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1. Dosulepin
2. Dothiepin
3. Hydrochloride, Dothiepin
4. Prothiaden
1. Dothiepin Hcl
2. Depresym
3. Dosulepin Hydrochloride
4. 897-15-4
5. Dopress
6. Dosulepine
7. Prothiadene
8. Dothep
9. Dothiepin Hydrochloride [usan]
10. Prothiaden
11. Nsc-172130
12. Dosulepin Chloride
13. Prothiadiene
14. 3h0042311v
15. 1-propanamine, 3-dibenzo(b,e)thiepin-11(6h)-ylidene-n,n-dimethyl-, Hydrochloride
16. Prothiaden Hydrochloride
17. Prothiadene Hydrochloride
18. Xerenal
19. Trans-dothiepin Hydrochloride
20. Idom
21. Chebi:36805
22. Trans-11-(3-dimethylaminopropylidene)-6,11-dihydrodibenzo(b,e)thiepin Hydrochloride
23. Thaden
24. Dosulepin Hydrochloride [jan]
25. (3e)-3-(6h-benzo[c][1]benzothiepin-11-ylidene)-n,n-dimethylpropan-1-amine;hydrochloride
26. Unii-3h0042311v
27. Einecs 212-978-8
28. Dothiepinhcl
29. Nsc 172130
30. Nsc172130
31. Schembl35428
32. Mls002153839
33. Dothiepin Hydrochloride- Bio-x
34. Chembl1711280
35. Dtxsid60873550
36. Amy40796
37. Dothiepin Hydrochloride [mi]
38. Ccg-220488
39. Dosulepin Hydrochloride [mart.]
40. 11-(3-dimethylaminopropylidene)-6,11-dihydrodibenzo(b,e)thiepine Hydrochloride
41. Dibenzo(b,e)thiepin-delta(sup 11(6h),gamma)-propylamine, N,n-dimethyl-, Hydrochloride, (e)-
42. Dosulepin Hydrochloride [who-dd]
43. N,n-dimethyldibenzo(b,e)thiepin-delta(sup 11(6h),gamma)-propylamine Hydrochloride
44. Bd164382
45. Smr001233202
46. Dosulepin Hydrochloride [ep Monograph]
47. Wln: T C676 Is&t&j B3n1&1 &gh
48. Sr-01000838836
49. Sr-01000838836-2
50. Q27116969
51. 11-[3-(dimethylamino)propylidene]-6,e]thiepin Hydrochloride
52. 11-[3-(dimethylamino)propylidene]-6,e]thiepine Hydrochloride
53. Dibenzo[b,.gamma.-propylamine, N,n-dimethyl-, Hydrochloride
54. N,e]thiepin-.delta.11(6h),.gamma.-propylamine, Hydrochloride
55. 1-propanamine,e]thiepin-11(6h)-ylidene-n,n-dimethyl-, Hydrochloride
56. Dibenzo(b,e)thiepin-delta(sup 11(6h),gamma)-propylamine, N,n-dimethyl-, Hydrochloride
57. Dibenzo(b,e)thiepin-delta11(6h),gamma-propylamine, N,n-dimethyl-, Hydrochloride
58. Dothiepin Hydrochloride (dosulepin Hydrochloride) 1.0 Mg/ml In Methanol (as Free Base)
59. (3e)-3-(dibenzo[b,e]thiepin-11(6h)-ylidene)-n,n-dimethylpropan-1-amine, Hydrogen Chloride (1:1)
60. Dothiepin (cis/trans) Hydrochloride Solution, 1.0 Mg/ml In Methanol (as Free Base), Ampule Of 1 Ml, Certified Reference Material
1. Dosulepin Chloride
2. Dothiepin Hcl
3. Idom
4. Prothiaden
5. Prothiadene
6. Xerenal
7. Dosulepin Hydrochloride
8. Dosulepine
9. Dosulepin
10. Dothiepin
| Molecular Weight | 331.9 g/mol |
|---|---|
| Molecular Formula | C19H22ClNS |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 331.1161486 g/mol |
| Monoisotopic Mass | 331.1161486 g/mol |
| Topological Polar Surface Area | 28.5 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 363 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
Adrenergic Uptake Inhibitors
Drugs that block the transport of adrenergic transmitters into axon terminals or into storage vesicles within terminals. The tricyclic antidepressants (ANTIDEPRESSIVE AGENTS, TRICYCLIC) and amphetamines are among the therapeutically important drugs that may act via inhibition of adrenergic transport. Many of these drugs also block transport of serotonin. (See all compounds classified as Adrenergic Uptake Inhibitors.)
Antidepressive Agents, Tricyclic
Substances that contain a fused three-ring moiety and are used in the treatment of depression. These drugs block the uptake of norepinephrine and serotonin into axon terminals and may block some subtypes of serotonin, adrenergic, and histamine receptors. However, the mechanism of their antidepressant effects is not clear because the therapeutic effects usually take weeks to develop and may reflect compensatory changes in the central nervous system. (See all compounds classified as Antidepressive Agents, Tricyclic.)
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