Reaction Details |
| Report a problem with these data |
Target | N-acetylated-alpha-linked acidic dipeptidase 2 |
---|
Ligand | BDBM50143073 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_71707 (CHEMBL680921) |
---|
Ki | 0.9±n/a nM |
---|
Citation | Kozikowski, AP; Zhang, J; Nan, F; Petukhov, PA; Grajkowska, E; Wroblewski, JT; Yamamoto, T; Bzdega, T; Wroblewska, B; Neale, JH Synthesis of urea-based inhibitors as active site probes of glutamate carboxypeptidase II: efficacy as analgesic agents. J Med Chem47:1729-38 (2004) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
N-acetylated-alpha-linked acidic dipeptidase 2 |
---|
Name: | N-acetylated-alpha-linked acidic dipeptidase 2 |
Synonyms: | N-acetylated-alpha-linked acidic dipeptidase 2 | N-acetylated-alpha-linked acidic dipeptidase II | NAALAD2 | NAALADase II | NALD2_HUMAN |
Type: | PROTEIN |
Mol. Mass.: | 83602.57 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_71707 |
Residue: | 740 |
Sequence: | MAESRGRLYLWMCLAAALASFLMGFMVGWFIKPLKETTTSVRYHQSIRWKLVSEMKAENI
KSFLRSFTKLPHLAGTEQNFLLAKKIQTQWKKFGLDSAKLVHYDVLLSYPNETNANYISI
VDEHETEIFKTSYLEPPPDGYENVTNIVPPYNAFSAQGMPEGDLVYVNYARTEDFFKLER
EMGINCTGKIVIARYGKIFRGNKVKNAMLAGAIGIILYSDPADYFAPEVQPYPKGWNLPG
TAAQRGNVLNLNGAGDPLTPGYPAKEYTFRLDVEEGVGIPRIPVHPIGYNDAEILLRYLG
GIAPPDKSWKGALNVSYSIGPGFTGSDSFRKVRMHVYNINKITRIYNVVGTIRGSVEPDR
YVILGGHRDSWVFGAIDPTSGVAVLQEIARSFGKLMSKGWRPRRTIIFASWDAEEFGLLG
STEWAEENVKILQERSIAYINSDSSIEGNYTLRVDCTPLLYQLVYKLTKEIPSPDDGFES
KSLYESWLEKDPSPENKNLPRINKLGSGSDFEAYFQRLGIASGRARYTKNKKTDKYSSYP
VYHTIYETFELVEKFYDPTFKKQLSVAQLRGALVYELVDSKIIPFNIQDYAEALKNYAAS
IYNLSKKHDQQLTDHGVSFDSLFSAVKNFSEAASDFHKRLIQVDLNNPIAVRMMNDQLML
LERAFIDPLGLPGKLFYRHIIFAPSSHNKYAGESFPGIYDAIFDIENKANSRLAWKEVKK
HISIAAFTIQAAAGTLKEVL
|
|
|
BDBM50143073 |
---|
n/a |
---|
Name | BDBM50143073 |
Synonyms: | (S)-2-{3-[(S)-1-Carboxy-3-(1H-tetrazol-5-yl)-propyl]-ureido}-pentanedioic acid | CHEMBL49669 |
Type | Small organic molecule |
Emp. Form. | C11H16N6O7 |
Mol. Mass. | 344.2807 |
SMILES | OC(=O)CC[C@H](NC(=O)N[C@@H](CCc1nnn[nH]1)C(O)=O)C(O)=O |
Structure |
|