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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 3157생성일: 2026년 10월 26일

Doxazosin

UK 33274 · UK 33,274 · DOXAZOSIN · Doxazosin base · DOXAZOSINMESYTL · DOXAZOSIN(CARDULAR) · Doxazosin USP/EP/BP · Doxazosin (UK 33274)

https://huagongshe.com/ko/chemical/3157

Doxazosin 분자 구조식

식별자 및 물리적 특성

CAS No.74191-85-8
분자식C23H25N5O5
평균 분자량451.5 g/mol
단동위원소 질량451.1855689 g/mol
SMILESCOc1cc2nc(N3CCN(C(=O)C4COc5ccccc5O4)CC3)nc(N)c2cc1OC
InChIKeyRUZYUOTYCVRMRZ-UHFFFAOYSA-N
PubChem CID3157
ChEMBLCHEMBL707
ChEBICHEBI:4708
EC No.616-059-6
DTXSIDDTXSID7022964

화학 및 물리적 성질

XLogP2.5
극성 표면적112
수소 결합 공여자 수1
수소 결합 수용자 수9
회전 가능 결합 수4
무거운 원자 수33
형식 전하0
복잡도678
의약품Pharmaceuticals -> Antihypertensives
LogP(분배 계수)2.13.38
용해도0.8%7.90e-01 g/LDMSO에 용해됨
Human DrugsBreast FeedingLactationMilk, HumanAdrenergic alpha-AntagonistsAntihypertensive Agents
녹는점275-277289 - 290 °C289-290°C
Physical DescriptionSolid
Dissociation Constants6.52
Collision Cross Section202.9 Ų [M+H]+ [CCS Type: TWMethod: Major Mix IMS/Tof Calibration Kit (Waters)]196.92 Ų [M+Na]+ [CCS Type: TWMethod: calibrated with polyalanine and drug standards]
끓는 점718.0±70.0 °C(Predicted)
밀도1.371±0.06 g/cm3(Predicted)
저장 조건Store at -20°C
물리적 상태가루
pKa(산도 계수)6.52±0.50(Predicted)
색상White to off-white

안전 및 규제

GHS 분류DangerH302 (20%): Harmful if swallowed [Warning Acute toxicity, oral]P260, P264, P270, P273, P280, P301+P317, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P319, P321, P330, P363, P391, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 5 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
규제 정보Status: Active Update: 01-07-2020 https://echa.europa.eu/registration-dossier/-/registered-dossier/31210
Hazard Classes and CategoriesSkin Corr. 1B (80%)
HepatotoxicityDoxazosin has been associated with a low rate of serum aminotransferase elevations that in controlled trials was no higher than with placebo therapy. These elevations were transient and did not require dose modification. No instances of clinically apparent acute liver injury due to doxazosin have been published in the literature, but reports of cholestatic hepatitis have been received by the sponsor. Among the alpha adrenergic receptor antagonists, the most frequently implicated agent in causing liver injury has been alfuzosin with only single, and not well documented cases linked to other alpha blockers. Thus, acute symptomatic liver injury due to doxazosin is quite rare, and severe hepatotoxicity must be exceeding rare, if it occurs at all.
유해 작용Dose-related Adverse Effects
독성 요약Reports with overdosage and toxicity with the alpha-1 antagonists, including doxazosin, remain very limited in the literature. There is a report of one case of acute doxazosin overdose in 2005. The study found that the patient presented to the emergency department (ED) with drowsiness, decreased blood pressure, and reflex tachycardia but did not have orthostatic hypotension or any other abnormalities. This patient was able to fully awaken with supportive therapy in 8 hours and was discharged 48 hours after admission to the ED. Although there are limited works of literature for the toxicity of doxazosin, it appears to have low acute toxicity.
Drug Induced Liver InjuryDrug-Induced Liver Injury Severity and Toxicity (DILIst)doxazosinDILI NegativeOralDOI:10.1016/j.drudis.2019.09.022
Effects During Pregnancy and Lactation◉ Summary of Use during Lactation
신호 어Danger
유해·위험 문구암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드 H302

용도

개요

Doxazosin mesylate is a selective alpha, blocker indicated for the treatment of hypertension, reportedly of special benefit as a first-line agent in the most hypertonic patient population. Another advantage of doxazosin is its favorable effect on blood lipids; it significantly increases the HDL/total cholesterol ratio and decreases the total cholesterol as well as triglycerides levels.

용도

ACIPHEX therapeutic Erosive or Ulcerative Gastroesophageal Reflux Disease

일반 설명

Doxazosin, 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(1,4-benzodioxan-2-ylcarbonyl)piperazine(Cardura), is a quinazoline compound that selectively inhibitsthe α1-subtype of α-adrenergic receptors. This agentis very useful in the management of hypertension associatedwith pheochromocytoma.