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SMR000146101

HCID 9550045
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기본 정보

CAS
3892-78-2
표준 SMILES
Cl.FC(F)(F)c1ccc2c(c1)N(CCCN1CCN(CCCl)CC1)c1ccccc1S2
InChIKey
KGXTXMNKUAOQHG-UHFFFAOYSA-N
분자식
C22H26Cl2F3N3S
평균 분자량
492.438 g/mol
단동위원소 질량
491.11765885

이름 및 식별자

우선 이름
SMR000146101
IUPAC
10-{3-[4-(2-Chloroethyl)piperazin-1-yl]propyl}-2-(trifluoromethyl)-10H-phenothiazine--hydrogen chloride (1/1)
영어명
Fluphenazine-N-2-chloroethane (hydrochloride)
분자식
C22H26Cl2F3N3S
분자량
492.4281496

이름 및 동의어

10-{3-[4-(2-Chloro-ethyl)-piperazin-1-yl]-propyl}-2-trifluoromethyl-10H-phenothiazine10-[3-[4-(2-chloroethyl)-1-piperazinyl]propyl]-2-(trifluoromethyl)-10H-phenothiazinedihydrochloride10-(3-(4-(2-chloroethyl)piperazin-1-yl)propyl)-2-(trifluoromethyl)-10H-phenothiazine dihydrochloride

데이터베이스 식별자

CAS
3892-78-2
PubChem CID
9550045
DTXSID
DTXSID30429563
ChEMBL
CHEMBL1519379

물성

물리화학적 성질

녹는점
224 · 224-225 °C
저장 조건
-20 °C · Store at -20°C
용해도
10 mg/ml; · DMF: 10 mg/ml; DMSO: 10 mg/ml; Ethanol: 1 mg/ml
물리적 상태
결정성 고체
색상
White to off-white

화학 및 산업

응용 분야 · 2건

개요Fluphenazine is a traditional antipsychotic compound that tightly binds the dopamine D2 receptor (Ki = 0.55 nM) and also reversibly inhibits calmodulin at micromolar concentrations. Fluphenazine-N-2-chloroethane is a derivative of fluphenazine that contains an alkylating chlorethylamine chain, which produces irreversible protein binding. It is a relatively selective, irreversible antagonist of D2 receptors both in vitro (IC50 = 100 nM) and in vivo, inactivating approximately 90% of D2 receptors in mice within 4 hours of treatment. Through this action, fluphenazine-B-2-chloroethane can be used to induce catalepsy in mice. It irreversibly inhibits calmodulin at higher doses (IC50 = 10 μM), which can sensitize cancer cells to TRAIL-induced apoptosis.

용도Fluphenazine is a traditional antipsychotic compound that tightly binds the dopamine D2 receptor (Ki = 0.55 nM) and also reversibly inhibits calmodulin at micromolar concentrations. Fluphenazine-N-2-chloroethane (hydrochloride) is a derivative of fluphenazine that contains an alkylating chlorethylamine chain, which produces irreversible protein binding. It is a relatively selective, irreversible antagonist of D2 receptors both in vitro (IC50 = 100 nM) and in vivo, inactivating approximately 90% of D2 receptors in mice within 4 hours of treatment. Through this action, fluphenazine-B-2-chloroethane can be used to induce catalepsy in mice. It irreversibly inhibits calmodulin at higher doses (IC50 = 10 μM), which can sensitize cancer cells to TRAIL-induced apoptosis.[Cayman Chemical]

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