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rhapontigenin

rhapontigenin Structure
CAS No.
500-65-2
Chemical Name:
rhapontigenin
Synonyms
Protigenin;rhapontigenin;3-benzenediol;Rhapontigenin >rhapontigenin USP/EP/BP;-5-(3-Hydroxy-4-methoxystyryl);COc2ccc(/C=C/c1cc(O)cc(O)c1)cc2O;(E)-4'-Methoxy-3,3',5-stilbenetriol;3,3',5-Trihydroxy-4'-methoxy-trans-stilbene;5-[(1E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]-1
CBNumber:
CB01309681
Molecular Formula:
C15H14O4
Molecular Weight:
258.27
MOL File:
500-65-2.mol
MSDS File:
SDS
Modify Date:
2024/4/25 13:42:50
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rhapontigenin Properties

Melting point 189.0 to 193.0 °C
Boiling point 503.6±38.0 °C(Predicted)
Density 1.345±0.06 g/cm3(Predicted)
storage temp. 4°C, protect from light
solubility ≤30mg/ml in ethanol;30mg/ml in DMSO;30mg/ml in dimethyl formamide
form powder to crystal
pka 9.17±0.10(Predicted)
color White to Light yellow
CAS DataBase Reference 500-65-2

SAFETY

Risk and Safety Statements

HS Code  2914.50.3000

rhapontigenin price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) R0089 Rhapontigenin min. 98.0 % 500-65-2 100MG ₹15700 2022-05-26 Buy
Product number Packaging Price Buy
R0089 100MG ₹15700 Buy

rhapontigenin Chemical Properties,Uses,Production

Description

Rhapontigenin is a natural analog of resveratrol with antioxidant and anti-cancer activity. It is a mechanism-based, selective inactivator of cytochrome P450 1A1 (IC50 = 400 nM), an aryl hydrocarbon hydroxylase which activates polycyclic aromatic hydrocarbons that act as procarcinogens. At higher concentrations, rhapontigenin inhibits the proliferation of HepG2 and HL-60R cancer cell lines (IC50 = 48 μM).

Uses

Rhapontigenin is a natural analog of resveratrol with antioxidant and anti-cancer activity. It is a mechanism-based, selective inactivator of cytochrome P450 1A1 (IC50 = 400 nM), an aryl hydrocarbon hydroxylase which activates polycyclic aromatic hydrocarbons that act as procarcinogens. At higher concentrations, rhapontigenin inhibits the proliferation of HepG2 and HL-60R cancer cell lines (IC50 = 48 μM).[Cayman Chemical]

rhapontigenin Preparation Products And Raw materials

Raw materials

Preparation Products

rhapontigenin Suppliers

Global( 170)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
BINBO BIOLOGICAL CO.,LTD +8618629063126 China 346 58 Inquiry
Chengdu Greenpure Biopharma CO.,Ltd 18283602253; +8618283602253 China 953 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29899 58 Inquiry
Zhejiang ZETian Fine Chemicals Co. LTD +8618957127338 China 2136 58 Inquiry
Chengdu GLP biotechnology Co Ltd 028-87075086 13350802083 CHINA 1824 58 Inquiry
Chengdu Biopurify Phytochemicals Ltd. +8618080483897 China 3772 58 Inquiry
Chongqing Chemdad Co., Ltd +86-023-6139-8061 +86-86-13650506873 China 39916 58 Inquiry
Hubei Ipure Biology Co., Ltd +8613367258412 China 10326 58 Inquiry
Supplier Advantage
A.J Chemicals 58
TCI Chemicals (India) Pvt. Ltd. 58
BINBO BIOLOGICAL CO.,LTD 58
Chengdu Greenpure Biopharma CO.,Ltd 58
career henan chemical co 58
Zhejiang ZETian Fine Chemicals Co. LTD 58
Chengdu GLP biotechnology Co Ltd 58
Chengdu Biopurify Phytochemicals Ltd. 58
Chongqing Chemdad Co., Ltd 58
Hubei Ipure Biology Co., Ltd 58

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rhapontigenin (E)-5-[2-(3-Hydroxy-4-methoxyphenyl)ethenyl]-1,3-benzenediol 3,3',5-Trihydroxy-4'-methoxy-trans-stilbene trans-1-(3,5-Dihydroxyphenyl)-2-(3-hydroxy-4-methoxyphenyl)ethylene (E)-4'-Methoxy-3,3',5-stilbenetriol (E)-5-(3-Hydroxy-4-Methoxystyryl)benzene-1,3-diol -5-(3-Hydroxy-4-methoxystyryl) 3-benzenediol 5-[(1E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]-1 5-[(1E)-2-(3-HYDROXY-4-METHOXYPHENYL)ETHENYL]-1;3-BENZENEDIOL 5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]benzene-1,3-diol Rhapontigenin > Protigenin 1,3-Benzenediol,5-[(1E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]- 3,3',5-Trihydroxy-4'-methoxy-trans-stilbene trans-1-(3,5-Dihydroxyphenyl)-2-(3-hydroxy-4-methoxyphenyl)ethylene rhapontigenin USP/EP/BP COc2ccc(/C=C/c1cc(O)cc(O)c1)cc2O 500-65-2