |
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GK8578-5MG | Glentham Life Sciences | 5 mg | EUR 333 |
![]() 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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20-abx076548 | Abbexa |
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![]() Y-27632 |
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E1KS1049 | EnoGene | 2 mg | EUR 325 |
![]() Y-27632 |
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HY-10071 | MedChemExpress | 100mg | EUR 1234 |
![]() 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]. |
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HY-10069 | MedChemExpress | 5mg | EUR 215 |
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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 |
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B3342-5.1 | ApexBio | 10 mM (in 1mL H2O) | EUR 168 |
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![]() Spectinomycin dihydrochloride |
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![]() Mizolastine dihydrochloride |
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B1116-100 | ApexBio | 100 mg | EUR 238 |
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![]() Mizolastine dihydrochloride |
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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. |