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Fasudil

Chemical Structure : Fasudil

CAS No.: 103745-39-7

Fasudil (AT-877;HA-1077;AT877;HA1077;AT 877;HA 1077)

Catalog No.: PC-42541Not For Human Use, Lab Use Only.

A potent and selective inhibitor of Rho kinase, displays less potent inhibiton over PKA, PKG, PKC and MLCK with Ki of 1.6, 1.6, 3.3, and 36 μM in cell-free assays, respectively.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

A potent and selective inhibitor of Rho kinase, displays less potent inhibiton over PKA, PKG, PKC and MLCK with Ki of 1.6, 1.6, 3.3, and 36 μM in cell-free assays, respectively; exhibits vasodilator actions by inhibition of 5-hydroxytryptamine, noradrenaline, histamine, angiotensin, and dopamine induced spiral strips contraction.

Physicochemical Properties

M.Wt 291.3687
Formula C14H17N3O2S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Isoquinoline, 5-[(hexahydro-1H-1,4-diazepin-1-yl)sulfonyl]-

References

1. Ono-Saito N, et al.1999 May-Jun;82(2-3):123-31.

2. Asano T, et al. J Pharmacol Exp Ther. 1987 Jun;241(3):1033-40.

3. Asano T, et al. Br J Pharmacol. 1989 Dec;98(4):1091-100.

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