Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA1784976
Max Phase: Preclinical
Molecular Formula: C19H28O3
Molecular Weight: 304.43
Molecule Type: Small molecule
Associated Items:
ID: ALA1784976
Max Phase: Preclinical
Molecular Formula: C19H28O3
Molecular Weight: 304.43
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCCCCCCC=Cc1cccc(OC)c1C(=O)OCC
Standard InChI: InChI=1S/C19H28O3/c1-4-6-7-8-9-10-11-13-16-14-12-15-17(21-3)18(16)19(20)22-5-2/h11-15H,4-10H2,1-3H3
Standard InChI Key: XCCGGEPEBJAUBK-UHFFFAOYSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 304.43 | Molecular Weight (Monoisotopic): 304.2038 | AlogP: 5.25 | #Rotatable Bonds: 10 |
Polar Surface Area: 35.53 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 0 |
#RO5 Violations: 1 | HBA (Lipinski): 3 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 5.97 | CX LogD: 5.97 |
Aromatic Rings: 1 | Heavy Atoms: 22 | QED Weighted: 0.44 | Np Likeness Score: 0.41 |
1. Pereira JM, Severino RP, Vieira PC, Fernandes JB, da Silva MF, Zottis A, Andricopulo AD, Oliva G, Corrêa AG.. (2008) Anacardic acid derivatives as inhibitors of glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi., 16 (19): [PMID:18789702] [10.1016/j.bmc.2008.08.057] |
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