Ethanone, 2-chloro-1-(3-indolyl)-

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CAS:28755-03-5
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Products Intro: Product Name:2-chloro-1-(1H-indol-3-yl)ethanone
CAS:28755-03-5
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Products Intro: Product Name:3-(Chloroacetyl)-1H-Indole
CAS:28755-03-5
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Ethanone, 2-chloro-1-(3-indolyl)- Basic information
Product Name:Ethanone, 2-chloro-1-(3-indolyl)-
Synonyms:Ethanone, 2-chloro-1-(3-indolyl)-;3-chloroacetylindole;2-chloro-1-(1H-indol-3-yl)ethanone(SALTDATA: FREE);2-Chloro-1-(1H-indol-3-yl)ethan-1-one, 3-(2-Chloroethanoyl)-1H-indole;3CAI;Chloromethyl indol-3-yl ketone;Ethanone, 2-chloro-1-(1H-indol-3-yl)-;Ethanone, 2-chloro-1H-indol-1-yl-
CAS:28755-03-5
MF:C10H8ClNO
MW:193.63
EINECS:
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Mol File:28755-03-5.mol
Ethanone, 2-chloro-1-(3-indolyl)- Structure
Ethanone, 2-chloro-1-(3-indolyl)- Chemical Properties
Melting point 212-214 °C(Solv: ethyl ether (60-29-7))
Boiling point 379.1±17.0 °C(Predicted)
density 1.337±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility DMSO: soluble5mg/mL, clear
form powder
pka15.08±0.30(Predicted)
color yellow to brown
Safety Information
Hazard Codes Xn
Risk Statements 22-36
Safety Statements 26
WGK Germany 3
HS Code 2933998090
MSDS Information
Ethanone, 2-chloro-1-(3-indolyl)- Usage And Synthesis
Uses3-(Chloroacetyl)indole is a reagent used in organic synthesis. Used in the preparation of 1,?2-?dihydroazepino[4,?5-?b]?indoles.
Biological Activity3cai is a potent allosteric and specific inhibitor of akt, which directly binds with akt1 or akt2 in an atp noncompetitive manner and shows 60% inhibition of akt1 kinase activity at 1 μm [1]. the serine/threonine kinase akt includes three members, akt1, akt2, and akt3. akt plays a critical role in promoting transformation and chemoresistance through inducing proliferation and inhibiting apoptosis. therefore, akt is regarded as a potential target for cancer therapy.
in vitro3cai (1 and 4 μm) significantly inhibited akt1 kinase activity and decreased expression of akt direct downstream targets including mtor and gsk3β, respectively. 3cai (4 μm) efficiently induced growth inhibition and apoptosis in hct116 or hct29 colon cancer cells [1].
in vivo3cai (30 mg/kg, oral administration) significantly suppressed colon cancer growth in an in vivo xenograft mouse model and inhibited the expression of akt-target protein such as mtor and gsk3βin hct116 colon tumor tissues [1].
targetakt
IC 501 μm
references1. kim dj, reddy k, kim mo, li y, nadas j, cho yy, et al. (3-chloroacetyl)-indole, a novel allosteric akt inhibitor, suppresses colon cancer growth in vitro and in vivo. cancer prev res (phila). 2011;4(11):1842-51.
Ethanone, 2-chloro-1-(3-indolyl)- Preparation Products And Raw materials
Preparation Products2-HYDROXY-1-(1H-INDOL-3-YL)ETHANONE
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