GSK269962 Hydrochloride
- Product Name
- GSK269962 Hydrochloride
- CAS No.
- 2095432-71-4
- Chemical Name
- GSK269962 Hydrochloride
- Synonyms
- GSK269962 HCl;GSK269962A HCl ,S7687;GSK269962 Hydrochloride;GSK269962A hydrochloride;N-(3-((2-(4-Amino-1,2,5-oxadiazol-3-yl)-1-ethyl-1H-imidazo[4,5-c]pyridin-6-yl)oxy)phenyl)-4-(2-morpholinoethoxy)benzamide hydrochloride
- CBNumber
- CB44672087
- Molecular Formula
- C29H31ClN8O5
- Formula Weight
- 607.07
- MOL File
- 2095432-71-4.mol
GSK269962 Hydrochloride Property
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- solubility
- DMSO: 100 mg/mL (164.73 mM);Ethanol: 28 mg/mL (46.12 mM)
- form
- Solid
- color
- Off-white to light yellow
- Water Solubility
- Water: Insoluble
N-Bromosuccinimide Price
- Product number
- 4701DN
- Product name
- GSK269962hydrochloride
- Packaging
- 100mg
- Price
- $598
- Updated
- 2021/12/16
- Product number
- 4701DN
- Product name
- GSK269962hydrochloride
- Packaging
- 1g
- Price
- $2751
- Updated
- 2021/12/16
- Product number
- CSN19208
- Product name
- GSK269962HCl
- Packaging
- 5mg
- Price
- $64
- Updated
- 2021/12/16
- Product number
- A105790
- Product name
- GSK269962hydrochloride
- Purity
- 98+%
- Packaging
- 5mg
- Price
- $194
- Updated
- 2021/12/16
- Product number
- AS428096
- Product name
- GSK269962hydrochloride
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $249
- Updated
- 2021/12/16
GSK269962 Hydrochloride Chemical Properties,Usage,Production
Uses
GSK269962A hydrochloride (GSK 269962 hydrochloride) is a potent ROCK inhibitor with IC50s of 1.6 and 4 nM for recombinant human ROCK1 and ROCK2 respectively. GSK269962A hydrochloride has anti-inflammatory and vasodilatory activities[1].
Biological Activity
GSK269962A HCl is a selective ROCK (Rho-associated protein kinase) inhibitor with IC50 of 1.6 nM and 4 nM for ROCK1 and ROCK2, respectively.
in vivo
GSK269962A is a potent antihypertensive agent. GSK269962A (0.3, 1, and 3 mg/kg; oral gavage) induces a dose-dependent reduction in blood pressure in spontaneously hypertensive rat (SHR). The reduction of blood pressure is acute and substantial[1].
| Animal Model: | Male Sprague-Dawley rats (350-400g)[1] |
| Dosage: | 0.3, 1, and 3 mg/kg |
| Administration: | Oral gavage; 12 hours |
| Result: | Induced a dose-dependent reduction in blood pressure. |
target
| Target | Value |
| ROCK1 (Cell-free assay) | 1.6 nM |
| ROCK2 (Cell-free assay) | 4 nM |
| 49 nM | |
| RSK1 (Cell-free assay) td> | 132 nM |
IC 50
ROCK1: 1.6 nM (IC50); ROCK2: 4 nM (IC50); RSK1: 132 nM (IC50); MSK1: 49 nM (IC50); AKT1: 955 nM (IC50); AKT2: 1350 nM (IC50); AKT3: 1510 nM (IC50); CDK2: 3500 nM (IC50); GSK3α: 1260 nM (IC50)
References
[1] Doe C, et al. Novel Rho kinase inhibitors with anti-inflammatory and vasodilatory activities. J Pharmacol Exp Ther. 2007 Jan;320(1):89-98. DOI:10.1124/jpet.106.110635
GSK269962 Hydrochloride Preparation Products And Raw materials
Raw materials
Preparation Products
GSK269962 Hydrochloride Suppliers
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