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ID: ALA4782080
Max Phase: Preclinical
Molecular Formula: C29H36ClN3O5S2
Molecular Weight: 569.75
Molecule Type: Unknown
Associated Items:
ID: ALA4782080
Max Phase: Preclinical
Molecular Formula: C29H36ClN3O5S2
Molecular Weight: 569.75
Molecule Type: Unknown
Associated Items:
Canonical SMILES: C=C1CN(S(=O)(=O)c2ccc(C)cc2)CCc2cc(OCC)cc(n2)CCN(S(=O)(=O)c2ccc(C)cc2)C1.Cl
Standard InChI: InChI=1S/C29H35N3O5S2.ClH/c1-5-37-27-18-25-14-16-31(38(33,34)28-10-6-22(2)7-11-28)20-24(4)21-32(17-15-26(19-27)30-25)39(35,36)29-12-8-23(3)9-13-29;/h6-13,18-19H,4-5,14-17,20-21H2,1-3H3;1H
Standard InChI Key: WFBTZGCKJZZDQM-UHFFFAOYSA-N
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: Unknown | 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: 569.75 | Molecular Weight (Monoisotopic): 569.2018 | AlogP: 4.13 | #Rotatable Bonds: 6 |
Polar Surface Area: 96.88 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 0 |
#RO5 Violations: 1 | HBA (Lipinski): 8 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: 5.36 | CX LogP: 4.39 | CX LogD: 4.38 |
Aromatic Rings: 3 | Heavy Atoms: 39 | QED Weighted: 0.41 | Np Likeness Score: -0.64 |
1. Lumangtad LA,Claeys E,Hamal S,Intasiri A,Basrai C,Yen-Pon E,Beenfeldt D,Vermeire K,Bell TW. (2020) Syntheses and anti-HIV and human cluster of differentiation 4 (CD4) down-modulating potencies of pyridine-fused cyclotriazadisulfonamide (CADA) compounds., 28 (24): [PMID:33181479] [10.1016/j.bmc.2020.115816] |
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