| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA1630008
Max Phase: Preclinical
Molecular Formula: C12H16O3
Molecular Weight: 208.26
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CC(C)=CC(O)C#CC#C[C@@H](O)[C@H](C)O
Standard InChI: InChI=1S/C12H16O3/c1-9(2)8-11(14)6-4-5-7-12(15)10(3)13/h8,10-15H,1-3H3/t10-,11?,12+/m0/s1
Standard InChI Key: OKPRDFLKKLSGAZ-ASKATJPDSA-N
Associated Targets(non-human)
Quinone oxidoreductase 288 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: 208.26 | Molecular Weight (Monoisotopic): 208.1099 | AlogP: 0.06 | #Rotatable Bonds: 2 |
| Polar Surface Area: 60.69 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 3 |
| #RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 12.40 | CX Basic pKa: | CX LogP: 0.95 | CX LogD: 0.95 |
| Aromatic Rings: 0 | Heavy Atoms: 15 | QED Weighted: 0.44 | Np Likeness Score: 2.39 |
References
| 1. Shin D, Yang JE, Lee SB, Nho CW.. (2010) SAR studies of gymnasterkoreayne derivatives with cancer chemopreventive activities., 20 (24): [PMID:21050753] [10.1016/j.bmcl.2010.07.066] |
Source
Source(1):