About: Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality

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About: Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality Goto Sponge NotDistinct Permalink

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scientific article published on 01 February 2001

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 2001 (uk) im Februar 2001 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en febreru de 2001 (ast) artikull shkencor i botuar më 01 shkurt 2001 (sq) scientific article published on 01 February 2001 (en)
publication date	wds:Q73566634-74C69318-2E0E-4E94-999D-A452B01DD43C
publication date	2001-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q73566634-00D3B390-DB38-48C7-A9FC-9CAABD67AE4F
language of work or name	English
cites work	wds:Q73566634-0272FB35-3FE0-4F64-86EC-ED40D25E170B wds:Q73566634-09D487E2-63F1-467F-908D-CF083CD5F1EB wds:Q73566634-238E6B3D-3F9D-4F4D-B20D-EEE663ACB304 wds:Q73566634-26FD8CEF-091B-48AA-BFAD-0AF9F8565179 wds:Q73566634-33E88A54-23AA-48F5-B529-E8B297F4FD18 wds:Q73566634-3DEF6731-D065-426F-BA5F-AFF634F07F54 wds:Q73566634-4BAFD41D-622F-4847-9944-595B35ABC95F wds:Q73566634-90226B19-1425-4C0A-8878-9AA4C99D0451 wds:Q73566634-9BDD1B9A-36BE-41ED-81A7-82FD5E1535E6 wds:Q73566634-A026C087-AEF3-4A5D-BCA6-BF95C28EF1DC wds:Q73566634-BD4D052D-407E-49E6-A48F-756E0F90D396 wds:Q73566634-D37E0D3C-E07D-47EB-8A12-2306864B85EB wds:Q73566634-D7E03718-02C7-488F-8677-356906C1ED8F wds:Q73566634-E0132845-22E4-4F7E-B29E-76A27C144845 wds:Q73566634-E0C178D2-1001-4AEC-9435-8B026B725506 wds:Q73566634-E789BDE2-B790-4B93-AE11-BC0747E96C10 wds:Q73566634-F9F19D97-C592-47FC-93C4-EB67129ECD01 wds:Q73566634-FC345A64-B193-4DE7-80AA-094E52594C81 wds:Q73566634-FE69DC69-22D6-4F07-BF6C-2CEF896C1A42 wds:Q73566634-FFDDDA7D-0377-489F-ABA2-F6B56870FECB
cites work	1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive Matrix metalloproteinase inhibitors: a structure-activity study Design and therapeutic application of matrix metalloproteinase inhibitors Stromelysin-1: three-dimensional structure of the inhibited catalytic domain and of the C-truncated proenzyme Cell-matrix interactions modulate interstitial collagenase expression by human keratinocytes actively involved in wound healing Collagenase 2 (MMP-8) expression in murine tissue-remodeling processes. Analysis of its potential role in postpartum involution of the uterus. Matrix metalloproteinases A novel coumarin-labelled peptide for sensitive continuous assays of the matrix metalloproteinases The significance of matrix metalloproteinases during early stages of tumor progression Matrix metalloproteinase inhibitors: present achievements and future prospects Matrix metalloproteinase inhibitors Metalloproteinase inhibitors and the prevention of connective tissue breakdown Demonstration of tissue collagenase activity in vivo and its relationship to inflammation severity in human gingiva Epidermal expression of collagenase delays wound-healing in transgenic mice. Gelatinase activity during wound healing Inhibition of bovine nasal cartilage degradation by selective matrix metalloproteinase inhibitors Inhibition of stromelysin-1 (MMP-3) by P1'-biphenylylethyl carboxyalkyl dipeptides Discovery of potent and selective succinyl hydroxamate inhibitors of matrix metalloprotease-3 (stromelysin-1). Structure-based design and synthesis of a series of hydroxamic acids with a quaternary-hydroxy group in P1 as inhibitors of matrix metalloproteinases Matlystatins, new inhibitors of typeIV collagenases from Actinomadura atramentaria. II. Biological activities
author name string	wds:Q73566634-76B050E7-22A3-416E-99E0-D71C1F461D82 wds:Q73566634-8050E17D-7FC6-43A2-8CA2-59E2594F2160 wds:Q73566634-E73EA298-7BA7-41A1-9B46-FDBC1CF11277
author name string	M F Burslem M J Fray R P Dickinson
rdfs:label	Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality (en) Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality (nl) Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality (sq)
skos:prefLabel	Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality (en) Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality (nl) Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality (sq)
name	Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality (en) Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality (nl) Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality (sq)
title	wds:Q73566634-C63F4110-F1F4-4F28-B2C3-2640EB97C11A
title	Selectivity of inhibition of matrix metalloproteases MMP-3 and MMP-2 by succinyl hydroxamates and their carboxylic acid analogues is dependent on P3' group chirality (en)
page(s)	wds:Q73566634-4DEC59E1-85B4-40C0-BAB6-DC5E867D8BC6
page(s)	567-570
instance of	wds:Q73566634-5FB36E39-A09D-49AF-B285-8EF3BCA6AF20
instance of	scholarly article
main subject	wds:Q73566634-BC54BF5C-48CD-448E-89AD-98295C37BB34
main subject	chirality
PubMed ID	wds:Q73566634-507AEE4A-4B44-4551-B188-70569F061DB5
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11229773
PubMed ID	11229773
published in	wds:Q73566634-46615DDD-3EF1-4DFE-8757-E3615B266393
published in	Bioorganic & Medicinal Chemistry Letters
issue	wds:Q73566634-64037E3F-7B67-48AC-BC11-EA76A3BCE62D
volume	wds:Q73566634-9D75F586-6ED8-494B-8B63-79CEE2AF2AD0
issue	4
volume	11
DOI	wds:Q73566634-B634023E-4D08-46B6-AC26-9A292D8BEAB8
DOI	http://dx.doi.org/10.1016/S0960-894X(00)00719-8
DOI	10.1016/S0960-894X(00)00719-8
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73566634
is cites work of	Heterocyclic zinc-binding groups for use in next-generation matrix metalloproteinase inhibitors: potency, toxicity, and reactivity Discovery of potent and selective succinyl hydroxamate inhibitors of matrix metalloprotease-3 (stromelysin-1). Hydroxamic acids as matrix metalloproteinase inhibitors
is cites work of	wds:Q38014073-E339CBDB-DD3F-4196-B3CA-A70963F6DDF2 wds:Q31028431-7AD992A3-3057-4C74-B5CE-542B22EEC5BD wds:Q32068355-90567A1C-1071-4751-BAF9-48AE351148D4

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