Reaction Details |
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Target | Steryl-sulfatase |
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Ligand | BDBM50528712 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1906080 (CHEMBL4408438) |
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IC50 | 33±n/a nM |
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Citation | Moi, D; Foster, PA; Rimmer, LG; Jaffri, A; Deplano, A; Balboni, G; Onnis, V; Potter, BVL Synthesis and in vitro evaluation of piperazinyl-ureido sulfamates as steroid sulfatase inhibitors. Eur J Med Chem182:0 (2019) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Steryl-sulfatase |
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Name: | Steryl-sulfatase |
Synonyms: | ARSC1 | ASC | Arylsulfatase C | STS | STS_HUMAN | Steroid sulfatase | Steryl-sulfate sulfohydrolase |
Type: | Enzyme |
Mol. Mass.: | 65503.66 |
Organism: | Homo sapiens (Human) |
Description: | P08842 |
Residue: | 583 |
Sequence: | MPLRKMKIPFLLLFFLWEAESHAASRPNIILVMADDLGIGDPGCYGNKTIRTPNIDRLAS
GGVKLTQHLAASPLCTPSRAAFMTGRYPVRSGMASWSRTGVFLFTASSGGLPTDEITFAK
LLKDQGYSTALIGKWHLGMSCHSKTDFCHHPLHHGFNYFYGISLTNLRDCKPGEGSVFTT
GFKRLVFLPLQIVGVTLLTLAALNCLGLLHVPLGVFFSLLFLAALILTLFLGFLHYFRPL
NCFMMRNYEIIQQPMSYDNLTQRLTVEAAQFIQRNTETPFLLVLSYLHVHTALFSSKDFA
GKSQHGVYGDAVEEMDWSVGQILNLLDELRLANDTLIYFTSDQGAHVEEVSSKGEIHGGS
NGIYKGGKANNWEGGIRVPGILRWPRVIQAGQKIDEPTSNMDIFPTVAKLAGAPLPEDRI
IDGRDLMPLLEGKSQRSDHEFLFHYCNAYLNAVRWHPQNSTSIWKAFFFTPNFNPVGSNG
CFATHVCFCFGSYVTHHDPPLLFDISKDPRERNPLTPASEPRFYEILKVMQEAADRHTQT
LPEVPDQFSWNNFLWKPWLQLCCPSTGLSCQCDREKQDKRLSR
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BDBM50528712 |
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n/a |
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Name | BDBM50528712 |
Synonyms: | CHEMBL4471248 |
Type | Small organic molecule |
Emp. Form. | C21H36N4O4S |
Mol. Mass. | 440.6 |
SMILES | CCCCCCCCCCN1CCN(CC1)C(=O)Nc1ccc(OS(N)(=O)=O)cc1 |
Structure |
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