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2D Structure
Also known as: 56-91-7, 4-carboxybenzylamine, Aminomethylbenzoic acid, 4-aminomethylbenzoic acid, Pamba, Styptopur
Molecular Formula
C8H9NO2
Molecular Weight
151.16  g/mol
InChI Key
QCTBMLYLENLHLA-UHFFFAOYSA-N
FDA UNII
68WG9JKC7L

Aminomethylbenzoic acid may be useful as an antifibrinolytic agent.
1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
4-(aminomethyl)benzoic acid
2.1.2 InChI
InChI=1S/C8H9NO2/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4H,5,9H2,(H,10,11)
2.1.3 InChI Key
QCTBMLYLENLHLA-UHFFFAOYSA-N
2.1.4 Canonical SMILES
C1=CC(=CC=C1CN)C(=O)O
2.2 Other Identifiers
2.2.1 UNII
68WG9JKC7L
2.3 Synonyms
2.3.1 MeSH Synonyms

1. 4-aminomethylbenzoic Acid

2. P-aminomethylbenzoic Acid

3. Pamba

4. Para-aminomethylbenzoic Acid

2.3.2 Depositor-Supplied Synonyms

1. 56-91-7

2. 4-carboxybenzylamine

3. Aminomethylbenzoic Acid

4. 4-aminomethylbenzoic Acid

5. Pamba

6. Styptopur

7. P-aminomethylbenzoic Acid

8. Gumbix

9. Benzoic Acid, 4-(aminomethyl)-

10. Benzylamine-4-carboxylic Acid

11. Alpha-amino-p-toluic Acid

12. P-(aminomethyl)benzoic Acid

13. 4-aminomethyl-benzoic Acid

14. Mfcd00010203

15. Nsc41629

16. Nsc-41629

17. 68wg9jkc7l

18. .alpha.-amino-p-toluic Acid

19. Chembl328875

20. P-toluic Acid, .alpha.-amino-

21. 4-(aminomethyl)benzoesaeure

22. Einecs 200-297-9

23. Nsc 41629

24. Unii-68wg9jkc7l

25. 4-(aminomethyl)benzoicacid

26. P-toluic Acid, Alpha-amino-

27. Gumbix (tn)

28. Pteroicacid

29. A-amino-p-toluic Acid

30. 4-aminomethylbezoic Acid

31. Alphaamino-p-toluic Acid

32. Tranexamic Acid Impurity D

33. 4-aminomethyl Benzoic Acid

34. 4-(aminomethyl)benzoic-acid

35. Ncistruc1_000124

36. Ncistruc2_000164

37. Oprea1_689394

38. Schembl38758

39. Cbdive_002627

40. 4-(aminomethyl) Benzoic Acid

41. 4-(aminomethyl)-benzoic Acid

42. Gtpl4702

43. Dtxsid20204568

44. Chebi:134774

45. Act00964

46. Bcp24445

47. Hy-b1258

48. Nci41629

49. 4-(aminomethyl)benzoic Acid, 97%

50. 4-(aminomethyl)phenylcarboxylic Acid

51. Bdbm50408790

52. Ccg-36812

53. Ncgc00013487

54. Stk246898

55. Zinc12359009

56. Akos000118982

57. Aminomethylbenzoic Acid [mart.]

58. Cs-4892

59. Db13244

60. Aminomethylbenzoic Acid [who-dd]

61. Ncgc00013487-02

62. Ncgc00096601-01

63. Ac-10932

64. As-13170

65. Nci60_003944

66. Sy002868

67. Tranexamic Acid Related Compound D

68. Db-008385

69. A0965

70. Am20060672

71. Ft-0616689

72. D07568

73. D70590

74. Tranexamic Acid Impurity D [ep Impurity]

75. Q695442

76. W-105499

77. Aminomethylbenzoic Acid 4-(aminomethyl)benzoic Acid

78. F1313-0009

79. Tranexamic Acid Related Compound D [usp Impurity]

80. 4az

2.4 Create Date
2005-03-26
3 Chemical and Physical Properties
Molecular Weight 151.16 g/mol
Molecular Formula C8H9NO2
XLogP3-1.6
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass151.063328530 g/mol
Monoisotopic Mass151.063328530 g/mol
Topological Polar Surface Area63.3 Ų
Heavy Atom Count11
Formal Charge0
Complexity139
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

Antifibrinolytic Agents

Agents that prevent fibrinolysis or lysis of a blood clot or thrombus. Several endogenous antiplasmins are known. The drugs are used to control massive hemorrhage and in other coagulation disorders. (See all compounds classified as Antifibrinolytic Agents.)


Protease Inhibitors

Compounds which inhibit or antagonize biosynthesis or actions of proteases (ENDOPEPTIDASES). (See all compounds classified as Protease Inhibitors.)


4.2 ATC Code

B - Blood and blood forming organs

B02 - Antihemorrhagics

B02A - Antifibrinolytics

B02AA - Amino acids

B02AA03 - Aminomethylbenzoic acid