ID: ALA4449514

Max Phase: Preclinical

Molecular Formula: C30H42N2O5

Molecular Weight: 510.68

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1ccc(CCCN(C)[C@@H]2CCC[C@H](N3CCc4cc(OC)c(OC)cc4CC3=O)C2)cc1OC

Standard InChI:  InChI=1S/C30H42N2O5/c1-31(14-7-8-21-11-12-26(34-2)27(16-21)35-3)24-9-6-10-25(20-24)32-15-13-22-17-28(36-4)29(37-5)18-23(22)19-30(32)33/h11-12,16-18,24-25H,6-10,13-15,19-20H2,1-5H3/t24-,25+/m1/s1

Standard InChI Key:  JBGCSKYMXGOCBY-RPBOFIJWSA-N

Associated Targets(Human)

Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4 92 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: 510.68Molecular Weight (Monoisotopic): 510.3094AlogP: 4.52#Rotatable Bonds: 10
Polar Surface Area: 60.47Molecular Species: BASEHBA: 6HBD: 0
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 10.13CX LogP: 4.17CX LogD: 1.50
Aromatic Rings: 2Heavy Atoms: 37QED Weighted: 0.47Np Likeness Score: -0.07

References

1. Romanelli MN, Del Lungo M, Guandalini L, Zobeiri M, Gyökeres A, Árpádffy-Lovas T, Koncz I, Sartiani L, Bartolucci G, Dei S, Manetti D, Teodori E, Budde T, Cerbai E..  (2019)  EC18 as a Tool To Understand the Role of HCN4 Channels in Mediating Hyperpolarization-Activated Current in Tissues.,  10  (4): [PMID:30996800] [10.1021/acsmedchemlett.8b00587]

Source