| Identification | Back Directory | [Name]
S-Etodolac | [CAS]
87249-11-4 | [Synonyms]
RAK 592
S-Etodolac
(+)-(S)-Etodolac
(S)-(+)-Etodolac
(S)-(+)-Etodolic acid
Etodolac Impurity 15 ((S)-(+)-Etodolac)
(1S)-1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid
Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-, (S)-
Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-, (1S)-
(S)-EtodolacQ: What is
(S)-Etodolac Q: What is the CAS Number of
(S)-Etodolac Q: What is the storage condition of
(S)-Etodolac Q: What are the applications of
(S)-Etodolac
(S)-Etodolac D4Q: What is
(S)-Etodolac D4 Q: What is the CAS Number of
(S)-Etodolac D4 Q: What is the storage condition of
(S)-Etodolac D4 Q: What are the applications of
(S)-Etodolac D4 | [Molecular Formula]
C17H21NO3 | [MDL Number]
MFCD00870723 | [MOL File]
87249-11-4.mol | [Molecular Weight]
287.35 |
| Chemical Properties | Back Directory | [Melting point ]
>133°C (dec.) | [storage temp. ]
-20°C Freezer | [solubility ]
Chloroform (Sparingly), DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [color ]
White to Off-White |
| Hazard Information | Back Directory | [Uses]
The S-enantiomer of Etodolac (E933090). Anti-inflammatory; analgesic. | [Definition]
ChEBI: (S)-etodolac is the S-enantiomer of etodolac. It is a preferential inhibitor of cyclo-oxygenase 2 and a non-steroidal anti-inflammatory, whereas the enantiomer, (R)-etodolac, is inactive. The racemate is commonly used for the treatment of rheumatoid arthritis and osteoarthritis, and for the alleviation of postoperative pain. It has a role as a cyclooxygenase 2 inhibitor and a non-narcotic analgesic. It is an enantiomer of a (R)-etodolac. |
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Ralington Pharma
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BOC Sciences
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guoyungurui
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