Solution synthesis of human peptide YY (hPYY)

DOI: 10.1248/cpb.38.1731

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1731 - 1734 (1990)

Update date:2022-08-02

Topics:

Authors:

Kitagawa

Tomoyasu

Futaki Futaki

Akita Akita

Higashide

I noue I noue

Tobe Tobe

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

Article abstract of DOI:10.1248/cpb.38.1731

Full text of DOI:10.1248/cpb.38.1731

NII-Electronic Library Service

Products guided by the article

Product name:Z(OMe)-Asn-Arg(Mts)-Tyr-Tyr-Ala-OMe

Cas No:130132-34-2

R&D Labs maybe for 130132-34-2

Lanzhou huibang biological chemical technology Co., LTD

Contact:0931-7843964

Address:NO.2011,Yannan Road,Chengguan,
shandong zhongke taidou chemical co.,ltd

Contact:86-531-88682301

Address:Jinan shandong Province CHina
Tianjin Ji Ping Jia Chemical Co., Ltd.

Contact:18622448868

Address:tianjin
Huayang chemical Co., LTD

Contact:+86-18653358619

Address:zibo
Jiacheng-Chem Enterprises Limited(expird)

Contact:86-571-86711508

Address:19 Floor, CIBC Holley International Building, No. 198,Wuxing Road, Hangzhou, China,310020

Relevant to this article

Regio- and Diastereoselective Access to 4-Imidazolidinones via an Aza-Mannich Initiated Cyclization of Sulfamate-Derived Cyclic Imines with α-Halo Hydroxamates

Doi:10.1021/acs.joc.9b01128
(2019)
Synthesis and reactivity of a 1-Aza-2,3-diphosphaallyl anion

Doi:10.1021/om00047a006
(1991)
Molecular recognition: A remarkably simple receptor for the selective complexation of dicarboxylic acids

Doi:10.1021/ja00176a048
(1990)
Chiral Br?nsted acid-catalyzed dynamic kinetic resolution of atropisomeric: Ortho -formyl naphthamides

Doi:10.1039/d0cc02380a
(2020)
α-Tributylstannylacetals: preparation via transacetalisation of diethoxymethyltributyltin, and use for the synthesis of new α-stannylated ethers

Doi:10.1016/0022-328X(90)80020-Z
(1990)
Fluorinated cyclopropanes: Synthesis and chemistry of the aryl α,β,β-trifluorocyclopropane motif

Doi:10.1039/c8cc04964e
(2018)

Article Doi