Reaction Details |
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Target | Nicotinamide phosphoribosyltransferase |
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Ligand | BDBM50254213 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_1686176 |
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Ki | 21±n/a nM |
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Citation | Curtin, ML; Heyman, HR; Clark, RF; Sorensen, BK; Doherty, GA; Hansen, TM; Frey, RR; Sarris, KA; Aguirre, AL; Shrestha, A; Tu, N; Woller, K; Pliushchev, MA; Sweis, RF; Cheng, M; Wilsbacher, JL; Kovar, PJ; Guo, J; Cheng, D; Longenecker, KL; Raich, D; Korepanova, AV; Soni, NB; Algire, MA; Richardson, PL; Marin, VL; Badagnani, I; Vasudevan, A; Buchanan, FG; Maag, D; Chiang, GG; Tse, C; Michaelides, MR SAR and characterization of non-substrate isoindoline urea inhibitors of nicotinamide phosphoribosyltransferase (NAMPT). Bioorg Med Chem Lett27:3317-3325 (2017) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Nicotinamide phosphoribosyltransferase |
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Name: | Nicotinamide phosphoribosyltransferase |
Synonyms: | NAMPT | NAMPT_HUMAN | NAmPRTase | Nicotinamide phosphoribosyltransferase | Nicotinamide phosphoribosyltransferase (NAMPT) | PBEF | PBEF1 | Pre-B-cell colony-enhancing factor 1 |
Type: | Enzyme |
Mol. Mass.: | 55524.98 |
Organism: | Homo sapiens (Human) |
Description: | P43490 |
Residue: | 491 |
Sequence: | MNPAAEAEFNILLATDSYKVTHYKQYPPNTSKVYSYFECREKKTENSKLRKVKYEETVFY
GLQYILNKYLKGKVVTKEKIQEAKDVYKEHFQDDVFNEKGWNYILEKYDGHLPIEIKAVP
EGFVIPRGNVLFTVENTDPECYWLTNWIETILVQSWYPITVATNSREQKKILAKYLLETS
GNLDGLEYKLHDFGYRGVSSQETAGIGASAHLVNFKGTDTVAGLALIKKYYGTKDPVPGY
SVPAAEHSTITAWGKDHEKDAFEHIVTQFSSVPVSVVSDSYDIYNACEKIWGEDLRHLIV
SRSTQAPLIIRPDSGNPLDTVLKVLEILGKKFPVTENSKGYKLLPPYLRVIQGDGVDINT
LQEIVEGMKQKMWSIENIAFGSGGGLLQKLTRDLLNCSFKCSYVVTNGLGINVFKDPVAD
PNKRSKKGRLSLHRTPAGNFVTLEEGKGDLEEYGQDLLHTVFKNGKVTKSYSFDEIRKNA
QLNIELEAAHH
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BDBM50254213 |
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n/a |
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Name | BDBM50254213 |
Synonyms: | CHEMBL4076641 |
Type | Small organic molecule |
Emp. Form. | C21H18N2O3S |
Mol. Mass. | 378.444 |
SMILES | O=C(Nc1ccc(cc1)S(=O)(=O)c1ccccc1)N1Cc2ccccc2C1 |
Structure |
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