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Alminoprofen

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ACTIVE PHARMA INGREDIENTS

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Alminoprofen

Synopsis

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Chemistry

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Also known as: 39718-89-3, Alminoprofene, Alminoprofeno, Alminoprofenum, Minalfen, Eb-382

Molecular Formula

C₁₃H₁₇NO₂

Molecular Weight

219.28 g/mol

InChI Key

FPHLBGOJWPEVME-UHFFFAOYSA-N

FDA UNII

0255AHR9GJ

structure given in first source; RN given refers to parent cpd without isomeric designation

1 2D Structure

Alminoprofen

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

2-[4-(2-methylprop-2-enylamino)phenyl]propanoic acid

2.1.2 InChI

InChI=1S/C13H17NO2/c1-9(2)8-14-12-6-4-11(5-7-12)10(3)13(15)16/h4-7,10,14H,1,8H2,2-3H3,(H,15,16)

2.1.3 InChI Key

FPHLBGOJWPEVME-UHFFFAOYSA-N

2.2 Other Identifiers

2.2.1 UNII

0255AHR9GJ

2.3 Synonyms

2.3.1 MeSH Synonyms

1. 2-(4-((2-methyl-2-propenyl)amino)phenyl)propionic Acid

2. 2-(4-methylallylaminophenyl)propionic Acid

3. Eb 382

4. Eb-382

2.3.2 Depositor-Supplied Synonyms

1. 39718-89-3

2. Alminoprofene

3. Alminoprofeno

4. Alminoprofenum

5. Minalfen

6. Eb-382

7. P-((2-methylallyl)amino)hydratropic Acid

8. Eb 382

9. Brn 2373633

10. 2-(4-((2-methylallyl)amino)phenyl)propansaeure

11. 0255ahr9gj

12. Chebi:31190

13. Benzeneacetic Acid, Alpha-methyl-4-((2-methyl-2-propenyl)amino)-

14. Acide (methallylamino-4 Phenyl)-2 Propionique

15. 2-{4-[(2-methylprop-2-en-1-yl)amino]phenyl}propanoic Acid

16. Alpha-methyl-4-((2-methyl-2-propenyl)amino)benzeneacetic Acid

17. 2-{4-[(2-methylprop-2-en-1-yl)amino]phenyl}propionic Acid

18. Alpha-methyl-4-[(2-methyl-2-propenyl)amino]benzeneacetic Acid

19. 2-(4-((2-methylprop-2-en-1-yl)amino)phenyl)propanoic Acid

20. 2-(4-((2-methylprop-2-en-1-yl)amino)phenyl)propionic Acid

21. 2-(4-methylallylaminophenyl)propionic Acid

22. Refchem:554938

23. 2-(4-((2-methyl-2-propenyl)amino)phenyl)propionic Acid

24. M01ae16

25. (2rs)-2-((4-(2-methylprop-2-en-1-yl)amino)phenyl)propanoic Acid

26. 254-604-6

27. Minalfene

28. 2-(4-((2-methylallyl)amino)phenyl)propanoic Acid

29. Rac Alminoprofen

30. Racalminoprofen-d3

31. 54362-71-9

32. Alminoprofen, (+)-

33. 2-[4-(2-methylprop-2-enylamino)phenyl]propanoic Acid

34. 2-[4-(2-methylallylamino)phenyl]propanoic Acid

35. Alminoprofeno [spanish]

36. Alminoprofen [inn:jan]

37. Alminoprofene [inn-french]

38. Alminoprofenum [inn-latin]

39. Alminoprofeno [inn-spanish]

40. (+/-)-alminoprofen;eb 382; Minalfene

41. (+/-)-alminoprofen

42. Einecs 254-604-6

43. Unii-0255ahr9gj

44. 4-((2-methylallyl)amino)hydratropasaeure

45. 2-(4-(methallylamino)phenyl)propionic Acid

46. Minalfen (tn)

47. Mfcd00866084

48. Acide (methallylamino-4 Phenyl)-2 Propionique [french]

49. Alminoprofen (standard)

50. Alminoprofen [mi]

51. Alminoprofen [inn]

52. Alminoprofen [jan]

53. Alminoprofen (jp17/inn)

54. Propionic Acid, 2-(4-(methallylamino)phenyl)-

55. Schembl26940

56. Alminoprofen [mart.]

57. Alminoprofen [who-dd]

58. Orb1703760

59. Chembl1765293

60. Dtxsid90865968

61. Fphlbgojwpevme-uhfffaoysa-n

62. Bcp11016

63. Uwc97721

64. Hy-17485r

65. ()-alminoprofen;eb 382; Minalfene

66. Akos016014146

67. Db13314

68. Ncgc00522017-01

69. As-78318

70. Da-60933

71. Hy-17485

72. ( Inverted Exclamation Marka)-alminoprofen

73. Cs-0009220

74. Ns00015369

75. D01513

76. F600577

77. Q3612806

2.4 Create Date

2005-03-25

3 Chemical and Physical Properties

Molecular Formula	C₁₃H₁₇NO₂
Molecular Weight	219.28 g/mol
XLogP3	3.2
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	5
Exact Mass	Da
Monoisotopic Mass	Da
Topological Polar Surface Area	49.3
Heavy Atom Count	16
Formal Charge	0
Complexity	255
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	1
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	1

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.

4.2 ATC Code

M - Musculo-skeletal system

M01 - Antiinflammatory and antirheumatic products

M01A - Antiinflammatory and antirheumatic products, non-steroids

M01AE - Propionic acid derivatives

M01AE16 - Alminoprofen

ATCvet Code

QM - Musculo-skeletal system

QM01 - Antiinflammatory and antirheumatic products

QM01A - Antiinflammatory and antirheumatic products, non-steroids

QM01AE - Propionic acid derivatives

QM01AE16 - Alminoprofen