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ID: ALA4874099
Max Phase: Preclinical
Molecular Formula: C30H30N3O7P
Molecular Weight: 575.56
Molecule Type: Unknown
Associated Items:
ID: ALA4874099
Max Phase: Preclinical
Molecular Formula: C30H30N3O7P
Molecular Weight: 575.56
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CC(C)C(NC(=O)Cn1cccc(NC(=O)Oc2ccccc2)c1=O)P(=O)(Oc1ccccc1)Oc1ccccc1
Standard InChI: InChI=1S/C30H30N3O7P/c1-22(2)28(41(37,39-24-15-8-4-9-16-24)40-25-17-10-5-11-18-25)32-27(34)21-33-20-12-19-26(29(33)35)31-30(36)38-23-13-6-3-7-14-23/h3-20,22,28H,21H2,1-2H3,(H,31,36)(H,32,34)
Standard InChI Key: QCRLFRZMKZDITK-UHFFFAOYSA-N
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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 |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 575.56 | Molecular Weight (Monoisotopic): 575.1821 | AlogP: 5.91 | #Rotatable Bonds: 11 |
Polar Surface Area: 124.96 | Molecular Species: NEUTRAL | HBA: 8 | HBD: 2 |
#RO5 Violations: 2 | HBA (Lipinski): 10 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 2 |
CX Acidic pKa: 11.19 | CX Basic pKa: | CX LogP: 5.20 | CX LogD: 5.20 |
Aromatic Rings: 4 | Heavy Atoms: 41 | QED Weighted: 0.21 | Np Likeness Score: -0.80 |
1. Hwang J, Strange N, Phillips MJA, Krause AL, Heywood A, Gamble AB, Huston WM, Tyndall JDA.. (2021) Optimization of peptide-based inhibitors targeting the HtrA serine protease in Chlamydia: Design, synthesis and biological evaluation of pyridone-based and N-Capping group-modified analogues., 224 [PMID:34265463] [10.1016/j.ejmech.2021.113692] |
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