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4-[N-(tert-butyloxycarbonyl)benzyloxyamino]-1-butylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1027408-37-2

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1027408-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1027408-37-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,4,0 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1027408-37:
(9*1)+(8*0)+(7*2)+(6*7)+(5*4)+(4*0)+(3*8)+(2*3)+(1*7)=122
122 % 10 = 2
So 1027408-37-2 is a valid CAS Registry Number.

1027408-37-2Relevant academic research and scientific papers

Identification of a gene cluster that directs putrebactin biosynthesis in Shewanella species: PubC catalyzes cyclodimerization of N-Hydroxy-N- succinylputrescine

Kadi, Nadia,Arbache, Simon,Song, Lijiang,Oves-Costales, Daniel,Challis, Gregory L.

, p. 10458 - 10459 (2008)

Putrebactin is a dihydroxamate iron chelator produced by the metabolically versatile marine bacterium Shewanella putrefaciens. It is a macrocyclic dimer of N-hydroxy-N-succinyl-putrescine (HSP) and is structurally related to desferrioxamine E, which is a

Design, Synthesis and Evaluation of AdSS Bisubstrate Inhibitors

Tibrewal, Nidhi,Elliott, Gregory I.

supporting information, p. 2269 - 2272 (2020/09/17)

Many cancers lack the expression of methylthioadenosine phosphorylase (MTAP). These cancers require adenylosuccinate synthetase (AdSS) for nucleic acid synthesis. By inhibiting adenylosuccinate synthetase, we potentially have a new therapeutic agent. Bisubstrate inhibitors were synthesized and evaluated against purified AdSS. The best activity was obtained with adenosine bearing a four-carbon linker that connects the N-formyl-N-hydroxy moiety to the 6-position of the purine nucleoside.

The preparation of a fully differentiated "multiwarhead" siderophore precursor

Murray, Aaron P.,Miller, Marvin J.

, p. 191 - 194 (2007/10/03)

A protected, fully differentiated siderophore analogue has been prepared so that "Trojan Horse"-like siderophore drug conjugates with different drugs can be synthesized. The key steps in the synthesis include controlled preparation of an unsymmetrical urea and its conversion to a fully differentiated isocyanurate by reaction with chloro(carbonyl) isocyanate.

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