dimethyl 5-(3-fluorophenyl)-1'',3''-dioxo-1'',3''-dihydro-5H-spiro[furan-2,2''-indene]-3,4-dicarboxylate

ID: ALA589734

Chembl Id: CHEMBL589734

PubChem CID: 2840573

Max Phase: Preclinical

Molecular Formula: C22H15FO7

Molecular Weight: 410.35

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Synonyms: SJ000296655 | SMR000116242|CBMicro_016937|MLS000525768|CHEMBL589734|SCHEMBL12325684|HMS2476C13|CCG-5711|AKOS000616871|AKOS016300968|dimethyl 5-(3-fluorophenyl)-1',3'-dioxo-1',3'-dihydro-5H-spiro[furan-2,2'-indene]-3,4-dicarboxylate|BIM-0016701.P001|EU-0011593|SJ000296655|SR-01000493157|SR-01000493157-1|3,4-DIMETHYL 5-(3-FLUOROPHENYL)-1',3'-DIOXO-1',3'-DIHYDRO-5H-SPIRO[FURAN-2,2'-INDENE]-3,4-DICARBOXYLATE

Canonical SMILES:  COC(=O)C1=C(C(=O)OC)C2(OC1c1cccc(F)c1)C(=O)c1ccccc1C2=O

Standard InChI:  InChI=1S/C22H15FO7/c1-28-20(26)15-16(21(27)29-2)22(30-17(15)11-6-5-7-12(23)10-11)18(24)13-8-3-4-9-14(13)19(22)25/h3-10,17H,1-2H3

Standard InChI Key:  BEYHXTRSACTXAI-UHFFFAOYSA-N

Associated Targets(Human)

NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 (95332 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KPNB1 Tbio Importin subunit beta-1/Snurportin-1 (25097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 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: 410.35Molecular Weight (Monoisotopic): 410.0802AlogP: 2.36#Rotatable Bonds: 3
Polar Surface Area: 95.97Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.12CX LogD: 3.12
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.57Np Likeness Score: -0.06

References

1. Guiguemde WA, Shelat AA, Bouck D, Duffy S, Crowther GJ, Davis PH, Smithson DC, Connelly M, Clark J, Zhu F, Jiménez-Díaz MB, Martinez MS, Wilson EB, Tripathi AK, Gut J, Sharlow ER, Bathurst I, El Mazouni F, Fowble JW, Forquer I, McGinley PL, Castro S, Angulo-Barturen I, Ferrer S, Rosenthal PJ, Derisi JL, Sullivan DJ, Lazo JS, Roos DS, Riscoe MK, Phillips MA, Rathod PK, Van Voorhis WC, Avery VM, Guy RK..  (2010)  Chemical genetics of Plasmodium falciparum.,  465  (7296): [PMID:20485428] [10.1038/nature09099]
2. PubChem BioAssay data set,