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Rhuscholide A, a natural product belonging to the tetracyclic triterpenoids group, is isolated from the leaves of Toxicodendron succedaneum (syn. Rhus succedanea). It exhibits a range of biological activities, such as anti-inflammatory, anti-tumor, and anti-viral properties, making it a promising candidate for pharmaceutical research and development.

944804-58-4

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944804-58-4 Usage

Uses

Used in Pharmaceutical Industry:
Rhuscholide A is used as a therapeutic agent for the treatment of inflammatory diseases and cancer due to its anti-inflammatory, anti-tumor, and anti-viral properties. Its mechanism of action involves modulation of various signaling pathways and inhibition of key cellular processes, which contribute to its potential as a promising pharmaceutical compound.
Used in Drug Development:
Rhuscholide A is used as a candidate for further research and development in the pharmaceutical field. Its diverse biological activities and potential as a therapeutic agent make it a valuable asset for the discovery of new drugs and treatment options for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 944804-58-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,8,0 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 944804-58:
(8*9)+(7*4)+(6*4)+(5*8)+(4*0)+(3*4)+(2*5)+(1*8)=194
194 % 10 = 4
So 944804-58-4 is a valid CAS Registry Number.

944804-58-4SDS

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 Rhuscholide A

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:944804-58-4 SDS

944804-58-4Downstream Products

944804-58-4Relevant academic research and scientific papers

First total synthesis of rhuscholide A, glabralide B and denudalide

Li, Tian-Ze,Geng, Chang-An,Chen, Ji-Jun

, (2019)

The first total synthesis of rhuscholide A, a benzofuran lactone possessing anti-HIV-1 activity, had been accomplished in 14 linear steps with 10.6% overall yield. In this synthesis, base-mediated phenol ortho-alkylation and piperidine promoted aldol condensation were exploited as key steps. The synthesis was flexible and allowed for the convenient preparation of two analogous natural products glabralide B and denudalide.

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