| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA439519
Max Phase: Preclinical
Molecular Formula: C17H22NO7P
Molecular Weight: 383.34
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CC(NC(=O)/C=C/c1ccccc1)P(=O)(O)CC(CCC(=O)O)C(=O)O
Standard InChI: InChI=1S/C17H22NO7P/c1-12(18-15(19)9-7-13-5-3-2-4-6-13)26(24,25)11-14(17(22)23)8-10-16(20)21/h2-7,9,12,14H,8,10-11H2,1H3,(H,18,19)(H,20,21)(H,22,23)(H,24,25)/b9-7+
Standard InChI Key: HQHPPIRCEQWDAV-VQHVLOKHSA-N
Associated Targets(non-human)
UDP-N-acetylmuramoylalanine--D-glutamate ligase 81 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: 383.34 | Molecular Weight (Monoisotopic): 383.1134 | AlogP: 2.00 | #Rotatable Bonds: 10 |
| Polar Surface Area: 141.00 | Molecular Species: ACID | HBA: 4 | HBD: 4 |
| #RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 4 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 1.55 | CX Basic pKa: | CX LogP: 0.73 | CX LogD: -7.58 |
| Aromatic Rings: 1 | Heavy Atoms: 26 | QED Weighted: 0.36 | Np Likeness Score: 0.41 |
References
| 1. Strancar K, Blanot D, Gobec S.. (2006) Design, synthesis and structure-activity relationships of new phosphinate inhibitors of MurD., 16 (2): [PMID:16271472] [10.1016/j.bmcl.2005.09.086] |
Source
Source(1):