COVID-19 Ontology

Last uploaded: February 25, 2021
Preferred Name

efavirenz
Synonyms

(S)-6-chloro-4-cyclopropylethynyl-4-trifluoromethyl-1,4-dihydro-benzo[d][1,3]oxazin-2-one

(S)-6-chloro-4-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one

6-chloro-4-(2-cyclopropyl-1-ethynyl)-4-trifluoromethyl-(4S)-1,4-dihydro-2H-benzo[d][1,3]oxazin-2-one

(-)-6-CHLORO-4-CYCLOPROPYLETHYNYL-4-TRIFLUOROMETHYL-1,4-DIHYDRO-2H-3,1-BENZOXAZIN-2-ONE

(4S)-6-chloro-4-(cyclopropylethynyl)-4-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-2-one

Efavirenz

Definitions

1,4-Dihydro-2H-3,1-benzoxazin-2-one substituted at the 4 position by cyclopropylethynyl and trifluoromethyl groups (S configuration) and at the 6 position by chlorine. A non-nucleoside reverse transcriptase inhibitor with activity against HIV, it is used with other antiretrovirals for combination therapy of HIV infection.

ID

http://purl.obolibrary.org/obo/CHEBI_119486

alternative_term

(4S)-6-chloro-4-(cyclopropylethynyl)-4-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-2-one

Efavirenz

charge

0

database_cross_reference

Beilstein:7387333

PDBeChem:EFZ

LINCS:LSM-5526

KEGG:D00896

PMID:25017682

DrugBank:DB00625

KEGG:C08088

PMID:10576692

HMDB:HMDB0014763

Patent:EP582455

CAS:154598-52-4

Drug_Central:989

PMID:10673109

Wikipedia:Efavirenz

Patent:US5519021

Reaxys:7387333

definition

1,4-Dihydro-2H-3,1-benzoxazin-2-one substituted at the 4 position by cyclopropylethynyl and trifluoromethyl groups (S configuration) and at the 6 position by chlorine. A non-nucleoside reverse transcriptase inhibitor with activity against HIV, it is used with other antiretrovirals for combination therapy of HIV infection.

formula

C14H9ClF3NO2

fromPubMed

true

has_alternative_id

CHEBI:190461

CHEBI:47396

CHEBI:4760

has_obo_namespace

chebi_ontology

has_related_synonym

(S)-6-chloro-4-cyclopropylethynyl-4-trifluoromethyl-1,4-dihydro-benzo[d][1,3]oxazin-2-one

(S)-6-chloro-4-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one

6-chloro-4-(2-cyclopropyl-1-ethynyl)-4-trifluoromethyl-(4S)-1,4-dihydro-2H-benzo[d][1,3]oxazin-2-one

(-)-6-CHLORO-4-CYCLOPROPYLETHYNYL-4-TRIFLUOROMETHYL-1,4-DIHYDRO-2H-3,1-BENZOXAZIN-2-ONE

id

CHEBI:119486

imported from

http://purl.obolibrary.org/obo/chebi.owl

in_subset

http://purl.oboInOwllibrary.org/oboInOwl/chebi#3_STAR

inchi

InChI=1S/C14H9ClF3NO2/c15-9-3-4-11-10(7-9)13(14(16,17)18,21-12(20)19-11)6-5-8-1-2-8/h3-4,7-8H,1-2H2,(H,19,20)/t13-/m0/s1

inchikey

XPOQHMRABVBWPR-ZDUSSCGKSA-N

label

efavirenz

mass

315.67500

monoisotopicmass

315.02739

notation

CHEBI:119486

oboInOwl:hasDbXRef

https://www.ncbi.nlm.nih.gov/pubmed/32232214

preferred label

efavirenz

prefLabel

efavirenz

smiles

FC(F)(F)[C@]1(OC(=O)Nc2ccc(Cl)cc12)C#CC1CC1

textual definition

1,4-Dihydro-2H-3,1-benzoxazin-2-one substituted at the 4 position by cyclopropylethynyl and trifluoromethyl groups (S configuration) and at the 6 position by chlorine. A non-nucleoside reverse transcriptase inhibitor with activity against HIV, it is used with other antiretrovirals for combination therapy of HIV infection.

subClassOf

http://purl.obolibrary.org/obo/CHEBI_23888

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/CHEBI_119486 OBA SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 DRON SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 PDRO SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 FIDEO SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 CCONT SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 HOIP SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 DINTO SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 EFO SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 BERO SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 HUPSON SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 DDSS SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 TXPO SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 BIOMODELS SAME_URI
http://purl.obolibrary.org/obo/CHEBI_119486 CHEBI SAME_URI
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http://purl.obolibrary.org/obo/CHEBI_119486 PDRO LOOM
http://purl.obolibrary.org/obo/CHEBI_119486 FIDEO LOOM
http://purl.obolibrary.org/obo/CHEBI_119486 CCONT LOOM
http://purl.obolibrary.org/obo/CHEBI_119486 HOIP LOOM
http://purl.obolibrary.org/obo/CHEBI_119486 DINTO LOOM
http://purl.obolibrary.org/obo/CHEBI_119486 EFO LOOM
http://purl.obolibrary.org/obo/CHEBI_119486 BERO LOOM
http://purl.obolibrary.org/obo/CHEBI_119486 HUPSON LOOM
http://purl.obolibrary.org/obo/CHEBI_119486 DDSS LOOM
http://purl.obolibrary.org/obo/CHEBI_119486 TXPO LOOM
http://purl.obolibrary.org/obo/CHEBI_119486 BIOMODELS LOOM
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http://purl.jp/bio/4/id/200906045925420948 IOBC LOOM
http://www.co-ode.org/ontologies/galen#Efavirenz GALEN LOOM
http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000148587 ODAE LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0674428 OCHV LOOM
http://stirdf.jst.go.jp/id/200907063104639153 IOBC LOOM
https://go.drugbank.com/drugs/DB00625 MDM LOOM
http://purl.obolibrary.org/obo/DRON_00017693 ODNAE LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#42573 OCHV LOOM
http://purl.bioontology.org/ontology/MESH/C098320 MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00026003 PMAPP-PMO LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/387001004 SNOMEDCT LOOM
http://purl.bioontology.org/ontology/RXNORM/195085 RXNORM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C098320 RH-MESH LOOM
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http://purl.bioontology.org/ontology/LNC/LP21310-5 LOINC LOOM
http://purl.bioontology.org/ontology/LNC/MTHU013845 LOINC LOOM
http://purl.bioontology.org/ontology/CSP/5000-0023 CRISP LOOM
http://www.semanticweb.org/zchero/ontologies/2023/11/SepsisOntology#Efavirenz SEPON LOOM
http://purl.bioontology.org/ontology/VANDF/4021133 VANDF LOOM
http://purl.bioontology.org/ontology/ATC/J05AG03 ATC LOOM