CAS 632-85-9|Wogonin

Introduction：Basic information about CAS 632-85-9|Wogonin, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Wogonin BiologicalActivity
3. Chemical & Physical Properties
4. Toxicological Information
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
MUTATION DATA
5. Safety Information
6. Synonyms

Common Name	Wogonin
CAS Number	632-85-9	Molecular Weight	284.263
Density	1.4±0.1 g/cm3	Boiling Point	518.8±50.0 °C at 760 mmHg
Molecular Formula	C₁₆H₁₂O₅	Melting Point	203-206°C
MSDS	USA	Flash Point	198.4±23.6 °C

Names

Name	wogonin
Synonym	More Synonyms

Wogonin BiologicalActivity

Description	Wogonin is a naturally occurring mono-flavonoid, can inhibit the activity of CDK8 and Wnt, and exhibits anti-inflammatory and anti-tumor effects.
Related Catalog	Signaling Pathways >>Autophagy >>AutophagySignaling Pathways >>Stem Cell/Wnt >>WntResearch Areas >>Inflammation/ImmunologyResearch Areas >>CancerNatural Products >>Flavonoids
Target	CDK8 Wnt
In Vitro	Wogonin (0-200 μM) exhibits a dose- and time- dependent reduces in cell viability of caco-2, SW1116 and HCT116 cells. Wogonin (10-40 μM) induces G1 phase arrest in HCT-116 cells. Wogonin also supresses Wnt signaling pathway in HCT116 cells. Wogonin interfers in the activity of transcription factor TCF/Lef family. Moreover, Wogonin inhibits β-catenin-mediated transcription through suppressing the activity of CDK8[1]. Wogonin shows cytotoxic and antiproliferative effects on HeLa cells. Wogonin (90 µM) induces cell cycle arrest at G0-G1 phase, and suppresses the levels of cyclin D1 and Cdk4 markedly in HeLa cells[2]. Wogonin (1.25, 2.5, 5, 10, 20 μg/ml) suppresses EtOH-induced inflammatory response in RAW264.7 cells[3].
In Vivo	Wogonin (30, 60 mg/kg) reduces tumor growth of HCT116 cells in a xenograft model[1]. Wogonin (25, 50, 100 mg/kg) protects against liver injury and pathological characteristics of ALD in mice. Wogonin activates PPAR-γ expression in mice with ALD and EtOH induced RAW264.7 cells[3].
Cell Assay	HCT116 cells are planted on a 96-well plate (1 × 105 cells per well). Different concentrations of wogonin are added and incubated for 24 h. Subsequently, 20 μL of MTT solution (5 mg/mL) is transferred to each well and the plates are incubated for 4 h at 37°C and 5% CO2. The supernatant is aspirated off and 100 μL DMSO is added to dissolve the formazan crystal. The mixture is shaken and measured at 570 nm using a universal microplate reader.
Animal Admin	C57BL/6 mice, male, 6-8 weeks old, weighing 18-22 g mice are housed at comfortable environment and are acclimatized for 3 days before the experiment. A total of 48 mice are randomLy divided into six groups of 8 animals, respectively control diet (CD)-fed mice, EtOH-fed mice, wogonin-treated mice at the dose of 25, 50, 100 mg/kg/day and the positive (dexamethasone, 1 mg/kg/day)-treated mice. Modeling process has a total of 16 days including a liquid diet adaptation period for 3 days and modeling for 13 days. The EtOH-fed mice are fed containing 5% v/v ethanol liquid diets adding certain vitamin and choline for 16 days, and mice are gavaged with a single binge ethanol administration (5 g/kg, body weight, 20% ethanol) at last day. At the same time, the wogonin-treated mice and the positive-treated mice are not only plus the ethanol administration, but also plus the medicines by gavage daily, whereas the CD-fed mice are fed with control liquid diets and gavaged with isocaloric maltose-dextrin at last day. All diets are prepared fresh daily. 9 h after the last gavage alcohol, mice are sacrificed under anaesthesia, the liver tissues and blood are collected for further analysis.
References	[1]. He L, et al. Wogonin induced G1 cell cycle arrest by regulating Wnt/β-catenin signaling pathway and inactivating CDK8 in human colorectal cancer carcinoma cells. Toxicology. 2013 Oct 4;312:36-47. [2]. Yang L, et al. Wogonin induces G1 phase arrest through inhibiting Cdk4 and cyclin D1 concomitant with an elevation in p21Cip1 in human cervical carcinoma HeLa cells. Biochem Cell Biol. 2009 Dec;87(6):933-42. [3]. Li HD, et al. Wogonin attenuates inflammation by activating PPAR-γ in alcoholic liver disease. Int Immunopharmacol. 2017 Sep;50:95-106.

Chemical & Physical Properties

Density	1.4±0.1 g/cm3
Boiling Point	518.8±50.0 °C at 760 mmHg
Melting Point	203-206°C
Molecular Formula	C₁₆H₁₂O₅
Molecular Weight	284.263
Flash Point	198.4±23.6 °C
Exact Mass	284.068481
PSA	79.90000
LogP	2.14
Vapour Pressure	0.0±1.4 mmHg at 25°C
Index of Refraction	1.669
InChIKey	XLTFNNCXVBYBSX-UHFFFAOYSA-N
SMILES	COc1c(O)cc(O)c2c(=O)cc(-c3ccccc3)oc12
Storage condition	2-8°C

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :: LK8331000

CHEMICAL NAME :: Flavone, 5,7-dihydroxy-8-methoxy-

CAS REGISTRY NUMBER :: 632-85-9

BEILSTEIN REFERENCE NO. :: 0287152

LAST UPDATED :: 199612

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: C16-H12-O5

MOLECULAR WEIGHT :: 284.28

WISWESSER LINE NOTATION :: T66 BO EVJ CR& GQ IQ JO1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :: Mutation in microorganisms

TEST SYSTEM :: Bacteria - Salmonella typhimurium

DOSE/DURATION :: 20 nmol/plate

REFERENCE :: MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 135,77,1984

Safety Information

Hazard Codes	Xn
Risk Phrases	R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . R36/37/38:Irritating to eyes, respiratory system and skin .
Safety Phrases	S26-S36/37/39-S45
RIDADR	3145
RTECS	SJ8922500
Packaging Group	III
Hazard Class	8

Synonyms

Norwogonin 8-methyl ether

5,7-DIHYDROXY-8-METHOXYFLAVON

5,7-Dihydroxy-8-methoxy-2-phenyl-chromen-4-on

Wogonin

5,7-Dihydroxy-8-methoxy-2-phenyl-4H-chromen-4-one

5,7-dihydroxy-8-methoxy-2-phenyl-chromen-4-one

4H-1-Benzopyran-4-one, 5,7-dihydroxy-8-methoxy-2-phenyl-

MFCD00017736

5,7-dihydroxy-8-methoxyflavone

vogonin

WOOGONIN

WILDYAMP.E

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