| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA540875
Max Phase: Preclinical
Molecular Formula: C14H18ClN3O2S
Molecular Weight: 291.38
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cl.NCCc1cnc(S)n1[C@H]1COc2ccc(O)cc2C1
Standard InChI: InChI=1S/C14H17N3O2S.ClH/c15-4-3-10-7-16-14(20)17(10)11-5-9-6-12(18)1-2-13(9)19-8-11;/h1-2,6-7,11,18H,3-5,8,15H2,(H,16,20);1H/t11-;/m1./s1
Standard InChI Key: RLTDDJMELMLUDK-RFVHGSKJSA-N
Associated Targets(Human)
Dopamine beta-hydroxylase 131 Activities
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 |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 291.38 | Molecular Weight (Monoisotopic): 291.1041 | AlogP: 1.55 | #Rotatable Bonds: 3 |
| Polar Surface Area: 73.30 | Molecular Species: BASE | HBA: 6 | HBD: 3 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 7.68 | CX Basic pKa: 9.66 | CX LogP: 1.04 | CX LogD: 0.68 |
| Aromatic Rings: 2 | Heavy Atoms: 20 | QED Weighted: 0.75 | Np Likeness Score: 0.07 |
References
| 1. Beliaev A, Learmonth DA, Soares-da-Silva P.. (2006) Synthesis and biological evaluation of novel, peripherally selective chromanyl imidazolethione-based inhibitors of dopamine beta-hydroxylase., 49 (3): [PMID:16451083] [10.1021/jm051051f] |
Source
Source(1):