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15404-76-9

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15404-76-9 Usage

General Description

Fuscaxanthone C is a natural chemical compound found in the fungus Phomopsis sp. It belongs to the xanthone class of compounds and is characterized by its yellow coloration. Fuscaxanthone C has been studied for its potential pharmacological properties, including its antioxidant, anti-inflammatory, and cytotoxic activities. Research has shown that fuscaxanthone C may have potential as a therapeutic agent for the treatment of various diseases, such as cancer and inflammation. Fuscaxanthone C is of interest to scientists and researchers for its unique chemical structure and potential medicinal properties.

Check Digit Verification of cas no

The CAS Registry Mumber 15404-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15404-76:
(7*1)+(6*5)+(5*4)+(4*0)+(3*4)+(2*7)+(1*6)=89
89 % 10 = 9
So 15404-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C26H30O6/c1-14(2)8-10-16-18(29-5)12-20-23(24(16)27)25(28)22-17(11-9-15(3)4)26(31-7)21(30-6)13-19(22)32-20/h8-9,12-13,27H,10-11H2,1-7H3

15404-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-3,6,7-trimethoxy-2,8-bis(3-methylbut-2-enyl)xanthen-9-one

1.2 Other means of identification

Product number -
Other names 3,6-Dimethylmangostin

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:15404-76-9 SDS

15404-76-9Relevant articles and documents

Yates,Bhat

, p. 3770 (1968)

Acetyl- and O-alkyl- derivatives of β-mangostin from Garcinia mangostana and their anti-inflammatory activities

Karunakaran, Thiruventhan,Ee, Gwendoline Cheng Lian,Ismail, Intan Safinar,Mohd Nor, Siti Mariam,Zamakshshari, Nor Hisam

, p. 1 - 5 (2017)

Pure β-mangostin (1) was isolated from the stem bark of Garcinia mangostana L. One monoacetate (2) and five O-alkylated β-mangostin derivatives (3–7) were synthesised from β-mangostin. The structures of these compounds were elucidated and determined using spectroscopic techniques such as 1D NMR and MS. The cytotoxicities and anti-inflammatory activities of these five compounds against RAW cell 264.7 were tested. The structural-activity relationship studies indicated that β-mangostin showed a significant activity against the LPS-induced RAW cell 264.7, while the acetyl- as well as the O-alkyl- β-mangostin derivatives did not give good activity. Naturally occurring β-mangostin demonstrated comparatively better anti-inflammatory activity than its synthetic counterparts.

Design, synthesis and structure-activity relationships of mangostin analogs as cytotoxic agents

Chi, Xiao-Qian,Zi, Cheng-Ting,Li, Hong-Mei,Yang, Liu,Lv, Yong-Feng,Li, Jin-Yu,Hou, Bo,Ren, Fu-Cai,Hu, Jiang-Miao,Zhou, Jun

, p. 41377 - 41388 (2019/01/03)

In order to better understand the structure-activity relationship of mangostin, a series of xanthone derivatives based on α-mangostin were designed and synthesized. All the compounds were evaluated for their cytotoxicity against a panel of five human canc

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