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SAR407899

Catalog No. T7391   CAS 923359-38-0

SAR407899 is Rho kinase inhibitor potently inhibits endothelin-1-induced constriction of renal resistance arteries.

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SAR407899 Chemical Structure
SAR407899, CAS 923359-38-0
Pack Size Availability Price/USD Quantity
2 mg In stock $ 33.00
5 mg In stock $ 52.00
10 mg In stock $ 85.00
25 mg In stock $ 153.00
50 mg In stock $ 247.00
100 mg In stock $ 393.00
1 mL * 10 mM (in DMSO) In stock $ 57.00
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Purity: 99.91%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description SAR407899 is Rho kinase inhibitor potently inhibits endothelin-1-induced constriction of renal resistance arteries.
Targets&IC50 ROCK2:102 nM (IC50), ROCK1:276 nM (IC50)
In vivo In vivo, SAR407899 dose-dependently induced rabbit penile erection, with greater potency and longer duration of action than sildenafil[1].
Animal Research Compared the effects of SAR407899, the Rho-kinase inhibitor Y-27632 and the PDE5 inhibitor sildenafil for their ability to relax corpus cavernosum strips contracted with phenylephrine in healthy and diabetic animals. Strips were obtained from WKY, spontaneous hypertensive (SHR), control CD, and diabetic CD rats, humans, control and diabetic rabbits. Diabetes was induced by streptozotocin or alloxan injection. In vivo penile erection (length) induced by drugs was measured in conscious rabbits[1].
Molecular Weight 244.29
Formula C14H16N2O2
CAS No. 923359-38-0

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 6 mg/mL (24.56 mM)

TargetMolReferences and Literature

1. Guagnini F , Ferazzini M , Grasso M , et al. Erectile properties of the Rho-kinase inhibitor SAR407899 in diabetic animals and human isolated corpora cavernosa[J]. Journal of Translational Medicine, 2012, 10(1):59-0. 2. Grisk O, Schlüter T, Reimer N, et al.The Rho kinase inhibitor SAR407899 potently inhibits endothelin-1-induced constriction of renal resistance arteries[J].J Hypertens. 2012 May;30(5):980-9.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Drug Repurposing Compound Library TGF-beta/Smad Compound Library Anti-Cancer Drug Library Anti-Cancer Clinical Compound Library Clinical Compound Library Anti-Diabetic Compound Library Cell Cycle Compound Library Kinase Inhibitor Library Cytoskeletal Signaling Pathway Compound Library

Related Products

Related compounds with same targets
ROCK-IN-2 Y-27632 CID-5056270 CKI-7 ZINC00881524 CCG-232964 Neoprzewaquinone A URMC-099

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Keywords

SAR407899 923359-38-0 Cell Cycle/Checkpoint Cytoskeletal Signaling Stem Cells ROCK Rho Rho-associated kinase ROK SAR-407899 Rho-kinase Rho-associated protein kinase SAR 407899 inhibit Inhibitor inhibitor

 

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