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N-(2,3-Dihydro-1H-inden-5-yl)-4-methylpyrrolidin-2-imine Hydrochloride
ID: ALA3408295
Chembl Id: CHEMBL3408295
PubChem CID: 89964736
Max Phase: Preclinical
Molecular Formula: C14H19ClN2
Molecular Weight: 214.31
Molecule Type: Small molecule
Associated Items:
Names and Identifiers
Canonical SMILES: CC1CN/C(=N\c2ccc3c(c2)CCC3)C1.Cl
Standard InChI: InChI=1S/C14H18N2.ClH/c1-10-7-14(15-9-10)16-13-6-5-11-3-2-4-12(11)8-13;/h5-6,8,10H,2-4,7,9H2,1H3,(H,15,16);1H
Standard InChI Key: QJIXIZZLHVPLNG-UHFFFAOYSA-N
Associated Targets(Human)
Associated Targets(non-human)
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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Calculated Properties
Molecular Weight: 214.31 | Molecular Weight (Monoisotopic): 214.1470 | AlogP: 2.83 | #Rotatable Bonds: 1 |
Polar Surface Area: 24.39 | Molecular Species: BASE | HBA: 1 | HBD: 1 |
#RO5 Violations: ┄ | HBA (Lipinski): 2 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): ┄ |
CX Acidic pKa: ┄ | CX Basic pKa: 10.25 | CX LogP: 2.97 | CX LogD: 1.22 |
Aromatic Rings: 1 | Heavy Atoms: 16 | QED Weighted: 0.76 | Np Likeness Score: -0.40 |
References
1. Gasparik V, Greney H, Schann S, Feldman J, Fellmann L, Ehrhardt JD, Bousquet P.. (2015) Synthesis and biological evaluation of 2-aryliminopyrrolidines as selective ligands for I1 imidazoline receptors: discovery of new sympatho-inhibitory hypotensive agents with potential beneficial effects in metabolic syndrome., 58 (2): [PMID:25521963] [10.1021/jm501456p] |