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Assay Detail

CHEMBL4137333

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of [3H]BMS-488043 binding to HIV-1 JRFL gp120 after 1 hr by scintillation counting method
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human immunodeficiency virus 1
Confidence 9 — Direct single protein target
Curated By Intermediate

Target

Envelope glycoprotein gp160 (CHEMBL1293311)
Type SINGLE PROTEIN
Organism Human immunodeficiency virus 1

Publication

Discovery of the Human Immunodeficiency Virus Type 1 (HIV-1) Attachment Inhibitor Temsavir and Its Phosphonooxymethyl Prodrug Fostemsavir.
Wang T, Ueda Y, Zhang Z, Yin Z, Matiskella J, Pearce BC, Yang Z, Zheng M, Parker DD, Yamanaka GA, Gong YF, Ho HT, Colonno RJ, Langley DR, Lin PF, Meanwell NA, Kadow JF.
J Med Chem (2018) 61 : 6308 -6327
PubMed 29920093 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 2 8.40 9.08

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3301620 TEMSAVIR 2.0 1 9.08
CHEMBL238103 1 7.72

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3301620 TEMSAVIR Kd = 0.83 nM 9.08
CHEMBL238103 Kd = 19.0 nM 7.72