Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0SZ9E
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| Former ID |
DNC008864
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| Drug Name |
8(S)-amino-2(R)-methyl-7-oxononanoic acid
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| Synonyms |
8(S)-Amino-2(R)-methyl-7-oxononanoic acid; CHEMBL465576; Nonanoic acid, 8-amino-2-methyl-7-oxo-, (S-(R*,S*))-; 181886-81-7; SCHEMBL4098289; AC1L42P6; DTXSID90171213; BDBM50292361; (2R,8S)-8-amino-2-methyl-7-oxononanoic acid; (2R,8S)-2-Methyl-7-oxo-8-aminononanoic acid
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C10H19NO3
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| Canonical SMILES |
CC(CCCCC(=O)C(C)N)C(=O)O
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| InChI |
1S/C10H19NO3/c1-7(10(13)14)5-3-4-6-9(12)8(2)11/h7-8H,3-6,11H2,1-2H3,(H,13,14)/t7-,8+/m1/s1
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| InChIKey |
YBWPFLPQZXWNNM-SFYZADRCSA-N
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| CAS Number |
CAS 181886-81-7
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|
| REF 1 | Isolation and structure of leukotriene-A4 hydrolase inhibitor: 8(S)-amino-2(R)-methyl-7-oxononanoic acid produced by Streptomyces diastaticus. J Nat Prod. 1996 Oct;59(10):962-4. | |||
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