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ID: ALA4863666
Max Phase: Preclinical
Molecular Formula: C32H47N3O6
Molecular Weight: 569.74
Molecule Type: Unknown
Associated Items:
ID: ALA4863666
Max Phase: Preclinical
Molecular Formula: C32H47N3O6
Molecular Weight: 569.74
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CC(C)C[C@H](NC(=O)[C@@H]1Cc2ccc(cc2)OCCCCCCCCC(=O)N2CCC[C@H]2C(=O)N1)C(=O)[C@@]1(C)CO1
Standard InChI: InChI=1S/C32H47N3O6/c1-22(2)19-25(29(37)32(3)21-41-32)33-30(38)26-20-23-13-15-24(16-14-23)40-18-9-7-5-4-6-8-12-28(36)35-17-10-11-27(35)31(39)34-26/h13-16,22,25-27H,4-12,17-21H2,1-3H3,(H,33,38)(H,34,39)/t25-,26-,27-,32+/m0/s1
Standard InChI Key: GRRBHLUBSJAWQE-GZNUUUAQSA-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: 569.74 | Molecular Weight (Monoisotopic): 569.3465 | AlogP: 3.72 | #Rotatable Bonds: 6 |
Polar Surface Area: 117.34 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 2 |
#RO5 Violations: 1 | HBA (Lipinski): 9 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: 12.19 | CX Basic pKa: | CX LogP: 4.27 | CX LogD: 4.27 |
Aromatic Rings: 1 | Heavy Atoms: 41 | QED Weighted: 0.50 | Np Likeness Score: 0.78 |
1. Lee MJ, Bhattarai D, Jang H, Baek A, Yeo IJ, Lee S, Miller Z, Lee S, Hong JT, Kim DE, Lee W, Kim KB.. (2021) Macrocyclic Immunoproteasome Inhibitors as a Potential Therapy for Alzheimer's Disease., 64 (15.0): [PMID:34309393] [10.1021/acs.jmedchem.1c00291] |
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