캠페롤

캠페롤
캠페롤 구조식 이미지
카스 번호:
520-18-3
한글명:
캠페롤
동의어(한글):
캠페롤;캠퍼롤
상품명:
Kaempferol
동의어(영문):
ASARONE;kaempherol;kempferol;KAEMPFEROL 98%;3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4H-chroMen-4-one;campherol;pelargidenolon;Kaempferol Hydrate;3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one;3,4'
CBNumber:
CB5223176
분자식:
C15H10O6
포뮬러 무게:
286.24
MOL 파일:
520-18-3.mol
MSDS 파일:
SDS

캠페롤 속성

녹는점
276°C
끓는 점
348.61°C (rough estimate)
밀도
1.2981 (rough estimate)
굴절률
1.4413 (estimate)
저장 조건
2-8°C
용해도
에탄올: 20mg/mL
산도 계수 (pKa)
6.34±0.40(Predicted)
물리적 상태
가루
색상 색인 번호
75640
색상
노란색
Merck
14,5274
BRN
304401
안정성
솔루션이 불안정함
InChIKey
IYRMWMYZSQPJKC-UHFFFAOYSA-N
LogP
2.685 (est)
CAS 데이터베이스
520-18-3(CAS DataBase Reference)
IARC
3 (Vol. 31, Sup 7) 1987
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi,T
위험 카페고리 넘버 36/37/38-68-25
안전지침서 26-36-45-36/37-36/37/38-22
유엔번호(UN No.) 2811
WGK 독일 -
RTECS 번호 LK9275200
F 고인화성물질 8-10-23
HS 번호 29329990
유해 물질 데이터 520-18-3(Hazardous Substances Data)
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
예방조치문구:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
0
2 0

캠페롤 MSDS


3,4',5,7-Tetrahydroxyflavone

캠페롤 C화학적 특성, 용도, 생산

화학적 성질

Yellow Solid

용도

Kaempferol, is used as an inhibitor of Fatty Acid Synthase, Cox-1 activity, and Topo I. It also Induces caspase-9-mediated apoptosis in a variety of cancer cell lines via downregulation of polo-like kinase 1 (PLK1) expression. Exhibits antioxidant activity and attenuates osteoclastic bone reabsorption in vitro. Also blocks EGF-induced histone H3Ser10 phosphorylation in mouse epidermal JB6 C141 cells.

일반 설명

Kaempferol is a polyphenolic antioxidant abundantly present in vegetables and fruits. It has a diphenylpropane structure. In many plants, it is present as a glycosidic form namely, kaempferol-3-O-glucoside.

생물학적 활성

Naturally occurring flavonoid found in Gingko biloba and red wines that activates the mitochondrial Ca 2+ uniporter (EC 50 = 7 μ M). Induces caspase-9-mediated apoptosis in a variety of cancer cell lines via downregulation of polo-like kinase 1 (PLK1) expression. Exhibits antioxidant activity and attenuates osteoclastic bone reabsorption in vitro .

Anticancer Research

Kaempferol is one of the secondary metabolites found in some plants, plant-derivedfoods, and traditional medicines. It is a flavonoid compound obtained from someedible plants including grapes, tea, strawberries, broccoli, tomato, cabbage, leek,kale, endive, and beans. It inhibits growth and migration of pancreatic cancer cellsby acting on proto-oncogene tyrosine kinase (Src), ERK1/2, and AKT pathways(Singh et al. 2016a). It is being investigated in pancreatic and lung cancers toevaluate its antiangiogenic, anticancer, and radical scavenging activities. It showsmoderate cytostatic activity in PC3, HeLa, and K562 human cancer cells. It isidentified as aryl hydrocarbon receptor antagonist and acts against ABCG2 (ATP-bindingcassette subfamily G member 2)-mediated multidrug resistance bypreventing the ABCG2 upregulation in esophageal carcinoma. It induces theapoptosis of ovarian cancer cell by activating p53 in intrinsic pathway mechanism.It is an inhibitor of breast cancer resistance protein (BCRP), quinine reductase-2,and a substrate of BCRP (Calderon-Montano et al. 2011; Wang et al. 2012).

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