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TargetEquilibrative nucleoside transporter 1
LigandBDBM21221
Substrate/Competitorn/a
Meas. Tech.ChEMBL_181682 (CHEMBL786456)
Ki 15200±n/a nM
Citation Kim, HOJi, XDSiddiqi, SMOlah, MEStiles, GLJacobson, KA 2-Substitution of N6-benzyladenosine-5'-uronamides enhances selectivity for A3 adenosine receptors. J Med Chem37:3614-21 (1994) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Equilibrative nucleoside transporter 1
Name:Equilibrative nucleoside transporter 1
Synonyms:Ent1 | S29A1_RAT | Slc29a1
Type:PROTEIN
Mol. Mass.:50023.68
Organism:Rattus norvegicus
Description:ChEMBL_181682
Residue:457
Sequence:
MTTSHQPQDRYKAVWLIFFVLGLGTLLPWNFFITATQYFTSRLNTSQNISLVTNQSCEST
EALADPSVSLPARSSLSAIFNNVMTLCAMLPLLIFTCLNSFLHQKVSQSLRILGSLLAIL
LVFLVTATLVKVQMDALSFFIITMIKIVLINSFGAILQASLFGLAGVLPANYTAPIMSGQ
GLAGFFTSVAMICAVASGSKLSESAFGYFITACAVVILAILCYLALPWMEFYRHYLQLNL
AGPAEQETKLDLISEGEEPRGGREESGVPGPNSLPANRNQSIKAILKSIWVLALSVCFIF
TVTIGLFPAVTAEVESSIAGTSPWKNCYFIPVACFLNFNVFDWLGRSLTAICMWPGQDSR
WLPVLVACRVVFIPLLMLCNVKQHHYLPSLFKHDVWFITFMAAFAFSNGYLASLCMCFGP
KKVKPAEAETAGNIMSFFLCLGLALGAVLSFLLRALV
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM21221
n/a
NameBDBM21221
Synonyms:(2S,3S,4R,5R)-5-(2-chloro-6-{[(3-iodophenyl)methyl]amino}-9H-purin-9-yl)-3,4-dihydroxy-N-methyloxolane-2-carboxamide | 2-Cl-IB-MECA | 2-chloro-N6-(3-iodobenzyl)adenosine-5-N-methylcarboxamide | C-IBzA-MU | C1-IB-MECA | CHEMBL431733 | CI-IB-MECA | Cl-IB-MECA | US20230364057, Compound 76
TypeSmall organic molecule
Emp. Form.C18H18ClIN6O4
Mol. Mass.544.731
SMILESCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NCc3cccc(I)c3)nc(Cl)nc12
Structure
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