Reaction Details |
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Target | Hemagglutinin-neuraminidase |
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Ligand | BDBM50341457 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_741750 (CHEMBL1769849) |
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IC50 | 2000000±n/a nM |
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Citation | Nishino, R; Ikeda, K; Hayakawa, T; Takahashi, T; Suzuki, T; Sato, M Syntheses of 2-deoxy-2,3-didehydro-N-acetylneuraminic acid analogues modified by N-sulfonylamidino groups at the C-4 position and biological evaluation as inhibitors of human parainfluenza virus type 1. Bioorg Med Chem19:2418-27 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Hemagglutinin-neuraminidase |
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Name: | Hemagglutinin-neuraminidase |
Synonyms: | n/a |
Type: | PROTEIN |
Mol. Mass.: | 64031.12 |
Organism: | Human parainfluenza virus 1 |
Description: | ChEMBL_741750 |
Residue: | 575 |
Sequence: | MAEKGKTNSSYWSTTRNDNSTVNTYIDTPAGKTHIWLLIATTMHTILSFIIMILCIDLII
KQDTCMKTNIITISSMNESAKTIKETITELIRQEVISRTINIQSSVQSGIPILLNKQSRD
LTQLIEKSCNRQELAQICENTNAIHHADGISPLDPHDFWRCPVGEPLLSDNPNISLLPGP
SLLSGSTTISGCVRLPSLSIGDAIYAYSSNLITQGCADIGKSYQVLQLGYISLNSDMYPD
LNPVISHTYDINDNRKSCSVIAAGTRGYQLCSLPTVNETTDYSSEGIEDLVFDILDLKGK
TKSHRYKNEDITFDHPFSAMYPSVGSGIKIENTLIFLGYGGLTTPLQGDTKCVTNRCANV
NQSVCNDALKITWRLKKRQVNVLIRINNYLSDRPKIVVETIPITQNYLGAEGRLLKLGKK
IYIYTRSSGWHSHLQIGSLDINNPMTIKWAPHEVLSRPGNQDCNWYNRCPRECISGVYTD
AYPLSPDAVNVATTTLYANTSRVNPTIMYSNTSEIINMLRLKNVQLEAAYTTTSCITHFG
KGYCFHIVEINQTSLNTLQPMLFKTSIPKICKITS
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BDBM50341457 |
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n/a |
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Name | BDBM50341457 |
Synonyms: | 5-Acetamido-2,6-anhydro-3,5-dideoxy-4-[2-(thiophen-2-yl)-N'-(methylsulfonyl)acetimidamido]-D-glycero-D-galactonon-2-enonic acid | CHEMBL1767335 |
Type | Small organic molecule |
Emp. Form. | C18H25N3O9S2 |
Mol. Mass. | 491.536 |
SMILES | CC(=O)N[C@H]1[C@@H](OC(=C[C@@H]1N=C(Cc1cccs1)NS(C)(=O)=O)C(O)=O)[C@H](O)[C@H](O)CO |r,w:11.19,c:7| |
Structure |
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