| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Stagonolide G
ID: ALA2251288
Max Phase: Preclinical
Molecular Formula: C10H16O4
Molecular Weight: 200.23
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C[C@H]1OC(=O)CC[C@H](O)C/C=C\[C@H]1O
Standard InChI: InChI=1S/C10H16O4/c1-7-9(12)4-2-3-8(11)5-6-10(13)14-7/h2,4,7-9,11-12H,3,5-6H2,1H3/b4-2-/t7-,8-,9-/m1/s1
Standard InChI Key: YTPQADMIIIZGDS-UJNGWYBVSA-N
Associated Targets(non-human)
Cirsium arvense 30 Activities
Molecule Features
| Natural Product: Yes | 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: 200.23 | Molecular Weight (Monoisotopic): 200.1049 | AlogP: 0.38 | #Rotatable Bonds: 0 |
| Polar Surface Area: 66.76 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 13.80 | CX Basic pKa: | CX LogP: 0.12 | CX LogD: 0.12 |
| Aromatic Rings: 0 | Heavy Atoms: 14 | QED Weighted: 0.44 | Np Likeness Score: 2.91 |
References
| 1. Evidente A, Cimmino A, Berestetskiy A, Andolfi A, Motta A.. (2008) Stagonolides G-I and modiolide A, nonenolides produced by Stagonospora cirsii, a potential mycoherbicide for Cirsium arvense., 71 (11): [PMID:18959441] [10.1021/np800415w] |
Source
Source(1):