diethyl (1RS,3aRS,6aRS)-5-cyclohexyl-4,6-dioxo-1,3a,4,5,6,6a-hexahydropyrrolo[3,4-c]pyrrol-1-ylphosphonate

ID: ALA4483022

Chembl Id: CHEMBL4483022

PubChem CID: 78114597

Max Phase: Preclinical

Molecular Formula: C16H25N2O5P

Molecular Weight: 356.36

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  CCOP(=O)(OCC)C1N=CC2C(=O)N(C3CCCCC3)C(=O)C21

Standard InChI:  InChI=1S/C16H25N2O5P/c1-3-22-24(21,23-4-2)14-13-12(10-17-14)15(19)18(16(13)20)11-8-6-5-7-9-11/h10-14H,3-9H2,1-2H3

Standard InChI Key:  CIWHQJBTCNPDOW-UHFFFAOYSA-N

Associated Targets(Human)

NISCH Tclin Nischarin (304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 356.36Molecular Weight (Monoisotopic): 356.1501AlogP: 2.60#Rotatable Bonds: 6
Polar Surface Area: 85.27Molecular Species: NEUTRALHBA: 6HBD:
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: 11.52CX Basic pKa: 2.61CX LogP: 1.31CX LogD: 1.31
Aromatic Rings: Heavy Atoms: 24QED Weighted: 0.54Np Likeness Score: -0.02

References

1. Abás S, Rodríguez-Arévalo S, Bagán A, Griñán-Ferré C, Vasilopoulou F, Brocos-Mosquera I, Muguruza C, Pérez B, Molins E, Luque FJ, Pérez-Lozano P, de Jonghe S, Daelemans D, Naesens L, Brea J, Loza MI, Hernández-Hernández E, García-Sevilla JA, García-Fuster MJ, Radan M, Djikic T, Nikolic K, Pallàs M, Callado LF, Escolano C..  (2020)  Bicyclic α-Iminophosphonates as High Affinity Imidazoline I2 Receptor Ligands for Alzheimer's Disease.,  63  (7): [PMID:32150414] [10.1021/acs.jmedchem.9b02080]

Source