Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H23N5O2.2ClH |
| Molecular Weight | 402.319 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.Cl.COC1=CC2=C(C=C1OC)C(N)=NC(=N2)N3CCN(CC=C)CC3
InChI
InChIKey=LJEPCGWMLNUFDA-UHFFFAOYSA-N
InChI=1S/C17H23N5O2.2ClH/c1-4-5-21-6-8-22(9-7-21)17-19-13-11-15(24-3)14(23-2)10-12(13)16(18)20-17;;/h4,10-11H,1,5-9H2,2-3H3,(H2,18,19,20);2*1H
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C17H23N5O2 |
| Molecular Weight | 329.3968 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Quinazosin is a diaminoquinazoline derivative patented by Pfizer, Chas., and Co., Inc. as a hypotensive agent. Quinazosin acts as adrenoreceptor antagonist and in preclinical studies lowered systolic blood pressure in conscious hypertensive dogs, without having any significant effect on their heart rate. Quinazosin lowered blood pressure and reduced total peripheral vascular resistance, while the duration of these effects was dose-dependent. In cats, Quinazosin reduced or reversed the pressor effects of epinephrine, but did not alter those of angiotensin amide.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:18:22 GMT 2025
by
admin
on
Mon Mar 31 18:18:22 GMT 2025
|
| Record UNII |
2N2LI66RRO
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
| Name | Type | Language | ||
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Preferred Name | English | ||
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Official Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Code | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C270
Created by
admin on Mon Mar 31 18:18:22 GMT 2025 , Edited by admin on Mon Mar 31 18:18:22 GMT 2025
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DTXSID00222947
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7262-00-2
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CHEMBL2111007
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C73813
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160354
Created by
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2N2LI66RRO
Created by
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300000055042
Created by
admin on Mon Mar 31 18:18:22 GMT 2025 , Edited by admin on Mon Mar 31 18:18:22 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |