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ID: ALA4082015
Max Phase: Preclinical
Molecular Formula: C20H24N2O
Molecular Weight: 308.43
Molecule Type: Small molecule
Associated Items:
ID: ALA4082015
Max Phase: Preclinical
Molecular Formula: C20H24N2O
Molecular Weight: 308.43
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: O=C(NCC12CC3CC(CC(C3)C1)C2)c1cc2ccccc2[nH]1
Standard InChI: InChI=1S/C20H24N2O/c23-19(18-8-16-3-1-2-4-17(16)22-18)21-12-20-9-13-5-14(10-20)7-15(6-13)11-20/h1-4,8,13-15,22H,5-7,9-12H2,(H,21,23)
Standard InChI Key: BDJVODHBHWDKRK-UHFFFAOYSA-N
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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: 308.43 | Molecular Weight (Monoisotopic): 308.1889 | AlogP: 4.11 | #Rotatable Bonds: 3 |
Polar Surface Area: 44.89 | Molecular Species: NEUTRAL | HBA: 1 | HBD: 2 |
#RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 3.49 | CX LogD: 3.49 |
Aromatic Rings: 2 | Heavy Atoms: 23 | QED Weighted: 0.88 | Np Likeness Score: -0.67 |
1. Franz ND, Belardinelli JM, Kaminski MA, Dunn LC, Calado Nogueira de Moura V, Blaha MA, Truong DD, Li W, Jackson M, North EJ.. (2017) Design, synthesis and evaluation of indole-2-carboxamides with pan anti-mycobacterial activity., 25 (14): [PMID:28545813] [10.1016/j.bmc.2017.05.015] |
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