Reaction Details |
| Report a problem with these data |
Target | Histone-lysine N-methyltransferase SMYD3 |
---|
Ligand | BDBM378447 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | SMYD3 Biochemical Assay |
---|
IC50 | 0.900±n/a nM |
---|
Citation | Foley, MA; Kuntz, KW; Mills, JE; Mitchell, LH; Munchhof, MJ; Harvey, DM Substituted 1,2,3-triazoles as SMYD inhibitors for treating cancer US Patent US10266526 Publication Date 4/23/2019 |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Histone-lysine N-methyltransferase SMYD3 |
---|
Name: | Histone-lysine N-methyltransferase SMYD3 |
Synonyms: | SET and MYND domain-containing protein 3 | SMYD3 | SMYD3_HUMAN | ZMYND1 | ZNFN3A1 | Zinc finger MYND domain-containing protein 1 |
Type: | Enzyme |
Mol. Mass.: | 49101.22 |
Organism: | Homo sapiens (Human) |
Description: | Q9H7B4-2 |
Residue: | 428 |
Sequence: | MEPLKVEKFATAKRGNGLRAVTPLRPGELLFRSDPLAYTVCKGSRGVVCDRCLLGKEKLM
RCSQCRVAKYCSAKCQKKAWPDHKRECKCLKSCKPRYPPDSVRLLGRVVFKLMDGAPSES
EKLYSFYDLESNINKLTEDKKEGLRQLVMTFQHFMREEIQDASQLPPAFDLFEAFAKVIC
NSFTICNAEMQEVGVGLYPSISLLNHSCDPNCSIVFNGPHLLLRAVRDIEVGEELTICYL
DMLMTSEERRKQLRDQYCFECDCFRCQTQDKDADMLTGDEQVWKEVQESLKKIEELKAHW
KWEQVLAMCQAIISSNSERLPDINIYQLKVLDCAMDACINLGLLEEALFYGTRTMEPYRI
FFPGSHPVRGVQVMKVGKLQLHQGMFPQAMKNLRLAFDIMRVTHGREHSLIEDLILLLEE
CDANIRAS
|
|
|
BDBM378447 |
---|
n/a |
---|
Name | BDBM378447 |
Synonyms: | N-((2S,4S)-1-((4-aminopiperidin-1-yl)sulfonyl)-2-methylpiperidin-4-yl)-2-oxoindoline-5-carboxamide | US10266526, Compound 580 |
Type | Small organic molecule |
Emp. Form. | C20H29N5O4S |
Mol. Mass. | 435.54 |
SMILES | C[C@H]1C[C@H](CCN1S(=O)(=O)N1CCC(N)CC1)NC(=O)c1ccc2NC(=O)Cc2c1 |r| |
Structure |
|