| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4862309
Max Phase: Preclinical
Molecular Formula: C25H22N2O7
Molecular Weight: 462.46
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: COc1cc2c(cc1O)CC1c3c(cc(OC)c(O)c3-2)CCN1C(=O)c1ccc([N+](=O)[O-])cc1
Standard InChI: InChI=1S/C25H22N2O7/c1-33-20-12-17-15(10-19(20)28)9-18-22-14(11-21(34-2)24(29)23(17)22)7-8-26(18)25(30)13-3-5-16(6-4-13)27(31)32/h3-6,10-12,18,28-29H,7-9H2,1-2H3
Standard InChI Key: GGXFLMKMDUVNQF-UHFFFAOYSA-N
Associated Targets(non-human)
EL4 235 Activities
Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Unknown | 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: 462.46 | Molecular Weight (Monoisotopic): 462.1427 | AlogP: 3.99 | #Rotatable Bonds: 4 |
| Polar Surface Area: 122.37 | Molecular Species: NEUTRAL | HBA: 7 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 9 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 9.30 | CX Basic pKa: | CX LogP: 3.80 | CX LogD: 3.79 |
| Aromatic Rings: 3 | Heavy Atoms: 34 | QED Weighted: 0.44 | Np Likeness Score: 0.39 |
References
| 1. Chang L, Zhang Q, Tang Y, Fang Y, Dou R, Chu Y, Xia Y, Wei Z, Chen L, Dai Y.. (2021) Synthesis of norisoboldine derivatives and bioactivity assay for inducing the generation of regulatory T cells., 37 [PMID:33556569] [10.1016/j.bmcl.2021.127844] |
Source
Source(1):