Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA58644
Max Phase: Preclinical
Molecular Formula: C25H25FN2O
Molecular Weight: 388.49
Molecule Type: Small molecule
Associated Items:
ID: ALA58644
Max Phase: Preclinical
Molecular Formula: C25H25FN2O
Molecular Weight: 388.49
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Cc1ccc(N[C@H]2C[C@@H](C)N(C(=O)c3cccc(F)c3)c3ccc(C)cc32)cc1
Standard InChI: InChI=1S/C25H25FN2O/c1-16-7-10-21(11-8-16)27-23-14-18(3)28(24-12-9-17(2)13-22(23)24)25(29)19-5-4-6-20(26)15-19/h4-13,15,18,23,27H,14H2,1-3H3/t18-,23+/m1/s1
Standard InChI Key: AAKMQRFRNKSENC-JPYJTQIMSA-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: 388.49 | Molecular Weight (Monoisotopic): 388.1951 | AlogP: 6.03 | #Rotatable Bonds: 3 |
Polar Surface Area: 32.34 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 1 |
#RO5 Violations: 1 | HBA (Lipinski): 3 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: 4.14 | CX LogP: 5.66 | CX LogD: 5.66 |
Aromatic Rings: 3 | Heavy Atoms: 29 | QED Weighted: 0.59 | Np Likeness Score: -1.22 |
1. Smith HC, Cavanaugh CK, Friz JL, Thompson CS, Saggers JA, Michelotti EL, Garcia J, Tice CM.. (2003) Synthesis and SAR of cis-1-benzoyl-1,2,3,4-tetrahydroquinoline ligands for control of gene expression in ecdysone responsive systems., 13 (11): [PMID:12749904] [10.1016/s0960-894x(03)00317-2] |
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