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Moroxydine Hydrochloride

Moroxydine Hydrochloride

Synopsis, Chemistry

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Also known as: 3160-91-6, Moroxydine hcl, Abob hydrochloride, Flumidin, Virustat, Influcol

Molecular Formula

C₆H₁₄ClN₅O

Molecular Weight

207.66 g/mol

InChI Key

FXYZDFSNBBOHTA-UHFFFAOYSA-N

FDA UNII

6Y9698W0XT

1 2D Structure

Moroxydine Hydrochloride

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

N-(diaminomethylidene)morpholine-4-carboximidamide;hydrochloride

2.1.2 InChI

InChI=1S/C6H13N5O.ClH/c7-5(8)10-6(9)11-1-3-12-4-2-11;/h1-4H2,(H5,7,8,9,10);1H

2.1.3 InChI Key

FXYZDFSNBBOHTA-UHFFFAOYSA-N

2.1.4 Canonical SMILES

C1COCCN1C(=N)N=C(N)N.Cl

2.2 Other Identifiers

2.2.1 UNII

6Y9698W0XT

2.3 Synonyms

2.3.1 MeSH Synonyms

1. 4-morpholinocarboximidoylguanidine

2. Flumidine

3. Influmine

4. Moroxidine

5. Moroxydine

6. Moroxydine Monohydrochloride

7. N-amidino-4-morpholinecarboxamidine

8. Skf 8898-a

9. Skf-8898-a

10. Skf-8898a

11. Vironil

12. Virustat

2.3.2 Depositor-Supplied Synonyms

1. 3160-91-6

2. Moroxydine Hcl

3. Abob Hydrochloride

4. Flumidin

5. Virustat

6. Influcol

7. Spenitol

8. Virusmin

9. N-carbamimidoylmorpholine-4-carboximidamide Hydrochloride

10. Moroxidine Hydrochloride

11. Moroxydine (hydrochloride)

12. Morpholinobiguanide Hydrochloride

13. Morpholinobiguanide Monohydrochloride

14. 4-(amidinoamidino)morpholine, Hydrochloride

15. N-amidinomorpholine-4-carboxamidine Hydrochloride

16. N-[amino(imino)methyl]morpholine-4-carboximidamide Hydrochloride

17. 6y9698w0xt

18. 1-(morpholine-4-carboximidoyl)guanidine Hydrochloride

19. Nsc-43840

20. Nsc-47838

21. Nsc-52355

22. Nsc-63755

23. Nsc-407204

24. Flumadon

25. N-(diaminomethylidene)morpholine-4-carboximidamide;hydrochloride

26. Dsstox_cid_25376

27. Dsstox_rid_80837

28. Dsstox_gsid_45376

29. Flumidin (van)

30. Smr000718626

31. 4-morpholinecarboxamidine, Monohydrochloride

32. Sr-01000841820

33. Ncgc00016623-01

34. Einecs 221-612-6

35. Cas-3160-91-6

36. Nsc 43840

37. Nsc 47838

38. Nsc 52355

39. Nsc 63755

40. N-carbamimidoylmorpholine-4-carboximidamide;hydrochloride

41. Nsc 407204

42. N1,n1-anhydrobis(.beta.-hydroxyethyl)biguanide Hydrochloride

43. Unii-6y9698w0xt

44. Ai3-51320

45. Influcol, Spenitol

46. Prestwick_547

47. Einecs 231-039-3

48. 4-morpholinecarboxamidine, N-amidino-, Monohydrochloride

49. N-amidinomorpholine-4-carboxamidine Hcl

50. N1,n1-anhydrobis(beta-hydroxyethyl)biguanide Hydrochloride

51. Biguanide, 1,1-anhydrobis(beta-hydroxyethyl)-, Hydrochloride

52. 4-morpholinecarboximidamide, N-(aminoiminomethyl)-, Monohydrochloride

53. N(sup 1),n(sup 1)-anhydrobis(beta-hydroxyethyl)biguanide Hydrochloride

54. Schembl92735

55. Moroxydine Hydrochloride,(s)

56. Mls001032033

57. Mls002154194

58. Moroxydine Hydrochloride, 99%

59. Dtxsid1045376

60. Schembl14973476

61. Hy-b0420a

62. Hms1568a10

63. Pharmakon1600-01506078

64. 1-morpholinobiguanide Hydrochloride

65. Nsc43840

66. Nsc47838

67. Nsc52355

68. Nsc63755

69. Tox21_110532

70. Mfcd00012798

71. Moroxydine Hydrochloride [mi]

72. Nsc407204

73. Nsc759315

74. S2486

75. Akos005256937

76. Akos037515708

77. Tox21_110532_1

78. Ccg-213951

79. Nsc-759315

80. S10381

81. Moroxydine Hydrochloride [who-dd]

82. Ncgc00016623-05

83. Ac-14457

84. As-13339

85. Ft-0698221

86. M2443

87. Sw196730-3

88. 4-chloro-3-(trifluoromethyl)phenylboronicacid

89. 160m916

90. A875839

91. J-018491

92. Moroxydine Hydrochloride 100 Microg/ml In Methanol

93. Sr-01000841820-2

94. Sr-01000841820-3

95. Q27265715

96. N''-(morpholine-4-carboximidoyl)guanidine Hydrochloride

97. Z2160887313

2.4 Create Date

2005-07-28

3 Chemical and Physical Properties

Molecular Formula	C₆H₁₄ClN₅O
Molecular Weight	207.66 g/mol
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	2
Exact Mass	207.0886878 g/mol
Monoisotopic Mass	207.0886878 g/mol
Topological Polar Surface Area	101 Å²
Heavy Atom Count	13
Formal Charge	0
Complexity	192
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	2

4 Pharmacology and Biochemistry

4.1 MeSH Pharmacological Classification

Antiviral Agents

Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly. (See all compounds classified as Antiviral Agents.)