Welcome to LookChem.com Sign In|Join Free
  • or
7,2',4',5'-Tetramethoxyflavone is a naturally occurring flavonoid compound characterized by the presence of four methoxy groups at the 7, 2', 4', and 5' positions on its molecular structure. Flavonoids are a class of polyphenolic compounds found in plants, known for their antioxidant properties and potential health benefits. This specific flavone is derived from various plant sources, such as the bark of the Artocarpus altilis tree, and has been studied for its potential anti-inflammatory, anti-cancer, and anti-viral activities. The chemical structure of 7,2',4',5'-tetramethoxyflavone consists of a flavone backbone with two phenyl rings and a heterocyclic ring, which contributes to its diverse biological activities and potential applications in pharmaceutical and nutraceutical industries.

4253-02-5

Post Buying Request

4253-02-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

4253-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4253-02-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,5 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4253-02:
(6*4)+(5*2)+(4*5)+(3*3)+(2*0)+(1*2)=65
65 % 10 = 5
So 4253-02-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H18O6/c1-21-11-5-6-12-16(7-11)25-10-14(19(12)20)13-8-17(23-3)18(24-4)9-15(13)22-2/h5-10H,1-4H3

4253-02-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methoxy-3-(2,4,5-trimethoxyphenyl)chromen-4-one

1.2 Other means of identification

Product number -
Other names 7,2',4',5'-tetramethoxyisoflavone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4253-02-5 SDS

4253-02-5Downstream Products

4253-02-5Relevant academic research and scientific papers

Synthesis, structure-activity relationships and biological evaluation of barbigerone analogues as anti-proliferative and anti-angiogenesis agents

Wang, Guangcheng,Wang, Fang,Cao, Dong,Liu, Yibin,Zhang, Ronghong,Ye, Haoyu,Li, Xiuxia,He, Lin,Yang, Zhuang,Ma, Liang,Peng, Aihua,Xiang, Mingli,Wei, Yuquan,Chen, Lijuan

, p. 3158 - 3163 (2014/06/24)

A series of barbigerone analogues (7a-7w, 13a-13x) were designed, synthesized and biologically evaluated for their anti-proliferative and anti-angiogenic activities. Among these compounds, compound 13a exhibited the most potent inhibitory effect on the proliferation of HUVECs, HepG2, A375, U251, B16, and HCT116 cells (IC50 = 3.80, 0.28, 1.58, 3.50, 1.09 and 0.68 μM, respectively). Compound 13a inhibited the angiogenesis in zebrafish embryo assay in a concentration-dependent manner. Furthermore, 13a also effectively inhibited the migration and capillary like tube formation of human umbilical vein endothelial cell in vitro. These results support the further investigation of this class of compounds as potential anti-proliferative and anti-angiogenesis agents.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 4253-02-5