Amino acids and peptides. XLIV. Synthesis of stereoisomeric pentapeptides of thiol proteinase inhibitor

DOI: 10.1248/cpb.44.1599

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1599 - 1602 (1996)

Update date:2022-08-02

Topics:

Authors:

Iguchi, Shin

Hirano, Kenichi

Okamoto, Hiroshi

Okamoto, Yoshiko

Okada, Yoshio

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1248/cpb.44.1599

Stereoisomers of thiol proteinase inhibitor (TPI) were synthesized by a conventional solution method. Among them, iNoc-D-Gln-Val-Val-Ala-Ala-pNA weakly inhibited the amidolytic activity of papain, although iNoc-Gln-Val- Val-Ala-Ala-pNA inhibited papain ac

Full text of DOI:10.1248/cpb.44.1599

NII-Electronic Library Service

Products guided by the article

Product name:{(S)-3-Carbamoyl-1-[(R)-2-methyl-1-((S)-2-methyl-1-{(S)-1-[(S)-1-(4-nitro-phenylcarbamoyl)-ethylcarbamoyl]-ethylcarbamoyl}-propylcarbamoyl)-propylcarbamoyl]-propyl}-carbamic acid tert-butyl ester

Cas No:181119-81-3

R&D Labs maybe for 181119-81-3

Allright GC (Jinan) Biotechnology Ltd.

website:https://www.argcbiotech.com/

Contact:86-18405413579-

Address: No.27566 of Jingshiroad, Huaiyin District, Jinan City(250011), Shandong Province, China.
Shanghai better-in Medical Technology Co.,LTD.

Contact:+86-21-38921049

Address:Lane 720 zhangjianggaoke cailun road, Pudong, Shanghai, room 513
Kaiping Genuine Biochemical Pharmaceutical Co.,Ltd.

Contact:+86-750-2881198

Address:No.1, Xinke Road, Shatang Town, Kaiping, Guangdong Province, P.R.China
Hangzhou Yanshan Chemical Co.,Ltd.

Contact:86-571- 87698076

Address:Room 1001, #1 Building, Zhongtian MCC, No.2 Youzhinong, Wenyi West Road, Xihu District, Hangzhou, China
Tianjin Boron PharmaTech Co.,Ltd.(expird)

Contact:86-022-59845187

Address:B9-401, Tianda Science Park,No.80,4th Avenue,TEDA,Tianjin, China

Relevant to this article

Doi:10.1016/S0040-4020(01)97350-8
(1974)
Doi:10.1002/zaac.19744030214
(1974)
PdCl₂ and NiCl₂-catalyzed hydrogen-halogen exchange for the convenient preparation of bromo- and iodosilanes and germanes

Doi:10.1016/S0022-328X(02)02147-2
(2003)
A ring-transformation/ring-annulation strategy for the synthesis of the DHFR inhibitor, TNP-351: A correction

Doi:10.1021/jo961230s
(1996)
Sodium dithionite initiated addition of CF₂Br₂, CF₃I and (CF₃)₂CFI to allylaromatics. Synthesis and the reactivity of 4-aryl-1,1-difluorodienes and 4-aryl-1,1-bis(trifluoromethyl)dienes

Doi:10.1016/j.jfluchem.2007.04.028
(2007)
Synthesis and Structure-Activity Relationship Studies of C2-Modified Analogs of the Antimycobacterial Natural Product Pyridomycin

Doi:10.1021/acs.jmedchem.9b01457
(2020)

Article Doi