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12-EPI-SCALARADIAL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72300-72-2

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72300-72-2 Usage

Origin

Derived from marine organisms

Family

Scalarane sesterterpenes

Chemical structure

Unique, featuring a 12-epi configuration

Biological activities

Exhibits anticancer, antifungal, and antibacterial properties

Additional effects

Anti-inflammatory

Potential applications

Pharmaceutical and biomedical

Research significance

Promising candidate for the development of new drugs to treat various diseases

Therapeutic uses

Diverse bioactive properties make it intriguing for further research and potential therapeutic applications

Check Digit Verification of cas no

The CAS Registry Mumber 72300-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,0 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72300-72:
(7*7)+(6*2)+(5*3)+(4*0)+(3*0)+(2*7)+(1*2)=92
92 % 10 = 2
So 72300-72-2 is a valid CAS Registry Number.

72300-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 12-epi-scalaradial

1.2 Other means of identification

Product number -
Other names 12-episcalaradial

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:72300-72-2 SDS

72300-72-2Downstream Products

72300-72-2Relevant academic research and scientific papers

Scalarane sesterterpenoids: Semisynthesis and biological activity

Kamel, Haidy N.,Kim, Young B.,Rimoldi, John M.,Fronczek, Frank R.,Ferreira, Daneel,Slattery, Marc

, p. 1492 - 1496 (2009)

Aiming to improve the potency and selectivity of scalarane sesterterpenoids, a series of natural and semisynthetic analogues, derived from the cytotoxic naturally abundant sesterterpene heteronemin (1), were evaluated for their in vitro antimicrobial and

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