http://rdf.ncbi.nlm.nih.gov/pubchem/reference/25370593

Outgoing Links

Predicate Object
contentType Journal Article
endingPage 398
issn 0006-2952
issueIdentifier 4
pageRange 387-398
publicationName Biochemical Pharmacology
startingPage 387
bibliographicCitation Junquero D, Pilon A, Carilla-Durand E, Patoiseau J, Tarayre J, Torpier G, Staels B, Fruchart J, Colpaert FC, Clavey V, Delhon A. Lack of toxic effects of F 12511, a novel potent inhibitor of acyl-coenzyme A: cholesterol O-acyltransferase, on human adrenocortical cells in culture11Abbreviations: ACAT, acyl-coenzyme A: cholesterol O-acyltransferase; F 12511, (S)-2′,3′,5′-trimethyl-4′-hydroxy-α-dodecylthio-phenylacetanilide; DMEM, Dulbecco’s modified Eagle medium; FBS, fetal bovine serum; LDL, low-density lipoprotein; HDL, high-density lipoprotein; SR-BI, scavenger receptor class B, type I; P450scc, cytochrome P450 cholesterol side-chain cleavage; P450c17, cytochrome P450 17 α-hydroxylase; P450c21, cytochrome P450 21-hydroxylase; PMA, phorbol 12-myristate 13-acetate; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; cAMP, adenosine 3′5′-cyclic monophosphate; ITS, insulin-transferrin-linoleic acid; and MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide. Biochemical Pharmacology. 2001 Feb;61(4):387–98. doi: 10.1016/s0006-2952(00)00555-4.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0f2c5f1dbb96ef7458362d27a42e472a
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_fd80619882a9ae70a32c91cda3bc404d
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7a5994291e371a802cbd792635f658f0
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_b6789604ecb613db2a462bf0d2d82ed4
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0d90d0c66a2a0ddf1502bd218b627d07
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_441cc4a0a58235ebb29422014a17f12f
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_c264e2f3cfc85d679f648429cc94e4d9
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f07f91f3a49ac84312b0d83a84dbefd7
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_37253df8df8d4475a68df8f143313dca
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_44e26393a2c185fa9e6a1a5e443b3c5b
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_24cc1b7a628fbf9bb132c699cd77f691
date 2001-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://doi.org/10.1016/s0006-2952%2800%2900555-4
https://pubmed.ncbi.nlm.nih.gov/11226372
isPartOf http://rdf.ncbi.nlm.nih.gov/pubchem/journal/1015
https://portal.issn.org/resource/ISSN/0006-2952
language English
source https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/
title Lack of toxic effects of F 12511, a novel potent inhibitor of acyl-coenzyme A: cholesterol O-acyltransferase, on human adrenocortical cells in culture11Abbreviations: ACAT, acyl-coenzyme A: cholesterol O-acyltransferase; F 12511, (S)-2′,3′,5′-trimethyl-4′-hydroxy-α-dodecylthio-phenylacetanilide; DMEM, Dulbecco’s modified Eagle medium; FBS, fetal bovine serum; LDL, low-density lipoprotein; HDL, high-density lipoprotein; SR-BI, scavenger receptor class B, type I; P450scc, cytochrome P450 cholesterol side-chain cleavage; P450c17, cytochrome P450 17 α-hydroxylase; P450c21, cytochrome P450 21-hydroxylase; PMA, phorbol 12-myristate 13-acetate; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; cAMP, adenosine 3′5′-cyclic monophosphate; ITS, insulin-transferrin-linoleic acid; and MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide.
discusses http://id.nlm.nih.gov/mesh/M0020527
http://id.nlm.nih.gov/mesh/M0376294
http://id.nlm.nih.gov/mesh/M0001214
http://id.nlm.nih.gov/mesh/M0007520
http://id.nlm.nih.gov/mesh/M0027310
http://id.nlm.nih.gov/mesh/M0004270
http://id.nlm.nih.gov/mesh/M0012584
http://id.nlm.nih.gov/mesh/M0012590
http://id.nlm.nih.gov/mesh/M0004268
hasPrimarySubjectTerm http://id.nlm.nih.gov/mesh/D000813Q000494
http://id.nlm.nih.gov/mesh/D004791Q000494
http://id.nlm.nih.gov/mesh/D002785Q000037
http://id.nlm.nih.gov/mesh/D000311Q000187
hasSubjectTerm http://id.nlm.nih.gov/mesh/D018110Q000378
http://id.nlm.nih.gov/mesh/D000306
http://id.nlm.nih.gov/mesh/D001665
http://id.nlm.nih.gov/mesh/D014407
http://id.nlm.nih.gov/mesh/D008075Q000378
http://id.nlm.nih.gov/mesh/D001692
http://id.nlm.nih.gov/mesh/D013256Q000378
http://id.nlm.nih.gov/mesh/D002785Q000378
http://id.nlm.nih.gov/mesh/D002470Q000187
http://id.nlm.nih.gov/mesh/D002784Q000378
http://id.nlm.nih.gov/mesh/D000311Q000201
http://id.nlm.nih.gov/mesh/D006801
http://id.nlm.nih.gov/mesh/D005786Q000187
http://id.nlm.nih.gov/mesh/D050356
http://id.nlm.nih.gov/mesh/D008077Q000378
discussesAsDerivedByTextMining http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9804740
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5839
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/EC_2.3.1.26
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_ca54abf2cd66a50d865124263a58c5b7
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID47936
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/EC_1.14.14.1
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_c25c5bef0fa0efbec10a882f149a99d6
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5997
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6076
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5283632
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_f6774a09cb253115e3ecb689d9e1c872
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_005ef34c8ba989d84eb20cdc3a19dd7c
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_5d730d822392d752f46e1dd4a1fbcc62
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_a83ab8aaf9c09255e4d00c76c58f5173
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5754

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128808200
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128954713
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128814610
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID247161207
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128344927
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID136296502
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128121087

Total number of triples: 78.