Undecylprodigiosin
기본 정보
- CAS
13129-81-2- 표준 SMILES
CCCCCCCCCCCc1ccc(/C=C2\N=C(c3ccc[nH]3)C=C2OC)[nH]1- InChIKey
HIYSWASSDOXZLC-MOHJPFBDSA-N- 분자식
- C25H35N3O
- 평균 분자량
- 393.6 g/mol
개요
Undecylprodigiosin is a member of the class of tripyrroles that is 1H-pyrrole substituted by (4'-methoxy-1H,5'H-[2,2'-bipyrrol]-5'-ylidene)methyl and undecyl groups at positions 2 and 5, respectively. It is a pigment produced by Stveptomyces coelicolor. It has a role as a radiosensitizing agent, a biological pigment, an antibacterial agent, an antineoplastic agent, an immunosuppressive agent, an apoptosis inducer and a bacterial metabolite. It is an alkaloid, an aromatic ether and a tripyrrole.
이름 및 식별자
- 우선 이름
- Undecylprodigiosin
- IUPAC
- (2Z)-3-methoxy-5-(1H-pyrrol-2-yl)-2-[(5-undecyl-1H-pyrrol-2-yl)methylidene]pyrrole
- 영어명
- 2-(5-Undecyl-2-pyrrolylmethylene)-3-methoxy-5-(2-pyrrolyl)-2H-pyrrole
- 분자량
- 0
이름 및 동의어
undecylprodigiosin52340-48-4ZQ2HK5E6ZG2-((3-Methoxy-5-(1H-pyrrol-2-yl)-2H-pyrrol-2-ylidene)methyl)-5-undecyl-1H-pyrroleCHEBI:29702DTXSID001315967(5'Z)-4'-methoxy-5'-[(5-undecyl-1H-pyrrol-2-yl)methylidene]-1H,5'H-2,2'-bipyrrole(5'Z)-4'-methoxy-5'-((5-undecyl-1H-pyrrol-2-yl)methylidene)-1H,5'H-2,2'-bipyrroleRefChem:933809DTXCID301745846(2E)-3-methoxy-5-(1H-pyrrol-2-yl)-2-((5-undecyl-1H-pyrrol-2-yl)methylidene)pyrrole2-(5-Undecyl-2-pyrrolylmethylene)-3-methoxy-5-(2-pyrrolyl)-2H-pyrrole
이름 더 보기
UndecylprodiginineUndecylprodigiosin, Apoptotic and anticancer agent2-[3-Methoxy-2-(5-undecyl-1H-pyrrol-2-ylmethylene)-2H-pyrrol-5-yl]-1H-pyrrole2-(5-Undecyl-1H-pyrrole-2-ylmethylene)-3-methoxy-5-(1H-pyrrole-2-yl)-2H-pyrrole2-[[3-Methoxy-5-(1H-pyrrol-2-yl)-2H-pyrrol-2-ylidene]methyl]-5-undecyl-1H-pyrrole
(2Z)-3-methoxy-5-(1H-pyrrol-2-yl)-2-[(5-undecyl-1H-pyrrol-2-yl)methylidene]pyrrole(2Z,5Z)-3-methoxy-5-pyrrol-2-ylidene-2-[(5-undecyl-1H-pyrrol-2-yl)methylidene]pyrroleundecylprodigininprodigiosin-25 cUNII-ZQ2HK5E6ZGorb17026902,2'-Bipyrrole, 4-methoxy-5-[(5-undecyl-2H-pyrrol-2-ylidene)methyl]-2,2'-Bi-1H-pyrrole, 4-methoxy-5-[(5-undecyl-2H-pyrrol-2-ylidene)methyl]-
물성
구조 계산 물성
- XLogP
- 7.2
- 극성 표면적
- 53.2 Ų
- 수소 결합 공여자 수
- 2
- 수소 결합 수용자 수
- 2
- 회전 가능 결합 수
- 13
- 무거운 원자 수
- 29
- 형식 전하
- 0
- 복잡도
- 581
화학 및 산업
약리 정보
MeSH Pharmacological Classification
Agents that suppress immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-CELLS or by inhibiting the activation of HELPER CELLS. While immunosuppression has been brought about in the past primarily to prevent rejection of transplanted organs, new applications involving mediation of the effects of INTERLEUKINS and other CYTOKINES are emerging.
Substances that inhibit the growth or reproduction of BACTERIA.
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