BDBM1355 (9bR)-9b-phenyl-2H,3H,5H,9bH-isoindolo[1,2-b][1,3]thiazol-5-one::(R)-9b-Phenyl-2,3-dihydrothiazolo[2,3-a]isoindol-5(9bH)-one::Thiazoloisoindol-5-one deriv. 1R
SMILES: O=C1N2CCS[C@@]2(c2ccccc12)c1ccccc1
InChI Key: InChIKey=CTGFADZNCCTVMP-MRXNPFEDSA-N
Data: 1 IC50
PDB links: 2 PDB IDs contain this monomer as substructures. 2 PDB IDs contain inhibitors having a similarity of 90% to this monomer.
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
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HIV-1 Reverse Transcriptase (Human immunodeficiency virus type 1) | BDBM1355 ((9bR)-9b-phenyl-2H,3H,5H,9bH-isoindolo[1,2-b][1,3]...) | PDB MMDB B.MOAD GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 280 | n/a | n/a | n/a | n/a | 7.7 | 37 |
Boehringer Mannheim GmbH | Assay Description The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro. | J Med Chem 36: 2526-35 (1993) Article DOI: 10.1021/jm00069a011 BindingDB Entry DOI: 10.7270/Q2BR8QCZ | |||||||||||
More data for this Ligand-Target Pair | 3D Structure (docked) |