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25438-22-6

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25438-22-6 Usage

Heterocyclic compound

Contains a thiazole ring and a carboxylic acid group

Aminomethyl group

Attached to the 2-position of the thiazole ring

Uses

Synthesis of pharmaceuticals and agrochemicals, exhibits antibacterial and antiviral properties

Building block

Used in organic synthesis and drug discovery efforts

Check Digit Verification of cas no

The CAS Registry Mumber 25438-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,3 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25438-22:
(7*2)+(6*5)+(5*4)+(4*3)+(3*8)+(2*2)+(1*2)=106
106 % 10 = 6
So 25438-22-6 is a valid CAS Registry Number.

25438-22-6Upstream product

25438-22-6Relevant articles and documents

Pagoamide A, a Cyclic Depsipeptide Isolated from a Cultured Marine Chlorophyte, Derbesia sp., Using MS/MS-Based Molecular Networking

Cottrell, Garrison W.,Fang, Fang,Gerwick, Lena,Gerwick, William H.,Glukhov, Evgenia,Guan, Huashi,Kim, Hyunwoo,Leao, Tiago,Li, Yueying,Mao, Huanru Henry,Murray, Thomas F.,Pierce, Marsha L.,Yu, Hao-Bing,Zhang, Chen,Zhang, Yi

supporting information, (2020/01/31)

A thiazole-containing cyclic depsipeptide with 11 amino acid residues, named pagoamide A (1), was isolated from laboratory cultures of a marine Chlorophyte, Derbesia sp. This green algal sample was collected from America Samoa, and pagoamide A was isolated using guidance by MS/MS-based molecular networking. Cultures were grown in a light- and temperature-controlled environment and harvested after several months of growth. The planar structure of pagoamide A (1) was characterized by detailed 1D and 2D NMR experiments along with MS and UV analysis. The absolute configurations of its amino acid residues were determined by advanced Marfey's analysis following chemical hydrolysis and hydrazinolysis reactions. Two of the residues in pagoamide A (1), phenylalanine and serine, each occurred twice in the molecule, once in the d- and once in the l-configuration. The biosynthetic origin of pagoamide A (1) was considered in light of other natural products investigations with coenocytic green algae.

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