BioBioPha
China
Product Name: Galangin
Price: ￥Inquiry/50mg
Purity: 98.0%
Stocking Period: 1 Day
Contact: Xueping-Zheng

Shanghai Jizhi Biochemical Technology Co., Ltd
China
Product Name: Galangin
Price: ￥1698.0/100mg ￥468.0/25mg ￥588.0/20mg
Purity: 98.0%
Stocking Period: 1 Day
Contact: Liu jia

DC Chemicals Limited
China
Product Name: 3,5,7-Trihydroxyflavone
Price: $280.0/20mg
Purity: 98.0%
Stocking Period: 3 Day
Contact: Tony Cao

Henan Tianfu Chemical Co., Ltd.
China
Product Name: Galangin
Price: $Inquiry/1kg $Inquiry/25kg $Inquiry/1000kg $Inquiry/10ton
Purity: 99.0%
Stocking Period: Inquiry
Contact: Anson

548-83-4

548-83-4 structure

548-83-4 structure

Name: Galangin
Chemical Name: galangin
CAS Number: 548-83-4
Molecular Formula: C₁₅H₁₀O₅
Molecular Weight: 270.237
Catalog: Natural product Flavonoids
Create Date: 2018-06-16 18:25:37
Modify Date: 2024-01-02 11:28:10
Galangin is an agonist/antagonist of the arylhydrocarbon receptor, and also shows inhibition of CYP1A1 activity.

Name	galangin
Synonyms	EINECS 208-960-4 3,5,7-trihydroxyflavone Galangin teptochrysin Galengin 3,5,7-trihydroxy-2-phenyl-chromen-4-one 3,5,7-trihydroxy-flavon 3,5,7-Trihydroxy-2-phenyl-4H-chromen-4-one 3,5,7-Trihydroxy-Flavone galangine 5,7-dihydroxyflavonol 4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-phenyl- NORIZALPININ 3,5,7-trihydroxyfalvone MFCD00006833 3,5,7-Trihydroxy-2-phenyl-4H-1-benzopyran-4-one

Description	Galangin is an agonist/antagonist of the arylhydrocarbon receptor, and also shows inhibition of CYP1A1 activity.
Related Catalog	Signaling Pathways >> Autophagy >> Autophagy Signaling Pathways >> Metabolic Enzyme/Protease >> Cytochrome P450 Research Areas >> Cancer Natural Products >> Flavonoids
In Vitro	Galangin inhibits the catabolic breakdown of DMBA, as measured by thin-layer chromatography, in a dose-dependent manner. Galangin also inhibits the formation of DMBA-DNA adducts, and prevents DMBA-induced inhibition of cell growth. Galangin causes a potent, dose-dependent inhibition of CYP1A1 activity, as measured by ethoxyresorufin-O-deethylase activity, in intact cells and in microsomes isolated from DMBA-treated cells. Analysis of the inhibition kinetics by double-reciprocal plot demonstrates that galangin inhibits CYP1A1 activity in a noncompetitive manner. Galangin causes an increase in the level of CYP1A1 mRNA, indicating that it may be an agonist of the aryl hydrocarbon receptor, but it inhibits the induction of CYP1A1 mRNA by DMBA or by 2,3,5,7-tetrachlorodibenzo-p-dioxin (TCDD). Galangin also inhibits the DMBA- or TCDD-induced transcription of a reporter vector containing the CYP1A1 promoter[1]. Galangin treatment inhibits cell proliferation and induced autophagy (130 μM) and apoptosis (370 μM). In particular, galangin treatment in HepG2 cells causes (1) an accumulation of autophagosomes, (2) elevated levels of microtubule-associated protein light chain 3, and (3) an increased percentage of cells with vacuoles. p53 expression is also increased. The galangin-induced autophagy is attenuated by the inhibition of p53 in HepG2 cells, and overexpression of p53 in Hep3B cells restored the galangin-induced higher percentage of cells with vacuoles to normal level[2].
Cell Assay	Cells (5.0×103) are seeded and treated with different concentrations of galangin for different periods of time in 96-well plates. The number of viable cells in each well is determined by adding 10 µL of 5 mg/mL MTT solution. Following the 4 hour incubation at 37°C, the cells are dissolved in a 100 µL solution containing 20% SDS and 50% dimethy formamide. The optical densities are quantified at a test wavelength of 570 nm with a reference wavelength of 630 nm using a Varioskan Flash Reader spectrophotometer.
References	[1]. Ciolino HP, et al. The flavonoid galangin is an inhibitor of CYP1A1 activity and an agonist/antagonist of the aryl hydrocarbon receptor. Br J Cancer. 1999 Mar;79(9-10):1340-6. [2]. Wen M, et al. Galangin induces autophagy through upregulation of p53 in HepG2 cells. Pharmacology. 2012;89(5-6):247-55.

Density	1.6±0.1 g/cm3
Boiling Point	518.6±50.0 °C at 760 mmHg
Melting Point	214-215 °C(lit.)
Molecular Formula	C₁₅H₁₀O₅
Molecular Weight	270.237
Flash Point	202.0±23.6 °C
Exact Mass	270.052826
PSA	90.90000
LogP	2.83
Vapour Pressure	0.0±1.4 mmHg at 25°C
Index of Refraction	1.748

CHEMICAL IDENTIFICATION

RTECS NUMBER :: LK9275500

CHEMICAL NAME :: Flavone, 3,5,7-trihydroxy-

CAS REGISTRY NUMBER :: 548-83-4

BEILSTEIN REFERENCE NO. :: 0272179

LAST UPDATED :: 199803

DATA ITEMS CITED :: 8

MOLECULAR FORMULA :: C15-H10-O5

MOLECULAR WEIGHT :: 270.25

WISWESSER LINE NOTATION :: T66 BO EVJ CR& DQ GQ IQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD - Lethal dose

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: >1500 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

TYPE OF TEST :: Micronucleus test

TYPE OF TEST :: Micronucleus test

MUTATION DATA

TYPE OF TEST :: Mutation in mammalian somatic cells

TEST SYSTEM :: Rodent - hamster Ovary

DOSE/DURATION :: 20 mg/L

REFERENCE :: MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 113,45,1983

Symbol	GHS07
Signal Word	Warning
Hazard Statements	H315-H319-H335
Precautionary Statements	P261-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes	Xi:Irritant;
Risk Phrases	R36/37/38
Safety Phrases	S26-S37/39
RIDADR	NONH for all modes of transport
WGK Germany	3
RTECS	LK9275500
HS Code	2914400090

Precursor 8
26964-29-4 500-99-2 17874-42-9 82451-30-7
480-66-0 100-52-7 65982-77-6 93-97-0
DownStream 9
487-70-7 65-85-0 1707-75-1 83-30-7
480-14-8 70786-48-0 6665-74-3 42193-83-9
144-62-7

HS Code	2914400090
Summary	2914400090 other ketone-alcohols and ketone-aldehydes。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%