.
luminespib - Ontology Report - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

CHEBI ONTOLOGY - ANNOTATIONS

The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/. The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/). For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.
Term:luminespib
go back to main search page
Accession:CHEBI:83656 term browser browse the term
Definition:A monocarboxylic acid amide obtained by formal condensation of the carboxy group of 5-(2,4-dihydroxy-5-isopropylphenyl)-4-[4-(morpholin-4-ylmethyl)phenyl]-1,2-oxazole-3-carboxylic acid with the amino group of ethylamine.
Synonyms:exact_synonym: 5-(2,4-dihydroxy-5-isopropylphenyl)-N-ethyl-4-[4-(morpholin-4-ylmethyl)phenyl]-1,2-oxazole-3-carboxamide
 related_synonym: Formula=C26H31N3O5;   InChI=1S/C26H31N3O5/c1-4-27-26(32)24-23(18-7-5-17(6-8-18)15-29-9-11-33-12-10-29)25(34-28-24)20-13-19(16(2)3)21(30)14-22(20)31/h5-8,13-14,16,30-31H,4,9-12,15H2,1-3H3,(H,27,32);   InChIKey=NDAZATDQFDPQBD-UHFFFAOYSA-N;   NVP-AUY922;   SMILES=CCNC(=O)c1noc(c1-c1ccc(CN2CCOCC2)cc1)-c1cc(C(C)C)c(O)cc1O
 xref: CAS:747412-49-3;   PMID:22286776;   PMID:22523597;   PMID:22619113;   PMID:22753713;   PMID:22810956;   PMID:23016912;   PMID:23064324;   PMID:23196876;   PMID:23340178;   PMID:23356405;   PMID:23493311;   PMID:24090817;   PMID:24551261;   PMID:24796583;   PMID:25027745;   PMID:25072314;   PMID:25085789;   PMID:25263741;   Reaxys:12046798;   Wikipedia:NVP-AUY922

 Loading Annotations... 
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
X
Y
MT

show annotations for term's descendants           Sort by:
Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 5181
    role 5148
      application 964
        pharmaceutical 800
          drug 800
            antineoplastic agent 245
              luminespib 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 5181
    subatomic particle 5171
      composite particle 5171
        hadron 5171
          baryon 5171
            nucleon 5171
              atomic nucleus 5171
                atom 5171
                  main group element atom 5144
                    p-block element atom 5141
                      carbon group element atom 5059
                        carbon atom 5058
                          organic molecular entity 5058
                            heteroorganic entity 4906
                              organochalcogen compound 4860
                                organooxygen compound 4825
                                  carbon oxoacid 405
                                    carboxylic acid 401
                                      carboacyl group 223
                                        univalent carboacyl group 223
                                          carbamoyl group 220
                                            carboxamide 220
                                              monocarboxylic acid amide 99
                                                luminespib 0
paths to the root