Structure–activity relationships within a series of caspase inhibitors. Part 2: Heterocyclic warheads-Reference-Cited by-同舟云学术

Structure–activity relationships within a series of caspase inhibitors. Part 2: Heterocyclic warheads

Published:2005-08 Issue:15 Volume:15 Page:3632-3636
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Ullman Brett R.,Aja Teresa,Chen Ning,Diaz Jose-Luis,Gu Xin,Herrmann Julia,Kalish Vincent J.,Karanewsky Donald S.,Kodandapani Lalitha,Krebs Joseph J.,Linton Steven D.,Meduna Steven P.,Nalley Kip,Robinson Edward D.,Roggo Silvio P.,Sayers Robert O.,Schmitz Albert,Ternansky Robert J.,Tomaselli Kevin J.,Wu Joe C.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference16 articles.

1. The C. elegans cell death gene ced-3 encodes a protein similar to mammalian interleukin-1β-converting enzyme

2. Induction of apoptosis in fibroblasts by IL-1β-converting enzyme, a mammalian homolog of the C. elegans cell death gene ced-3

3. The protein structures that shape caspase activity, specificity, activation and inhibition

4. Cell Death Studies Yield Cancer Clues

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Carbon-based catalysts: advances in synthesizing N-heterocyclic compounds using graphene family and graphite oxide;Research on Chemical Intermediates;2024-01-05

2. Chemoselective O-Alkylation of 4-(Trifluoromethyl)pyrimidin-2(1H)-ones Using 4-(Iodomethyl)pyrimidines;ACS Omega;2022-05-24

3. Substituent-Driven Selective N-/O-Alkylation of 4-(Trihalomethyl)pyrimidin-2(1H)-ones Using Brominated Enones;The Journal of Organic Chemistry;2022-03-14

4. Ultrasound-assisted synthesis of pyrimidines and their fused derivatives: A review;Ultrasonics Sonochemistry;2021-11

5. Diazocarbonyl derivatives of amino acids: unique chiral building blocks for the synthesis of biologically active compounds;Russian Chemical Reviews;2019-03-01