ID: ALA2179894

Max Phase: Preclinical

Molecular Formula: C35H50O5

Molecular Weight: 550.78

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=C(c1ccccc1)[C@@H]1CO[C@@]2(CC[C@@]3(C)[C@H](CC[C@@H]4[C@@H]3CC[C@]3(C)[C@@H]([C@H](C)CCC(=O)OC)CC[C@@H]43)C2)OO1

Standard InChI:  InChI=1S/C35H50O5/c1-23(11-16-32(36)37-5)28-14-15-29-27-13-12-26-21-35(20-19-33(26,3)30(27)17-18-34(28,29)4)38-22-31(39-40-35)24(2)25-9-7-6-8-10-25/h6-10,23,26-31H,2,11-22H2,1,3-5H3/t23-,26-,27+,28-,29+,30+,31+,33+,34-,35+/m1/s1

Standard InChI Key:  MVVAPRVWTVJCMA-SHFWOMIJSA-N

Associated Targets(non-human)

Plasmodium yoelii nigeriensis 1119 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 550.78Molecular Weight (Monoisotopic): 550.3658AlogP: 7.99#Rotatable Bonds: 6
Polar Surface Area: 53.99Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 2HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 8.13CX LogD: 8.13
Aromatic Rings: 1Heavy Atoms: 40QED Weighted: 0.27Np Likeness Score: 1.66

References

1. Singh C, Hassam M, Verma VP, Singh AS, Naikade NK, Puri SK, Maulik PR, Kant R..  (2012)  Bile acid-based 1,2,4-trioxanes: synthesis and antimalarial assessment.,  55  (23): [PMID:23163291] [10.1021/jm301323k]
2. Singh C, Hassam M, Verma VP, Singh AS, Naikade NK, Puri SK, Maulik PR, Kant R..  (2012)  Bile acid-based 1,2,4-trioxanes: synthesis and antimalarial assessment.,  55  (23): [PMID:23163291] [10.1021/jm301323k]

Source