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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 4008생성일: 2026년 10월 27일

마니디핀

마니디핀 · Manidipine (Manyper) · Artedil · Iperten · Manidipine · Franidipine · Manidipine 6300 · Manidipine(base)

https://huagongshe.com/ko/chemical/4008

마니디핀 분자 구조식

식별자 및 물리적 특성

CAS No.89226-50-6
분자식C35H38N4O6
평균 분자량610.7 g/mol
단동위원소 질량610.27913494 g/mol
SMILESCOC(=O)C1=C(C)NC(C)=C(C(=O)OCCN2CCN(C(c3ccccc3)c3ccccc3)CC2)C1c1cccc([N+](=O)[O-])c1
InChIKeyANEBWFXPVPTEET-UHFFFAOYSA-N
PubChem CID4008
ChEMBLCHEMBL1085699
ChEBICHEBI:135849
EC No.855-394-4
DTXSIDDTXSID2043745
현지명마니디핀

화학 및 물리적 성질

XLogP5.6
극성 표면적117
수소 결합 공여자 수1
수소 결합 수용자 수9
회전 가능 결합 수11
무거운 원자 수45
형식 전하0
복잡도1,090
용해도<1mg/mLSoluble in DMSO > 10 mM
녹는점125-128°C
끓는 점722.0±60.0 °C(Predicted)
밀도1.232±0.06 g/cm3(Predicted)
저장 조건Sealed in dry,2-8°C
물리적 상태가루
pKa(산도 계수)6.12±0.10(Predicted)
색상Light yellow to yellow
LogP(분배 계수)4.135

화학적 성질

Light Yellow Crystalline Solid

안전 및 규제

GHS 분류DangerH301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]P264, P270, P301+P316, P321, P330, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 3 reports by companies from 1 notifications to the ECHA C&L Inventory.Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
규제 정보Status: Active Update: 11-04-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/33372
Hazard Classes and CategoriesAcute Tox. 3 (100%)
Drug Induced Liver InjuryDrug-Induced Liver Injury Severity and Toxicity (DILIst)ManidipineDILI PositiveDOI:10.1016/j.drudis.2019.09.022
신호 어Warning
유해·위험 문구암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드 H302

용도

개요

Manidipine is a dihydropyridine L- and T-type calcium channel blocker. It blocks recombinant rabbit L-type (α1Cα2/δβ1a) and human T-type (α1H) calcium channels expressed in Xenopus oocytes and native L-type channels in dissociated guinea pig cardiac ventricular cells (IC50 = 2.6 nM). Manidipine inhibits intracellular calcium increases induced by endothelin-1 (ET-1; ) in A7r5 rat vascular smooth muscle cells (ED50 = 1 nM) and potassium-induced contraction of isolated dog femoral and portal veins (IC50s = 24 and 2.1 nM, respectively). In vivo, it lowers blood pressure in spontaneously hypertensive rats (SHRs) when administered at a dose of 10 mg/kg and inhibits left ventricular hypertrophy in rats induced by isoproterenol when administered at a dose of 3 mg/kg. Formulations containing manidipine have been used in the treatment of hypertension.

용도

Manidipine (Manyper) is a lipophilic, third-generation, highly vasoselective dihydropyridine calcium antagonist with an IC50 of 2.6 nM. It causes systemic vasodilation by inhibiting the voltage-dependent calcium inward currents in smooth muscle cells. It