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ID: ALA2271416
Max Phase: Preclinical
Molecular Formula: C22H26ClN3O4S
Molecular Weight: 463.99
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCOCCOC(=O)/C(C#N)=C(\NCc1ccc(OCc2cnc(Cl)s2)cc1)C(C)C
Standard InChI: InChI=1S/C22H26ClN3O4S/c1-4-28-9-10-29-21(27)19(11-24)20(15(2)3)25-12-16-5-7-17(8-6-16)30-14-18-13-26-22(23)31-18/h5-8,13,15,25H,4,9-10,12,14H2,1-3H3/b20-19-
Standard InChI Key: SLKDNQRYGCKYDO-VXPUYCOJSA-N
Associated Targets(non-human)
Brassica napus 1186 Activities
Amaranthus retroflexus 1838 Activities
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Medicago sativa 511 Activities
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Photosystem Q(B) protein 185 Activities
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Molecule Features
| 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 |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 463.99 | Molecular Weight (Monoisotopic): 463.1333 | AlogP: 4.48 | #Rotatable Bonds: 12 |
| Polar Surface Area: 93.47 | Molecular Species: NEUTRAL | HBA: 8 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 0.28 | CX LogP: 4.20 | CX LogD: 4.20 |
| Aromatic Rings: 2 | Heavy Atoms: 31 | QED Weighted: 0.21 | Np Likeness Score: -1.24 |
References
| 1. Wang T, Bing G, Zhang X, Qin Z, Yu H, Qin X, Dai H, Miao W, Wu S, Fang J.. (2010) Synthesis and herbicidal activities of 2-cyano-3-benzylaminoacrylates containing thiazole moiety., 20 (11): [PMID:20452764] [10.1016/j.bmcl.2010.04.027] |
Source
Source(1):