Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D0R3DP
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| Former ID |
DNC013248
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| Drug Name |
L-valyl-L-proline hexylamide
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| Synonyms |
CHEMBL375490; L-valyl-L-proline hexylamide; SCHEMBL6245007
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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 |
C16H31N3O2
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| Canonical SMILES |
CCCCCCNC(=O)C1CCCN1C(=O)C(C(C)C)N
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| InChI |
1S/C16H31N3O2/c1-4-5-6-7-10-18-15(20)13-9-8-11-19(13)16(21)14(17)12(2)3/h12-14H,4-11,17H2,1-3H3,(H,18,20)/t13-,14-/m0/s1
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| InChIKey |
BWJSLNXXZBEGLH-KBPBESRZSA-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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