5-(4-fluorophenyl)-1-((3R,5aS,6R,8aS,9R,10R,12R,12aR)-3,6,9-trimethyldecahydro-3H-3,12-epoxy[1,2]dioxepino[4,3-i]isochromen-10-yl)-1H-1,2,3-triazole

ID: ALA5272263

Chembl Id: CHEMBL5272263

Max Phase: Preclinical

Molecular Formula: C23H28FN3O4

Molecular Weight: 429.49

Associated Items:

Names and Identifiers

Canonical SMILES:  C[C@H]1[C@H](n2nncc2-c2ccc(F)cc2)O[C@@H]2O[C@@]3(C)CC[C@H]4[C@H](C)CC[C@@H]1[C@@]24OO3

Standard InChI:  InChI=1S/C23H28FN3O4/c1-13-4-9-18-14(2)20(27-19(12-25-26-27)15-5-7-16(24)8-6-15)28-21-23(18)17(13)10-11-22(3,29-21)30-31-23/h5-8,12-14,17-18,20-21H,4,9-11H2,1-3H3/t13-,14-,17+,18+,20-,21-,22-,23-/m1/s1

Standard InChI Key:  AYAMKYTUMJIURS-DUFGVIJSSA-N

Alternative Forms

  1. Parent:

    ALA5272263

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Associated Targets(Human)

DLD-1 (17511 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SiHa (2051 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A 172 (535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

B16 (5829 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: 429.49Molecular Weight (Monoisotopic): 429.2064AlogP: 4.46#Rotatable Bonds: 2
Polar Surface Area: 67.63Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 0.45CX LogP: 5.09CX LogD: 5.09
Aromatic Rings: 2Heavy Atoms: 31QED Weighted: 0.66Np Likeness Score: 1.38

References

1. Gao F, Sun Z, Kong F, Xiao J..  (2020)  Artemisinin-derived hybrids and their anticancer activity.,  188  [PMID:31945642] [10.1016/j.ejmech.2020.112044]

Source