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-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

TMB dihydrochloride
TB0514 1g
EUR 85.06

1400W dihydrochloride
2055-25 each
EUR 405.6

1400W dihydrochloride
2055-5 each
EUR 151.2

DMPQ Dihydrochloride
20-abx076714
  • EUR 693.60
  • EUR 326.40
  • 25 mg
  • 5 mg

IT1t dihydrochloride
B5650-10 10 mg
EUR 385.2
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
B5650-100 100 mg
EUR 2100
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
B5650-25 25 mg
EUR 710.4
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
B5650-5 5 mg
EUR 243.6
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
B5650-5.1 10 mM (in 1mL DMSO)
EUR 261.6
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
B5650-50 50 mg
EUR 1232.4
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.

DMPQ dihydrochloride
B6642-10 10 mg
EUR 223.2

DMPQ dihydrochloride
B6642-5 5 mg
EUR 184.8

GNTI dihydrochloride
B6669-10 10 mg
EUR 459.6

GNTI dihydrochloride
B6669-50 50 mg
EUR 1746

1400W dihydrochloride
B6730-10 10 mg
EUR 170.4
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
B6730-100 100 mg
EUR 873.6
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
B6730-50 50 mg
EUR 525.6
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
GK6799-100MG 100 mg
EUR 661.2

1400W dihydrochloride
GK6799-25MG 25 mg
EUR 274.8

1400W dihydrochloride
GK6799-5MG 5 mg
EUR 136.8

PAβN (dihydrochloride)
HY-101444A 10mM/1mL
EUR 154.8

IT1t (dihydrochloride)
HY-101458A 10mg
EUR 308.4

1400W (Dihydrochloride)
HY-18731 10mM/1mL
EUR 151.2

DAPI (dihydrochloride)
HY-D0814 50mg
EUR 439.2

CP 31398 dihydrochloride
A4476-10 10 mg
EUR 381.6
Description: CP 31398 dihydrochloride is a potent activator of p53 with maximum tolerated dose of 400 ppm [2].Tumor protein p53 (p53) is a crucial protein in multicellular organisms and plays an important role in preventing cancer formation.

CP 31398 dihydrochloride
A4476-50 50 mg
EUR 1413.6
Description: CP 31398 dihydrochloride is a potent activator of p53 with maximum tolerated dose of 400 ppm [2].Tumor protein p53 (p53) is a crucial protein in multicellular organisms and plays an important role in preventing cancer formation.

AZ 12080282 dihydrochloride
A8657-10 10 mg
EUR 498
Description: AZ 12080282 dihydrochloride is a selective inhibitor of Hh with IC50 value <0.012 ?M [1]. It is also reported that AZ 12080282 also has a selective inhibition to p38? with low nanomolar potency [1].

AZ 12080282 dihydrochloride
A8657-50 50 mg
EUR 1900.8
Description: AZ 12080282 dihydrochloride is a selective inhibitor of Hh with IC50 value <0.012 ?M [1]. It is also reported that AZ 12080282 also has a selective inhibition to p38? with low nanomolar potency [1].

AY 9944 dihydrochloride
A8658-10 10 mg
EUR 289.2
Description: AY 9944 dihydrochloride is a selective inhibitor of ?7-sterol reductase with IC50 value of 13 nM [1].?7-sterol reductase (Dhcr7) is an enzyme and plays an important role in catalyzing the production of cholesterol from 7-Dehydrocholesterol through using NADPH [2, 3].

AY 9944 dihydrochloride
A8658-25 25 mg
EUR 582
Description: AY 9944 dihydrochloride is a selective inhibitor of ?7-sterol reductase with IC50 value of 13 nM [1].?7-sterol reductase (Dhcr7) is an enzyme and plays an important role in catalyzing the production of cholesterol from 7-Dehydrocholesterol through using NADPH [2, 3].

AY 9944 dihydrochloride
A8658-5 5 mg
EUR 184.8
Description: AY 9944 dihydrochloride is a selective inhibitor of ?7-sterol reductase with IC50 value of 13 nM [1].?7-sterol reductase (Dhcr7) is an enzyme and plays an important role in catalyzing the production of cholesterol from 7-Dehydrocholesterol through using NADPH [2, 3].

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.

A 412997 dihydrochloride
B5639-5 5 mg
EUR 212.4
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