Ki Summary

Reaction Details

Report a problem with these data

Target

Bifunctional epoxide hydrolase 2

Ligand

BDBM50196662

Substrate/Competitor

n/a

Meas. Tech.

ChEMBL_432025 (CHEMBL918224)

IC50

100±n/a nM

Citation

Kim, IH; Nishi, K; Tsai, HJ; Bradford, T; Koda, Y; Watanabe, T; Morisseau, C; Blanchfield, J; Toth, I; Hammock, BD Design of bioavailable derivatives of 12-(3-adamantan-1-yl-ureido)dodecanoic acid, a potent inhibitor of the soluble epoxide hydrolase. Bioorg Med Chem15:312-23 (2006) [PubMed] Article

More Info.:

Get all data from this article, Assay Method

Bifunctional epoxide hydrolase 2

Name:

Bifunctional epoxide hydrolase 2

Synonyms:

Type:

Enzyme

Mol. Mass.:

62613.07

Organism:

Homo sapiens (Human)

Description:

P34913

Residue:

555

Sequence:

MTLRAAVFDLDGVLALPAVFGVLGRTEEALALPRGLLNDAFQKGGPEGATTRLMKGEITL
SQWIPLMEENCRKCSETAKVCLPKNFSIKEIFDKAISARKINRPMLQAALMLRKKGFTTA
ILTNTWLDDRAERDGLAQLMCELKMHFDFLIESCQVGMVKPEPQIYKFLLDTLKASPSEV
VFLDDIGANLKPARDLGMVTILVQDTDTALKELEKVTGIQLLNTPAPLPTSCNPSDMSHG
YVTVKPRVRLHFVELGSGPAVCLCHGFPESWYSWRYQIPALAQAGYRVLAMDMKGYGESS
APPEIEEYCMEVLCKEMVTFLDKLGLSQAVFIGHDWGGMLVWYMALFYPERVRAVASLNT
PFIPANPNMSPLESIKANPVFDYQLYFQEPGVAEAELEQNLSRTFKSLFRASDESVLSMH
KVCEAGGLFVNSPEEPSLSRMVTEEEIQFYVQQFKKSGFRGPLNWYRNMERNWKWACKSL
GRKILIPALMVTAEKDFVLVPQMSQHMEDWIPHLKRGHIEDCGHWTQMDKPTEVNQILIK
WLDSDARNPPVVSKM

BDBM50196662

n/a

Name

BDBM50196662

Synonyms:

12-(3-adamantan-1-yl-ureido)decanoic acid[1-(2,3,4-trihydroxy-5-hydroxymethyl-cyclohexylcarbamoyl)-nonyl]amide | CHEMBL224266

Type

Small organic molecule

Emp. Form.

C38H68N4O8

Mol. Mass.

708.9685

SMILES

CCCCCCCC(NC(=O)CCCCCCCCCCCNC(=O)NC12CC3CC(CC(C3)C1)C2)C(=O)N[C@H]1O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]1O |TLB:25:26:29:33.32.31,THB:27:28:31:35.26.34,27:26:29.28.33:31,34:26:29:33.32.31,34:32:29:35.27.26|

Structure