CHEBI:63608 - maraviroc

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ChEBI Name maraviroc
ChEBI ID CHEBI:63608
Definition A monocarboxylic acid amide obtained by formal condensation of the carboxy group of 4,4-difluorocyclohexanecarboxylic acid and the primary amino group of (1S)-3-[(3-exo)-3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]oct-8-yl]-1-phenylpropylamine. An antiretroviral drug, it prevents the interaction of HIV-1 gp120 and chemokine receptor 5 (CCR5) necessary for CCR5-tropic HIV-1 to enter cells.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Anonymous
Supplier Information No supplier information found for this compound.
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Sodium aurothiosulfate, or sanocrysin, is the inorganic compound with the formula Na3[Au(S2O3)2]·2H2O. It is the trisodium salt of the coordination complex of gold(I), [Au(S2O3)2]3−. The dihydrate, which is colorless, crystallizes with two waters of crystallization. The compound has some medicinal properties as well as potential for hydrometallurgy.
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Formula C29H41F2N5O
Net Charge 0
Average Mass 513.66550
Monoisotopic Mass 513.32792
InChI InChI=1S/C29H41F2N5O/c1-19(2)27-34-33-20(3)36(27)25-17-23-9-10-24(18-25)35(23)16-13-26(21-7-5-4-6-8-21)32-28(37)22-11-14-29(30,31)15-12-22/h4-8,19,22-26H,9-18H2,1-3H3,(H,32,37)/t23-,24+,25-,26-/m0/s1
InChIKey GSNHKUDZZFZSJB-QYOOZWMWSA-N
SMILES CC(C)c1nnc(C)n1[C@H]1C[C@@H]2CC[C@H](C1)N2CC[C@H](NC(=O)C1CCC(F)(F)CC1)c1ccccc1
Roles Classification
Biological Role(s): chemokine receptor 5 antagonist
An antogonist that blocks chemokine receptor 5 (CCR5).
antiviral drug
A substance used in the prophylaxis or therapy of virus diseases.
HIV fusion inhibitor
A drug which interferes with the binding, fusion and entry of an HIV virion to a human cell. By blocking this step in HIV's replication cycle, such agents slow the progression from HIV infection to AIDS.
Application(s): antiviral drug
A substance used in the prophylaxis or therapy of virus diseases.
HIV fusion inhibitor
A drug which interferes with the binding, fusion and entry of an HIV virion to a human cell. By blocking this step in HIV's replication cycle, such agents slow the progression from HIV infection to AIDS.
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ChEBI Ontology
Outgoing maraviroc (CHEBI:63608) has role antiviral drug (CHEBI:36044)
maraviroc (CHEBI:63608) has role chemokine receptor 5 antagonist (CHEBI:63673)
maraviroc (CHEBI:63608) has role HIV fusion inhibitor (CHEBI:59886)
maraviroc (CHEBI:63608) is a azabicycloalkane (CHEBI:38295)
maraviroc (CHEBI:63608) is a monocarboxylic acid amide (CHEBI:29347)
maraviroc (CHEBI:63608) is a organofluorine compound (CHEBI:37143)
maraviroc (CHEBI:63608) is a triazoles (CHEBI:35727)
IUPAC Name
4,4-difluoro-N-{(1S)-3-[(3-exo)-3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]oct-8-yl]-1-phenylpropyl}cyclohexanecarboxamide
INNs Sources
maraviroc WHO MedNet
maraviroc WHO MedNet
maraviroc WHO MedNet
maraviroc KEGG DRUG
maravirocum WHO MedNet
Manual Xrefs Databases
D06670 KEGG DRUG
DB04835 DrugBank
Maraviroc Wikipedia
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Registry Numbers Types Sources
10131963 Reaxys Registry Number Reaxys
376348-65-1 CAS Registry Number ChemIDplus
376348-65-1 CAS Registry Number KEGG DRUG
Citations Types Sources
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Last Modified
22 February 2017