| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4281983
Max Phase: Preclinical
Molecular Formula: C28H29N3O2
Molecular Weight: 439.56
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COc1ncccc1-c1ccnc2cc(C)c(-c3ccc(CN4CCOCC4)cc3)c(C)c12
Standard InChI: InChI=1S/C28H29N3O2/c1-19-17-25-27(23(10-12-29-25)24-5-4-11-30-28(24)32-3)20(2)26(19)22-8-6-21(7-9-22)18-31-13-15-33-16-14-31/h4-12,17H,13-16,18H2,1-3H3
Standard InChI Key: UZZZVJSAHCZPAS-UHFFFAOYSA-N
Associated Targets(non-human)
Long-chain-fatty-acid--AMP ligase FadD32 36 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: 439.56 | Molecular Weight (Monoisotopic): 439.2260 | AlogP: 5.42 | #Rotatable Bonds: 5 |
| Polar Surface Area: 47.48 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
| #RO5 Violations: 1 | HBA (Lipinski): 5 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: | CX Basic pKa: 7.19 | CX LogP: 5.39 | CX LogD: 5.18 |
| Aromatic Rings: 4 | Heavy Atoms: 33 | QED Weighted: 0.42 | Np Likeness Score: -0.87 |
References
| 1. Fang C, Lee KK, Nietupski R, Bates RH, Fernandez-Menendez R, Lopez-Roman EM, Guijarro-Lopez L, Yin Y, Peng Z, Gomez JE, Fisher S, Barros-Aguirre D, Hubbard BK, Serrano-Wu MH, Hung DT.. (2018) Discovery of heterocyclic replacements for the coumarin core of anti-tubercular FadD32 inhibitors., 28 (22): [PMID:30316633] [10.1016/j.bmcl.2018.09.037] |
Source
Source(1):