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TargetATP receptor
LigandBDBM85682
Substrate/Competitorn/a
Ki 770±n/a nM
CommentsPDSP_3351
Citation Rettinger, JSchmalzing, GDamer, SMüller, GNickel, PLambrecht, G The suramin analogue NF279 is a novel and potent antagonist selective for the P2X(1) receptor. Neuropharmacology39:2044-53 (2000) [PubMed]  Article
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ATP receptor
Name:ATP receptor
Synonyms:Purinergic, P2X2
Type:Enzyme Catalytic Domain
Mol. Mass.:41254.50
Organism:Xenopus
Description:Purinergic, P2X2 0 Xenopus::F6VH38
Residue:367
Sequence:
CRTRSMSWIGQLWSYETPKVIVVKNRRLGTIYRLLQLLIVVYFVWYVFVVQKGYQAQETG
PESAVITKVKGVSTSKGPRGIKKIWDVAEYVKPPEGGSVFTIITRIESTKLQTMGTCPES
RTVPNALCVSDEDCNRGEMHILGNGEQTGRCIIAGRGSLRTCEIYAWCPLEDETAISESL
QDYVQNFTILIKNNIHFPQFGFSKGNIEGQGFLRNCTYHPVLSPSCPIFTVGFIVSEAGA
NFTELAKKVRLPIIKCDLDFIEIVKSMKYFLELASNYAPVSFVPSFRFAKYYNNNGTETR
TLIKVYGIRIDVIVHGQAGKFSLIPTIINLATALTSIGVGSVLCDWILLTFMNKDRTYSL
RKFDEVI
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BDBM85682
n/a
NameBDBM85682
Synonyms:CAS_5311315 | NF279 | NSC_5311315
TypeSmall organic molecule
Emp. Form.C49H30N6O23S6
Mol. Mass.1263.182
SMILES[O-]S(=O)(=O)c1cc(c2c(NC(=O)c3ccc(NC(=O)c4ccc(NC(=O)Nc5ccc(cc5)C(=O)Nc5ccc(cc5)C(=O)Nc5ccc(c6cc(cc(c56)S([O-])(=O)=O)S([O-])(=O)=O)S([O-])(=O)=O)cc4)cc3)ccc(c2c1)S([O-])(=O)=O)S([O-])(=O)=O
Structure
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