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10172-02-8

(-)-Limacine is a chemical compound that belongs to the class of alkaloids and is found in certain species of plants. It is known for its potent antifungal and antibacterial properties, making it a potentially valuable compound for use in pharmaceutical and agricultural applications. Studies have shown that (-)-Limacine has activity against a variety of fungal and bacterial pathogens, including those that are resistant to traditional antibiotics. Additionally, it has also been investigated for its potential as an anti-cancer agent, as it has been shown to inhibit the growth of cancer cells in laboratory studies. Overall, the unique chemical properties and potential therapeutic uses of (-)-Limacine make it an intriguing and promising compound for further research and development.

10172-02-8

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10172-02-8 Usage

Uses

Used in Pharmaceutical Applications:
(-)-Limacine is used as an antifungal and antibacterial agent for its potent activity against a variety of fungal and bacterial pathogens, including those resistant to traditional antibiotics.
Used in Agricultural Applications:
(-)-Limacine is used as a biopesticide for its ability to combat fungal and bacterial infections in crops, potentially reducing the need for chemical pesticides.
Used in Anticancer Applications:
(-)-Limacine is used as a potential anti-cancer agent for its demonstrated ability to inhibit the growth of cancer cells in laboratory studies, warranting further research into its therapeutic potential in oncology.

Check Digit Verification of cas no

The CAS Registry Mumber 10172-02-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,7 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10172-02:
(7*1)+(6*0)+(5*1)+(4*7)+(3*2)+(2*0)+(1*2)=48
48 % 10 = 8
So 10172-02-8 is a valid CAS Registry Number.

10172-02-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name AC1MJ1UI

1.2 Other means of identification

Product number -
Other names (S,S)-(+)-tetrandine

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:10172-02-8 SDS

10172-02-8Relevant articles and documents

Design, synthesis and in vitro anticancer research of novel tetrandrine and fangchinoline derivatives

Gao, Xiu-zheng,Lv, Xu-tao,Zhang, Rui-rui,Luo, Yang,Wang, Mu-xuan,Chen, Jia-shu,Zhang, Yu-kai,Sun, Bin,Sun, Jin-yue,Liu, Yu-fa,Liu, Chao

, (2021)

Cancer treatment is one of the major public health issues in the world. Tetrandrine (Tet) and fangchinoline (d-Tet) are two bis-benzyl isoquinoline alkaloids extracted from Stephania tetrandra S. Moore, and their antitumor activities have been confirmed.

Bioactive bisbenzylisoquinoline alkaloids from the roots of Stephania tetrandra

Li, Jiayuan,Li, Li,Li, Xuyu,Liu, Yanfei,Shi, Guoru,Wang, Renzhong,Yu, Dequan,Yuan, Jiqiao,Zhou, Jie

, (2020/03/17)

Ten new bisbenzylisoquinoline alkaloids (1–10) and eight known analogues (11–18) were obtained from the roots of Stephania tetrandra. The structures of these compounds were determined by spectroscopic methods, single-crystal X-ray diffraction, electronic

REGIOSELECTIVE O-DEMETHYLATION OF BISBENZYLISOQUINOLINE ALKALOIDS

Kunitomo, Jun-ichi,Oshikata, Megumi,Akasu, Michinori,Ishii, Hisashi

, p. 937 - 942 (2007/10/02)

The cleavage of methyl ethers of several bisbenzylisoquinoline alkaloids was studied and regioselective O-demethylation was observed.

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