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358721-33-2

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358721-33-2 Usage

Description

Apocynol A, a naturally occurring chemical compound, is derived from the roots of Apocynum venetum, a medicinal plant traditionally used in Chinese medicine. Recognized for its potential as an anti-cancer agent, it demonstrates the ability to inhibit the growth of various cancer cells, particularly in breast and lung cancer. Additionally, Apocynol A exhibits antioxidant and anti-inflammatory properties, positioning it as a promising candidate for the development of new drugs for cancer and other diseases. Ongoing research is focused on understanding its mechanisms of action and potential side effects.

Uses

Used in Pharmaceutical Industry:
Apocynol A is used as an anti-cancer agent for its ability to inhibit the growth of cancer cells in various types of cancer, such as breast and lung cancer. Its potential in this application is attributed to its direct effects on tumor growth and the modulation of oncological signaling pathways.
Used in Antioxidant and Anti-inflammatory Applications:
Apocynol A is used as a therapeutic agent for its antioxidant and anti-inflammatory properties, which may contribute to the treatment and management of various diseases and conditions where oxidative stress and inflammation play a significant role.
Used in Drug Development Research:
Apocynol A is used as a subject of research for the development of new drugs, given its potential in cancer treatment and other therapeutic areas. Ongoing studies aim to elucidate its mechanisms of action and assess its safety and efficacy for clinical use.

Check Digit Verification of cas no

The CAS Registry Mumber 358721-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,8,7,2 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 358721-33:
(8*3)+(7*5)+(6*8)+(5*7)+(4*2)+(3*1)+(2*3)+(1*3)=162
162 % 10 = 2
So 358721-33-2 is a valid CAS Registry Number.

358721-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(2E)-2-Buten-1-yl]-2-isopropyl-4-{[2'-(1H-tetrazol-5-yl)-4-bip henylyl]methyl}-2,4-dihydro-3H-1,2,4-triazol-3-one

1.2 Other means of identification

Product number -
Other names -

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:358721-33-2 SDS

358721-33-2Upstream product

358721-33-2Downstream Products

358721-33-2Relevant articles and documents

Glochidionionosides A-D: Megastigmane glucosides from leaves of Glochidion zeylanicum (Gaertn.) A. Juss

Otsuka, Hideaki,Kijima, Hidehiko,Hirata, Eiji,Shinzato, Takakazu,Takushi, Anki,Bando, Masahiko,Takeda, Yoshio

, p. 286 - 290 (2003)

Five megastigmane glucosides were isolated from the leaves of Glochidion zeylanicum. One of them was a known compound, blumenol C O-β-D- glucopyranoside (1), and the structures of the four new compounds, glochidionionosides A-D (2-5), were mainly elucidated by spectroscopic methods, including a modified Mosher's method. The absolute configurations of the six-membered ring of glochidionionoside D (5) were deduced by β-D-glucopyranosylation-induced shift trends in the 13C-NMR spectra and confirmed by X-ray analysis as its pbromobenzoate (5b), and the axis chirality of C-7 was determined to be R.

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