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2D Structure
Also known as: 72895-88-6, Telzenac, Eltenac [inn], Eltenac (inn), 2-[4-(2,6-dichloroanilino)thiophen-3-yl]acetic acid, 4-(2,6-dichloroanilino)-3-thiopheneacetic acid
Molecular Formula
C12H9Cl2NO2S
Molecular Weight
302.2  g/mol
InChI Key
AELILMBZWCGOSB-UHFFFAOYSA-N
FDA UNII
A153L3JA99

1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
2-[4-(2,6-dichloroanilino)thiophen-3-yl]acetic acid
2.1.2 InChI
InChI=1S/C12H9Cl2NO2S/c13-8-2-1-3-9(14)12(8)15-10-6-18-5-7(10)4-11(16)17/h1-3,5-6,15H,4H2,(H,16,17)
2.1.3 InChI Key
AELILMBZWCGOSB-UHFFFAOYSA-N
2.1.4 Canonical SMILES
C1=CC(=C(C(=C1)Cl)NC2=CSC=C2CC(=O)O)Cl
2.2 Other Identifiers
2.2.1 UNII
A153L3JA99
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Telzenac

2.3.2 Depositor-Supplied Synonyms

1. 72895-88-6

2. Telzenac

3. Eltenac [inn]

4. Eltenac (inn)

5. 2-[4-(2,6-dichloroanilino)thiophen-3-yl]acetic Acid

6. 4-(2,6-dichloroanilino)-3-thiopheneacetic Acid

7. A153l3ja99

8. Eltenacum [latin]

9. 2-(4-((2,6-dichlorophenyl)amino)thiophen-3-yl)acetic Acid

10. Eltenaco

11. Eltenacum

12. Eltenaco [spanish]

13. Unii-a153l3ja99

14. Telzenac (tn)

15. Eltenac-13c,d3

16. Starbld0009574

17. Eltenac [mart.]

18. Schembl145080

19. 4-[(2,6-dichlorophenyl)amino]-3-thiopheneacetic Acid

20. Zinc1346

21. 3-thiopheneacetic Acid, 4-[(2,6-dichlorophenyl)amino]-

22. Chembl2104561

23. Dtxsid30223184

24. Sb23043

25. Hy-106093

26. Cs-0024841

27. Ft-0667838

28. 4-(2,6-dichloroanilino)-3-thiophenacetic Acid

29. D07888

30. Q27273482

2.4 Create Date
2005-08-08
3 Chemical and Physical Properties
Molecular Weight 302.2 g/mol
Molecular Formula C12H9Cl2NO2S
XLogP33.9
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count4
Exact Mass300.9731051 g/mol
Monoisotopic Mass300.9731051 g/mol
Topological Polar Surface Area77.6 Ų
Heavy Atom Count18
Formal Charge0
Complexity296
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

Anti-Inflammatory Agents, Non-Steroidal

Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)