Reaction Details |
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Target | Aryl hydrocarbon receptor |
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Ligand | BDBM50185305 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1587673 (CHEMBL3825787) |
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EC50 | 2300±n/a nM |
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Citation | Smutny, T; Nova, A; Drechslerová, M; Carazo, A; Hyrsova, L; Hru?ková, ZR; Kune?, J; Pour, M; ?pulák, M; Pavek, P 2-(3-Methoxyphenyl)quinazoline Derivatives: A New Class of Direct Constitutive Androstane Receptor (CAR) Agonists. J Med Chem59:4601-10 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Aryl hydrocarbon receptor |
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Name: | Aryl hydrocarbon receptor |
Synonyms: | AHR | AHR_HUMAN | BHLHE76 | Class E basic helix-loop-helix protein 76 | aryl hydrocarbon receptor precursor |
Type: | PROTEIN |
Mol. Mass.: | 96143.77 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1503828 |
Residue: | 848 |
Sequence: | MNSSSANITYASRKRRKPVQKTVKPIPAEGIKSNPSKRHRDRLNTELDRLASLLPFPQDV
INKLDKLSVLRLSVSYLRAKSFFDVALKSSPTERNGGQDNCRAANFREGLNLQEGEFLLQ
ALNGFVLVVTTDALVFYASSTIQDYLGFQQSDVIHQSVYELIHTEDRAEFQRQLHWALNP
SQCTESGQGIEEATGLPQTVVCYNPDQIPPENSPLMERCFICRLRCLLDNSSGFLAMNFQ
GKLKYLHGQKKKGKDGSILPPQLALFAIATPLQPPSILEIRTKNFIFRTKHKLDFTPIGC
DAKGRIVLGYTEAELCTRGSGYQFIHAADMLYCAESHIRMIKTGESGMIVFRLLTKNNRW
TWVQSNARLLYKNGRPDYIIVTQRPLTDEEGTEHLRKRNTKLPFMFTTGEAVLYEATNPF
PAIMDPLPLRTKNGTSGKDSATTSTLSKDSLNPSSLLAAMMQQDESIYLYPASSTSSTAP
FENNFFNESMNECRNWQDNTAPMGNDTILKHEQIDQPQDVNSFAGGHPGLFQDSKNSDLY
SIMKNLGIDFEDIRHMQNEKFFRNDFSGEVDFRDIDLTDEILTYVQDSLSKSPFIPSDYQ
QQQSLALNSSCMVQEHLHLEQQQQHHQKQVVVEPQQQLCQKMKHMQVNGMFENWNSNQFV
PFNCPQQDPQQYNVFTDLHGISQEFPYKSEMDSMPYTQNFISCNQPVLPQHSKCTELDYP
MGSFEPSPYPTTSSLEDFVTCLQLPENQKHGLNPQSAIITPQTCYAGAVSMYQCQPEPQH
THVGQMQYNPVLPGQQAFLNKFQNGVLNETYPAELNNINNTQTTTHLQPLHHPSEARPFP
DLTSSGFL
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BDBM50185305 |
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n/a |
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Name | BDBM50185305 |
Synonyms: | CHEMBL3822867 |
Type | Small organic molecule |
Emp. Form. | C16H14N2OS |
Mol. Mass. | 282.36 |
SMILES | COc1cccc(c1)-c1nc(SC)c2ccccc2n1 |
Structure |
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