Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3585797
Max Phase: Preclinical
Molecular Formula: C14H22ClN3O3
Molecular Weight: 315.80
Molecule Type: Small molecule
Associated Items:
ID: ALA3585797
Max Phase: Preclinical
Molecular Formula: C14H22ClN3O3
Molecular Weight: 315.80
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCCCc1nc(Cl)c(C(=O)N[C@H](C(=O)O)C(C)C)n1C
Standard InChI: InChI=1S/C14H22ClN3O3/c1-5-6-7-9-16-12(15)11(18(9)4)13(19)17-10(8(2)3)14(20)21/h8,10H,5-7H2,1-4H3,(H,17,19)(H,20,21)/t10-/m0/s1
Standard InChI Key: XTNBFEHIQYHKMS-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: 315.80 | Molecular Weight (Monoisotopic): 315.1350 | AlogP: 2.26 | #Rotatable Bonds: 7 |
Polar Surface Area: 84.22 | Molecular Species: ACID | HBA: 4 | HBD: 2 |
#RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 3.65 | CX Basic pKa: 2.64 | CX LogP: 2.15 | CX LogD: -0.84 |
Aromatic Rings: 1 | Heavy Atoms: 21 | QED Weighted: 0.81 | Np Likeness Score: -0.88 |
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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