Reaction Details |
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Target | Reverse transcriptase |
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Ligand | BDBM50478732 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_552634 (CHEMBL957279) |
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IC50 | 740±n/a nM |
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Citation | Cesarini, S; Spallarossa, A; Ranise, A; Schenone, S; Bruno, O; La Colla, P; Casula, L; Collu, G; Sanna, G; Loddo, R Parallel one-pot synthesis and structure-activity relationship study of symmetric formimidoester disulfides as a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors. Bioorg Med Chem16:6353-63 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Reverse transcriptase |
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Name: | Reverse transcriptase |
Synonyms: | n/a |
Type: | Protein |
Mol. Mass.: | 29598.37 |
Organism: | Human immunodeficiency virus 1 |
Description: | Q9WKE8 |
Residue: | 254 |
Sequence: | PISPITVPVKLKPGMDGPKVKQWPLTEEKIKALTEICTEMEKEGKIEKIGPENPYNTPVF
AIKKKDSTKWRKVVDFRELNKRTQDFWEVQLGIPHPAGLKKKKSVTVLDVGDAYFSVPLD
KDFRKYTAFTIPSINNETPGIRYQYNVLPQGWKGSPAIFQSSMTKILEPFRKQNPDIVIY
QYMDDLYVGSDLEIEQHRAKIEELRQHLLRWGFTTPDKKHQKEPPFLWMGYELHPDKWTV
QPIVLPEKDSWTVN
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BDBM50478732 |
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n/a |
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Name | BDBM50478732 |
Synonyms: | CHEMBL443403 |
Type | Small organic molecule |
Emp. Form. | C34H24Br2N4O6S2 |
Mol. Mass. | 808.516 |
SMILES | Brc1ccc(cc1)\N=C(/OCCN1C(=O)c2ccccc2C1=O)SS\C(OCCN1C(=O)c2ccccc2C1=O)=N\c1ccc(Br)cc1 |
Structure |
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