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BAY-549

BAY-549 (Azaindole 1), a chemical probe, is an orally active and ATP-competitive ROCK inhibitor with IC50s of 0.6 and 1.1 nM for human ROCK-1 and ROCK-2, respectively[1].

Product Specifications

CAS Number

867017-68-3

Product Name Alternative

ROCK-IN-2; Azaindole 1; TC-S 7001

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

ROCK

Type

Reference compound

Related Pathways

Cell Cycle/DNA Damage; Cytoskeleton; Stem Cell/Wnt; TGF-beta/Smad

Applications

COVID-19-anti-virus

Field of Research

Cardiovascular Disease

Assay Protocol

https://www.medchemexpress.com/bay-549.html

Purity

99.46

Solubility

DMSO : 33.33 mg/mL (ultrasonic)

Smiles

NC1=NC(Cl)=CC(NC2=CC(F)=C(OC3=C4C(NC=C4C)=NC=C3)C(F)=C2)=N1

Molecular Formula

C18H13ClF2N6O

Molecular Weight

402.79

Precautions

H302, H315, H319, H335

References & Citations

[1]Kast R, et al. Cardiovascular effects of a novel potent and highly selective azaindole-based inhibitor of Rho-kinase. Br J Pharmacol. 2007 Dec;152 (7) :1070-80. Epub 2007 Oct 15.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

ROCK1; ROCK2

Available Sizes

Frequently Asked Questions

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