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118160-59-1

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118160-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118160-59-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,1,6 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 118160-59:
(8*1)+(7*1)+(6*8)+(5*1)+(4*6)+(3*0)+(2*5)+(1*9)=111
111 % 10 = 1
So 118160-59-1 is a valid CAS Registry Number.
InChI:InChI=1/C39H44N2O6/c1-7-45-38-36(44-6)22-27-15-17-41(3)31-19-25-10-13-32(42-4)34(20-25)46-28-11-8-24(9-12-28)18-30-29-23-35(47-39(38)37(27)31)33(43-5)21-26(29)14-16-40(30)2/h8-13,20-23,30-31H,7,14-19H2,1-6H3/t30-,31-/m0/s1

118160-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Tjn 220

1.2 Other means of identification

Product number -
Other names 7-O-Ethylfangchinoline

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:118160-59-1 SDS

118160-59-1Downstream Products

118160-59-1Relevant articles and documents

Design, synthesis and biological activities of tetrandrine and fangchinoline derivatives as antitumer agents

Li, Dechao,Liu, Haizheng,Liu, Yufa,Zhang, Qikun,Liu, Chao,Zhao, Shuhua,Jiao, Bo

, p. 533 - 536 (2017)

The isolation and modification of natural products is always a very important resources to anti-tumor drugs. Therefore, a novel series of tetrandrine and fangchinoline derivatives were designed and synthesized, and their antiproliferative activities against HepG2, MCF-7 cells were evaluated and described. From the activity result obtained, high to very high activity in vitro has been found, one of the tested compounds (compound 5d) exhibited the most significant cytotoxic effects. Compound 5d increased 29.2, 7.37 times anti-proliferative activity for HepG2 cells and MCF-7 cells compared to sunitinib (IC50?=?16.06?μM and 25.41?μM). Finally flow cytometry determined that compound 5d could indeed inhibit the proliferation of HepG2 cells via inducing apoptosis.

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