Reaction Details |
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Target | Chondroitin sulfate N-acetylgalactosaminyltransferase 1 |
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Ligand | BDBM50386148 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_824644 (CHEMBL2045702) |
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IC50 | 69000±n/a nM |
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Citation | Jadhav, RD; Kadam, KS; Kandre, S; Guha, T; Reddy, MM; Brahma, MK; Deshmukh, NJ; Dixit, A; Doshi, L; Potdar, N; Enose, AA; Vishwakarma, RA; Sivaramakrishnan, H; Srinivasan, S; Nemmani, KV; Gupte, A; Gangopadhyay, AK; Sharma, R Synthesis and biological evaluation of isoxazole, oxazole, and oxadiazole containing heteroaryl analogs of biaryl ureas as DGAT1 inhibitors. Eur J Med Chem54:324-42 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Chondroitin sulfate N-acetylgalactosaminyltransferase 1 |
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Name: | Chondroitin sulfate N-acetylgalactosaminyltransferase 1 |
Synonyms: | Beta4GalNAcT-1 | CGAT1_HUMAN | CHGN | CSGALNACT1 | Chondroitin beta-1,4-N-acetylgalactosaminyltransferase 1 | CsGalNAcT-1 | GALNACT1 |
Type: | PROTEIN |
Mol. Mass.: | 61307.78 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_824644 |
Residue: | 532 |
Sequence: | MMMVRRGLLAWISRVVVLLVLLCCAISVLYMLACTPKGDEEQLALPRANSPTGKEGYQAV
LQEWEEQHRNYVSSLKRQIAQLKEELQERSEQLRNGQYQASDAAGLGLDRSPPEKTQADL
LAFLHSQVDKAEVNAGVKLATEYAAVPFDSFTLQKVYQLETGLTRHPEEKPVRKDKRDEL
VEAIESALETLNSPAENSPNHRPYTASDFIEGIYRTERDKGTLYELTFKGDHKHEFKRLI
LFRPFGPIMKVKNEKLNMANTLINVIVPLAKRVDKFRQFMQNFREMCIEQDGRVHLTVVY
FGKEEINEVKGILENTSKAANFRNFTFIQLNGEFSRGKGLDVGARFWKGSNVLLFFCDVD
IYFTSEFLNTCRLNTQPGKKVFYPVLFSQYNPGIIYGHHDAVPPLEQQLVIKKETGFWRD
FGFGMTCQYRSDFINIGGFDLDIKGWGGEDVHLYRKYLHSNLIVVRTPVRGLFHLWHEKR
CMDELTPEQYKMCMQSKAMNEASHGQLGMLVFRHEIEAHLRKQKQKTSSKKT
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BDBM50386148 |
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n/a |
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Name | BDBM50386148 |
Synonyms: | CHEMBL2042350 |
Type | Small organic molecule |
Emp. Form. | C23H23FN4O5 |
Mol. Mass. | 454.4509 |
SMILES | CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2cc(F)ccc2C)cc1)C(O)=O |r| |
Structure |
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