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112652-46-7

112652-46-7

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112652-46-7 Usage

General Description

Fragransin A2 is a natural compound derived from the marine bacterium Microbulbifer sp. Its structure consists of a linear peptide composed of 14 amino acids containing several unusual modifications, making it an interesting molecule for potential pharmaceutical applications. Fragransin A2 has been found to exhibit potent antifungal and antibacterial properties, making it a promising candidate for the development of new antimicrobial agents. Additionally, it has shown potential for use in the agricultural industry as a biocontrol agent against plant-pathogenic fungi. Overall, Fragransin A2 presents a unique chemical structure and promising bioactivity that merits further exploration for potential therapeutic and agricultural applications.

Check Digit Verification of cas no

The CAS Registry Mumber 112652-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,5 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112652-46:
(8*1)+(7*1)+(6*2)+(5*6)+(4*5)+(3*2)+(2*4)+(1*6)=97
97 % 10 = 7
So 112652-46-7 is a valid CAS Registry Number.

112652-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-[(2R,3R,4R,5R)-3,4-Dimethyltetrahydrofuran-2,5-diyl]bis(2-me thoxyphenol)

1.2 Other means of identification

Product number -
Other names Nectandrin B

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:112652-46-7 SDS

112652-46-7Relevant articles and documents

Synthesis of all stereoisomers of 3,3′-dimethoxy-7,7′- epoxylignane-4,4′-diol and their plant growth inhibitory activity

Nishiwaki, Hisashi,Nakayama, Kumiko,Shuto, Yoshihiro,Yamauchi, Satoshi

, p. 651 - 659 (2014/02/14)

All stereoisomers of 3,3′-dimethoxy-7,7′-epoxylignane-4, 4′-diol were synthesized to examine the effect of stereochemistry on their plant growth inhibitory activity using lettuce and Italian ryegrass. The effect of structural modifications such as dehydro

Glycosides from the bark of Machilus robusta

Bu, Peng-Bin,Li, Yan-Ru,Jiang, Ming,Wang, Fang,Wang, Xiao-Liang,Lin, Sheng,Zhu, Cheng-Gen,Shi, Jian-Gong

, p. 482 - 491 (2013/09/02)

Six new glycosidic constituents (1-6), together with 10 known analogs, have been isolated from the bark of Machilus robusta. Structures of the new compounds, including the absolute configurations, were determined by spectroscopic and chemical methods as (

Analysis of HIF-1 inhibition by manassantin A and analogues with modified tetrahydrofuran configurations

Kasper, Amanda C.,Moon, Eui Jung,Hu, Xiangqian,Park, Yongho,Wooten, Ceshea M.,Kim, Hyoungsu,Yang, Weitao,Dewhirst, Mark W.,Hong, Jiyong

scheme or table, p. 3783 - 3786 (2010/03/01)

We have shown that manassantin A downregulated the HIF-1α expression and inhibited the secretion of VEGF. We have also demonstrated that the 2,3-cis-3,4-trans-4,5-cis-configuration of the tetrahydrofuran is critical to the HIF-1 inhibition of manassantin

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