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136684-40-7

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136684-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136684-40-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,6,8 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 136684-40:
(8*1)+(7*3)+(6*6)+(5*6)+(4*8)+(3*4)+(2*4)+(1*0)=147
147 % 10 = 7
So 136684-40-7 is a valid CAS Registry Number.

136684-40-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 23-hydroxybetulonic acid

1.2 Other means of identification

Product number -
Other names benzyl 3-oxo-23-hydroxy-lup-20(29)-en-28-oic acid

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:136684-40-7 SDS

136684-40-7Upstream product

136684-40-7Downstream Products

136684-40-7Relevant articles and documents

Synthesis and antitumor activity of novel 3-oxo-23-hydroxybetulinic acid derivatives

Zhang, Hengyuan,Zhu, Peiqing,Liu, Jie,Yang, Xue,Xu, Shengtao,Yao, Hequan,Jiang, Jieyun,Ye, Wencai,Wu, Xiaoming,Xu, Jinyi

, p. 159 - 167 (2014)

A series of novel derivatives of 3-oxo-23-hydroxybetulinic acid was designed, synthesized, and evaluated for their antiproliferative activity against a panel of cancer cell lines (HL-60, BEL-7402, SF-763, HeLa, B16 and A375). The results indicated that majority of the derivatives exhibited more significant antitumor activity than the parent compound. In particular compound 10e showed the most potent activity with IC50values of 5.85, 6.23 and 7.22 μM against B16, SF-763 and BEL-7402 cells, respectively. Furthermore, 10e inhibited tumor growth by 51.8% and 62.7% (w/w) in H22 and B16 xenograft mouse models, comparable to cyclophosphamide and 5-fluorouracil, respectively.

NMDA AND MC RECEPTOR ANTAGONISTS EXHIBITING NEUROPROTECTIVE AND MEMORY ENHANCING ACTIVITIES

-

, (2009/01/20)

The present invention provides therapeutically active compounds and compositions as NMDA and MC receptor antagonists, which are useful in preventing and treating central nervous system disorders by inhibiting over-activation of NMDA and/or MC receptors. In one aspect, the present invention provides methods of treating and/or preventing neurodegenerative diseases and neuropathological disorders, methods of providing neuroprotection under stress conditions such as a stroke, methods of enhancing the brain's cognitive functions and methods of treating depression, anxiety and cachexia induced by a chronic disease in mammals and humans.

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