Reaction Details |
| Report a problem with these data |
Target | Polyunsaturated fatty acid lipoxygenase ALOX12 |
---|
Ligand | BDBM50240865 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_636732 (CHEMBL1167021) |
---|
IC50 | 22000±n/a nM |
---|
Citation | Robinson, SJ; Hoobler, EK; Riener, M; Loveridge, ST; Tenney, K; Valeriote, FA; Holman, TR; Crews, P Using enzyme assays to evaluate the structure and bioactivity of sponge-derived meroterpenes. J Nat Prod72:1857-63 (2009) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Polyunsaturated fatty acid lipoxygenase ALOX12 |
---|
Name: | Polyunsaturated fatty acid lipoxygenase ALOX12 |
Synonyms: | 12-LOX | 12-Lipoxygenase (12-LOX) | 12LO | ALOX12 | Arachidonate 12-lipoxygenase | Arachidonate 12-lipoxygenase, 12S-type | LOG12 | LOX12_HUMAN | Platelet 12-lipoxygenase | Platelet-type lipoxygenase 12 |
Type: | Protein |
Mol. Mass.: | 75689.18 |
Organism: | Homo sapiens (Human) |
Description: | P18054 |
Residue: | 663 |
Sequence: | MGRYRIRVATGAWLFSGSYNRVQLWLVGTRGEAELELQLRPARGEEEEFDHDVAEDLGLL
QFVRLRKHHWLVDDAWFCDRITVQGPGACAEVAFPCYRWVQGEDILSLPEGTARLPGDNA
LDMFQKHREKELKDRQQIYCWATWKEGLPLTIAADRKDDLPPNMRFHEEKRLDFEWTLKA
GALEMALKRVYTLLSSWNCLEDFDQIFWGQKSALAEKVRQCWQDDELFSYQFLNGANPML
LRRSTSLPSRLVLPSGMEELQAQLEKELQNGSLFEADFILLDGIPANVIRGEKQYLAAPL
VMLKMEPNGKLQPMVIQIQPPNPSSPTPTLFLPSDPPLAWLLAKSWVRNSDFQLHEIQYH
LLNTHLVAEVIAVATMRCLPGLHPIFKFLIPHIRYTMEINTRARTQLISDGGIFDKAVST
GGGGHVQLLRRAAAQLTYCSLCPPDDLADRGLLGLPGALYAHDALRLWEIIARYVEGIVH
LFYQRDDIVKGDPELQAWCREITEVGLCQAQDRGFPVSFQSQSQLCHFLTMCVFTCTAQH
AAINQGQLDWYAWVPNAPCTMRMPPPTTKEDVTMATVMGSLPDVRQACLQMAISWHLSRR
QPDMVPLGHHKEKYFSGPKPKAVLNQFRTDLEKLEKEITARNEQLDWPYEYLKPSCIENS
VTI
|
|
|
BDBM50240865 |
---|
n/a |
---|
Name | BDBM50240865 |
Synonyms: | (4aS,6aS,12aR,12bS)-10-Hydroxy-4,4,6a,12b-tetramethyl-1,2,3,4,4a,5,6,6a,12a,12b-decahydro-benzo[a]xanthen-9-one | CHEMBL157844 | PUUPEHENONE |
Type | Small organic molecule |
Emp. Form. | C21H28O3 |
Mol. Mass. | 328.4452 |
SMILES | CC1(C)CCC[C@@]2(C)[C@H]1CC[C@]1(C)OC3=CC(=O)C(=O)CC3=C[C@H]21 |r,c:23,t:15| |
Structure |
|