Reaction Details |
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Target | Ceramide glucosyltransferase |
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Ligand | BDBM50602025 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2238979 (CHEMBL5152875) |
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IC50 | 3.6±n/a nM |
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Citation | Wang, J; Reynolds, M; Ibáñez, I; Sasaki, Y; Tanaka, Y; Kikuchi, F; Ohashi, T; Sato, S; Miyabayashi, M; Fujii, T; Tanaka, Y Photoredox-based late-stage functionalization in SAR study for in vivo potent glucosylceramide synthase inhibitor. Bioorg Med Chem Lett77:0 (2022) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Ceramide glucosyltransferase |
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Name: | Ceramide glucosyltransferase |
Synonyms: | CEGT_HUMAN | GCS | GLCT-1 | Glucosylceramide synthase | UDP-glucose ceramide glucosyltransferase | UDP-glucose:N-acylsphingosine D-glucosyltransferase | UGCG |
Type: | PROTEIN |
Mol. Mass.: | 44859.25 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1435474 |
Residue: | 394 |
Sequence: | MALLDLALEGMAVFGFVLFLVLWLMHFMAIIYTRLHLNKKATDKQPYSKLPGVSLLKPLK
GVDPNLINNLETFFELDYPKYEVLLCVQDHDDPAIDVCKKLLGKYPNVDARLFIGGKKVG
INPKINNLMPGYEVAKYDLIWICDSGIRVIPDTLTDMVNQMTEKVGLVHGLPYVADRQGF
AATLEQVYFGTSHPRYYISANVTGFKCVTGMSCLMRKDVLDQAGGLIAFAQYIAEDYFMA
KAIADRGWRFAMSTQVAMQNSGSYSISQFQSRMIRWTKLRINMLPATIICEPISECFVAS
LIIGWAAHHVFRWDIMVFFMCHCLAWFIFDYIQLRGVQGGTLCFSKLDYAVAWFIRESMT
IYIFLSALWDPTISWRTGRYRLRCGGTAEEILDV
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BDBM50602025 |
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n/a |
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Name | BDBM50602025 |
Synonyms: | CHEMBL5181454 |
Type | Small organic molecule |
Emp. Form. | C28H27F3N2O4 |
Mol. Mass. | 512.5202 |
SMILES | CC(C)(O)c1ccc(cc1)N1Cc2c(cc(nc2-c2ccccc2OCC(F)(F)F)C2(C)COC2)C1=O |
Structure |
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