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3CAI is an inhibitor of Akt1 and Akt2 with anticancer activity. It inhibits Akt1 and Akt2 in a kinase assay in a concentration-dependent manner, but has no effect on MEK1, JNK1, ERK1, or PDZ binding kinase (PBK) when used at a concentration of 1 µM. 3CAI (4 µM) increases apoptosis in HCT116 and HT-29 colon cancer cells and inhibits the growth of HCT116 cells in vitro in a concentration-dependent manner. Oral administration of 3CAI (30 mg/kg) reduces tumor growth in an HCT116 mouse xenograft model. It also decreases status epilepticus-induced vasogenic edema to 0.46-fold of vehicle control levels and reduces increases in endothelial nitric oxide synthase (eNOS) levels in the piriform cortex in rats when administered at a dose of 25 µM.Formal Name: 2-chloro-1-(1H-indol-3-yl)-ethanone. CAS Number: 28755-03-5. Synonyms: 3-chloroacetyl Indole. Molecular Formula: C10H8ClNO. Formula Weight: 193.6. Purity: >95%. Formulation: (Request formulation change), A crystalline solid. Solubility: DMF: 50 mg/ml, DMF:PBS (pH 7.2), (1:7): 0.125 mg/ml, DMSO: 33 mg/ml, Ethanol: 17 mg/ml. lambdamax: 244, 304 nm. SMILES: O=C(CCl)C1=CNC2=CC=CC=C21. InChi Code: InChI=1S/C10H8ClNO/c11-5-10(13)8-6-12-9-4-2-1-3-7(8)9/h1-4,6,12H,5H2. InChi Key: LLZQFAXTCYDVTR-UHFFFAOYSA-N.
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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