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35795-16-5

35795-16-5 structure
35795-16-5 structure
  • Name: Trimazosin
  • Chemical Name: (2-hydroxy-2-methylpropyl) 4-(4-amino-6,7,8-trimethoxyquinazolin-2-yl)piperazine-1-carboxylate
  • CAS Number: 35795-16-5
  • Molecular Formula: C20H29N5O6
  • Molecular Weight: 435.47
  • Catalog: Signaling Pathways GPCR/G Protein Adrenergic Receptor
  • Create Date: 2018-05-26 08:00:00
  • Modify Date: 2024-01-06 20:52:59
  • Trimazosin is an orally active, quinazoline derivative which is structurally related to prazosin. Trimazosin shows hypotensive effect by selectively block α1-adrenoceptors[1][2].

Name (2-hydroxy-2-methylpropyl) 4-(4-amino-6,7,8-trimethoxyquinazolin-2-yl)piperazine-1-carboxylate
Synonyms trimazosine
TRIMAZOSIN
EINECS 252-732-7
Description Trimazosin is an orally active, quinazoline derivative which is structurally related to prazosin. Trimazosin shows hypotensive effect by selectively block α1-adrenoceptors[1][2].
Related Catalog
Target

α1-adrenergic receptor

In Vivo Trimazosin (10–30 mg/kg; i.h.; once) produces graded decreases in blood pressure[3]. Animal Model: Conscious spontaneously hypertensive rats (SHR)[3] Dosage: 10–30 mg/kg Administration: Subcutaneous administration, once Result: Produced graded decreases in blood pressure.
References

[1]. J Vincent, et al. The cardiovascular effects of trimazosin and prazosin in the rabbit. Clin Exp Pharmacol Physiol. 1986 Aug;13(8):593-608.

[2]. H L Elliott, et al. Trimazosin in normotensive subjects. Clin Pharmacol Ther. 1984 Feb;35(2):156-60.

[3]. J. P. Buyniski, et al. Effects of Tiodazosin, Prazosin, Trimazosin and Phentolamine on Blood Pressure, Heart Rate and on Pre- and Postsynaptic α-Adrenergic Receptors in the Rat. Clinical and Experimental Hypertension , 1980, Vol.2(6), p.1039-1066.

Density 1.31g/cm3
Boiling Point 648.2ºC at 760mmHg
Molecular Formula C20H29N5O6
Molecular Weight 435.47
Flash Point 345.8ºC
Exact Mass 435.21200
PSA 132.50000
LogP 1.85140
Index of Refraction 1.606