| Reaction Details |
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 | Report a problem with these data |
| Target | Uromodulin |
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| Ligand | BDBM534921 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | In-Vitro Assay |
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| IC50 | 4.00±n/a nM |
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| Citation |  Sharma, R; Iyer, P; Agarwal, S Substituted sulfoximine compounds US Patent US11236045 Publication Date 2/1/2022 |
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| More Info.: | Get all data from this article, Assay Method |
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| Uromodulin |
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| Name: | Uromodulin |
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| Synonyms: | THP | Tamm-Horsfall urinary glycoprotein | UMOD | UROM_HUMAN |
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| Type: | Protein |
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| Mol. Mass.: | 69744.65 |
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| Organism: | Human |
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| Description: | P07911 |
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| Residue: | 640 |
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| Sequence: | MGQPSLTWMLMVVVASWFITTAATDTSEARWCSECHSNATCTEDEAVTTCTCQEGFTGDG
LTCVDLDECAIPGAHNCSANSSCVNTPGSFSCVCPEGFRLSPGLGCTDVDECAEPGLSHC
HALATCVNVVGSYLCVCPAGYRGDGWHCECSPGSCGPGLDCVPEGDALVCADPCQAHRTL
DEYWRSTEYGEGYACDTDLRGWYRFVGQGGARMAETCVPVLRCNTAAPMWLNGTHPSSDE
GIVSRKACAHWSGHCCLWDASVQVKACAGGYYVYNLTAPPECHLAYCTDPSSVEGTCEEC
SIDEDCKSNNGRWHCQCKQDFNITDISLLEHRLECGANDMKVSLGKCQLKSLGFDKVFMY
LSDSRCSGFNDRDNRDWVSVVTPARDGPCGTVLTRNETHATYSNTLYLADEIIIRDLNIK
INFACSYPLDMKVSLKTALQPMVSALNIRVGGTGMFTVRMALFQTPSYTQPYQGSSVTLS
TEAFLYVGTMLDGGDLSRFALLMTNCYATPSSNATDPLKYFIIQDRCPHTRDSTIQVVEN
GESSQGRFSVQMFRFAGNYDLVYLHCEVYLCDTMNEKCKPTCSGTRFRSGSVIDQSRVLN
LGPITRKGVQATVSRAFSSLGLLKVWLPLLLSATLTLTFQ
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| BDBM534921 |
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| n/a |
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| Name | BDBM534921 |
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| Synonyms: | N′-cyano-1-(4-cyanophenyl)-N-((1,2,3,5,6,7-hexahydro-s-indacen-4-yl)carbamoyl)-methanesulfonimidamide | US11236045, Example 66 |
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| Type | Small organic molecule |
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| Emp. Form. | C22H21N5O2S |
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| Mol. Mass. | 419.499 |
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| SMILES | O=C(Nc1c2CCCc2cc2CCCc12)NS(=O)(Cc1ccc(cc1)C#N)=NC#N |
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| Structure | 
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