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Ruboxistaurin hydrochloride

Chemical Structure : Ruboxistaurin hydrochloride

CAS No.: 169939-93-9

Ruboxistaurin hydrochloride (LY333531 hydrochloride, LY-333531 hydrochloride)

Catalog No.: PC-42441Not For Human Use, Lab Use Only.

Ruboxistaurin hydrochloride (LY333531) is a potent, selective, ATP-competitive, orally available PKC beta (PKCβ) inhibitor with IC50 of 4.7 and 5.9 nM for PKCβ I and PKCβ II, respectively.

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

Biological Activity

Ruboxistaurin hydrochloride (LY333531) is a potent, selective, ATP-competitive, orally available PKC beta (PKCβ) inhibitor with IC50 of 4.7 and 5.9 nM for PKCβ I and PKCβ II, respectively.
Ruboxistaurin hydrochloride (LY333531) displays >60-fold selectivity over PKCα, and other ATP dependent kinases (PKA, Calcium calmodulin, Caesin kinase and Src).
Ruboxistaurin hydrochloride (LY333531) ameliorates the glomerular filtration rate, albumin excretion rate, and retinal circulation in diabetic rats.

Physicochemical Properties

M.Wt 505.0079
Formula C28H29ClN4O3
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

DMSO: 6.8 mg/mL (Need ultrasonic and warming)

Chemical Name/SMILES

9H,18H-5,21:12,17-Dimethenodibenzo[e,k]pyrrolo[3,4-h][1,4,13]oxadiazacyclohexadecine-18,20(19H)-dione, 9-[(dimethylamino)methyl]-6,7,10,11-tetrahydro-, monohydrochloride, (9S)- (9CI)

References

1. Jirousek MR, et al. J Med Chem. 1996 Jul 5;39(14):2664-71.

2. Ishii H, et al. Science. 1996 May 3;272(5262):728-31.

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