Vicriviroc

Vicriviroc
Names
IUPAC name
5-({4-[(3S)-4-{2-methoxy-1-[4-(trifluoromethyl)phenyl]ethyl}-3-methylpiperazin-1-yl]-4-methylpiperidin-1-yl}carbonyl)-4,6-dimethylpyrimidine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
MeSH Vicriviroc
UNII
  • InChI=1S/C28H38F3N5O2/c1-19-16-35(14-15-36(19)24(17-38-5)22-6-8-23(9-7-22)28(29,30)31)27(4)10-12-34(13-11-27)26(37)25-20(2)32-18-33-21(25)3/h6-9,18-19,24H,10-17H2,1-5H3/t19-,24?/m0/s1 checkY
    Key: CNPVJJQCETWNEU-XGLRFROISA-N checkY
  • InChI=1/C28H38F3N5O2/c1-19-16-35(14-15-36(19)24(17-38-5)22-6-8-23(9-7-22)28(29,30)31)27(4)10-12-34(13-11-27)26(37)25-20(2)32-18-33-21(25)3/h6-9,18-19,24H,10-17H2,1-5H3/t19-,24?/m0/s1
    Key: CNPVJJQCETWNEU-XGLRFROIBK
  • FC(F)(F)c1ccc(cc1)[C@H](COC)N2CCN(C[C@@H]2C)C3(C)CCN(CC3)C(=O)c4c(C)ncnc4C
Properties
C28H38F3N5O2
Molar mass 533.629 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Vicriviroc, previously named SCH 417690 and SCH-D, is a pyrimidine CCR5 entry inhibitor of HIV-1. It was developed by the pharmaceutical company Schering-Plough. Merck decided to not pursue regulatory approval for use in treatment-experienced patients because the drug did not meet primary efficacy endpoints in late stage trials. Clinical trials continue in patients previously untreated for HIV.