S-Diclofenac

HCID 11948307

Grundinformationen

CAS
912758-00-0
Standard-SMILES
O=C(Cc1ccccc1Nc1c(Cl)cccc1Cl)Oc1ccc(-c2cc(=S)ss2)cc1
InChIKey
BRDUXOHVEZVAHI-UHFFFAOYSA-N
Summenformel
C23H15Cl2NO2S3
Durchschnittliche Molmasse
504,5 g/mol
Monoisotopische Masse
502,96419708

Überblick

an NSAID; structure in first source

Namen und Bezeichner

Bevorzugter Name
S-Diclofenac
IUPAC
[4-(5-sulfanylidenedithiol-3-yl)phenyl] 2-[2-(2,6-dichloroanilino)phenyl]acetate
Englischer Name
ATB-337
Summenformel
C23H15Cl2NO2S3
Molmasse
504.47

Namen und Synonyme

S-diclofenac912758-00-0DTXSID7013180052-((2,6-dichlorophenyl)amino)benzeneacetic acid 4-(3H-1,2-dithiol-3-thione-5-yl)phenyl esterRefChem:180656DTXCID301747797ATB-337ACS 15Benzeneacetic acid, 2-((2,6-dichlorophenyl)amino)-, 4-(3H-1,2-dithiol-3-thione-5-yl)phenyl esterC23H15Cl2NO2S3ACS 15,S-Diclofenacorb1704919
Weitere Namen anzeigen
Benzeneacetic acid, 2-[(2,6-dichlorophenyl)amino]-, 4-(3-thioxo-3H-1,2-dithiol-5-yl)phenyl ester
SCHEMBL2880811BRDUXOHVEZVAHI-UHFFFAOYSA-NHMS3648K05MFCD11976903[4-(5-sulfanylidenedithiol-3-yl)phenyl] 2-[2-(2,6-dichloroanilino)phenyl]acetateHY-15035CS-0003711T21939

Datenbank-Bezeichner

CAS
912758-00-0
PubChem CID
11948307
DTXSID
DTXSID701318005

Eigenschaften

Berechnete Struktureigenschaften

XLogP
6,9
Polarare Oberfläche (TPSA)
121 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
6
Frei drehbare Bindungen
7
Schwere Atome
31

Physikochemische Eigenschaften

storage temp.
-20 °C · Store at -20°C
Löslichkeit
10 mg/ml · ≤10mg/ml in DMSO;10mg/ml in dimethyl formamide
Aggregatzustand
crystalline solid
Farbe
Reddish brown to red

Chemie und Industrie

Anwendungen · 1 Eintrag

VerwendenHydrogen sulfide (H2S) is a naturally occurring gasotransmitter with vasodilator and inflammatory modulating activity. Non-steroidal anti-inflammatory drugs (NSAIDs), such as indomethacin, diclofenac, and ibuprofen, are some of the most commonly used anti-inflammatory drugs available but exhibit significant side effects, particularly gastric damage, when used chronically. ATB-337 is a hybrid molecule of an H2S donor and the NSAID diclofenac. In rats, diclofenac at 10-50 μmol/kg caused significant gastrointestinal damage, whereas no damage was observed with ATB-337 treatment at the same dose. ATB-337 at 50 μmol/kg does not promote leukocyte adherence to vascular endothelium, an effect observed with diclofenac treatment alone. COX-1 and COX-2 were inhibited with similar efficacy by diclofenac and ABT-337. An increase in expression of the pro-inflammatory mediator TNF-α, as well as, the adhesion molecules ICAM-1 and LFA-1 were not observed in rats treated with 50 μmol/kg ABT-337, effects seen with equimolar doses of diclofenac. These results indicate that H2S-releasing derivatives of NSAIDs may prove to be more effective anti-inflammatory agents than traditional NSAIDs alone.[Cayman Chemical]

Anbieter8 Anbieter

杭州摩库生物医药科技有限公司+86-057181025280; +8617767106207 · [email protected]
InvivoChem中国13549236410 · [email protected]
MedBio脉铂医药021-69568360 18916172912 · [email protected]
AdooQ BioScience, LLC+1 (866) 930-6790 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]

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