tert-Butyl 7-(4-chlorophenyl)-2-(4-methoxyphenyl)-3-methyl-5-oxo-2,3,7,8-tetrahydro-3,8a-epidioxypyrano[3,2-c]pyridine-6(5H)-carboxylate

ID: ALA2435083

PubChem CID: 73356984

Max Phase: Preclinical

Molecular Formula: C27H28ClNO7

Molecular Weight: 513.97

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  COc1ccc(C2O[C@]34CC(c5ccc(Cl)cc5)N(C(=O)OC(C)(C)C)C(=O)C3=C[C@@]2(C)OO4)cc1

Standard InChI:  InChI=1S/C27H28ClNO7/c1-25(2,3)34-24(31)29-21(16-6-10-18(28)11-7-16)15-27-20(23(29)30)14-26(4,35-36-27)22(33-27)17-8-12-19(32-5)13-9-17/h6-14,21-22H,15H2,1-5H3/t21?,22?,26-,27+/m1/s1

Standard InChI Key:  WIJCDIIWFBZSNY-PGJSQRTPSA-N

Molfile:  

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M  END

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)

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

Calculated Properties

Molecular Weight: 513.97Molecular Weight (Monoisotopic): 513.1554AlogP: 5.67#Rotatable Bonds: 3
Polar Surface Area: 83.53Molecular Species: NEUTRALHBA: 7HBD:
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): #RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 5.97CX LogD: 5.97
Aromatic Rings: 2Heavy Atoms: 36QED Weighted: 0.49Np Likeness Score: 0.37

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