Ki Summary

Reaction Details

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Target

Peroxisome proliferator-activated receptor alpha

Ligand

BDBM50373916

Substrate/Competitor

n/a

Meas. Tech.

ChEMBL_468712 (CHEMBL929848)

EC50

300±n/a nM

Citation

Asaki, T; Aoki, T; Hamamoto, T; Sugiyama, Y; Ohmachi, S; Kuwabara, K; Murakami, K; Todo, M Structure-activity studies on 1,3-dioxane-2-carboxylic acid derivatives, a novel class of subtype-selective peroxisome proliferator-activated receptor alpha (PPARalpha) agonists. Bioorg Med Chem16:981-94 (2008) [PubMed] Article

More Info.:

Get all data from this article, Assay Method

Peroxisome proliferator-activated receptor alpha

Name:

Peroxisome proliferator-activated receptor alpha

Synonyms:

Type:

Enzyme

Mol. Mass.:

52222.08

Organism:

Homo sapiens (Human)

Description:

Q07869

Residue:

468

Sequence:

MVDTESPLCPLSPLEAGDLESPLSEEFLQEMGNIQEISQSIGEDSSGSFGFTEYQYLGSC
PGSDGSVITDTLSPASSPSSVTYPVVPGSVDESPSGALNIECRICGDKASGYHYGVHACE
GCKGFFRRTIRLKLVYDKCDRSCKIQKKNRNKCQYCRFHKCLSVGMSHNAIRFGRMPRSE
KAKLKAEILTCEHDIEDSETADLKSLAKRIYEAYLKNFNMNKVKARVILSGKASNNPPFV
IHDMETLCMAEKTLVAKLVANGIQNKEAEVRIFHCCQCTSVETVTELTEFAKAIPGFANL
DLNDQVTLLKYGVYEAIFAMLSSVMNKDGMLVAYGNGFITREFLKSLRKPFCDIMEPKFD
FAMKFNALELDDSDISLFVAAIICCGDRPGLLNVGHIEKMQEGIVHVLRLHLQSNHPDDI
FLFPKLLQKMADLRQLVTEHAQLVQIIKKTESDAALHPLLQEIYRDMY

BDBM50373916

n/a

Name

BDBM50373916

Synonyms:

CHEMBL273036

Type

Small organic molecule

Emp. Form.

C21H24F3NO5

Mol. Mass.

427.4142

SMILES

Cc1ccc(cc1)-c1nc(CCCC[C@H]2CO[C@](C)(OC2)C(O)=O)c(o1)C(F)(F)F |wU:14.14,17.22,wD:17.18,(-11.55,-40.45,;-10.01,-40.46,;-9.25,-41.78,;-7.72,-41.79,;-6.96,-40.47,;-7.72,-39.14,;-9.25,-39.14,;-5.41,-40.47,;-4.51,-41.72,;-3.04,-41.24,;-1.8,-42.15,;-.39,-41.53,;.85,-42.43,;2.26,-41.81,;3.51,-42.72,;4.9,-42.09,;6.15,-43,;5.98,-44.54,;5.97,-46.08,;4.57,-45.15,;3.33,-44.25,;7.51,-44.54,;8.28,-45.86,;8.28,-43.2,;-3.04,-39.7,;-4.5,-39.23,;-1.79,-38.8,;-.47,-38.02,;-2.64,-37.51,;-.95,-40.09,)|

Structure