http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15314421

Outgoing Links

Predicate Object
contentType Journal Article|Research Support, N.I.H., Extramural|Research Support, Non-U.S. Gov't
endingPage 1005
issn 0006-291X
issueIdentifier 4
pageRange 1000-1005
publicationName Biochemical and Biophysical Research Communications
startingPage 1000
hasFundingAgency http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_eb4f340a1767b2ff28113b9d3c67834b
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_81157022b5fdeefce124d8c945a814a4
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_e84350a65e9a47198640404e26ee8ec4
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_5a0eb2fadabf1dffb4d70280b760adba
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_2ea80026665e031b7380448129ca3b62
isSupportedBy http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_16bf5ea5e93935d571155c8acdbb1e75
http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_317ba22d0079f0930bbcb1789dfa3b71
http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_98b46ddacfe0557e0361f005b4f26a7c
bibliographicCitation Matsuo AL, Carmona AK, Silva LS, Cunha CEL, Nakayasu ES, Almeida IC, Juliano MA, Puccia R. C-Npys (S-3-nitro-2-pyridinesulfenyl) and peptide derivatives can inhibit a serine-thiol proteinase activity from Paracoccidioides brasiliensis. Biochemical and Biophysical Research Communications. 2007 Apr;355(4):1000–5. doi: 10.1016/j.bbrc.2007.02.070.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e71983dc2b2656de03a008ab5bd0d473
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_4dfce544b8d87ad0f36fbf82d01ae3d0
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_89edfd593274033f254385e01873446a
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7f720c77c3e38801eb6955f8ea1eb6f8
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_57409c83f26b49e232f62c703dec96a9
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_32588ff9a723d49cfec14496063b48be
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_567f3f1b14c8b6475511f8863fdbedb5
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_43498c1d1b4309c6745784fee872780c
date 2007-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://doi.org/10.1016/j.bbrc.2007.02.070
https://pubmed.ncbi.nlm.nih.gov/PMC3606896
https://pubmed.ncbi.nlm.nih.gov/17328865
isPartOf http://rdf.ncbi.nlm.nih.gov/pubchem/journal/1008
https://portal.issn.org/resource/ISSN/0006-291X
language English
source https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/
title C-Npys (S-3-nitro-2-pyridinesulfenyl) and peptide derivatives can inhibit a serine-thiol proteinase activity from Paracoccidioides brasiliensis
discusses http://id.nlm.nih.gov/mesh/M0180298
http://id.nlm.nih.gov/mesh/M0005542
http://id.nlm.nih.gov/mesh/M0024260
http://id.nlm.nih.gov/mesh/M0016238
http://id.nlm.nih.gov/mesh/M0024280
http://id.nlm.nih.gov/mesh/M0019678
http://id.nlm.nih.gov/mesh/M0018233
hasPrimarySubjectTerm http://id.nlm.nih.gov/mesh/D015842Q000494
http://id.nlm.nih.gov/mesh/D010228Q000201
http://id.nlm.nih.gov/mesh/D015853Q000494
http://id.nlm.nih.gov/mesh/D012697Q000378
http://id.nlm.nih.gov/mesh/D003546Q000378
http://id.nlm.nih.gov/mesh/D011725Q000494
http://id.nlm.nih.gov/mesh/D010455Q000494
hasSubjectTerm http://id.nlm.nih.gov/mesh/D015853Q000737
http://id.nlm.nih.gov/mesh/D015842Q000737
http://id.nlm.nih.gov/mesh/D011725Q000737
http://id.nlm.nih.gov/mesh/D015394
http://id.nlm.nih.gov/mesh/D010455Q000737
discussesAsDerivedByTextMining http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53717739
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID168833
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID108459
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID439352
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID402
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11966311
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1725
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID129283

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129031960
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129742316
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129475384
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128643942

Total number of triples: 65.