Name | N,N-dimethyl-1-pyrido[3,2-b][1,4]benzothiazin-10-ylpropan-2-amine |
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Synonyms |
Actapront
Odantol Nilergex Isothipendylum isothiopendyl Isothipendyl Udantol Andanton |
Description | Isothipendyl (AY 56012), an azaphenothiazine derivative, is a potent histamine 1 (H1) receptor antagonist. Isothipendyl is a primary metabolite[1]. |
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Related Catalog | |
Target |
Human Endogenous Metabolite |
Density | 1.167g/cm3 |
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Boiling Point | 421.3ºC at 760mmHg |
Molecular Formula | C16H19N3S |
Molecular Weight | 285.40700 |
Flash Point | 208.6ºC |
Exact Mass | 285.13000 |
PSA | 44.67000 |
LogP | 3.69940 |
Vapour Pressure | 2.63E-07mmHg at 25°C |
Index of Refraction | 1.62 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
~% 482-15-5 |
Literature: Yale; Sowinski Journal of the American Chemical Society, 1958 , vol. 80, p. 1651,1653 |
~% 482-15-5 |
Literature: Yale; Sowinski Journal of the American Chemical Society, 1958 , vol. 80, p. 1651,1653 |
~% 482-15-5 |
Literature: Yale; Sowinski Journal of the American Chemical Society, 1958 , vol. 80, p. 1651,1653 |
~% 482-15-5 |
Literature: Yale; Sowinski Journal of the American Chemical Society, 1958 , vol. 80, p. 1651,1653 |
~% 482-15-5 |
Literature: Yale; Sowinski Journal of the American Chemical Society, 1958 , vol. 80, p. 1651,1653 |
~% 482-15-5 |
Literature: Schuler,W.A.; Klebe,H. Justus Liebigs Annalen der Chemie, 1962 , vol. 653, p. 172 - 180 |
~% 482-15-5 |
Literature: Schuler,W.A.; Klebe,H. Justus Liebigs Annalen der Chemie, 1962 , vol. 653, p. 172 - 180 |
Precursor 7 | |
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DownStream 0 |