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ID: ALA4101536
Max Phase: Preclinical
Molecular Formula: C23H30N2O
Molecular Weight: 350.51
Molecule Type: Small molecule
Associated Items:
ID: ALA4101536
Max Phase: Preclinical
Molecular Formula: C23H30N2O
Molecular Weight: 350.51
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Cc1cc(C)c2cc(C(=O)NC(C)C34CC5CC(CC(C5)C3)C4)[nH]c2c1
Standard InChI: InChI=1S/C23H30N2O/c1-13-4-14(2)19-9-21(25-20(19)5-13)22(26)24-15(3)23-10-16-6-17(11-23)8-18(7-16)12-23/h4-5,9,15-18,25H,6-8,10-12H2,1-3H3,(H,24,26)
Standard InChI Key: FOWMNNSUMIYLDC-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: 350.51 | Molecular Weight (Monoisotopic): 350.2358 | AlogP: 5.12 | #Rotatable Bonds: 3 |
Polar Surface Area: 44.89 | Molecular Species: NEUTRAL | HBA: 1 | HBD: 2 |
#RO5 Violations: 1 | HBA (Lipinski): 3 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 4.94 | CX LogD: 4.94 |
Aromatic Rings: 2 | Heavy Atoms: 26 | QED Weighted: 0.79 | Np Likeness Score: -0.78 |
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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