| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4163047
Max Phase: Preclinical
Molecular Formula: C8H14O3
Molecular Weight: 158.20
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CC(C)C[C@H](C(=O)O)[C@H]1CO1
Standard InChI: InChI=1S/C8H14O3/c1-5(2)3-6(8(9)10)7-4-11-7/h5-7H,3-4H2,1-2H3,(H,9,10)/t6-,7+/m0/s1
Standard InChI Key: RYZINPYPTVDRHP-NKWVEPMBSA-N
Associated Targets(non-human)
Carboxypeptidase A1 174 Activities
Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Small molecule | Topical: No | First In Class: No | Black Box: No |
| Chirality: No | Availability: No | Prodrug: No |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 158.20 | Molecular Weight (Monoisotopic): 158.0943 | AlogP: 1.13 | #Rotatable Bonds: 4 |
| Polar Surface Area: 49.83 | Molecular Species: ACID | HBA: 2 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 4.57 | CX Basic pKa: | CX LogP: 1.45 | CX LogD: -1.31 |
| Aromatic Rings: 0 | Heavy Atoms: 11 | QED Weighted: 0.62 | Np Likeness Score: 1.28 |
References
| 1. Testero SA, Granados C, Fernández D, Gallego P, Covaleda G, Reverter D, Vendrell J, Avilés FX, Pallarès I, Mobashery S.. (2017) Discovery of Mechanism-Based Inactivators for Human Pancreatic Carboxypeptidase A from a Focused Synthetic Library., 8 (10): [PMID:29057062] [10.1021/acsmedchemlett.7b00346] |
Source
Source(1):