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394735-26-3

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  • hot sale (1R,2S,5S)-Methyl 3-((S)-2-(3-(t-butyl)ureido)-3,3-diMethyl butanoyl)-6,6-diMethyl-3-azabicyclo [3.1.0]hexane-2-carboxylate

    Cas No: 394735-26-3

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  • (1R,2S,5S)-METHYL 3-((S)-2(3-(TERT-BUTYL)UREIDO)-3,3, DIMETHYLBUTANOYL)-6,6-DIMETHYL-3-AZABICYCLO[3.1.0]HEXANE-2-CARBOXYLATE

    Cas No: 394735-26-3

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  • 3-Azabicyclo[3.1.0]hexane-2-carboxylic acid, 3-[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-3,3-dimethyl-1-oxobutyl] -6,6-dimethyl-, methyl ester, (1R,2S,5S)-

    Cas No: 394735-26-3

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  • (1R,2S,5S)-methyl 3-((S)-2-(3- (t-butyl)ureido)-3,3-dimethyl butanoyl)-6,6-dimethyl-3-azabicyclo [3.1.0]hexane-2-carboxylate

    Cas No: 394735-26-3

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394735-26-3 Usage

General Description

The chemical compound "(1R,2S,5S)-Methyl 3-((S)-2-(3-(t-butyl)ureido)-3,3-diMethyl butanoyl)-6,6-diMethyl-3-azabicyclo [3.1.0]hexane-2-carboxylate" is a complex molecule with a three-dimensional structure. It contains a methyl ester group, a ureido group, and a bicyclic azabicyclohexane ring. The compound is formed by the combination of various functional groups and has a unique stereochemistry. It is likely to have specific biological or pharmaceutical properties due to its intricate structure and potentially high potency as a drug or chemical agent.

Check Digit Verification of cas no

The CAS Registry Mumber 394735-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,4,7,3 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 394735-26:
(8*3)+(7*9)+(6*4)+(5*7)+(4*3)+(3*5)+(2*2)+(1*6)=183
183 % 10 = 3
So 394735-26-3 is a valid CAS Registry Number.

394735-26-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[2-(3-tert-butylureido)-3,3-dimethylbutyryl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names boc-tert-Leu

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:394735-26-3 SDS

394735-26-3Relevant articles and documents

FUNCTIONALIZED PEPTIDES AS ANTIVIRAL AGENTS

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Page/Page column 73, (2022/02/05)

The present invention discloses compounds of Formula (I), and pharmaceutically acceptable salts, thereof: which inhibit coronavirus replication activity. The invention further relates to pharmaceutical compositions comprising a compound of Formula (I) or a pharmaceutically acceptable salt thereof, and methods of treating or preventing a coronavirus infection in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of Formula (I) or a pharmaceutically acceptable salt thereof.

PROTEASE INHIBITORS FOR TREATMENT OR PREVENTION OF CORONAVIRUS DISEASE

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Page/Page column 28, (2021/11/13)

Provided are protease inhibitor compounds that find use in treating or preventing coronavirus disease. In some embodiments, the coronavirus disease is COVID-19. Also provided are compositions and kits comprising the compounds, as well methods of using the

Discovery of potent sulfonamide P4-capped ketoamide second generation inhibitors of hepatitis C virus NS3 serine protease with favorable pharmacokinetic profiles in preclinical species

Bogen, Stéphane L.,Arasappan, Ashok,Velazquez, Francisco,Blackman, Melissa,Huelgas, Regina,Pan, Weidong,Siegel, Elise,Nair, Latha G.,Venkatraman, Srikanth,Guo, Zhuyan,Doll, Ronald,Shih, Neng-Yang,George Njoroge

scheme or table, p. 1854 - 1865 (2010/05/17)

Hepatitis is a disease characterized by inflammation of the liver, usually producing swelling and, in many cases, permanent damage to liver tissues. Viral hepatitis C (HCV), a small (+)-RNA virus, infects chronically 3% of the world's population. Boceprevir, SCH 503034, (1) our first generation HCV inhibitor, has already established proof-of- concept and is currently in late stage (phase III) clinical trials. In view of the positive data from our first generation compound, further work aimed at optimizing its overall profile was undertaken. Herein, we report that extension of our earlier inhibitor to the P4 pocket by introducing a new sulfonamide moiety and optimization of the P1/P1′ capping led to the discovery of a novel series of inhibitors of the HCV NS3 serine protease. Optimization of the P1 residue significantly improved potency and selectivity. The combination of optimal moieties led to the discovery of compound 47 which, in addition to being a potent inhibitor of HCV subgenomic RNA replication, was also found to have good PK profile in rat, dog and monkey.

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