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Chemistry

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Also known as: Flector, Diclofenac hydroxyethylpyrrolidine, Diep, Dhep, Diclofenac epolaminum, Diclofenac-epolamine
Molecular Formula
C20H24Cl2N2O3
Molecular Weight
411.3  g/mol
InChI Key
DCERVXIINVUMKU-UHFFFAOYSA-N
FDA UNII
X5F8EKL9ZG

Diclofenac Epolamine
1 2D Structure

Diclofenac Epolamine

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
2-[2-(2,6-dichloroanilino)phenyl]acetic acid;2-pyrrolidin-1-ylethanol
2.1.2 InChI
InChI=1S/C14H11Cl2NO2.C6H13NO/c15-10-5-3-6-11(16)14(10)17-12-7-2-1-4-9(12)8-13(18)19;8-6-5-7-3-1-2-4-7/h1-7,17H,8H2,(H,18,19);8H,1-6H2
2.1.3 InChI Key
DCERVXIINVUMKU-UHFFFAOYSA-N
2.1.4 Canonical SMILES
C1CCN(C1)CCO.C1=CC=C(C(=C1)CC(=O)O)NC2=C(C=CC=C2Cl)Cl
2.2 Other Identifiers
2.2.1 UNII
X5F8EKL9ZG
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Dhep

2. Diclofenac 1-(2-hydroxyethyl)pyrrolidinium Salt

3. Diclofenac Hydroxyethylpyrrolidine

4. Diclofenac-epolamine

5. Diclofenac-n-(2-hydroxyethyl) Pyrrolidine

6. Diep

7. Flector

8. N-(2-hydroxyethyl)pyrrolidinium (2-((2,6-dichlorophenyl)amino)phenyl)acetate

2.3.2 Depositor-Supplied Synonyms

1. Flector

2. Diclofenac Hydroxyethylpyrrolidine

3. Diep

4. Dhep

5. Diclofenac Epolaminum

6. Diclofenac-epolamine

7. X5f8ekl9zg

8. 2-[2-(2,6-dichloroanilino)phenyl]acetic Acid;2-pyrrolidin-1-ylethanol

9. N-(2-hydroxyethyl)pyrrolidinium (2-((2,6-dichlorophenyl)amino)phenyl)acetate

10. 2-((2,6-dichlorophenyl)amino)benzeneacetic Acid, Compd. With 1-pyrrolidineethanol (1:1)

11. Diclofenac 1-(2-hydroxyethyl)pyrrolidinium Salt

12. Dhep Plaster

13. Benzeneacetic Acid, 2-((2,6-dichlorophenyl)amino)-, Compd. With 1-pyrrolidineethanol (1:1)

14. Chebi:48296

15. Unii-x5f8ekl9zg

16. Flector (tn)

17. Licart

18. Diclofenac-n-(2-hydroxyethyl) Pyrrolidine

19. Schembl1006944

20. Chembl1201180

21. Dtxsid80152531

22. Diclofenac Epolamine [vandf]

23. Diclofenac Epolamine [mart.]

24. S5737

25. Diclofenac Epolamine [who-dd]

26. Diclofenac Hydroxyethylpirrolidine

27. Diclofenac Epolamine [orange Book]

28. D07818

29. 528d502

30. Diclofenac Acid N-(2-hydroxyetheyl) Pyrrolidine Salt

31. Q27121125

2.4 Create Date
2005-08-08
3 Chemical and Physical Properties
Molecular Weight 411.3 g/mol
Molecular Formula C20H24Cl2N2O3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count6
Exact Mass410.1163980 g/mol
Monoisotopic Mass410.1163980 g/mol
Topological Polar Surface Area72.8 Ų
Heavy Atom Count27
Formal Charge0
Complexity363
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Drug and Medication Information
4.1 Drug Information
1 of 2  
Drug NameFlector
PubMed HealthDiclofenac
Drug ClassesAnalgesic, Anti-Inflammatory, Antimigraine, Antirheumatic, Central Nervous System Agent, Musculoskeletal Agent, Ophthalmologic Agent
Drug LabelFlector Patch (10 cm x 14 cm) is comprised of an adhesive material containing 1.3% diclofenac epolamine which is applied to a non-woven polyester felt backing and coveredwith a polypropylene film release liner. The release liner is emoved prior to...
Active IngredientDiclofenac epolamine
Dosage FormPatch
RouteTopical
Strength1.3%
Market StatusPrescription
CompanyInst Biochem

2 of 2  
Drug NameFlector
PubMed HealthDiclofenac
Drug ClassesAnalgesic, Anti-Inflammatory, Antimigraine, Antirheumatic, Central Nervous System Agent, Musculoskeletal Agent, Ophthalmologic Agent
Drug LabelFlector Patch (10 cm x 14 cm) is comprised of an adhesive material containing 1.3% diclofenac epolamine which is applied to a non-woven polyester felt backing and coveredwith a polypropylene film release liner. The release liner is emoved prior to...
Active IngredientDiclofenac epolamine
Dosage FormPatch
RouteTopical
Strength1.3%
Market StatusPrescription
CompanyInst Biochem

5 Pharmacology and Biochemistry
5.1 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.)


5.2 FDA Pharmacological Classification
5.2.1 Pharmacological Classes
Cyclooxygenase Inhibitors [MoA]; Decreased Prostaglandin Production [PE]; Nonsteroidal Anti-inflammatory Drug [EPC]; Anti-Inflammatory Agents, Non-Steroidal [CS]

API Reference Price

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06-Feb-2024
27-Aug-2024
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