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Kaempferol

Kaempferol Structure
CAS No.
520-18-3
Chemical Name:
Kaempferol
Synonyms
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';asurone
CBNumber:
CB5223176
Molecular Formula:
C15H10O6
Molecular Weight:
286.24
MOL File:
520-18-3.mol
MSDS File:
SDS
Modify Date:
2024/6/11 13:57:21

Kaempferol Properties

Melting point 276°C
Boiling point 348.61°C (rough estimate)
Density 1.2981 (rough estimate)
refractive index 1.4413 (estimate)
storage temp. 2-8°C
solubility ethanol: 20 mg/mL
pka 6.34±0.40(Predicted)
form powder
Colour Index 75640
color yellow
Merck 14,5274
BRN 304401
Stability Unstable in Solution
InChIKey IYRMWMYZSQPJKC-UHFFFAOYSA-N
LogP 2.685 (est)
CAS DataBase Reference 520-18-3(CAS DataBase Reference)
IARC 3 (Vol. 31, Sup 7) 1987

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P501
Hazard Codes  Xi,T
Risk Statements  36/37/38-68-25
Safety Statements  26-36-45-36/37-36/37/38-22
RIDADR  2811
WGK Germany  -
RTECS  LK9275200
8-10-23
HS Code  29329990
NFPA 704
0
2 0

Kaempferol price More Price(14)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) K0133 Kaempferol ≥90% (HPLC), powder 520-18-3 10MG ₹6743.98 2022-06-14 Buy
Sigma-Aldrich(India) K0133 Kaempferol ≥90% (HPLC), powder 520-18-3 50MG ₹22364.45 2022-06-14 Buy
Sigma-Aldrich(India) K0133 Kaempferol ≥90% (HPLC), powder 520-18-3 100MG ₹28329.03 2022-06-14 Buy
Sigma-Aldrich(India) PHR2705 Kaempferol Pharmaceutical Secondary Standard; Certified Reference Material, certified reference material, pharmaceutical secondary standard, pkg of 30?mg 520-18-3 30MG ₹34066.28 2022-06-14 Buy
Sigma-Aldrich(India) K0133 Kaempferol ≥90% (HPLC), powder 520-18-3 500MG ₹83255.08 2022-06-14 Buy
Product number Packaging Price Buy
K0133 10MG ₹6743.98 Buy
K0133 50MG ₹22364.45 Buy
K0133 100MG ₹28329.03 Buy
PHR2705 30MG ₹34066.28 Buy
K0133 500MG ₹83255.08 Buy

Kaempferol Chemical Properties,Uses,Production

Chemical Properties

Yellow Solid

Uses

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.

General Description

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.

Biological Activity

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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