| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4862033
Max Phase: Preclinical
Molecular Formula: C22H45NO2
Molecular Weight: 355.61
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: CCCCCCCCCCCCCC[C@H](O)[C@H](C)NC(=O)C(C)(C)C
Standard InChI: InChI=1S/C22H45NO2/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-20(24)19(2)23-21(25)22(3,4)5/h19-20,24H,6-18H2,1-5H3,(H,23,25)/t19-,20-/m0/s1
Standard InChI Key: GLEMCDBVEMXTRQ-PMACEKPBSA-N
Associated Targets(Human)
Acid ceramidase 411 Activities
Associated Targets(non-human)
Alkaline ceramidase 3 54 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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: 355.61 | Molecular Weight (Monoisotopic): 355.3450 | AlogP: 5.99 | #Rotatable Bonds: 15 |
| Polar Surface Area: 49.33 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 2 |
| #RO5 Violations: 1 | HBA (Lipinski): 3 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 6.99 | CX LogD: 6.99 |
| Aromatic Rings: 0 | Heavy Atoms: 25 | QED Weighted: 0.35 | Np Likeness Score: 0.38 |
References
| 1. Bielsa N, Casasampere M, Aseeri M, Casas J, Delgado A, Abad JL, Fabriàs G.. (2021) Discovery of deoxyceramide analogs as highly selective ACER3 inhibitors in live cells., 216 [PMID:33677352] [10.1016/j.ejmech.2021.113296] |
Source
Source(1):