Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4790280
Max Phase: Preclinical
Molecular Formula: C26H27N5O4S
Molecular Weight: 505.60
Molecule Type: Unknown
Associated Items:
ID: ALA4790280
Max Phase: Preclinical
Molecular Formula: C26H27N5O4S
Molecular Weight: 505.60
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CCCCN1C(=O)/C(=C/c2ccc(OCCn3c([N+](=O)[O-])cnc3C)cc2)S/C1=N\c1ccccc1
Standard InChI: InChI=1S/C26H27N5O4S/c1-3-4-14-30-25(32)23(36-26(30)28-21-8-6-5-7-9-21)17-20-10-12-22(13-11-20)35-16-15-29-19(2)27-18-24(29)31(33)34/h5-13,17-18H,3-4,14-16H2,1-2H3/b23-17-,28-26-
Standard InChI Key: QXBLGWCPGIHJRC-BXCHBZDESA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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: 505.60 | Molecular Weight (Monoisotopic): 505.1784 | AlogP: 5.58 | #Rotatable Bonds: 10 |
Polar Surface Area: 102.86 | Molecular Species: NEUTRAL | HBA: 8 | HBD: 0 |
#RO5 Violations: 2 | HBA (Lipinski): 9 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 2 |
CX Acidic pKa: | CX Basic pKa: 3.58 | CX LogP: 5.36 | CX LogD: 5.36 |
Aromatic Rings: 3 | Heavy Atoms: 36 | QED Weighted: 0.20 | Np Likeness Score: -1.76 |
1. Ansari MF,Inam A,Ahmad K,Fatima S,Agarwal SM,Azam A. (2020) Synthesis of metronidazole based thiazolidinone analogs as promising antiamoebic agents., 30 (23): [PMID:32927029] [10.1016/j.bmcl.2020.127549] |
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