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153088-76-7

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153088-76-7 Usage

General Description

Z-Aspartic acid (OTBU)-bromomethylketone, also known as Z-ASP(OTBU)-BROMOMETHYLKETONE, is a compound used in biochemical research as an irreversible inhibitor of aspartic proteases. It is a specific inhibitor of cathepsin D, a lysosomal protease involved in protein degradation. The compound works by irreversibly binding to the active site of the enzyme, blocking its function and leading to a halt in protein degradation. Z-Aspartic acid (OTBU)-bromomethylketone is commonly utilized in studies exploring the mechanisms of aspartic proteases and in drug development targeting these enzymes.

Check Digit Verification of cas no

The CAS Registry Mumber 153088-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,0,8 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 153088-76:
(8*1)+(7*5)+(6*3)+(5*0)+(4*8)+(3*8)+(2*7)+(1*6)=137
137 % 10 = 7
So 153088-76-7 is a valid CAS Registry Number.

153088-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (3S)-5-bromo-4-oxo-3-(phenylmethoxycarbonylamino)pentanoate

1.2 Other means of identification

Product number -
Other names 5-benzyloxycarbonylamino-5-bromo-4-oxolpentanoic acid 4-tert-butyl ester

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:153088-76-7 SDS

153088-76-7Relevant articles and documents

Caspase inhibitor and pharmaceutical composition, application and treatment method thereof

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Paragraph 0037-0040, (2019/05/28)

The invention provides a compound serving as a caspase inhibitor and particularly relates to a novel compound with caspase inhibition activity or a pharmaceutically acceptable salt of the novel compound, a preparation method of the novel compound and a ph

CASPASE INHIBITOR AND PHARMACEUTICAL COMPOSITION, USE AND THERAPEUTIC METHOD THEREOF

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Paragraph 0073; 0078, (2019/04/05)

Disclosed are a class of compounds as a caspase inhibitor, and in particular the compound as shown in formula (I) or a pharmaceutically acceptable salt thereof, and the use of the compound in treating caspase-related diseases.

Synthesis of N-urethane protected α-aminoalkyl-α-cyanomethyl ketones; Application to the synthesis of 3-substituted 5-amino-1H-pyrazole tethered peptidomimetics

Sharnabai,Nagendra,Sureshbabu, Vommina V.

, p. 1913 - 1918 (2012/09/25)

The preparation of N-protected amino/peptide α-cyanomethyl ketones through cyanation of the corresponding α-bromomethyl ketones is described. The utility of the resulting α-cyanomethyl ketones in the synthesis of 3-substituted-5-amino-1H-pyrazoles has also been demonstrated. In both steps a wide range of N-protected amino/peptide acids has been employed and the products are obtained in good yield. The enantiomeric purity of both the α-cyanomethyl ketones and pyrazoles were confirmed by chiral HPLC analysis of the corresponding Z-protected d- and l-Ala-OH as model substrates. The synthesis of peptide pyrazolecarboxamides is also delineated. Georg Thieme Verlag Stuttgart · New York.

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