Y-27632 dihydrochloride 

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Y-27632, dihydrochloride
1596-50
EUR 2469

Y-27632 dihydrochloride
A3008-10 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
A3008-200 200 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
A3008-5.1 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
A3008-50 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)
HY-10583 50mg
EUR 291

Y-27632 dihydrochloride
GK8578-1MG 1 mg
EUR 142

Y-27632 dihydrochloride
GK8578-25MG 25 mg
EUR 788

Y-27632 dihydrochloride
GK8578-5MG 5 mg
EUR 333

Y-27632
B1293-10 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
B1293-200 200 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
B1293-5.1 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
B1293-50 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
20-abx076548
  • EUR 272.00
  • EUR 523.00
  • 1 mg
  • 5 mg
  • Shipped within 5-12 working days.

Y-27632
E1KS1049 2 mg
EUR 325

Y-27632
HY-10071 100mg
EUR 1234

EZSolution? Y-27632
1784-5
EUR 446

EZSolution? Y-27632, Sterile-Filtered
1994-1
EUR 359

Y 27632 (ROCK kinase inhibitor)
SIH-486-1MG 1 mg
EUR 149
  • Y 27632 is a very potent and selective ROCK1 and ROCK2 inhibitor. Y 27632 is cell permeable and is an ATP competitive inhibitor.
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)
SIH-486-5MG 5 mg
EUR 328
  • Y 27632 is a very potent and selective ROCK1 and ROCK2 inhibitor. Y 27632 is cell permeable and is an ATP competitive inhibitor.
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
B1176-10 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
B1176-100 100 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
B1176-5 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
B1176-50 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)
HY-10069 5mg
EUR 215

SNRPF Polyclonal Antibody
27632-100ul 100ul
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SNRPF Polyclonal Antibody
27632-50ul 50ul
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Vatalanib Dihydrochloride
2025-25
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Vatalanib Dihydrochloride
2025-5
EUR 126

1400W dihydrochloride
2055-25
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1400W dihydrochloride
2055-5
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Norquetiapine dihydrochloride
2362-250
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Berbamine dihydrochloride
2520-100
EUR 131

Berbamine dihydrochloride
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Antipain dihydrochloride
2834-25
EUR 327

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2834-5
EUR 120

Dorsmorphin dihydrochloride
2835-25
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Dorsmorphin dihydrochloride
2835-5
EUR 185

GGACK Dihydrochloride
1847-5 5 mg
EUR 319
  • Frequently asked questions for this product: Is the GGACK Dihydrochloride cell-permeable? - No
  • Is this item a salt form of GGACK Dihydrochloride? - Yes
  • Does this product have/require an MSDS? - Yes
  • What is the biological function of this molecul
  • Show more
Description: A potent and irreversible inhibitor of Urokinase (uPA (IC??<1 µM), Factor VIIa, Factor IXa, Factor Xa, and trypsin.

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Vanoxerine dihydrochloride
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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
B3248-25 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
B3248-50 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.

Spectinomycin dihydrochloride
B3342-1000 1 g
EUR 150
Description: Spectinomycin Dihydrochloride is a new parenteral antibiotic prepared from Streptomyces spectabilis.

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B3342-5.1 10 mM (in 1mL H2O)
EUR 168
Description: Spectinomycin Dihydrochloride is a new parenteral antibiotic prepared from Streptomyces spectabilis.

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B3342-5000 5 g
EUR 283
Description: Spectinomycin Dihydrochloride is a new parenteral antibiotic prepared from Streptomyces spectabilis.

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EUR 128
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B1116-100 100 mg
EUR 238
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.

Mizolastine dihydrochloride
B1116-200 200 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.

Y-27632 dihydrochloride