Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
ID: ALA3355294
Max Phase: Preclinical
Molecular Formula: C19H26O3
Molecular Weight: 302.41
Molecule Type: Small molecule
Associated Items:
ID: ALA3355294
Max Phase: Preclinical
Molecular Formula: C19H26O3
Molecular Weight: 302.41
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COc1ccc(CC(=O)OC/C=C(/C)CCC=C(C)C)cc1
Standard InChI: InChI=1S/C19H26O3/c1-15(2)6-5-7-16(3)12-13-22-19(20)14-17-8-10-18(21-4)11-9-17/h6,8-12H,5,7,13-14H2,1-4H3/b16-12-
Standard InChI Key: CRQXDVJVYHHKFY-VBKFSLOCSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
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 |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
---|
Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
---|
Molecular Weight: 302.41 | Molecular Weight (Monoisotopic): 302.1882 | AlogP: 4.47 | #Rotatable Bonds: 8 |
Polar Surface Area: 35.53 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 4.62 | CX LogD: 4.62 |
Aromatic Rings: 1 | Heavy Atoms: 22 | QED Weighted: 0.52 | Np Likeness Score: 1.09 |
1. Ortar G, Schiano Moriello A, Morera E, Nalli M, Di Marzo V, De Petrocellis L.. (2014) Effect of acyclic monoterpene alcohols and their derivatives on TRP channels., 24 (23): [PMID:25455494] [10.1016/j.bmcl.2014.10.012] |
Source(1):