ID: ALA4459907

Max Phase: Preclinical

Molecular Formula: C27H38N2O6

Molecular Weight: 486.61

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1c1ccc(OCCN2CCCCC2)c(OC)c1

Standard InChI:  InChI=1S/C27H38N2O6/c1-6-33-26(30)23-18(3)28-19(4)24(27(31)34-7-2)25(23)20-11-12-21(22(17-20)32-5)35-16-15-29-13-9-8-10-14-29/h11-12,17,25,28H,6-10,13-16H2,1-5H3

Standard InChI Key:  SVKVYOGDWRHZIJ-UHFFFAOYSA-N

Associated Targets(Human)

Voltage-gated L-type calcium channel 709 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Histamine H3 receptor 10389 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acetylcholine receptor protein epsilon chain 95 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

Properties

Molecular Weight: 486.61Molecular Weight (Monoisotopic): 486.2730AlogP: 3.92#Rotatable Bonds: 10
Polar Surface Area: 86.33Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.47CX LogP: 3.14CX LogD: 2.04
Aromatic Rings: 1Heavy Atoms: 35QED Weighted: 0.50Np Likeness Score: -0.69

References

1. Malek R, Arribas RL, Palomino-Antolin A, Totoson P, Demougeot C, Kobrlova T, Soukup O, Iriepa I, Moraleda I, Diez-Iriepa D, Godyń J, Panek D, Malawska B, Głuch-Lutwin M, Mordyl B, Siwek A, Chabchoub F, Marco-Contelles J, Kiec-Kononowicz K, Egea J, de Los Ríos C, Ismaili L..  (2019)  New Dual Small Molecules for Alzheimer's Disease Therapy Combining Histamine H3 Receptor (H3R) Antagonism and Calcium Channels Blockade with Additional Cholinesterase Inhibition.,  62  (24): [PMID:31724859] [10.1021/acs.jmedchem.9b00937]

Source