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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 190863생성일: 2026년 10월 31일

벤조말빈A

벤조말빈A · benzomalvin A · Quinazolino[3,2-a][1,4]benzodiazepine-5,13-dione, 6,7-dihydro-6-methyl-7-(phenylmethyl)-, (6S,7S)-

https://huagongshe.com/ko/chemical/190863

벤조말빈A 분자 구조식

식별자 및 물리적 특성

CAS No.157047-96-6
분자식C24H19N3O2
평균 분자량381.435 g/mol
단동위원소 질량381.14772685 g/mol
SMILESCN1C(=O)c2ccccc2-n2c(nc3ccccc3c2=O)C1Cc1ccccc1
InChIKeyYYWUABJYAOCACI-UHFFFAOYSA-N
PubChem CID190863
DTXSIDDTXSID90935599
현지명벤조말빈A

화학 및 물리적 성질

끓는 점599.3±60.0 °C(Predicted)
밀도1.28±0.1 g/cm3(Predicted)
저장 조건Store at -20°C
용해도DMF: SolubleDMSO: SolubleEthanol: SolubleMethanol: Soluble
물리적 상태고체
pKa(산도 계수)-0.46±0.40(Predicted)

용도

개요

Benzomalvin A is a fungal metabolite produced by Penicillium. It inhibits yeast α-glucosidase in vitro (IC50 = 383.2 μM). In vivo, benzomalvin A (3.1-31.6 mg/kg) decreases plasma glucose levels in mice following administration of sucrose. It also decreases the plasma glucose postprandial peak in nicotinamide-streptozotocin-induced hyperglycemic mice when administered at a dose of 10 mg/kg. Benzomalvin A also acts as an antagonist of neurokinin-1 (NK1) receptors, inhibiting binding of substance P to guinea pig, rat, and human NK1 (Kis = 12, 42, and 43 μM, respectively).