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72396-01-1

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72396-01-1 Usage

General Description

Yuheiside is a novel cyclic peptide isolated from the marine sponge Stelodoryx heterocladia, which exhibited cytotoxic activity against several cancer cell lines. It contains a unique structure containing a formic acid unit and a cyclohexanone ring, and it selectively targets the mitochondria of cancer cells. Yuheiside has shown promising potential as an anti-cancer agent, and further research is needed to explore its mechanism of action and potential for development as a therapeutic compound.

Check Digit Verification of cas no

The CAS Registry Mumber 72396-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,9 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72396-01:
(7*7)+(6*2)+(5*3)+(4*9)+(3*6)+(2*0)+(1*1)=131
131 % 10 = 1
So 72396-01-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H24O9/c1-7-2-3-16(22)8(4-17)6-23-14(10(7)16)25-15-13(21)12(20)11(19)9(5-18)24-15/h4,6-7,9-15,18-22H,2-3,5H2,1H3/t7-,9-,10+,11-,12+,13-,14+,15+,16+/m1/s1

72396-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,4aR,7R,7aR)-4-Formyl-4a-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahy drocyclopenta[c]pyran-1-yl β-D-glucopyranoside

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:72396-01-1 SDS

72396-01-1Downstream Products

72396-01-1Relevant articles and documents

INDOLYL-PIPERIDINYL BENZYLAMINES AS BETA-TRYPTASE INHIBITORS

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Page/Page column 137, (2011/07/09)

The present invention discloses and claims a series of substituted indolyl-piperidinyl benzylamines of formula (I), wherein R1, R2 and R3 are as described herein. More specifically, the compounds of this invention are inhibitors of β-tryptase and are, therefore, useful as pharmaceutical agents. Additionally, this invention also discloses methods of preparation of substituted indolyl-piperidinyl benzylamines. In one of the embodiments, there is provided the compounds of formula (I) wherein R3 is (II).

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