Y-27632 dihydrochloride

Y-27632 dihydrochloride

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Y-27632 dihydrochloride
A3008-200 200 mg
EUR 1284
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
A3008-5.1 10 mM (in 1mL DMSO)
EUR 177.6
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
A3008-50 50 mg
EUR 505.2
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
GK8578-1MG 1 mg
EUR 170.4

Y-27632 dihydrochloride
GK8578-25MG 25 mg
EUR 945.6

Y-27632 dihydrochloride
GK8578-5MG 5 mg
EUR 399.6

Y-27632 (dihydrochloride)
HY-10583 50mg
EUR 349.2

Y-27632 dihydrochloride
GK8578-1 1
EUR 98.4

Y-27632 dihydrochloride
GK8578-10 10
EUR 234

Y-27632 dihydrochloride
GK8578-25 25
EUR 428.6

Y-27632 dihydrochloride
GK8578-5 5
EUR 145.5

Y-39983 dihydrochloride
B1176-10 10 mg
EUR 494.4
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
B1176-100 100 mg
EUR 2881.2
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
B1176-5 5 mg
EUR 320.4
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
B1176-50 50 mg
EUR 1796.4
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)
HY-10069 5mg
EUR 258

H89 Dihydrochloride
20-abx076747
  • EUR 811.20
  • EUR 360.00
  • 25 mg
  • 5 mg

MPP dihydrochloride
B6910-10 10 mg
EUR 381.6

MPP dihydrochloride
B6910-50 50 mg
EUR 1413.6

SAG dihydrochloride
GL1175-1MG 1 mg
EUR 234

SAG dihydrochloride
GL1175-5MG 5 mg
EUR 688.8

TMB (dihydrochloride)
HY-15930A 10mM/1mL
EUR 135.6

SAG dihydrochloride
GL1175-1 1
EUR 98.4

SAG dihydrochloride
GL1175-25 25
EUR 334.3

SAG dihydrochloride
GL1175-5 5
EUR 169

TMB dihydrochloride
TB0514 1g
EUR 85.06

GBR 12935 dihydrochloride
B4661-10 10 mg
EUR 129.6

GBR 12935 dihydrochloride
B4661-100 100 mg
EUR 296.4

GBR 12935 dihydrochloride
B4661-50 50 mg
EUR 192

ETP 45835 dihydrochloride
B4938-10 10 mg
EUR 428.4

ETP 45835 dihydrochloride
B4938-50 50 mg
EUR 1608

AZ 10606120 dihydrochloride
B5410-10 10 mg
EUR 408
Description: KD: 1.4 nM and 1.9 nM for human and rat P2X7 receptors, respectivleyThe P2X7 receptor has intriguing biophysical properties, activates a diverse range of cellular events and mediates a wide range of functional effects.

AZ 10606120 dihydrochloride
B5410-50 50 mg
EUR 1531.2
Description: KD: 1.4 nM and 1.9 nM for human and rat P2X7 receptors, respectivleyThe P2X7 receptor has intriguing biophysical properties, activates a diverse range of cellular events and mediates a wide range of functional effects.

CP 99994 dihydrochloride
B5422-10 10 mg
EUR 478.8

CP 99994 dihydrochloride
B5422-50 50 mg
EUR 1824

SB 243213 dihydrochloride
B5444-10 10 mg
EUR 486

SB 243213 dihydrochloride
B5444-50 50 mg
EUR 1802.4

JNJ 5207852 dihydrochloride
B5513-10 10 mg
EUR 289.2

JNJ 5207852 dihydrochloride
B5513-5 5 mg
EUR 180

JNJ 5207852 dihydrochloride
B5513-50 50 mg
EUR 1021.2

A 412997 dihydrochloride
B5639-25 25 mg
EUR 642
Description: A 412997 dihydrochloride is a selective agonist of dopamine D4 receptor with Ki values of 7.9 and 12.1 nM for human and rat D4 receptors, respectively [1]. Dopamine D4 receptor is a G protein-coupled receptor and is activated by dopamine.

Y-27632 dihydrochloride