Synthesis and properties of gramicidin S analogs containing Pro-D-Phe sequence in place of D-Phe-Pro sequence in the β-turn part of the antibiotic

DOI: 10.1246/bcsj.58.1469

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1469 - 1472 (1985)

Update date:2022-09-26

Topics:

Authors:

Tamaki Tamaki

Takimoto

Muramatsu

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

Article abstract of DOI:10.1246/bcsj.58.1469

Two analogs of gramicidin S, [L-Pro⁴, D-Phe⁵]-gramicidin S and [L-Pro(4,4'), D-Phe(5,5')]-gramicidin S, were synthesized in order to investigate the relationships among positions of Pro residues, antibiotic activity and CD spectra. [

Full text of DOI:10.1246/bcsj.58.1469

Products guided by the article

Product name:cyclo<-D-Phe-Val-Orn(Z)-Leu-Pro->2

Cas No:97475-33-7

R&D Labs maybe for 97475-33-7

Shanghai Mintchem Development ., Ltd

Contact:0086 21 5190 8570

Address:R602,4#,89Nong, Mudan Road Pudong Shanghai China
Chinapeptides Co,. Ltd

Contact:+86-021-50792271

Address:Building 24A, 300 Chuantu Road, Chuansha, Pudong new area, Shanghai, China, 201202
miao tie sheng

Contact:0311-13263231263

Address:jian hua street,Shijiazhuang City, China
Shanghai PuYi Chem-Tech Co.,Ltd.

Contact:+86-21-57687505-227

Address:3 Floor, Building 11, No 201 MinYi Road, Songjiang District, Shanghai 201612, China
Twin International Co., Limited

Contact:+86-21-80309280

Address:No.345 Jinxiang Road, Jinqiao Export Processing Zone

Relevant to this article

Synthesis and properties of oligonucleotides with iodo-substituted aromatic aglycons: Investigation of possible halogen bonding base pairs

Doi:10.1021/jo701634t
(2008)
Benzimidazol-2-yl or benzimidazol-2-ylthiomethyl benzoylguanidines as novel Na⁺/H⁺ exchanger inhibitors, synthesis and protection against ischemic-reperfusion injury

Doi:10.1016/j.bmcl.2007.02.035
(2007)
Doi:10.1039/jr9620003040
(1962)
Regioselective reactions of 1-alkylidene-2-oxyallyl cations with furan: Control of [4 + 3] cycloaddition, [3 + 2] cycloaddition, and electrophilic substitution

Doi:10.1021/ol061655t
(2006)
The chemistry of 5-oxodihydroisoxazoles. XVI* a new synthesis of pyrroles, furans, thiophens and their benzo analogues

Doi:10.1071/CH9961315
(1996)
Further studies on imidazo[4,5-b]pyridine AT₁ angiotensin II receptor antagonists. Effects of the transformation of the 4-phenylquinoline backbone into 4-phenylisoquinolinone or 1-phenylindene scaffolds

Doi:10.1021/jm0603163
(2006)

Article Doi