Drug Information
Drug General Information | Top | |||
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Drug ID |
D0N6TC
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Former ID |
DNC008544
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Drug Name |
N5-[4-(2-phenylethoxy)phenyl]-L-glutamine
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Synonyms |
CHEMBL478993; Modified amino acid analog, 8i; BDBM24274; (2S)-2-amino-4-{[4-(2-phenylethoxy)phenyl]carbamoyl}butanoic acid
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C19H22N2O4
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Canonical SMILES |
C1=CC=C(C=C1)CCOC2=CC=C(C=C2)NC(=O)CCC(C(=O)O)N
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InChI |
1S/C19H22N2O4/c20-17(19(23)24)10-11-18(22)21-15-6-8-16(9-7-15)25-13-12-14-4-2-1-3-5-14/h1-9,17H,10-13,20H2,(H,21,22)(H,23,24)/t17-/m0/s1
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InChIKey |
LXNLZSBSUTWVJA-KRWDZBQOSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Leukotriene A-4 hydrolase (LTA4H) | Target Info | Inhibitor | [1] |
BioCyc | Leukotriene biosynthesis | |||
KEGG Pathway | Arachidonic acid metabolism | |||
Metabolic pathways | ||||
Pathwhiz Pathway | Arachidonic Acid Metabolism | |||
WikiPathways | Arachidonic acid metabolism | |||
Eicosanoid Synthesis |
References | Top | |||
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REF 1 | Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A4 hydrolase. Bioorg Med Chem. 2008 May 1;16(9):4963-83. |
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