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

ID: ALA5288606

Max Phase: Preclinical

Molecular Formula: C32H42FN3O6

Molecular Weight: 583.70

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(F)c2c1

Standard InChI:  InChI=1S/C32H42FN3O6/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:  OLVUNYPSRIBIGZ-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

 42 48  0  0  0  0  0  0  0  0999 V2000
    0.5255   -1.3058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0054   -0.6654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2999    0.1051    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1145    0.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4090    1.0060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2235    1.1363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5182    1.9069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9981    2.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3328    2.0372    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8530    1.3968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6677    1.5268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1857    0.8880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8911    0.1171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0807   -0.0140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5572    0.6229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8672   -0.8108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0703   -1.0244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0014    1.0179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2909    1.7872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7741    2.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9616    2.2924    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.5848    0.4345    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8092   -0.7957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1037   -1.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9183   -1.6966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4385   -1.0562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1440   -0.2856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3293   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7329   -1.8268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5476   -1.9571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0678   -1.3168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7732   -0.5461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9586   -0.4158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3705   -2.0928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1329   -2.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7390   -1.9876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4321   -1.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6666   -0.7519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4454   -0.7519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7301   -1.4896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1485   -1.9964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5848   -1.9082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 11 10  2  0
 12 11  1  0
 13 12  2  0
 14 13  1  0
 15 14  2  0
 10 15  1  0
 14 16  1  0
 16 17  1  0
 12 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 11 21  1  0
 18 22  1  0
 23  2  1  0
 24 23  1  0
 25 24  1  0
 26 25  1  0
 26 27  1  0
 28 27  1  0
 23 28  1  0
 29 26  1  0
 30 29  1  0
 31 30  1  0
 31 32  1  0
 33 32  1  0
 26 33  1  0
 34 31  1  0
 35 34  1  0
 36 35  1  0
 36 37  1  0
 37 38  1  0
 31 38  1  0
 38 39  1  0
 40 39  1  0
 40 41  1  0
 41 34  1  0
 42 40  1  0
 42 36  1  0
M  END

Alternative Forms

  1. Parent:

    ALA5288606

    ---

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: 583.70Molecular Weight (Monoisotopic): 583.3058AlogP: 6.03#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: 3.47CX LogP: 5.61CX LogD: 5.61
Aromatic Rings: 2Heavy Atoms: 42QED Weighted: 0.29Np Likeness Score: -0.10

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