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1. Hydrochloride, Pargyline
2. Pargyline
1. 306-07-0
2. Pargyline Hcl
3. Eutonyl
4. N-methyl-n-propargylbenzylamine Hydrochloride
5. Eutonyl-ten
6. N-methyl-n-2-propynylbenzylamine Hydrochloride
7. N-benzyl-n-methylprop-2-yn-1-amine Hydrochloride
8. Pargyline Chloride
9. Pargyline, Hcl
10. Pargyline (hydrochloride)
11. Usaf A-19120
12. Benzylmethylpropynylamine Hydrochloride
13. Methylbenzylpropynylamine Hydrochloride
14. Mo-911
15. Benzenemethanamine, N-methyl-n-2-propynyl-, Hydrochloride
16. Pargyline Hydrochloride [usan]
17. Mfcd00012492
18. N-benzyl-n-methyl-2-propynylamine Hydrochloride
19. Nsc-43798
20. A-19120
21. N-benzyl-n-methylprop-2-yn-1-amine;hydrochloride
22. W70v6i2omy
23. Mls000028460
24. Benzylamine, N-methyl-n-2-propynyl-, Hydrochloride
25. Smr000058367
26. Dsstox_cid_24647
27. Dsstox_rid_80375
28. Dsstox_gsid_44647
29. Pargyline Hydrochloride (usan)
30. Nsc43798
31. Pargylamine Hydrochloride
32. Sr-01000003035
33. Ncgc00015841-02
34. Cas-306-07-0
35. Einecs 206-175-1
36. Nsc 43798
37. Unii-w70v6i2omy
38. Ai3-62178
39. N-methyl-n-(2-propynyl)benzylamine Hydrochloride
40. N-methyl-n-propargylbenzylamine Hcl
41. Prestwick_377
42. 2-propynylamine, N-benzyl-n-methyl-, Hydrochloride
43. Eutonyl (tn)
44. Pargyline Hydrochloride [usan:usp]
45. Opera_id_404
46. N-methyl-n-propargylbenzylaminehydrochloride
47. Mls001076511
48. Pargyline Hydrochloride, 99%
49. Schembl121111
50. 2-propynylamine, Hydrochloride
51. Chembl1200425
52. Dtxsid1044647
53. Hms1568f07
54. Pharmakon1600-01500462
55. Amy20608
56. Bcp21320
57. Hy-a0091
58. Pargyline Hydrochloride [mi]
59. Tox21_110241
60. Tox21_302678
61. Tox21_501022
62. Ccg-40239
63. Nsc757264
64. S3690
65. Akos015950558
66. Tox21_110241_1
67. Lp01022
68. Nsc-757264
69. Pargyline Hydrochloride [mart.]
70. Pargyline Hydrochloride [vandf]
71. Wln: 1uu2n1 & 1r & Gh
72. Pargyline Hydrochloride [who-dd]
73. Ncgc00015841-11
74. Ncgc00094313-01
75. Ncgc00094313-02
76. Ncgc00094313-03
77. Ncgc00256654-01
78. Ncgc00261707-01
79. Ac-18917
80. As-16929
81. Sy005867
82. Db-047811
83. Eu-0101022
84. Ft-0631924
85. Pargyline Hydrochloride [orange Book]
86. Bim-0050995.0001
87. D02564
88. Eutron Component Pargyline Hydrochloride
89. P 8013
90. A820454
91. A935225
92. Pargyline Hydrochloride Component Of Eutron
93. N-benzyl-n-methylprop-2-yn-1-amine;hydron;chloride
94. Sr-01000003035-2
95. Sr-01000003035-7
96. Q27292421
97. Sr-01000003035-11
98. N-methyl-n-(phenylmethyl)-2-propyn-1-amine Hydrochloride
99. N-methyl-n-(phenylmethyl)prop-2-yn-1-amine Hydrochloride
100. 4-(3-methylpyrazin-2-yl)-6-methyl-pyrimidin-2-amine
101. Benzenemethanamine, N-methyl-n-2-propyn-1-yl-, Hydrochloride (1:1)
102. Benzenemethanamine,n-methyl-n-2-propyn-1-yl-, Hydrochloride (1:1);
103. Pargyline Hydrochloride, United States Pharmacopeia (usp) Reference Standard
104. N-benzyl-n-methylprop-2-yn-1-amine Hydrochloride; Eutonyl-ten; N-methyl-n-propargylbenzylamine Hydrochloride; Pargyline Hcl
| Molecular Weight | 195.69 g/mol |
|---|---|
| Molecular Formula | C11H14ClN |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 3 |
| Exact Mass | 195.0814771 g/mol |
| Monoisotopic Mass | 195.0814771 g/mol |
| Topological Polar Surface Area | 3.2 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 159 |
| 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 |
Antihypertensive Agents
Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS. (See all compounds classified as Antihypertensive Agents.)
Monoamine Oxidase Inhibitors
A chemically heterogeneous group of drugs that have in common the ability to block oxidative deamination of naturally occurring monoamines. (From Gilman, et al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed, p414) (See all compounds classified as Monoamine Oxidase Inhibitors.)
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