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ID: ALA4290701
Max Phase: Preclinical
Molecular Formula: C30H23ClN4O4S2
Molecular Weight: 603.13
Molecule Type: Small molecule
Associated Items:
ID: ALA4290701
Max Phase: Preclinical
Molecular Formula: C30H23ClN4O4S2
Molecular Weight: 603.13
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Cc1ccc(S(=O)(=O)c2nnn(CCn3c(-c4ccccc4)c(-c4ccccc4)oc3=O)c2-c2ccc(Cl)s2)cc1
Standard InChI: InChI=1S/C30H23ClN4O4S2/c1-20-12-14-23(15-13-20)41(37,38)29-27(24-16-17-25(31)40-24)35(33-32-29)19-18-34-26(21-8-4-2-5-9-21)28(39-30(34)36)22-10-6-3-7-11-22/h2-17H,18-19H2,1H3
Standard InChI Key: UGPQENQXHNZGLN-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: 603.13 | Molecular Weight (Monoisotopic): 602.0849 | AlogP: 6.59 | #Rotatable Bonds: 8 |
Polar Surface Area: 99.99 | Molecular Species: NEUTRAL | HBA: 9 | HBD: 0 |
#RO5 Violations: 2 | HBA (Lipinski): 8 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 2 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 6.84 | CX LogD: 6.84 |
Aromatic Rings: 6 | Heavy Atoms: 41 | QED Weighted: 0.19 | Np Likeness Score: -1.37 |
1. Ramírez-Villalva A, González-Calderón D, Rojas-García RI, González-Romero C, Tamaríz-Mascarúa J, Morales-Rodríguez M, Zavala-Segovia N, Fuentes-Benítes A.. (2017) Synthesis and antifungal activity of novel oxazolidin-2-one-linked 1,2,3-triazole derivatives., 8 (12): [PMID:30108741] [10.1039/C7MD00442G] |
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