Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D0G2NF
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| Former ID |
DNC013233
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| Drug Name |
(2S)-aminobutyryl-(R)-pipecolinic acid amide
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| Synonyms |
CHEMBL225617; (2S)-aminobutyryl-(R)-pipecolinic acid amide
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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 |
C10H19N3O2
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| Canonical SMILES |
CCC(C(=O)N1CCCCC1C(=O)N)N
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| InChI |
1S/C10H19N3O2/c1-2-7(11)10(15)13-6-4-3-5-8(13)9(12)14/h7-8H,2-6,11H2,1H3,(H2,12,14)/t7-,8+/m0/s1
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| InChIKey |
CRFULCBPWYMTAL-JGVFFNPUSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Tripeptidyl-peptidase II (TPP2) | Target Info | Inhibitor | [1] |
| Reactome | Antigen processing: Ubiquitination & Proteasome degradation | |||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Inhibitors of tripeptidyl peptidase II. 3. Derivation of butabindide by successive structure optimizations leading to a potential general approach ... J Med Chem. 2005 Nov 17;48(23):7333-42. | |||
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