| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA3233290
Max Phase: Preclinical
Molecular Formula: C19H26N2O4
Molecular Weight: 346.43
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C/C1=C\CC[C@@]2(C)O[C@@H]2[C@H]2OC(=O)[C@@H](Cn3cnc(CO)c3)[C@@H]2CC1
Standard InChI: InChI=1S/C19H26N2O4/c1-12-4-3-7-19(2)17(25-19)16-14(6-5-12)15(18(23)24-16)9-21-8-13(10-22)20-11-21/h4,8,11,14-17,22H,3,5-7,9-10H2,1-2H3/b12-4+/t14-,15-,16-,17+,19+/m0/s1
Standard InChI Key: LEZDFUSTWQETNC-JDNHZJQCSA-N
Associated Targets(non-human)
Oocyte 84 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: 346.43 | Molecular Weight (Monoisotopic): 346.1893 | AlogP: 2.21 | #Rotatable Bonds: 3 |
| Polar Surface Area: 76.88 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 5.82 | CX LogP: 1.56 | CX LogD: 1.55 |
| Aromatic Rings: 1 | Heavy Atoms: 25 | QED Weighted: 0.52 | Np Likeness Score: 2.24 |
References
| 1. Janganati V, Penthala NR, Cragle CE, MacNicol AM, Crooks PA.. (2014) Heterocyclic aminoparthenolide derivatives modulate G(2)-M cell cycle progression during Xenopus oocyte maturation., 24 (8): [PMID:24656611] [10.1016/j.bmcl.2014.02.067] |
Source
Source(1):