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2D Structure
Also known as: 1255909-03-5, Hemay005, 4qx9bk9e7p, Hemay-005, Refchem:159992, Mufemilast [inn]
Molecular Formula
C20H22N2O7S2
Molecular Weight
466.5  g/mol
InChI Key
PRSNGWLHNWGOKD-CQSZACIVSA-N
FDA UNII
4QX9BK9E7P

a PDE4 inhibitor for the treatment of psoriasis
1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
N-[5-[(1S)-1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4,6-dioxothieno[3,4-c]pyrrol-3-yl]acetamide
2.1.2 InChI
InChI=1S/C20H22N2O7S2/c1-5-29-16-8-12(6-7-15(16)28-3)14(10-31(4,26)27)22-19(24)13-9-30-18(21-11(2)23)17(13)20(22)25/h6-9,14H,5,10H2,1-4H3,(H,21,23)/t14-/m1/s1
2.1.3 InChI Key
PRSNGWLHNWGOKD-CQSZACIVSA-N
2.2 Other Identifiers
2.2.1 UNII
4QX9BK9E7P
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Hemay005

2.3.2 Depositor-Supplied Synonyms

1. 1255909-03-5

2. Hemay005

3. 4qx9bk9e7p

4. Hemay-005

5. Refchem:159992

6. Mufemilast [inn]

7. Unii-4qx9bk9e7p

8. Acetamide, N-(5-((1s)-1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl)-5,6-dihydro-4,6-dioxo-4h-thieno(3,4-c)pyrrol-1-yl)-

9. Mufemilast [who-dd]

10. Orb1687054

11. Chembl5095240

12. Schembl20580068

13. Glxc-26950

14. Da-55763

15. Hy-145583

16. Cs-0376450

17. N-[5-[(1s)-1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4,6-dioxothieno[3,4-c]pyrrol-3-yl]acetamide

2.4 Create Date
2019-03-16
3 Chemical and Physical Properties
Molecular Weight 466.5 g/mol
Molecular Formula C20H22N2O7S2
XLogP31.9
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count8
Rotatable Bond Count8
Exact Mass Da
Monoisotopic Mass Da
Topological Polar Surface Area156
Heavy Atom Count31
Formal Charge0
Complexity813
Isotope Atom Count0
Defined Atom Stereocenter Count1
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

Dermatologic Agents

Drugs used to treat or prevent skin disorders or for the routine care of skin.


Phosphodiesterase 4 Inhibitors

Compounds that specifically inhibit PHOSPHODIESTERASE 4.