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TargetNeuraminidase
LigandBDBM4995
Substrate/CompetitorBDBM4702
Meas. Tech.Neuraminidase Inhibition Assay
IC50 3±n/a nM
Citation Kim, CULew, WWilliams, MAWu, HZhang, LChen, XEscarpe, PAMendel, DBLaver, WGStevens, RC Structure-activity relationship studies of novel carbocyclic influenza neuraminidase inhibitors. J Med Chem41:2451-60 (1998) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Neuraminidase
Name:Neuraminidase
Synonyms:Influenza B Virus Neuraminidase | NA | NRAM_INBLE | Neuraminidase | Neuraminidase B
Type:Enzyme
Mol. Mass.:51446.67
Organism:Influenza B virus (B/Lee/40)
Description:n/a
Residue:466
Sequence:
MLPSTVQTLTLLLTSGGVLLSLYVSASLSYLLYSDVLLKFSSTKTTAPTMSLECTNASNA
QTVNHSATKEMTFPPPEPEWTYPRLSCQGSTFQKALLISPHRFGEIKGNSAPLIIREPFV
ACGPKECRHFALTHYAAQPGGYYNGTRKDRNKLRHLVSVKLGKIPTVENSIFHMAAWSGS
ACHDGREWTYIGVDGPDNDALVKIKYGEAYTDTYHSYAHNILRTQESACNCIGGDCYLMI
TDGSASGISKCRFLKIREGRIIKEILPTGRVEHTEECTCGFASNKTIECACRDNSYTAKR
PFVKLNVETDTAEIRLMCTKTYLDTPRPDDGSIAGPCESNGDKWLGGIKGGFVHQRMASK
IGRWYSRTMSKTNRMGMELYVKYDGDPWTDSDALTLSGVMVSIEEPGWYSFGFEIKDKKC
DVPCIGIEMVHDGGKDTWHSAATAIYCLMGSGQLLWDTVTGVDMAL
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  Blast E-value cutoff:
BDBM4995
BDBM4702
NameBDBM4995
Synonyms:(3R,4R,5S)-4-Acetamido-5-amino-3-[[(1S)-1-ethylbut-3-enyl]oxy]-1-cyclohexene-1-carboxylic Acid | (3R,4R,5S)-5-amino-4-acetamido-3-[(3S)-hex-5-en-3-yloxy]cyclohex-1-ene-1-carboxylic acid | Carbocyclic Analogue 45
TypeSmall organic molecule
Emp. Form.C15H24N2O4
Mol. Mass.296.3621
SMILESCC[C@@H](CC=C)O[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(O)=O |r,c:8|
Structure
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