Reaction Details |
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Target | Equilibrative nucleoside transporter 1 |
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Ligand | BDBM21221 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_181682 (CHEMBL786456) |
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Ki | 15200±n/a nM |
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Citation | Kim, HO; Ji, XD; Siddiqi, SM; Olah, ME; Stiles, GL; Jacobson, KA 2-Substitution of N6-benzyladenosine-5'-uronamides enhances selectivity for A3 adenosine receptors. J Med Chem37:3614-21 (1994) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Equilibrative nucleoside transporter 1 |
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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
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BDBM21221 |
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n/a |
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Name | BDBM21221 |
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 |
Type | Small organic molecule |
Emp. Form. | C18H18ClIN6O4 |
Mol. Mass. | 544.731 |
SMILES | CNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NCc3cccc(I)c3)nc(Cl)nc12 |
Structure |
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