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ID: ALA3759036
Max Phase: Preclinical
Molecular Formula: C26H23N3O2
Molecular Weight: 409.49
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCCOc1ccc(-c2cccc(-c3noc(Cc4c[nH]c5ccccc45)n3)c2)cc1
Standard InChI: InChI=1S/C26H23N3O2/c1-2-14-30-22-12-10-18(11-13-22)19-6-5-7-20(15-19)26-28-25(31-29-26)16-21-17-27-24-9-4-3-8-23(21)24/h3-13,15,17,27H,2,14,16H2,1H3
Standard InChI Key: MOMNCAQJHZECEQ-UHFFFAOYSA-N
Associated Targets(Human)
PTPN1 Tchem Protein-tyrosine phosphatase 1B (8528 Activities)
PTPN2 Tchem T-cell protein-tyrosine phosphatase (1317 Activities)
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PTPN6 Tchem Protein-tyrosine phosphatase 1C (687 Activities)
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PTPN11 Tchem Protein-tyrosine phosphatase 2C (2297 Activities)
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PTPRF Tchem Receptor-type tyrosine-protein phosphatase F (LAR) (718 Activities)
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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 |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 409.49 | Molecular Weight (Monoisotopic): 409.1790 | AlogP: 6.26 | #Rotatable Bonds: 7 |
| Polar Surface Area: 63.94 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 1 |
| #RO5 Violations: 1 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 6.59 | CX LogD: 6.59 |
| Aromatic Rings: 5 | Heavy Atoms: 31 | QED Weighted: 0.34 | Np Likeness Score: -1.23 |
References
| 1. Zhang L, Jiang CS, Gao LX, Gong JX, Wang ZH, Li JY, Li J, Li XW, Guo YW.. (2016) Design, synthesis and in vitro activity of phidianidine B derivatives as novel PTP1B inhibitors with specific selectivity., 26 (3): [PMID:26774579] [10.1016/j.bmcl.2015.12.097] |
Source
Source(1):