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  • China
  • Product Name: Oroxin A
  • Price: ¥Inquiry/5mg
  • Purity: 98.0%
  • Stocking Period: 10 Day
  • Contact: Xueping-Zheng


57396-78-8

57396-78-8 structure
57396-78-8 structure
  • Name: Oroxin A
  • Chemical Name: 5,6-Dihydroxy-4-oxo-2-phenyl-4H-chromen-7-yl β-D-glucopyranoside
  • CAS Number: 57396-78-8
  • Molecular Formula: C21H20O10
  • Molecular Weight: 432.378
  • Catalog: Signaling Pathways Cell Cycle/DNA Damage PARP
  • Create Date: 2018-07-25 22:13:37
  • Modify Date: 2024-01-04 19:52:36
  • Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE), activates peroxisome proliferator-activated receptor γ (PPARγ) by docking into the PPARγ protein ligand-binding domain. Oroxin A exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2].

Name 5,6-Dihydroxy-4-oxo-2-phenyl-4H-chromen-7-yl β-D-glucopyranoside
Synonyms 5,6-dihydroxyflavone-7-glucoside
B-Aethyl-boracycloheptan
5,6-Dihydroxy-4-oxo-2-phenyl-4H-chromen-7-yl β-D-glucopyranoside
1-ethyl-borepane
4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-5,6-dihydroxy-2-phenyl-
baicalein-7-O-glucoside
Borepane,1-ethyl
Baicalein 7-b-D-glucopyranoside
Oroxin A
Description Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE), activates peroxisome proliferator-activated receptor γ (PPARγ) by docking into the PPARγ protein ligand-binding domain. Oroxin A exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2].
Related Catalog
In Vitro Oroxin A (0.5- 100 μM; 24 hours) significantly increases the PPARγ transcription level and exhibits the strongest activation with 50 μM in HEK-293t cells[1].
References

[1]. Sun W, et al. Oroxin A from Oroxylum indicum prevents the progression from prediabetes to diabetes in streptozotocin and high-fat diet induced mice. Phytomedicine. 2018 Jan 1;38:24-34.

[2]. He J, et al. Oroxin A inhibits breast cancer cell growth by inducing robust endoplasmic reticulum stress and senescence. Anticancer Drugs. 2016 Mar;27(3):204-15.

Density 1.6±0.1 g/cm3
Boiling Point 784.0±60.0 °C at 760 mmHg
Molecular Formula C21H20O10
Molecular Weight 432.378
Flash Point 279.0±26.4 °C
Exact Mass 432.105652
PSA 170.05000
LogP 0.47
Vapour Pressure 0.0±2.9 mmHg at 25°C
Index of Refraction 1.717
Storage condition -20℃
Hazard Codes N

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57396-78-8 structure

57396-78-8

Literature: Mezey-Vandor, Gabriella; Farkas, Lorand; Kanzel, Ida; Nogradi, Mihaly Chemische Berichte, 1980 , vol. 113, # 5 p. 1945 - 1949

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57396-78-8 structure

57396-78-8

Literature: Mezey-Vandor, Gabriella; Farkas, Lorand; Kanzel, Ida; Nogradi, Mihaly Chemische Berichte, 1980 , vol. 113, # 5 p. 1945 - 1949

~%

57396-78-8 structure

57396-78-8

Literature: Mezey-Vandor, Gabriella; Farkas, Lorand; Kanzel, Ida; Nogradi, Mihaly Chemische Berichte, 1980 , vol. 113, # 5 p. 1945 - 1949

~%

57396-78-8 structure

57396-78-8

Literature: Mezey-Vandor, Gabriella; Farkas, Lorand; Kanzel, Ida; Nogradi, Mihaly Chemische Berichte, 1980 , vol. 113, # 5 p. 1945 - 1949

~%

57396-78-8 structure

57396-78-8

Literature: Mezey-Vandor, Gabriella; Farkas, Lorand; Kanzel, Ida; Nogradi, Mihaly Chemische Berichte, 1980 , vol. 113, # 5 p. 1945 - 1949