Basic information Safety Supplier Related

HYDROXYFASUDIL MONOHYDROCHLORIDE

Basic information Safety Supplier Related

HYDROXYFASUDIL MONOHYDROCHLORIDE Basic information

Product Name:
HYDROXYFASUDIL MONOHYDROCHLORIDE
Synonyms:
  • HA-1100 HYDROCHLORIDE;HA 1100 HYDROCHLORIDE;HA1100 HYDROCHLORIDE
  • 5-(1,4-diazepan-1-ylsulfonyl)-2h-isoquinolin-1-one
  • Hydroxyfasudil hydrochloride (HA-1100 hydrochloride)
  • Hydroxyfasudil - CAS 155558-32-0 - Calbiochem
  • Hydroxyfasudil HCl
  • 5-[(Hexahydro-1H-1,4-diazepin-1-yl)sulfonyl]-1(2H)-isoquinolinone
  • Hydroxyfasudil Hydrochloride
  • 1-(1-hydroxy-5-isoquinolinesulfonyl)homopiperazine monohydrochloride
CAS:
155558-32-0
MF:
C14H18ClN3O3S
MW:
343.82902
Product Categories:
  • Various Metabolites and Impurities
  • Intermediates & Fine Chemicals
  • Metabolites & Impurities
  • Pharmaceuticals
Mol File:
155558-32-0.mol
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HYDROXYFASUDIL MONOHYDROCHLORIDE Chemical Properties

Melting point:
>250 (dec.)
storage temp. 
Inert atmosphere,2-8°C
solubility 
H2O: >5mg/mL
form 
solid
color 
white
Water Solubility 
Soluble in water (20mM)
InChIKey
XWWFOUVDVJGNNG-UHFFFAOYSA-N
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
WGK Germany 
3
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HYDROXYFASUDIL MONOHYDROCHLORIDE Usage And Synthesis

Chemical Properties

Off-White Solid

Uses

A metabolite of Fasudil. A cell-permeable, hydroxylated metabolite of HA 1077 that displays anti-anginal properties. Reported to inhibit the Rho kinase-mediated (ROCK) contraction both in vitro and in vivo.

Uses

A metabolite of Fasudil. A cell-permeable, hydroxylated metabolite of HA 1077 that displays anti-anginal properties. Reported to inhibit the Rho kinase-mediated ( ROCK) contraction both in vitro and in vivo. A

General Description

A cell-permeable, hydroxylated metabolite of HA 1077 (Fasudil; Cat. No. 371970) that displays anti-anginal properties. Acts as an ATP-competitive and a reversible inhibitor of Rho-kinase (IC50 = 0.9 and 1.8 μM using a peptide and MLC as substrate, respectively) with ~100-fold greater selectivity over MLCK, MRCKβ, and PKC. Reported to inhibit the Rho kinase-mediated contraction both in vitro and in vivo.

Biochem/physiol Actions

Cell permeable: yes

storage

-20°C

HYDROXYFASUDIL MONOHYDROCHLORIDESupplier

Suzhou Ran enzyme Biotechnology Co., Ltd. Gold
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