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Apigenin 7-glucoside

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Products Intro: Product Name:Apigenin-7-O-β-D-glucopyranoside
CAS:578-74-5
Purity:HPLC>98% Package:20mg,100mg,500mg,1g
Company Name: Shaanxi Cuikang Pharmaceutical Technology Co., Ltd
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Products Intro: Product Name:Apigenin 7-glucoside
CAS:578-74-5
Purity:98% Package:5KG;1KG;100g;10g;g
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Products Intro: Product Name:Apigenin-7-O-β-D-glucopyranoside
CAS:578-74-5
Purity:98% Package:20MG;100MG;1G;10G
Company Name: Shaanxi Haibo Biotechnology Co., Ltd
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Products Intro: Product Name:Apigenin 7-glucoside
CAS:578-74-5
Purity:99% Package:25kg Remarks:White Powder
Company Name: Shanghai Zheyan Biotech Co., Ltd.
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Products Intro: Product Name:Apigenin-7-O-β-D-glucopyranoside
CAS:578-74-5
Purity:HPLC>=98% Package:5mg

Apigenin 7-glucoside manufacturers

Apigenin 7-glucoside Basic information
Product Name:Apigenin 7-glucoside
Synonyms:4H-1-Benzopyran-4-one,7-(β-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl);Apigenin 7-glucoside SynonyMs:Apigetrin;Apigenin 7-b-D-glucoside;4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-;Apigenin 7-glucoside, >=98%;Apigetrin(Apigenin-7-O-glucoside);COSMIIN;7-O-BETA-D-GLUCOPYRANOSYLOXY-4',5-DIHYDROXYFLAVONE
CAS:578-74-5
MF:C21H20O10
MW:432.38
EINECS:209-430-5
Product Categories:chemical reagent;phytochemical;Tri-substituted Flavones;Pharmaceutical intermediate;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Flavones
Mol File:578-74-5.mol
Apigenin 7-glucoside Structure
Apigenin 7-glucoside Chemical Properties
Melting point 230-237°C
Boiling point 788.9±60.0 °C(Predicted)
density 1.642±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,2-8°C
solubility DMSO (Slightly, Sonicated), Methanol (Slightly)
pka6.13±0.40(Predicted)
form Solid
color Pale Yellow to Yellow
BRN 65669
Stability:Hygroscopic
Major Applicationfood and beverages
InChI1S/C21H20O10/c22-8-16-18(26)19(27)20(28)21(31-16)29-11-5-12(24)17-13(25)7-14(30-15(17)6-11)9-1-3-10(23)4-2-9/h1-7,16,18-24,26-28H,8H2/t16-,18-,19+,20-,21-/m1/s1
InChIKeyKMOUJOKENFFTPU-YUVSVTSJNA-N
SMILESC1(C2=CC=C(O)C=C2)OC2=C(C(=CC(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C2)O)C(=O)C=1 |&1:17,20,22,24,r|
LogP-0.040 (est)
CAS DataBase Reference578-74-5(CAS DataBase Reference)
Safety Information
Safety Statements 34/35
WGK Germany 3
3-10
HS Code 29389090
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
Apigenin 7-glucoside Usage And Synthesis
Chemical PropertiesWhite crystals, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from patchouli, agrimony, water chestnut, and paper mulberry leaves.
UsesApigenin 7-Glucoside is a by-product during the synthesis of Isorhoifolin (I819700), a naturally occurring flavonoid that was shown to exhibit potential antidiabetic, antihyperlipidemic and antioxidant effects.
ApplicationApigenin 7-glucoside is a flavonoid with anti-inflammatory and anxiolytic activities. It inhibits LPS-induced nitric oxide production in RAW 264.7 cells when used at concentrations ranging from 0.16 to 10 μM. In vivo, apigenin 7-glucoside (10 mg/kg) reduces pulmonary edema and lung inflammation in a mouse model of LPS-induced acute lung injury. It also increases the number of entries and the time spent in the open arms of the elevated plus maze in rats, indicating anxiolytic activity.
DefinitionChEBI: A glycosyloxyflavone that is apigenin substituted by a beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage.
Biological Functions Apigenin 7-glucoside inhibited HL-60 cell growth, dose- and time-dependently, but did not cause apoptosis. The distribution of cells at different stages in the cell cycle indicated an accumulation of treated cells in the G2/M phase. Moreover, apigenin 7-glucoside induced granulocytic differentiation of HL-60 cells[1].
Synthesis
4H-1-Benzopyran-4-one, 5-hydroxy-2-(4-hydroxyphenyl)-7-[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)oxy]-

119249-30-8

Apigenin 7-glucoside

578-74-5

Compound 1 (CAS: 119249-30-8, 150 mg, 0.25 mmol) was dissolved in a mixture of methanol (20 mL) and 30% ammonia (5 mL) under stirring conditions. The reaction mixture was stirred continuously for 12 hours at room temperature. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The resulting residue was purified by silica gel column chromatography using ethyl acetate/methanol (3:1, v/v) as eluent to afford the target product 5-hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-benzopyran-4-one , a yellow solid (78 mg, 72% yield). The melting point of the product was 234-236°C (literature value: 238-239°C). The infrared spectrum (KBr pressed sheet, cm^-1 ) showed characteristic absorption peaks: 3440, 2918, 1615, 1563, 1452, 1346, 1273, 1245, 1146, 1103, 1072, 1024, 895. the NMR hydrogen spectrum (400 MHz, DMSO-d6) δ: 12.97 (s, 1H, OH-5), 10.48 (s, 1H, OH-5), 10.47 (s, 1H). 10.48 (s, 1H, OH-4'), 7.96 (d, J = 8.8 Hz, 2H, H-2', H-6'), 6.94 (d, J = 8.8 Hz, 2H, H-3', H-5'), 6.87 (s, 1H, H-3), 6.83 (d, J = 1.6 Hz, 1H, H-8), 6.45 (d, J = 1.6 Hz, 1H, H-6), 6.45 (d, J = 1.6 Hz, 1H, H-8), 6.45 (d, J = 1.6 Hz, 1.6 Hz, 1.6 Hz), 6.85 (d, J = 1.6 Hz, 1.6 Hz, 1.6 Hz, 1.6 Hz, 1.6 Hz). 1H, H-6), 5.42 (d, J = 8.0 Hz, 1H, H-1), 5.15 (s, 1H, OH-2), 5.08 (s, 1H, OH-3), 5.06 (s, 1H, OH-4), 4.63 (s, 1H, OH-6), 3.72-3.70 (m, 1H, H-2), 3.49-3.18 (m, 5H H-3,4,5,6). NMR carbon spectrum (100 MHz, DMSO-d6) δ: 60.6, 69.6, 73.1, 76.5, 77.2, 94.8, 99.6, 99.9, 103.1, 105.4, 116.0, 121.1, 128.6, 156.9, 161.1, 161.4, 163.0, 164.3, 180.1. The calculated value of [M + Na]+ C21H20O10Na by high resolution mass spectrometry (HRMS) was 455.3665 and the measured value was 455.3649.

References[1] Eri Nakazaki. “Proteomic study of granulocytic differentiation induced by apigenin 7-glucoside in human promyelocytic leukemia HL-60 cells.” European Journal of Nutrition 52 1 (2013): 25–35.
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