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Daphnodorin B is a bioactive sesquiterpene lactone isolated from the marine sponge Daphnella sp. It possesses a unique chemical structure and exhibits potent anti-inflammatory properties. Daphnodorin B has demonstrated promising inhibitory activity against the production of pro-inflammatory cytokines and has been studied for its potential use in treating inflammatory diseases. Furthermore, Daphnodorin B has shown cytotoxicity against certain cancer cell lines, indicating its potential as an anticancer drug candidate. Its biological activities and potential therapeutic applications make Daphnodorin B a compound of significant interest.

95733-02-1

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  • [(2R,3S)-3,5-dihydroxy-2,8-bis(4-hydroxyphenyl)-3,4-dihydro-2H-furo[2,3-h]chromen-9-yl]-(2,4,6-trihydroxyphenyl)methanone

    Cas No: 95733-02-1

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95733-02-1 Usage

Uses

Used in Pharmaceutical Industry:
Daphnodorin B is used as an anti-inflammatory agent for its ability to inhibit the production of pro-inflammatory cytokines, making it a potential treatment for inflammatory diseases.
Used in Anticancer Drug Development:
Daphnodorin B is used as a cytotoxic agent against certain cancer cell lines, indicating its potential as a candidate for the development of anticancer drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 95733-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,3 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95733-02:
(7*9)+(6*5)+(5*7)+(4*3)+(3*3)+(2*0)+(1*2)=151
151 % 10 = 1
So 95733-02-1 is a valid CAS Registry Number.
InChI:InChI=1/C30H22O10/c31-15-5-1-13(2-6-15)28-22(37)11-18-19(34)12-23-25(30(18)40-28)26(29(39-23)14-3-7-16(32)8-4-14)27(38)24-20(35)9-17(33)10-21(24)36/h1-10,12,22,28,31-37H,11H2/t22-,28+/m0/s1

95733-02-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3S)-3,5-dihydroxy-2,8-bis(4-hydroxyphenyl)-3,4-dihydro-2H-furo[2,3-h]chromen-9-yl]-(2,4,6-trihydroxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names Daphnodorin B

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:95733-02-1 SDS

95733-02-1Relevant articles and documents

Three biflavonoids from daphne odora

Taniguchi, Masahiko,Baba, Kimiye

, p. 1447 - 1453 (1996)

Three new biflavonoids, daphnodorins G-I, were isolated from the roots of Daphne odora and their structures established from spectral and chemical means. These are two C-7/C-2'', C-8/C-3'' biflavonoids (upper half apigenin, lower half: afzelechin), daphno

Construction of 2-substituted-3-functionalized benzofurans via intramolecular heck coupling: Application to enantioselective total synthesis of daphnodorin B

Yuan, Hu,Bi, Kai-Jian,Li, Bo,Yue, Rong-Cai,Ye, Ji,Shen, Yun-Heng,Shan, Lei,Jin, Hui-Zi,Sun, Qing-Yan,Zhang, Wei-Dong

, p. 4742 - 4745 (2013/10/08)

A novel approach was developed for the synthesis of 2-substituted-3- functionalized benzofurans, using an intramolecular Heck reaction which was further applied in the first enantioselective total synthesis of Daphnodorin B.

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