✦ LIBER ✦

Synthesis of Macrosphelides Containing a Heterocyclic Side Chain as a Novel Apoptosis Inducer

✍ Scribed by Matsuya, Yuji; Nemoto, Hideo; Hori, Ayana; Kawamura, Tomomi; F. Emam, Heba; Ahmed, Kanwal; Kondo, Takashi; Toyooka, Naoki

Book ID: 119965949
Publisher: Japan Institute of Heterocyclic Chemistry
Year: 2010
Tongue: English
Weight: 595 KB
Volume: 80
Category: Article
ISSN: 0385-5414
DOI: 10.3987/COM-09-S(S)82

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis of Macros

ChemInform Abstract: Synthesis of Macrosphelides Containing a Heterocyclic Side Chain as a Novel Apoptosis Inducer.

✍ Yuji Matsuya; Ayana Hori; Tomomi Kawamura; Heba F. Emam; Kanwal Ahmed; Da-Yong Y 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

Synthesis of Macrosphelides with a Thiaz

Synthesis of Macrosphelides with a Thiazole Side Chain: New Antitumor Candidates Having Apoptosis-Inducing Property

✍ Matsuya, Yuji; Kawaguchi, Takanori; Ishihara, Kentaro; Ahmed, Kanwal; Zhao, Qing 📂 Article 📅 2006 🏛 American Chemical Society 🌐 English ⚖ 100 KB

ChemInform Abstract: Artificial Macrosph

ChemInform Abstract: Artificial Macrosphelides as a Novel Apoptosis-Inducing Compounds

✍ Yuji Matsuya; Hideo Nemoto 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 15 KB

Mechanism of apoptosis induced by a newl

Mechanism of apoptosis induced by a newly synthesized derivative of macrosphelides with a thiazole side chain

✍ Kanwal Ahmed; Yuji Matsuya; Hideo Nemoto; Syed Faisal Haider Zaidi; Toshiro Sugi 📂 Article 📅 2009 🏛 Elsevier Science 🌐 English ⚖ 933 KB

Synthesis of a novel side-chain to side-

Synthesis of a novel side-chain to side-chain cyclized enkephalin analogue containing a carbonyl bridge

✍ Danuta Pawlak; Ngoc Nga Chung; Peter W. Schiller; Jan Izdebski 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 110 KB 👁 2 views

A novel type of cyclic opioid peptide analogue, cyclo[N epsilon,N epsilon'-carbonyl-D-Lys2,Lys5]enkephalinamide, was prepared from a linear precursor peptide. The peptide was synthesized on the Merrified resin and also by a combination of the solid-phase technique and the classical method in solutio

The enantiospecific synthesis of novel l

The enantiospecific synthesis of novel lysine analogues incorporating a pyrrolidine containing side chain

✍ Peter John Murray; Ian D. Starkey; John E. Davies 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 187 KB

Two novel analogues of lysine have been prepared in high enantiomeric and diastereomeric purity. These unnatural a-amino acids possess modified aminoalkyl side chains incorporating a pyrrolidine nucleus as a cyclic constraint.