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ID: ALA4743003
Max Phase: Preclinical
Molecular Formula: C28H34ClN3O5S2
Molecular Weight: 555.72
Molecule Type: Unknown
Associated Items:
ID: ALA4743003
Max Phase: Preclinical
Molecular Formula: C28H34ClN3O5S2
Molecular Weight: 555.72
Molecule Type: Unknown
Associated Items:
Canonical SMILES: C=C1CN(S(=O)(=O)c2ccc(C)cc2)CCc2cc(OC)cc(n2)CCN(S(=O)(=O)c2ccc(C)cc2)C1.Cl
Standard InChI: InChI=1S/C28H33N3O5S2.ClH/c1-21-5-9-27(10-6-21)37(32,33)30-15-13-24-17-26(36-4)18-25(29-24)14-16-31(20-23(3)19-30)38(34,35)28-11-7-22(2)8-12-28;/h5-12,17-18H,3,13-16,19-20H2,1-2,4H3;1H
Standard InChI Key: ZCXWTLWQAVJEAL-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: 555.72 | Molecular Weight (Monoisotopic): 555.1862 | AlogP: 3.74 | #Rotatable Bonds: 5 |
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: 5.39 | CX LogP: 4.03 | CX LogD: 4.03 |
Aromatic Rings: 3 | Heavy Atoms: 38 | QED Weighted: 0.45 | Np Likeness Score: -0.50 |
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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