ID: ALA2435082

Max Phase: Preclinical

Molecular Formula: C26H25ClN2O8

Molecular Weight: 528.95

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)(C)OC(=O)N1C(=O)C2=C[C@@]3(C)OO[C@]2(CC1c1ccc(Cl)cc1)OC3c1ccc([N+](=O)[O-])cc1

Standard InChI:  InChI=1S/C26H25ClN2O8/c1-24(2,3)35-23(31)28-20(15-5-9-17(27)10-6-15)14-26-19(22(28)30)13-25(4,36-37-26)21(34-26)16-7-11-18(12-8-16)29(32)33/h5-13,20-21H,14H2,1-4H3/t20?,21?,25-,26+/m1/s1

Standard InChI Key:  FXFRYWPTFDGJNU-IEZXYYGGSA-N

Associated Targets(Human)

A549 127892 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HCT-116 91556 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MV4-11 7307 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

L6 7924 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Plasmodium falciparum 966862 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

BALB/3T3 534 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: 528.95Molecular Weight (Monoisotopic): 528.1299AlogP: 5.57#Rotatable Bonds: 3
Polar Surface Area: 117.44Molecular Species: NEUTRALHBA: 8HBD: 0
#RO5 Violations: 2HBA (Lipinski): 10HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 6.07CX LogD: 6.07
Aromatic Rings: 2Heavy Atoms: 37QED Weighted: 0.29Np Likeness Score: 0.10

References

1. Hossain MI, Świtalska M, Peng W, Takashima M, Wang N, Kaiser M, Wietrzyk J, Dan S, Yamori T, Inokuchi T..  (2013)  Design, synthesis, and in vitro cancer cell growth inhibition evaluation and antimalarial testing of trioxanes installed in cyclic 2-enoate substructures.,  69  [PMID:24056020] [10.1016/j.ejmech.2013.08.008]

Source