Reaction Details |
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Target | Reverse transcriptase |
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Ligand | BDBM50187658 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_545151 (CHEMBL1018093) |
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IC50 | >703000±n/a nM |
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Citation | Tan, GT; Pezzuto, JM; Kinghorn, AD; Hughes, SH Evaluation of natural products as inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase. J Nat Prod54:143-54[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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BDBM50187658 |
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n/a |
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Name | BDBM50187658 |
Synonyms: | 4',5-dihydroxy-7-methoxy flavone | 4',5-dihydroxy-7-methoxyflavone | 5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-chromen-4-one | 7-O-methylapigenin | CHEMBL210635 | Gonkwanin | genkwanin |
Type | Small organic molecule |
Emp. Form. | C16H12O5 |
Mol. Mass. | 284.2635 |
SMILES | COc1cc(O)c2c(c1)oc(cc2=O)-c1ccc(O)cc1 |
Structure |
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