Reaction Details |
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Target | Peroxisome proliferator-activated receptor delta |
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Ligand | BDBM50383371 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_1541804 |
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IC50 | 29±n/a nM |
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Citation | Kaupang, Å; Kase, ET; Vo, CX; Amundsen, M; Vik, A; Hansen, TV Synthesis of 5-trifluoromethyl-2-sulfonylpyridine PPARß/d antagonists: Effects on the affinity and selectivity towards PPARß/d. Bioorg Med Chem24:247-60 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Peroxisome proliferator-activated receptor delta |
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Name: | Peroxisome proliferator-activated receptor delta |
Synonyms: | NR1C2 | NUC1 | NUCI | Nuclear hormone receptor 1 | Nuclear receptor subfamily 1 group C member 2 | PPAR delta | PPAR-beta | PPARB | PPARD | PPARD_HUMAN | Peroxisome proliferator-activated receptor | Peroxisome proliferator-activated receptor beta | Peroxisome proliferator-activated receptor delta |
Type: | Enzyme |
Mol. Mass.: | 49910.45 |
Organism: | Homo sapiens (Human) |
Description: | Q03181 |
Residue: | 441 |
Sequence: | MEQPQEEAPEVREEEEKEEVAEAEGAPELNGGPQHALPSSSYTDLSRSSSPPSLLDQLQM
GCDGASCGSLNMECRVCGDKASGFHYGVHACEGCKGFFRRTIRMKLEYEKCERSCKIQKK
NRNKCQYCRFQKCLALGMSHNAIRFGRMPEAEKRKLVAGLTANEGSQYNPQVADLKAFSK
HIYNAYLKNFNMTKKKARSILTGKASHTAPFVIHDIETLWQAEKGLVWKQLVNGLPPYKE
ISVHVFYRCQCTTVETVRELTEFAKSIPSFSSLFLNDQVTLLKYGVHEAIFAMLASIVNK
DGLLVANGSGFVTREFLRSLRKPFSDIIEPKFEFAVKFNALELDDSDLALFIAAIILCGD
RPGLMNVPRVEAIQDTILRALEFHLQANHPDAQYLFPKLLQKMADLRQLVTEHAQMMQRI
KKTETETSLHPLLQEIYKDMY
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BDBM50383371 |
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n/a |
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Name | BDBM50383371 |
Synonyms: | CHEMBL2030550 |
Type | Small organic molecule |
Emp. Form. | C20H20BrN3 |
Mol. Mass. | 382.297 |
SMILES | CN1CCN(CC1)c1ccc(\C=C(/C#N)c2ccccc2Br)cc1 |
Structure |
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