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857900-54-0

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857900-54-0 Usage

General Description

The chemical {(S)-1-[N'-((2S,3S)-3-amino-2-hydroxy-4-phenyl-butyl)-N'-(4-pyridin-2-yl-benzyl)-hydrazinocarbonyl]-2,2-dimethyl-propyl}-carbamic acid methyl ester is a complex compound consisting of a carbamic acid methyl ester attached to a specific arrangement of amino acids and other functional groups. It contains a hydrazinocarbonyl group, as well as phenyl, pyridin, and benzyl groups. The compound is chiral, with the (S)-configuration, and has a 2,2-dimethyl-propyl group. This chemical structure may have potential applications in pharmaceuticals or biotechnology, where its specific arrangement of functional groups and chirality may be important for its activity.

Check Digit Verification of cas no

The CAS Registry Mumber 857900-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,9,0 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 857900-54:
(8*8)+(7*5)+(6*7)+(5*9)+(4*0)+(3*0)+(2*5)+(1*4)=200
200 % 10 = 0
So 857900-54-0 is a valid CAS Registry Number.

857900-54-0Relevant articles and documents

PROTEASE INHIBITORS HAVING ENHANCED FEATURES

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, (2017/02/28)

Provided herein (among other things) are protease inhibitor compounds having enhanced features, along with methods for administering such compounds. For example, the subject compounds can be administered without concomitant administration of a CYP3A4 inhibitor, have increased therapeutic index and/or increased potency, and are low-resistance inducing in nature.

HIV PROTEASE INHIBITING COMPOUNDS

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Page/Page column 110, (2010/02/12)

A compound of the formula (I) is disclosed as an HIV protease inhibitor. Methods and compositions for inhibiting an HIV infection are also disclosed.

A facile and efficient synthesis of d3-labelled Reyataz

Zhang, Huiping,Bonacorsi Jr., Samuel J.,Chen, Bang-Chi,Leith, Leslie W.,Rinehart, J. Kent,Balasubramanian, Balu,Barrish, Joel C.

, p. 1041 - 1047 (2007/10/03)

A facile and efficient synthesis of d3-labelled Reyataz is described. The key step of synthesis involved the coupling of N-(d 3-methoxycarbonyl)-L-tert-leucine 2b with an advanced chiral non-racemic building block 4. The latter was synthesized in 4 steps from the readily accessible hydrazine derivative 8. Copyright

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