Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4567596
Max Phase: Preclinical
Molecular Formula: C24H20ClN5O5S3
Molecular Weight: 590.11
Molecule Type: Unknown
Associated Items:
ID: ALA4567596
Max Phase: Preclinical
Molecular Formula: C24H20ClN5O5S3
Molecular Weight: 590.11
Molecule Type: Unknown
Associated Items:
Canonical SMILES: NS(=O)(=O)NCc1nnc(C(c2nc3ccc(-c4cccc(Cl)c4)cc3s2)S(=O)(=O)Cc2ccccc2)o1
Standard InChI: InChI=1S/C24H20ClN5O5S3/c25-18-8-4-7-16(11-18)17-9-10-19-20(12-17)36-24(28-19)22(37(31,32)14-15-5-2-1-3-6-15)23-30-29-21(35-23)13-27-38(26,33)34/h1-12,22,27H,13-14H2,(H2,26,33,34)
Standard InChI Key: QTLKEMOUBMXNFP-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: 590.11 | Molecular Weight (Monoisotopic): 589.0315 | AlogP: 4.00 | #Rotatable Bonds: 9 |
Polar Surface Area: 158.14 | Molecular Species: NEUTRAL | HBA: 9 | HBD: 2 |
#RO5 Violations: 1 | HBA (Lipinski): 10 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: 8.76 | CX Basic pKa: 1.26 | CX LogP: 2.57 | CX LogD: 2.56 |
Aromatic Rings: 5 | Heavy Atoms: 38 | QED Weighted: 0.26 | Np Likeness Score: -1.69 |
1. Johnson JA, Tora G, Pi Z, Phillips M, Yin X, Yang R, Zhao L, Chen AY, Taylor DS, Basso M, Rose A, Behnia K, Onorato J, Chen XQ, Abell LM, Lu H, Locke G, Caporuscio C, Galella M, Adam LP, Gordon D, Wexler RR, Finlay HJ.. (2018) Sulfonylated Benzothiazoles as Inhibitors of Endothelial Lipase., 9 (12): [PMID:30613337] [10.1021/acsmedchemlett.8b00424] |
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