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Imidazolo-oxindole PKR inhibitor C16_Molecular_structure_CAS_608512-97-6)
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Imidazolo-oxindole PKR inhibitor C16

Catalog No. I9785 Name Sigma Aldrich
CAS Number 608512-97-6 Website http://www.sigmaaldrich.com
M. F. C13H8N4OS Telephone 1-800-521-8956
M. W. 268.29382 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 126303

SYNONYMS

IUPAC name
8-(1H-imidazol-4-ylmethylidene)-6H,7H,8H-[1,3]thiazolo[5,4-e]indol-7-one
IUPAC Traditional name
8-(1H-imidazol-4-ylmethylidene)-6H-[1,3]thiazolo[5,4-e]indol-7-one
Synonyms
6,8-Dihydro-8-(1H-imidazol-5-ylmethylene)-7H-pyrrolo[2,3-g]benzothiazol-7-one

DATABASE IDS

MDL Number MFCD06735404
CAS Number 608512-97-6

PROPERTIES

Empirical Formula (Hill Notation) C13H8N4OS
Purity ≥98% (HPLC)
Shipped in wet ice
Solubility DMSO: soluble12 mg/mL
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Other Notes
Protect from light and air.
Biochem/physiol Actions
Imidazolo-oxindole PKR inhibitor C16 is a selective inhibitor of RNA-dependent protein kinases (PKR, Eif2ak2). C16 is a first reported, potent and selective PKR inhibitor. Its inhibition effect on PKR is ATP-binding site directed. C16 specifically inhibits the apoptotic PKR/eIF2a signaling pathway without stimulating the proliferative mTOR/p70S6K signaling mechanism.
Description (简体中文)
Other Notes
Protect from light and air.
Biochem/physiol Actions
Imidazolo-oxindole PKR inhibitor C16 is a selective inhibitor of RNA-dependent protein kinases (PKR, Eif2ak2). C16 is a first reported, potent and selective PKR inhibitor. Its inhibition effect on PKR is ATP-binding site directed. C16 specifically inhibits the apoptotic PKR/eIF2a signaling pathway without stimulating the proliferative mTOR/p70S6K signaling mechanism.

REFERENCES