| Reaction Details |
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 | Report a problem with these data |
| Target | Proton-coupled folate transporter |
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| Ligand | BDBM50354833 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_771182 (CHEMBL1837099) |
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| pH | 5.5±n/a |
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| Ki | 130±n/a nM |
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| Comments | extracted |
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| Citation |  Wang, L; Desmoulin, SK; Cherian, C; Polin, L; White, K; Kushner, J; Fulterer, A; Chang, MH; Mitchell-Ryan, S; Stout, M; Romero, MF; Hou, Z; Matherly, LH; Gangjee, A Synthesis, biological, and antitumor activity of a highly potent 6-substituted pyrrolo[2,3-d]pyrimidine thienoyl antifolate inhibitor with proton-coupled folate transporter and folate receptor selectivity over the reduced folate carrier that inhibits b-glycinamide ribonucleotide formyltransferase. J Med Chem54:7150-64 (2011) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Proton-coupled folate transporter |
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| Name: | Proton-coupled folate transporter |
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| Synonyms: | G21 | HCP1 | Heme carrier protein 1 | PCFT | PCFT/HCP1 | PCFT_HUMAN | SLC46A1 | Solute carrier family 46 member 1 |
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| Type: | PROTEIN |
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| Mol. Mass.: | 49782.13 |
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| Organism: | Homo sapiens (Human) |
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| Description: | ChEMBL_1469597 |
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| Residue: | 459 |
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| Sequence: | MEGSASPPEKPRARPAAAVLCRGPVEPLVFLANFALVLQGPLTTQYLWHRFSADLGYNGT
RQRGGCSNRSADPTMQEVETLTSHWTLYMNVGGFLVGLFSSTLLGAWSDSVGRRPLLVLA
SLGLLLQALVSVFVVQLQLHVGYFVLGRILCALLGDFGGLLAASFASVADVSSSRSRTFR
MALLEASIGVAGMLASLLGGHWLRAQGYANPFWLALALLIAMTLYAAFCFGETLKEPKST
RLFTFRHHRSIVQLYVAPAPEKSRKHLALYSLAIFVVITVHFGAQDILTLYELSTPLCWD
SKLIGYGSAAQHLPYLTSLLALKLLQYCLADAWVAEIGLAFNILGMVVFAFATITPLMFT
GYGLLFLSLVITPVIRAKLSKLVRETEQGALFSAVACVNSLAMLTASGIFNSLYPATLNF
MKGFPFLLGAGLLLIPAVLIGMLEKADPHLEFQQFPQSP
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| BDBM50354833 |
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| n/a |
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| Name | BDBM50354833 |
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| Synonyms: | AGF94 | CHEMBL1834488 |
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| Type | Small organic molecule |
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| Emp. Form. | C19H21N5O6S |
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| Mol. Mass. | 447.465 |
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| SMILES | Nc1nc2[nH]c(CCCc3ccc(s3)C(=O)N[C@@H](CCC(O)=O)C(O)=O)cc2c(=O)[nH]1 |r| |
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| Structure | 
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