ID: ALA515834
Chembl Id: CHEMBL515834
PubChem CID: 44581624
Max Phase: Preclinical
Molecular Formula: C15H18F3NO4S2
Molecular Weight: 397.44
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: C[C@H](CS)C(=O)N[C@@H](CSCc1ccc(OC(F)(F)F)cc1)C(=O)O
Standard InChI: InChI=1S/C15H18F3NO4S2/c1-9(6-24)13(20)19-12(14(21)22)8-25-7-10-2-4-11(5-3-10)23-15(16,17)18/h2-5,9,12,24H,6-8H2,1H3,(H,19,20)(H,21,22)/t9-,12+/m1/s1
Standard InChI Key: KBMIDQAQIWEGNJ-SKDRFNHKSA-N
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| 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: Small molecule | 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: 397.44 | Molecular Weight (Monoisotopic): 397.0629 | AlogP: 2.95 | #Rotatable Bonds: 9 |
| Polar Surface Area: 75.63 | Molecular Species: ACID | HBA: 5 | HBD: 3 |
| #RO5 Violations: ┄ | HBA (Lipinski): 5 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): ┄ |
| CX Acidic pKa: 3.70 | CX Basic pKa: ┄ | CX LogP: 3.94 | CX LogD: 0.64 |
| Aromatic Rings: 1 | Heavy Atoms: 25 | QED Weighted: 0.56 | Np Likeness Score: -0.49 |
| 1. Enomoto H, Morikawa Y, Miyake Y, Tsuji F, Mizuchi M, Suhara H, Fujimura K, Horiuchi M, Ban M.. (2009) Synthesis and biological evaluation of N-mercaptoacylcysteine derivatives as leukotriene A4 hydrolase inhibitors., 19 (2): [PMID:19042128] [10.1016/j.bmcl.2008.11.042] |
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