reference/24841538

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/24841538

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	1213
issn	0968-0896
issueIdentifier	3
pageRange	1207-1213
publicationName	Bioorganic & Medicinal Chemistry
startingPage	1207
bibliographicCitation	Liu XH, Zhu J, Zhou AN, Song BA, Zhu HL, Bai LS, Bhadury PS, Pan CX. Synthesis, structure and antibacterial activity of new 2-(1-(2-(substituted-phenyl)-5-methyloxazol-4-yl)-3-(2-substitued-phenyl)-4,5-dihydro-1H-pyrazol-5-yl)-7-substitued-1,2,3,4-tetrahydroisoquinoline derivatives. Bioorg Med Chem. 2009 Feb 01;17(3):1207–13. doi: 10.1016/j.bmc.2008.12.034. PMID: 19147367.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f0140eb0f9fa7fdc1f45eb16f3c43170 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_abe8b64927ad5691d558313738a2f295 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ce0bc88b583d5666806c97c3eb577712 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7cec30c55a0e34589e75a28aaabed893 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_2e53740730b725d27bb44dda75fe6be9 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_cdeee10d5b8c612556f0b083dda09590 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_b37cd958a566b4a8d5f7a08fea443602 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_16df7beb84fde86d7ff7b318d4d30ef9
date	2009-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/19147367 https://doi.org/10.1016/j.bmc.2008.12.034
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/8539 https://portal.issn.org/resource/ISSN/0968-0896
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Synthesis, structure and antibacterial activity of new 2-(1-(2-(substituted-phenyl)-5-methyloxazol-4-yl)-3-(2-substitued-phenyl)-4,5-dihydro-1H-pyrazol-5-yl)-7-substitued-1,2,3,4-tetrahydroisoquinoline derivatives
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http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103630397_AID369074_PMID19147367_VALUE7
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103630828_AID369073_PMID19147367_VALUE42
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103466522_AID369075_PMID19147367_VALUE2
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103630330_AID369073_PMID19147367_VALUE5
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103630664_AID369074_PMID19147367_VALUE30
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103630614_AID369073_PMID19147367_VALUE21
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103630616_AID369073_PMID19147367_VALUE23
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103630520_AID369073_PMID19147367_VALUE12
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103630329_AID369075_PMID19147367_VALUE4
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103466522_AID369074_PMID19147367_VALUE2
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103630825_AID369072_PMID19147367_VALUE39
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103630614_AID369075_PMID19147367_VALUE21

Total number of triples: 230.