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Indomethacin heptyl ester_Molecular_structure_CAS_)
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Indomethacin heptyl ester

Catalog No. I7904 Name Sigma Aldrich
CAS Number Website http://www.sigmaaldrich.com
M. F. C26H30ClNO4 Telephone 1-800-521-8956
M. W. 455.9737 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 155591

SYNONYMS

IUPAC name
heptyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetate
IUPAC Traditional name
heptyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetate

DATABASE IDS

MDL Number MFCD03412025

PROPERTIES

Empirical Formula (Hill Notation) C26H30ClNO4
Potency 0.04 μM IC50 (for human recombinat COX-2)
Purity ≥98% (HPLC)
Shipped in wet ice
Apperance methyl acetate solution
Flash Point -16 °C
Flash Point 3 °F
European Hazard Symbols Flammable Flammable (F)
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
RID/ADR UN 1231 3/PG 2
Risk Statements 11-36-66-67
RTECS AI9100000
Safety Statements 16-26-29-33-36
Storage Temperature -20°C
Hazard Class 3
UN Number 1231
Packing Group 2
German water hazard class 1

DETAILS

Description (English)
Application
Used to inhibit COX-1 and COX-2. To achieve 50% inhibition of human recombinant COX-2 use I7904 at 0.04 uM/mL .
Biochem/physiol Actions
Potent cyclooxygenase-2 inhibitor. 1700 times greater activity against COX-2 than COX-1.
Other Notes
Derivatized indomethacin.
Description (简体中文)
Application
Used to inhibit COX-1 and COX-2. To achieve 50% inhibition of human recombinant COX-2 use I7904 at 0.04 uM/mL .
Biochem/physiol Actions
Potent cyclooxygenase-2 inhibitor. 1700 times greater activity against COX-2 than COX-1.
Other Notes
Derivatized indomethacin.

REFERENCES