Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3585791
Max Phase: Preclinical
Molecular Formula: C15H24ClN3O3S
Molecular Weight: 361.90
Molecule Type: Small molecule
Associated Items:
ID: ALA3585791
Max Phase: Preclinical
Molecular Formula: C15H24ClN3O3S
Molecular Weight: 361.90
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCCCc1nc(Cl)c(C(=O)N[C@@H](CCSC)C(=O)OC)n1C
Standard InChI: InChI=1S/C15H24ClN3O3S/c1-5-6-7-11-18-13(16)12(19(11)2)14(20)17-10(8-9-23-4)15(21)22-3/h10H,5-9H2,1-4H3,(H,17,20)/t10-/m0/s1
Standard InChI Key: VNIVWECYRGUVEE-JTQLQIEISA-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: 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: 361.90 | Molecular Weight (Monoisotopic): 361.1227 | AlogP: 2.44 | #Rotatable Bonds: 9 |
Polar Surface Area: 73.22 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 13.54 | CX Basic pKa: 2.83 | CX LogP: 2.45 | CX LogD: 2.45 |
Aromatic Rings: 1 | Heavy Atoms: 23 | QED Weighted: 0.68 | Np Likeness Score: -1.12 |
1. Jallapally A, Addla D, Bagul P, Sridhar B, Banerjee SK, Kantevari S.. (2015) Design, synthesis and evaluation of novel 2-butyl-4-chloroimidazole derived peptidomimetics as Angiotensin Converting Enzyme (ACE) inhibitors., 23 (13): [PMID:25922179] [10.1016/j.bmc.2015.04.024] |
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