Product classification

28608-75-5

Product Name：4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-8-b-D-glucopyranosyl-5,7-dihydroxy-
Molecular Formula：C₂₁H₂₀O₁₁
Purity：99%
Molecular Weight：

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Product Details;

CasNo： 28608-75-5

Molecular Formula： C₂₁H₂₀O₁₁

Appearance： yellow powder

Henan Wentao Chemical Product Co., Ltd. is a quality supplier and manufacturer of Plant Extract ORIENTIN 28608-75-5 In Medicine . You can buy high quality, low price ORIENTIN 28608-75-5 here. Contact us.

ORIENTIN 28608-75-5 Supplier

Molecular Formula:C₂₁H₂₀O₁₁
Molecular Weight:448.383
Appearance/Colour:yellow powder
Vapor Pressure:3.63E-28mmHg at 25°C
Melting Point:260-285 °C
Refractive Index:1.767
Boiling Point:816.1 °C at 760 mmHg
PKA:6.24±0.40(Predicted)
Flash Point:289.1 °C
PSA：201.28000
Density:1.759 g/cm³
LogP:-0.20270

Plant Extract ORIENTIN 28608-75-5 In Medicine Usage

Orientin, a C-glycosyl flavonoid, is known to have anxiolytic and antioxidative activity, while it's Molecular Formula is C21H20O11. One of the bioactive compounds isolable from medicinal plants, orientin, is often used in various bioactivity studies due to its extensive beneficial properties. Orientin has been isolated from various medicinal plants such as Ocimum sanctum, Phyllostachys species (bamboo leaves), Passiflora species (passion flowers), Trollius species (Golden Queen), and Jatropha gossypifolia (Bellyache Bush).

InChI:InChI=1/C21H20O11/c22-6-14-17(28)18(29)19(30)21(32-14)16-11(26)4-10(25)15-12(27)5-13(31-20(15)16)7-1-2-8(23)9(24)3-7/h1-5,14,17-19,21-26,28-30H,6H2/t14-,17-,18+,19-,21+/m1/s1

28608-75-5 Relevant articles

Orientin Inhibits High Glucose-Induced Vascular Inflammation In Vitro and In Vivo

SK Ku, S Kwak, JS Bae

Inflammation, 2014

In this study, we assessed whether orientin can suppress vascular inflammation induced by high glucose (HG) in human umbilical vein endothelial cells (HUVECs) and mice.

Orientin Attenuated d-GalN/LPS-Induced Liver Injury through the Inhibition of Oxidative Stress via Nrf2/Keap1 Pathway

Fuhua Li, Xia Liao, Ling Jiang, Jichun Zhao, Surui Wu, and Jian Ming*

J. Agric. Food Chem. 2022, 70, 26, 7953–7967

Orientin, a flavonoid component with antioxidant capacity, has been regarded as a promising nutraceutical for patients with liver damage. This study aimed to investigate the amelioration effect of orientin on d-galactosamine and lipopolysaccharides (d-GalN/LPS) induced liver injury in mice, with a focus on its underlying mechanisms by using the H2O2-induced oxidative damage model of HepG2 cells.

Orientin inhibits inflammation in chondrocytes and attenuates osteoarthritis through Nrf2/NF‐κB and SIRT6/NF‐κB pathway

Weiyi Xia, Jian Xiao, ChengLin Tong, Jiajie Lu, Yurong Tu, Sunlong Li, Libing Ni, Yifeng Shi, Peng Luo, Xiaolei Zhang, Xiangyang Wang

Journal of Orthopaedic Research, 25 April 2023

The natural flavonoid compound (Orientin) has anti-inflammatory bioactive properties in the treatment of various diseases. But studies have not explored whether Orientin modulates OA progression.

28608-75-5 Process route

: C₁₅H₁₂O₇

: UDP-glucose

: 4261-42-1
isoorientin

: 7480-94-6,28608-75-5
Luteolin-8-C-glucoside

Conditions

Conditions	Yield
With recombinant Oryza sativa C-glycosyltransferase; In ethanol; at 30 ℃; pH=7.5; Enzymatic reaction;	56% 43%

: 381686-07-3
2-(3,4-bis-benzyloxyphenyl)-7-benzyloxy-8-C-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-5-hydroxy-4H-1-benzopyran-4-one

: 7480-94-6,28608-75-5
Luteolin-8-C-glucoside