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D-Proline, N-[(1,1-dimethylethoxy)carbonyl]-L-isoleucyl-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

221187-05-9

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221187-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221187-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,1,8 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 221187-05:
(8*2)+(7*2)+(6*1)+(5*1)+(4*8)+(3*7)+(2*0)+(1*5)=99
99 % 10 = 9
So 221187-05-9 is a valid CAS Registry Number.

221187-05-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-L-Ile-D-Pro-OBzl

1.2 Other means of identification

Product number -
Other names (R)-1-((2S,3S)-2-tert-Butoxycarbonylamino-3-methyl-pentanoyl)-pyrrolidine-2-carboxylic acid benzyl 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:221187-05-9 SDS

221187-05-9Downstream Products

221187-05-9Relevant academic research and scientific papers

HISTONE DEACETYLASE INHIBITOR AND PROCESS FOR PRODUCING THE SAME

-

, (2008/06/13)

HDAC inhibitors represented by formula (1) show strong inhibitory activity against various subtypes of HDACs. The compounds of the present invention find utility as pharmaceutical agents for treating or preventing diseases associated with HDAC 1, 4, and 6

Histone deacetylase inhibitors and process for producing the same

-

Page/Page column 11-12, (2008/06/13)

Compounds represented by formula (1) have strong inhibitory activity that is selective towards HDAC1 and HDAC4. Therefore, the compounds of the present invention are useful as pharmaceutical agents for treating or preventing diseases caused by HDAC1 and HDAC4.

Cyclic Tetrapeptides Bearing a Sulfhydryl Group Potently Inhibit Histone Deacetylases

Nishino, Norikazu,Jose, Binoy,Okamura, Shinji,Ebisusaki, Shutoku,Kato, Tamaki,Sumida, Yuko,Yoshida, Minoru

, p. 5079 - 5082 (2007/10/03)

(Equation presented) New inhibitors of histone deacetylase (HDAC) containing a sulfhydryl group were designed on the basis of the corresponding hydroxamic acid (CHAP31) and FK228. Their disulfide dimers and hybrids exhibited potent HDAC inhibitory activity in vivo with potential as anticancer prodrugs.

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