Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4218248
Max Phase: Preclinical
Molecular Formula: C39H64N12O4
Molecular Weight: 765.02
Molecule Type: Small molecule
Associated Items:
ID: ALA4218248
Max Phase: Preclinical
Molecular Formula: C39H64N12O4
Molecular Weight: 765.02
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCN(CC)c1ccc(/N=N/c2ccc(C(=O)N[C@@H](CC(N)=O)C(=O)NCCCCCCCCCNCCCNC(=O)[C@@H](N)CCCNC(=N)N)cc2)cc1
Standard InChI: InChI=1S/C39H64N12O4/c1-3-51(4-2)32-21-19-31(20-22-32)50-49-30-17-15-29(16-18-30)36(53)48-34(28-35(41)52)38(55)46-25-11-9-7-5-6-8-10-23-44-24-13-27-45-37(54)33(40)14-12-26-47-39(42)43/h15-22,33-34,44H,3-14,23-28,40H2,1-2H3,(H2,41,52)(H,45,54)(H,46,55)(H,48,53)(H4,42,43,47)/b50-49+/t33-,34-/m0/s1
Standard InChI Key: OQXFUYHFWLMALK-ZAHVXGADSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
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: 765.02 | Molecular Weight (Monoisotopic): 764.5173 | AlogP: 3.46 | #Rotatable Bonds: 29 |
Polar Surface Area: 258.30 | Molecular Species: BASE | HBA: 10 | HBD: 9 |
#RO5 Violations: 2 | HBA (Lipinski): 16 | HBD (Lipinski): 12 | #RO5 Violations (Lipinski): 3 |
CX Acidic pKa: | CX Basic pKa: 12.20 | CX LogP: 2.54 | CX LogD: -3.47 |
Aromatic Rings: 2 | Heavy Atoms: 55 | QED Weighted: 0.03 | Np Likeness Score: -0.30 |
1. Nørager NG, Poulsen MH, Strømgaard K.. (2018) Controlling Ca2+ Permeable α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid (AMPA) Receptors with Photochromic Ion Channel Blockers., 61 (17): [PMID:30125106] [10.1021/acs.jmedchem.8b00756] |
Source(1):