(1r,3r,5r,7r)-N-(4-((4-chloro-6-methoxyquinolin-8-yl)amino)pentyl)dispiro[adamantane-2,3'-[1,2,4,5]tetraoxane-6',1

ID: ALA5269234

Max Phase: Preclinical

Molecular Formula: C32H42ClN3O6

Molecular Weight: 600.16

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  COc1cc(NC(C)CCCNC(=O)C2CCC3(CC2)OOC2(OO3)C3CC4CC(C3)CC2C4)c2nccc(Cl)c2c1

Standard InChI:  InChI=1S/C32H42ClN3O6/c1-19(36-28-18-25(38-2)17-26-27(33)7-11-34-29(26)28)4-3-10-35-30(37)22-5-8-31(9-6-22)39-41-32(42-40-31)23-13-20-12-21(15-23)16-24(32)14-20/h7,11,17-24,36H,3-6,8-10,12-16H2,1-2H3,(H,35,37)

Standard InChI Key:  QHFHDVNWYHMBSF-UHFFFAOYSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA5269234

    ---

Associated Targets(Human)

Caco-2 (12174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium berghei (192651 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

Calculated Properties

Molecular Weight: 600.16Molecular Weight (Monoisotopic): 599.2762AlogP: 6.54#Rotatable Bonds: 8
Polar Surface Area: 100.17Molecular Species: NEUTRALHBA: 8HBD: 2
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 2.90CX LogP: 6.08CX LogD: 6.08
Aromatic Rings: 2Heavy Atoms: 42QED Weighted: 0.26Np Likeness Score: -0.09

References

1. Sharma B, Singh P, Singh AK, Awasthi SK..  (2021)  Advancement of chimeric hybrid drugs to cure malaria infection: An overview with special emphasis on endoperoxide pharmacophores.,  219  [PMID:33989911] [10.1016/j.ejmech.2021.113408]

Source