에스쿨렌토사이드A

한글명:에스쿨렌토사이드A

카스 번호65497-07-6

상품명:Esculentoside A

CBNumberCB3983421

분자식C42H66O16

포뮬러 무게826.96

MOL 파일65497-07-6.mol

동의어(한글)

에스쿨렌토사이드A

화학적 성질

녹는점	>192°C (dec.)
끓는 점	936.7±65.0 °C(Predicted)
밀도	1.42±0.1 g/cm3(Predicted)
저장 조건	Hygroscopic, -20°C Freezer, Under inert atmosphere
용해도	DMSO(약간 용해됨), 메탄올(약간 용해됨)
산도 계수 (pKa)	4.39±0.70(Predicted)
물리적 상태	고체
물리적 상태	단단한 모양
색상	옅은 노랑
안정성	흡습성

위험 및 안전 성명

안전지침서	24/25
HS 번호	29389090

그림문자(GHS)

에스쿨렌토사이드A 화학적 특성, 용도, 생산

용도
Esculentoside A is a saponin isolated from the root of Phytolacca esculenta. Modulates the immune response. and effects cell proliferation and apoptosis in cells. Anti-inflammatory. 500
Pharmacokinetics
Esculentoside A is a triterpenoid saponin isolated from the root of Phytolacca esculenta. Studies have revealed that this triterpenoid exhibits a strong anti-inflammatory property. Ci et al. (2015) observed the anti-inflammatory potency of esculentoside A against allergic airway inflammation in a mouse model. They found that the drug enhanced nuclear Nrf-2 translocation in the lungs of ovalbumin-challenged mice and also decreased airway inflammation (Ci et al., 2015). Esculentoside A enhanced the intracellular anti-oxidant potentials, reduced Th2 cytokine level and down-regulated the expression of adhesion molecule mRNA in lung tissues. Zhang et al. (2014) found that esculentoside A could rectify carbon tetrachlorideinduced acute liver injury in mice. The drug successfully cured the histopathological damage induced by carbon tetrachloride. Rectification has been also noted through the down-regulation of inflammatory molecules and oxidative stresses associated with PPAR-γ, NF-κB and ERK signal pathways (Zhang et al., 2014). Ma et al. (2013) analyzed the role of esculentoside A on lupus nephritis-induced BXSB mice (where male SB/Le mice and female C57BL/6 mice were hybridized, creating a recombinant inbred species). They observed that esculentoside A application significantly reduced urine protein excretion and improved renal function by promoting apoptosis of glomerular intrinsic cells and renal tubular epithelial cells (Ma et al., 2013). The efficacy was also aided by the down-regulation of inflammatory cytokines.
Wang et al. (2016) elucidated the role of esculentoside A against acetaminophen-induced liver toxicity in mice and observed that Nrf2-regulated the survival mechanism via the AMPK/ Akt/GSK3β pathway.

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