ID: ALA5271603

Max Phase: Preclinical

Molecular Formula: C26H41N5O3

Molecular Weight: 471.65

Associated Items:

Representations

Canonical SMILES:  CCCC[C@@H](CO)Nc1nc(N)nc(C)c1Cc1ccc(CC(=O)OCCCCN(C)C)cc1

Standard InChI:  InChI=1S/C26H41N5O3/c1-5-6-9-22(18-32)29-25-23(19(2)28-26(27)30-25)16-20-10-12-21(13-11-20)17-24(33)34-15-8-7-14-31(3)4/h10-13,22,32H,5-9,14-18H2,1-4H3,(H3,27,28,29,30)/t22-/m0/s1

Standard InChI Key:  LKMYDUPUYAWYEG-QFIPXVFZSA-N

Associated Targets(Human)

Toll-like receptor 7 2626 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 471.65Molecular Weight (Monoisotopic): 471.3209AlogP: 3.35#Rotatable Bonds: 15
Polar Surface Area: 113.60Molecular Species: BASEHBA: 8HBD: 3
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.79CX LogP: 3.71CX LogD: 0.87
Aromatic Rings: 2Heavy Atoms: 34QED Weighted: 0.27Np Likeness Score: -0.33

References

1. Kaushik D, Kaur A, Petrovsky N, Salunke DB..  (2021)  Structural evolution of toll-like receptor 7/8 agonists from imidazoquinolines to imidazoles.,  12  (7.0): [PMID:34355178] [10.1039/D1MD00031D]

Source