ID: ALA4441969
Chembl Id: CHEMBL4441969
PubChem CID: 155515528
Max Phase: Preclinical
Molecular Formula: C16H24N6O8S
Molecular Weight: 460.47
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CC(C)[C@H](O)[C@@H](O)C(=O)NS(=O)(=O)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)C[C@@H]1O
Standard InChI: InChI=1S/C16H24N6O8S/c1-7(2)12(24)13(25)16(26)21-31(27,28)29-4-9-8(23)3-10(30-9)22-6-20-11-14(17)18-5-19-15(11)22/h5-10,12-13,23-25H,3-4H2,1-2H3,(H,21,26)(H2,17,18,19)/t8-,9+,10+,12-,13+/m0/s1
Standard InChI Key: MSWRFIYYJZVPAP-YQPPGCHHSA-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: Unknown | 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: 460.47 | Molecular Weight (Monoisotopic): 460.1376 | AlogP: -2.19 | #Rotatable Bonds: 8 |
| Polar Surface Area: 212.01 | Molecular Species: ACID | HBA: 13 | HBD: 5 |
| #RO5 Violations: 1 | HBA (Lipinski): 14 | HBD (Lipinski): 6 | #RO5 Violations (Lipinski): 2 |
| CX Acidic pKa: 2.68 | CX Basic pKa: 4.94 | CX LogP: -3.07 | CX LogD: -2.66 |
| Aromatic Rings: 2 | Heavy Atoms: 31 | QED Weighted: 0.28 | Np Likeness Score: 0.55 |
| 1. Yoon S, Kim SE, Kim JH, Yoon I, Tran PT, Ann J, Kim C, Byun WS, Lee S, Kim S, Lee J, Lee J.. (2019) Structure-activity relationship of leucyladenylate sulfamate analogues as leucyl-tRNA synthetase (LRS)-targeting inhibitors of Mammalian target of rapamycin complex 1 (mTORC1)., 27 (6): [PMID:30755350] [10.1016/j.bmc.2019.01.037] |
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