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About This Item

Empirical Formula (Hill Notation):
C15H8Br2INO2
CAS Number:
Molecular Weight:
520.94
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.28
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Quality Level

Assay

≥97% (HPLC)

form

solid

potency

9 nM IC50

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
protect from light

color

dark orange

solubility

DMSO: 200 mg/mL

shipped in

ambient

storage temp.

−20°C

SMILES string

Ic1cc2c(cc1)NC(=O)\C\2=C/c3cc(c(c(c3)Br)O)Br

InChI

1S/C15H8Br2INO2/c16-11-4-7(5-12(17)14(11)20)3-10-9-6-8(18)1-2-13(9)19-15(10)21/h1-6,20H,(H,19,21)/b10-3-

InChI key

LMXYVLFTZRPNRV-KMKOMSMNSA-N

General description

A potent, cell-permeable, reversible, and ATP-competitive cRAF1 kinase inhibitor (IC50 = 9 nM). Shows ≥100-fold selectivity for Raf kinase versus Cdk1, Cdk2, c-Src, ERK2, MEK, p38, Tie2, VEGFR2, and c-Fms. Predicted broad spectrum antitumor agents. A 10 mM (500 µg/96 µl) solution of Raf1 Inhibitor I (Cat. No. 553003) in DMSO is also available.

Biochem/physiol Actions

Cell permeable: yes
Primary Target
CRAFI kinase
Product competes with ATP.
Reversible: yes

Packaging

Packaged under inert gas

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.







From Catalog:

Desc. Field- added "Predicted broad spectrum antitumor agents."

Other Notes

Lackey, K., et al. 2000. Bioorg. Med. Chem. Lett.10, 223.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)

Storage Class Code

11 - Combustible Solids

WGK

WGK 3


Certificates of Analysis (COA)

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