봉크렉산

봉크렉산
봉크렉산 구조식 이미지
카스 번호:
11076-19-0
한글명:
봉크렉산
동의어(한글):
봉크렉산
상품명:
BONGKREKIC ACID
동의어(영문):
edioicacid;bongkrekicaci;BONGKREKIC ACID;bongkrekic acid solution;Bongkrekic Acid (AS SOLUTION);(r-(r*,s*(e,z,z,e,e,z,e)))--trimethyl;Bongkrekic Acid Solution (1.0mg/mL in 0.01 M Tris buffer, pH 7.5);3-carboxymethyl-17-methoxy-6,18,21-trimethyldocosa-2,4,8,12,14,18,20-heptaen;2,4,8,10,14,18,20-docosaheptaenedioicacid,20-(carboxymethyl)-6-methoxy-2,5,17;(2E,4Z,6R,8Z,10E,14E,17S,18Z,20E)-20-Carboxymethyl-6-methoxy-2,5,17-trimethyldocosa-2,4,8,10,14,18,20-heptaenedioic acid
CBNumber:
CB4140241
분자식:
C28H38O7
포뮬러 무게:
486.6
MOL 파일:
11076-19-0.mol

봉크렉산 속성

녹는점
50-60°
알파
D25 +162.5°
끓는 점
715.1±60.0 °C(Predicted)
밀도
1.114±0.06 g/cm3(Predicted)
저장 조건
-20°C
용해도
DMSO(최대 100mg/ml) 또는 물(최대 1mg/ml)에 용해됩니다.
물리적 상태
동결건조된 고체
산도 계수 (pKa)
4.15±0.10(Predicted)
안정성
제공된 대로 구매일로부터 2년 동안 안정적입니다. DMSO 또는 증류수 용액은 -20°에서 최대 3개월 동안 보관할 수 있습니다.

안전

WGK 독일 -
유해 물질 데이터 11076-19-0(Hazardous Substances Data)
독성 LD50 i.v. in mice: 1.41 mg/kg (Lijmbach)

봉크렉산 C화학적 특성, 용도, 생산

용도

Bongkrekic acid solution has been used as an adenine nucleotide translocator (ANT) inhibitor to find out a different approach for the inhibition of oxidative phosphorylation in intact T98G cells. It has also been used as an inhibitor of the permeabilization transition pore complex (PTPC) pore and a tool to explore the role of PTPC in induction of apoptosis.

정의

ChEBI: A tricarboxylic acid that is docosa-2,4,8,10,14,18,20-heptaenedioic acid substituted at positions 2 ,5 and 17 by methyl groups, at positions 6 by a methoxy group and at position 20 by a carboxymethyl group.

효소 저해제

This toxic tricarboxylic acid (FWfree-acid = 486.61 g/mol; CAS 11076-19-0), produced Pseudomonas cocovenenans, is a potent competitive inhibitor of the mitochondrial ATP-ADP translocator, effectively blocking nucleotide binding to the carrier. The name is derived from bongkrek, a moldy coconut product produced in Indonesia. The toxin accumulates when P. cocovenenans outgrows the mold. Klingenberg et al. investigated bongkrekate binding to mitochondrial membrane to examine the reorienting site mechanism. The inferred mode of inhibition requires bongkrekate to bind to the single carrier site only from the inner face of the mitochondrial membrane (i.e., the matrix side)). They confirmed the pH-dependent accumulation of [3H]bongkrekate inside the mitochondria which superimposes onto the binding at carrier sites. By breaking the membrane with Lubrol or sonication, binding to the carrier sites could be titrated, and a Kd value of approximately 5 x 10–8 M was determined. The presence of ADP or ATP increases the amount of binding but does not alter the Kd. [35S]Atractylate is displaced by [3H]bongkrekate at a 1:1 molar ratio; this displacement is dependent on ADP concentration with the Km = 0.5 x 10–6 M. See also Atractyloside The isomer known as isobongkrekic acid, which has a cis-double bond at the dicarboxylic acid end of the molecule, has similar biological activity. Target(s): Adenine nucleotide translocator, ADP/ATP carrier; ATPase; bromelain, stem; papain; ficain, or ficin.

봉크렉산 준비 용품 및 원자재

원자재

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