Reaction Details |
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Target | Glutamate carboxypeptidase 2 |
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Ligand | BDBM50106572 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_141138 (CHEMBL749038) |
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IC50 | 90±n/a nM |
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Citation | Jackson, PF; Tays, KL; Maclin, KM; Ko, YS; Li, W; Vitharana, D; Tsukamoto, T; Stoermer, D; Lu, XC; Wozniak, K; Slusher, BS Design and pharmacological activity of phosphinic acid based NAALADase inhibitors. J Med Chem44:4170-5 (2001) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Glutamate carboxypeptidase 2 |
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Name: | Glutamate carboxypeptidase 2 |
Synonyms: | FOLH1_RAT | Folh1 | Glutamate carboxypeptidase II | Naalad1 |
Type: | PROTEIN |
Mol. Mass.: | 84547.28 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_68365 |
Residue: | 752 |
Sequence: | MWNAQQDSDSAEALGRRQRWFCAGTLVLAFTGTFIIGFLFGWFIKPSNDSTSSVSYPGMK
KAFLQELKAENIKKFLYNFTRTPHLAGTQHNFELAKQIHAQWKEFGLDLVELSDYDVLLS
YPNKTHPNYISIINEDGNEIFKTSLAELSPPGYENISDVVPPYSAFSPQGTPEGDLVYVN
YARTEDFFKLERVMKINCSGKIVIARYGQVFRGNKVKNAQLAGAKGIILYSDPADYFVPG
VKSYPDGWNLPGGGVQRGNVLNLNGAGDPLTPGYPANEYAYRHEFTEAVGLPSIPVHPIG
YDDAQKLLEHMGGSAPPDSSWKGGLKVPYNVGPGFAGNFSKQKVKLHIHSYNKVTRIYNV
IGTLKGAVEPDRYVILGGHRDAWVFGGIDPQSGAAVVHEIVRTFGTLKKKGWRPRRTILF
ASWDAEEFGLLGSTEWAEEHSRLLQERGVAYINADSSIEGNYTLRVDCTPLMHSLVYNLT
KELPSPDEGFEGKSLYDSWKEKSPSTEFIGMPRISKLGSGNDFEVFFQRLGIASGRARYT
KNWKNNKVSSYPLYHSVYETYELVEKFYDPTFKYHLTVAQVRGAMVFELANSIVLPFDCQ
SYAVALKKHAETIYNISMNHPQEMKAYMISFDSLFSAVNNFTDVASKFNQRLQDLDKSNP
ILLRILNDQLMYLERAFIDPLGLPGRPFYRHIIYAPSSHNKYAGESFPGIYDALFDINNK
VDTSKAWREVKRQISIAAFTVQAAAETLREVD
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BDBM50106572 |
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n/a |
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Name | BDBM50106572 |
Synonyms: | 2-[Hydroxy-(4-methoxy-benzyl)-phosphinoylmethyl]-pentanedioic acid | CHEMBL134095 |
Type | Small organic molecule |
Emp. Form. | C14H19O7P |
Mol. Mass. | 330.2702 |
SMILES | COc1ccc(CP(O)(=O)CC(CCC(O)=O)C(O)=O)cc1 |
Structure |
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