| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA2418566
Max Phase: Preclinical
Molecular Formula: C23H22N2O6S
Molecular Weight: 454.50
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COC(=O)COc1ccccc1/C=C1\S/C(=N\c2cccc(C(=O)O)c2)N(C(C)C)C1=O
Standard InChI: InChI=1S/C23H22N2O6S/c1-14(2)25-21(27)19(12-15-7-4-5-10-18(15)31-13-20(26)30-3)32-23(25)24-17-9-6-8-16(11-17)22(28)29/h4-12,14H,13H2,1-3H3,(H,28,29)/b19-12-,24-23-
Standard InChI Key: SITHAAHUCLEMDN-BUCZYZBOSA-N
Associated Targets(non-human)
O-acetylserine sulfhydrylase 237 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: 454.50 | Molecular Weight (Monoisotopic): 454.1199 | AlogP: 3.95 | #Rotatable Bonds: 7 |
| Polar Surface Area: 105.50 | Molecular Species: ACID | HBA: 7 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 3.88 | CX Basic pKa: 2.48 | CX LogP: 3.83 | CX LogD: 0.79 |
| Aromatic Rings: 2 | Heavy Atoms: 32 | QED Weighted: 0.50 | Np Likeness Score: -1.35 |
References
| 1. Poyraz O, Jeankumar VU, Saxena S, Schnell R, Haraldsson M, Yogeeswari P, Sriram D, Schneider G.. (2013) Structure-guided design of novel thiazolidine inhibitors of O-acetyl serine sulfhydrylase from Mycobacterium tuberculosis., 56 (16): [PMID:23879381] [10.1021/jm400710k] |
Source
Source(1):