Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
ID: ALA5180339
Max Phase: Preclinical
Molecular Formula: C20H21NO7
Molecular Weight: 387.39
Associated Items:
ID: ALA5180339
Max Phase: Preclinical
Molecular Formula: C20H21NO7
Molecular Weight: 387.39
Associated Items:
Canonical SMILES: COc1c(O)cc(O)c2c(=O)cc(-c3ccc(N(CCO)CCO)cc3)oc12
Standard InChI: InChI=1S/C20H21NO7/c1-27-19-16(26)10-14(24)18-15(25)11-17(28-20(18)19)12-2-4-13(5-3-12)21(6-8-22)7-9-23/h2-5,10-11,22-24,26H,6-9H2,1H3
Standard InChI Key: BSCJMQSDEUZNHG-UHFFFAOYSA-N
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: | 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: 387.39 | Molecular Weight (Monoisotopic): 387.1318 | AlogP: 1.67 | #Rotatable Bonds: 7 |
Polar Surface Area: 123.60 | Molecular Species: NEUTRAL | HBA: 8 | HBD: 4 |
#RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 4 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 7.10 | CX Basic pKa: 0.79 | CX LogP: 1.58 | CX LogD: 1.10 |
Aromatic Rings: 3 | Heavy Atoms: 28 | QED Weighted: 0.48 | Np Likeness Score: 0.74 |
1. Tian Y, Liu K, Liu R, Qiu Z, Xu Y, Wei W, Xu X, Wang J, Ding H, Li Z, Bian J.. (2022) Discovery of Potent Small-Molecule USP8 Inhibitors for the Treatment of Breast Cancer through Regulating ERα Expression., 65 (13.0): [PMID:35786929] [10.1021/acs.jmedchem.2c00013] |
Source(1):