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116883-12-6

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116883-12-6 Usage

Uses

Boc-L-Lys-Amc (cas# 116883-12-6) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 116883-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,8,8 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116883-12:
(8*1)+(7*1)+(6*6)+(5*8)+(4*8)+(3*3)+(2*1)+(1*2)=136
136 % 10 = 6
So 116883-12-6 is a valid CAS Registry Number.

116883-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-LYS-AMC

1.2 Other means of identification

Product number -
Other names BOC-LYSINE-AMC

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:116883-12-6 SDS

116883-12-6Downstream Products

116883-12-6Relevant articles and documents

Profiling of substrates for zinc-dependent lysine deacylase enzymes: HDAC3 exhibits decrotonylase activity in vitro

Madsen, Andreas S.,Olsen, Christian A.

, p. 9083 - 9087 (2012)

Systematic screening of the activities of the eleven human zinc-dependent lysine deacylases against a series of fluorogenic substrates (see scheme) as well as kinetic evaluation revealed substrates for screenings of histone deacetylases HDAC10 and HDAC11 at reasonably low enzyme concentrations. Furthermore, HDAC3 in complex with nuclear receptor corepressor 1 (HDAC3-NCoR1) was shown to harbor decrotonylase activity in vitro. Copyright

First non-radioactive assay for in vitro screening of histone deacetylase inhibitors

Hoffmann,Brosch,Loidl,Jung

, p. 601 - 606 (2007/10/03)

Inhibitors of histone deacetylase (HD) are of great potential as new drugs due to their ability to influence transcriptional regulation and to induce apoptosis or differentiation in cancer cells. So far only radioactive enzyme activity assays or in vivo a

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