Reaction Details |
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Target | DNA polymerase beta |
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Ligand | BDBM50292441 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_546495 (CHEMBL1026664) |
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IC50 | 2200±n/a nM |
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Citation | Pengsuparp, T; Cai, L; Constant, H; Fong, HH; Lin, LZ; Kinghorn, AD; Pezzuto, JM; Cordell, GA; Ingolfsdöttir, K; Wagner, H; Hughes, SH Mechanistic Evaluation of New Plant-Derived Compounds That Inhibit HIV-1 Reverse Transcriptase J Nat Prod58:1024-1031 (1995) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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DNA polymerase beta |
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Name: | DNA polymerase beta |
Synonyms: | DNA polymerase beta (Pol β) | DPOLB_HUMAN | POLB |
Type: | Protein |
Mol. Mass.: | 38188.76 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 335 |
Sequence: | MSKRKAPQETLNGGITDMLTELANFEKNVSQAIHKYNAYRKAASVIAKYPHKIKSGAEAK
KLPGVGTKIAEKIDEFLATGKLRKLEKIRQDDTSSSINFLTRVSGIGPSAARKFVDEGIK
TLEDLRKNEDKLNHHQRIGLKYFGDFEKRIPREEMLQMQDIVLNEVKKVDSEYIATVCGS
FRRGAESSGDMDVLLTHPSFTSESTKQPKLLHQVVEQLQKVHFITDTLSKGETKFMGVCQ
LPSKNDEKEYPHRRIDIRLIPKDQYYCGVLYFTGSDIFNKNMRAHALEKGFTINEYTIRP
LGVTGVAGEPLPVDSEKDIFDYIQWKYREPKDRSE
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BDBM50292441 |
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n/a |
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Name | BDBM50292441 |
Synonyms: | 1beta-hydroxyaleuritolic acid 3-p-hydroxybenzoate | 1beta-hydroxyaleuritolic acid-3-p-hydroxybenzoate | CHEMBL454727 |
Type | Small organic molecule |
Emp. Form. | C37H52O6 |
Mol. Mass. | 592.8052 |
SMILES | CC1(C)CC[C@@]2(CC=C3[C@]4(C)CC[C@H]5C(C)(C)[C@H](C[C@@H](O)[C@]5(C)[C@H]4CC[C@@]3(C)[C@H]2C1)OC(=O)c1ccc(O)cc1)C(O)=O |r,t:7| |
Structure |
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