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2D Structure
Also known as: Androviron, Proviron, 1424-00-6, Mesteranum, Mestoranum, Testiwop
Molecular Formula
C20H32O2
Molecular Weight
304.5  g/mol
InChI Key
UXYRZJKIQKRJCF-TZPFWLJSSA-N
FDA UNII
0SRQ75X9I9

17 beta-Hydroxy-1 alpha-methyl-5 alpha-androstan-3-one. A synthetic steroid with anabolic and androgenic activities.
1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
(1S,5S,8R,9S,10S,13S,14S,17S)-17-hydroxy-1,10,13-trimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one
2.1.2 InChI
InChI=1S/C20H32O2/c1-12-10-14(21)11-13-4-5-15-16-6-7-18(22)19(16,2)9-8-17(15)20(12,13)3/h12-13,15-18,22H,4-11H2,1-3H3/t12-,13-,15-,16-,17-,18-,19-,20-/m0/s1
2.1.3 InChI Key
UXYRZJKIQKRJCF-TZPFWLJSSA-N
2.1.4 Canonical SMILES
CC1CC(=O)CC2C1(C3CCC4(C(C3CC2)CCC4O)C)C
2.1.5 Isomeric SMILES
C[C@H]1CC(=O)C[C@H]2[C@]1([C@H]3CC[C@]4([C@H]([C@@H]3CC2)CC[C@@H]4O)C)C
2.2 Other Identifiers
2.2.1 UNII
0SRQ75X9I9
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Proviron

2. Vistimon

2.3.2 Depositor-Supplied Synonyms

1. Androviron

2. Proviron

3. 1424-00-6

4. Mesteranum

5. Mestoranum

6. Testiwop

7. Sh 723

8. Mesterolon

9. 17-hydroxy-1-methyl-5-androstane-3 One

10. Sh-60723

11. Nsc-75054

12. Sh-723

13. 17beta-hydroxy-1alpha-methyl-5alpha-androstan-3-one

14. 0srq75x9i9

15. (1s,5s,8r,9s,10s,13s,14s,17s)-17-hydroxy-1,10,13-trimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one

16. 1.alpha.-methyl-5.alpha.-dihydrotestosterone

17. Nsc 75054

18. Androstan-3-one, 17-hydroxy-1-methyl-, (1a,5a,17b)-

19. Androstan-3-one, 17-hydroxy-1-methyl-, (1.alpha.,5.alpha.,17.beta.)-

20. Mesterolona

21. Mesterolonum

22. 17.beta.-hydroxy-1.alpha.-methyl-5.alpha.-androstan-3-one

23. Mesterolonum [inn-latin]

24. Mesterolona [inn-spanish]

25. Provirone 25

26. (1s,5s,8r,9s,10s,13s,14s,17s)-17-hydroxy-1,10,13-trimethylhexadecahydro-3h-cyclopenta[a]phenanthren-3-one

27. Mesterolone [usan:inn:ban]

28. Einecs 215-836-3

29. 1alpha-methyl-5alpha-dihydrotestosterone

30. Unii-0srq75x9i9

31. Sh 60723

32. 5.alpha.-androstan-3-one, 17.beta.-hydroxy-1.alpha.-methyl-

33. Pro-viron

34. 1a-methyl-5a-dihydrotestosterone

35. Testosterone, 4,5alpha-dihydro-1alpha-methyl-

36. 1-alpha-methyl-5-alpha-androstan-17-beta-ol-3-one

37. 1-alpha-methyl-17-beta-hydroxy-5-alpha-androstan-3-one

38. 17-beta-hydroxy-1-alpha-methyl-5-alpha-androstan-3-one

39. 5alpha-androstan-3-one, 17beta-hydroxy-1alpha-methyl-

40. Mesterolone [mi]

41. Androstan-3-one, 17-hydroxy-1-methyl-, (1alpha,5alpha,17beta)-

42. Mesterolone [inn]

43. Mesterolone (usan/inn)

44. Mesterolone [usan]

45. Ec 215-836-3

46. Mesterolone [mart.]

47. Mesterolone [who-dd]

48. Schembl148260

49. Chembl258918

50. Mesterolone, Analytical Standard

51. Dtxsid90878533

52. Mesterolone [ep Impurity]

53. Chebi:135293

54. Mesterolone [ep Monograph]

55. 5-alpha-androstan-3-one, 17-beta-hydroxy-1-alpha-methyl-

56. Nsc75054

57. Zinc3881977

58. Androstan-3-one, 17-hydroxy-1-methyl-, (1-alpha,5-alpha,17-beta)-

59. Bdbm50423551

60. Lmst02020107

61. S3946

62. Akos015894889

63. Ccg-267514

64. Db13587

65. Mesterolone 1.0 Mg/ml In Acetonitrile

66. 1a-methyl-5a-androstan-17b-ol-3-one

67. 17b-hydroxy-1a-methyl-5a-androstan-3-one

68. 1a-methyl-17b-hydroxy-5a-androstan-3-one

69. D04947

70. Mesterolone, 1.0 Mg/ml In 1,2-dimethoxyethane

71. Testosterone,5.alpha.-dihydro-1.alpha.-methyl-

72. 424m006

73. (1a,5a,17b)-17-hydroxy-1-methyl-androstan-3-one

74. Androstan-3-one, (1.alpha.,5.alpha.,17.beta.)-

75. Q4291328

76. Mesterolone, European Pharmacopoeia (ep) Reference Standard

2.4 Create Date
2005-03-26
3 Chemical and Physical Properties
Molecular Weight 304.5 g/mol
Molecular Formula C20H32O2
XLogP34.1
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass304.240230259 g/mol
Monoisotopic Mass304.240230259 g/mol
Topological Polar Surface Area37.3 Ų
Heavy Atom Count22
Formal Charge0
Complexity486
Isotope Atom Count0
Defined Atom Stereocenter Count8
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

Anabolic Agents

These compounds stimulate anabolism and inhibit catabolism. They stimulate the development of muscle mass, strength, and power. (See all compounds classified as Anabolic Agents.)


4.2 ATC Code

G03BB01

S76 | LUXPHARMA | Pharmaceuticals Marketed in Luxembourg | Pharmaceuticals marketed in Luxembourg, as published by d'Gesondheetskeess (CNS, la caisse nationale de sante, www.cns.lu), mapped by name to structures using CompTox by R. Singh et al. (in prep.). List downloaded from https://cns.public.lu/en/legislations/textes-coordonnes/liste-med-comm.html. Dataset DOI:10.5281/zenodo.4587355


G - Genito urinary system and sex hormones

G03 - Sex hormones and modulators of the genital system

G03B - Androgens

G03BB - 5-androstanon (3) derivatives

G03BB01 - Mesterolone