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Fasudil (Hydrochloride)

Fasudil (HA-1077; AT877) Hydrochloride is a nonspecific RhoA/ROCK inhibitor and also has inhibitory effect on protein kinases, with an Ki of 0.33 μM for ROCK1, IC50s of 0.158 μM and 4.58 μM, 12.30 μM, 1.650 μM for ROCK2 and PKA, PKC, PKG, respectively. Fasudil Hydrochloride is also a potent Ca2+ channel antagonist and vasodilator[1][2][3].

Product Specifications

CAS Number

[105628-07-7]

Product Name Alternative

HA-1077 (Hydrochloride) ; AT-877 (Hydrochloride)

UNSPSC

12352005

Hazard Statement

H302

Target

Autophagy; Calcium Channel; HIV; PKA; PKC; ROCK

Type

Reference compound

Related Pathways

Anti-infection; Autophagy; Cell Cycle/DNA Damage; Cytoskeleton; Epigenetics; Membrane Transporter/Ion Channel; Neuronal Signaling; Stem Cell/Wnt; TGF-beta/Smad

Applications

Cancer-Kinase/protease

Field of Research

Cancer

Assay Protocol

https://www.medchemexpress.com/Fasudil-Hydrochloride.html

Concentration

10mM

Purity

99.97

Solubility

DMSO : ≥ 31 mg/mL|H2O : 55 mg/mL (ultrasonic)

Smiles

O=S(C1=CC=CC2=C1C=CN=C2)(N3CCNCCC3)=O.Cl[H]

Molecular Formula

C14H18ClN3O2S

Molecular Weight

327.83

Precautions

H302

References & Citations

[1]Chen M, et al. Fasudil and its analogs: a new powerful weapon in the long war against central nervous system disorders? Expert Opin Investig Drugs. 2013 Apr;22 (4) :537-50.|[2]Huang XN, et al. The effects of fasudil on the permeability of the rat blood-brain barrier and blood-spinal cordbarrier following experimental autoimmune encephalomyelitis. J Neuroimmunol. 2011 Oct 28;239 (1-2) :61-7.|[3]Uehata M, et al. Calcium sensitization of smooth muscle mediated by a Rho-associated protein kinase in hypertension. Nature. 1997 Oct 30;389 (6654) :990-4.|[4]Fukushima M, et al. Fasudil hydrochloride hydrate, a Rho-kinase (ROCK) inhibitor, suppresses collagen production and enhances collagenase activity in hepatic stellate cells. Liver Int. 2005 Aug;25 (4) :829-38.|[5]Corbin KD, et al. Choline metabolism provides novel insights into nonalcoholic fatty liver disease and its progression. Curr Opin Gastroenterol. 2012 Mar;28 (2) :159-65.|[6]Zhang J, et al. Inhibition of the activity of Rho-kinase reduces cardiomyocyte apoptosis in heart ischemia/reperfusion via suppressing JNK-mediated AIF translocation. Clin Chim Acta. 2009 Mar;401 (1-2) :76-80.|[7]Sun X, et al. The selective Rho-kinase inhibitor Fasudil is protective and therapeutic in experimental autoimmune encephalomyelitis. J Neuroimmunol. 2006 Nov;180 (1-2) :126-34. Epub 2006 Sep 22.

Shipping Conditions

Room Temperature

Storage Conditions

4°C (Powder, sealed storage, away from moisture)

Scientific Category

Reference compound1

Clinical Information

Launched

Isoform

PKA; PKC; ROCK1; ROCK2

Citation 01

Aging Cell. 2024 Jun 2:e14209.|Aging Cell. 2025 Jan;24 (1) :e14366.|Biochem Pharmacol. 2025 Apr 8:116933.|Biomed Rep. 2015 May;3 (3) :361-364. |Cell Mol Immunol. 2023 Apr;20 (4) :351-364.|Cell Stem Cell. 2025 Apr 3;32 (4) :581-597.e11.|Diabetol Metab Syndr. 2025 Oct 3;17 (1) :374.|Eur J Pharmacol. 2024 May 13:975:176640.|J Cereb Blood Flow Metab. 2025 Jun;45 (6) :1191-1202.|Metab Brain Dis. 2025 Jan 7;40 (1) :91.|NPJ Precis Oncol. 2025 Nov 26;9 (1) :391.|Sci Rep. 2018 Feb 6;8 (1) :2477. |Transl Neurosci. 2020 Apr 20;11 (1) :75-86.|Adipocyte. 2019 Dec;8 (1) :114-124. |Br J Cancer. 2023 May;128 (10) :1941-1954.|Cell Signal. 2026 Feb:138:112275.|Clin Transl Med. 2022 Jul;12 (7) :e961.|Clin Transl Med. 2022 Oct;12 (10) :e1036.|Inflammopharmacology. 2023 Aug;31 (4) :2037-2047.|Int J Biol Sci. 2024 Jan 12;20 (3) :897-915.|J Exp Clin Cancer Res. 2020 Jun 16;39 (1) :113.|J Pharm Pharmacol. 2021 Jul 7;73 (8) :1118-1127.|Neural Regen Res. 2021 Dec;16 (12) :2512-2520.|Sci Transl Med. 2018 Jul 18;10 (450) :eaaq1093.|SSRN. 2023 Feb 24.

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