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Grundinformationen
- Standard-SMILES
CC(C(=O)O)c1ccc(C(=O)c2cccs2)cc1- InChIKey
MDKGKXOCJGEUJW-UHFFFAOYSA-N- Summenformel
- C14H12O3S
- Durchschnittliche Molmasse
- 260,314 g/mol
- Monoisotopische Masse
- 260,05071524
Namen und Bezeichner
- Bevorzugter Name
- Suprofen
- IUPAC
- 2-[4-(Thiophene-2-carbonyl)phenyl]propanoic acid
- Lokaler Name
- Suprofen
- Englischer Name
- Suprofen
- Summenformel
- C14H12O3S
- Molmasse
- 260.31
Namen und Synonyme
ProfenolSuprolTN 762r25061AnemetSrendamSuprocilTopalgicProfenalmaldocil
Datenbank-Bezeichner
- CAS
40828-46-4- PubChem CID
- 5359
- DTXSID
DTXSID5045469- ChEMBL
CHEMBL956- ChEBI
CHEBI:9362- UNII
- 988GU2F9PE
- EC Number
- 255-096-9
- Nikkaji
- J16.410K
Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 278 °C · 278°C
- Siedepunkt
- 373.57 °C · 373.57°C (rough estimate)
- Dichte
- 1.2959 · 1.2959 (rough estimate)
- Brechungsindex
- 1.505 · 1.5050 (estimate)
- storage temp.
- -20 °C · Keep in dark place,Sealed in dry,Store in freezer, under -20°C
- Löslichkeit
- 30 mg/ml; · DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 20 mg/ml; PBS (pH 7.2): 0.5 mg/ml
- pka
- 3.91 · 3.91(at 25℃)
- Aggregatzustand
- Powder
- Farbe
- White to off-white
- Wasserlöslichkeit
- soluble
- InChI
- InChI=1S/C14H12O3S/c1-9(14(16)17)10-4-6-11(7-5-10)13(15)12-3-2-8-18-12/h2-9H,1H3,(H,16,17)
- InChIKey
- MDKGKXOCJGEUJW-UHFFFAOYSA-N
- SMILES
- C1(=CC=C(C(C)C(=O)O)C=C1)C(=O)C1SC=CC=1
- CAS Datenbank
- 40828 · 40828-46-4(CAS DataBase Reference)
Sicherheit und Regulatorisches
Sicherheitsdaten
- wgk
- WGK 3
- ridadr
- 3249
- hs_code
- 2934990002
- Toxizität
- LD50 (7 days post-drug) in mice, rats, guinea pigs, dogs (mg/kg): 590, 353, 280, 160 orally (Niemegeers)
- hazard_class
- 6.1(b)
- packing_group
- III
- Speicherklasse
- 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
- Hazard Classifications
- Acute Tox. 3 Oral
Chemie und Industrie
Anwendungen
BeschreibungSuprofen is an arylpropionic acid analgesic/antiinflammatory agent with close structural resemblance to ketoprofen. It is more potent in many assays than indomethacin and ketoprofen and appears better tolerated.
VerwendenBridged pseudopelletierine derivative; specific serotonin (5HT3) receptor antagonist. Antiemetic.
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Ergänzende Hinweise
DefinitionChEBI: An aromatic ketone that is thiophene substituted at C-2 by a 4-(1-carboxyethyl)benzoyl group.
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