Reaction Details |
| Report a problem with these data |
Target | Neutral ceramidase |
---|
Ligand | BDBM50569051 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_2107504 (CHEMBL4816179) |
---|
Ki | 2000±n/a nM |
---|
Citation | Bielsa, N; Casasampere, M; Aseeri, M; Casas, J; Delgado, A; Abad, JL; Fabriās, G Discovery of deoxyceramide analogs as highly selective ACER3 inhibitors in live cells. Eur J Med Chem216:0 (2021) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Neutral ceramidase |
---|
Name: | Neutral ceramidase |
Synonyms: | ASAH2 | ASAH2_HUMAN | Acylsphingosine deacylase 2 | BCDase | HNAC1 | LCDase | N-CDase | N-acylsphingosine amidohydrolase 2 | NCDase | Neutral ceramidase soluble form | Non-lysosomal ceramidase | hCD |
Type: | PROTEIN |
Mol. Mass.: | 85523.37 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_947546 |
Residue: | 780 |
Sequence: | MAKRTFSNLETFLIFLLVMMSAITVALLSLLFITSGTIENHKDLGGHFFSTTQSPPATQG
STAAQRSTATQHSTATQSSTATQTSPVPLTPESPLFQNFSGYHIGVGRADCTGQVADINL
MGYGKSGQNAQGILTRLYSRAFIMAEPDGSNRTVFVSIDIGMVSQRLRLEVLNRLQSKYG
SLYRRDNVILSGTHTHSGPAGYFQYTVFVIASEGFSNQTFQHMVTGILKSIDIAHTNMKP
GKIFINKGNVDGVQINRSPYSYLQNPQSERARYSSNTDKEMIVLKMVDLNGDDLGLISWF
AIHPVSMNNSNHLVNSDNVGYASYLLEQEKNKGYLPGQGPFVAAFASSNLGDVSPNILGP
RCINTGESCDNANSTCPIGGPSMCIAKGPGQDMFDSTQIIGRAMYQRAKELYASASQEVT
GPLASAHQWVDMTDVTVWLNSTHASKTCKPALGYSFAAGTIDGVGGLNFTQGKTEGDPFW
DTIRDQILGKPSEEIKECHKPKPILLHTGELSKPHPWHPDIVDVQIITLGSLAITAIPGE
FTTMSGRRLREAVQAEFASHGMQNMTVVISGLCNVYTHYITTYEEYQAQRYEAASTIYGP
HTLSAYIQLFRNLAKAIATDTVANLSRGPEPPFFKQLIVPLIPSIVDRAPKGRTFGDVLQ
PAKPEYRVGEVAEVIFVGANPKNSVQNQTHQTFLTVEKYEATSTSWQIVCNDASWETRFY
WHKGLLGLSNATVEWHIPDTAQPGIYRIRYFGHNRKQDILKPAVILSFEGTSPAFEVVTI
|
|
|
BDBM50569051 |
---|
n/a |
---|
Name | BDBM50569051 |
Synonyms: | CHEMBL4865548 |
Type | Small organic molecule |
Emp. Form. | C25H49NO2 |
Mol. Mass. | 395.6621 |
SMILES | CCCCCCCCCCCC\C=C\[C@@H](O)[C@@H](C)NC(=O)CCCCCCC |r| |
Structure |
|