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Chemical Structure| 476-34-6 Chemical Structure| 476-34-6
Chemical Structure| 476-34-6

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Isoindigo inhibits proliferation in various leukemia and cancer cell lines, displaying anticancer activity. Isoindigo and its derivatives may also bind the aryl hydrocarbon receptor (AhR). Additionally, similar compounds show chemotherapeutic benefits in animal models of leukemia.

Synonyms: Isoindigotin

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of Isoindigo

CAS No. :476-34-6
Formula : C16H10N2O2
M.W : 262.26
SMILES Code : O=C1NC2=C(C=CC=C2)/C1=C3C(NC4=C\3C=CC=C4)=O
Synonyms :
Isoindigotin
English Name :[3,3'-Biindolinylidene]-2,2'-dione
MDL No. :MFCD00423577
InChI Key :VBMISAYWIMDRCV-UHFFFAOYSA-N
Pubchem ID :164610

Safety of Isoindigo

Application In Synthesis of Isoindigo

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 476-34-6 ]

[ 476-34-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 476-34-6 ]
  • [ 595-05-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 8 steps 1.1: sodium hydride / tetrahydrofuran / 0.5 h 1.2: 1 h / 0 - 25 °C 2.1: glacial acetic acid; zinc powder / 1 h / 25 °C 3.1: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1S)-(6-methoxyquinolin-4-yl)(5-vinylquinuclidin-2-yl)methyl)thiourea / acetonitrile / 0.08 h / 25 °C 3.2: 72 h / 25 °C 4.1: Caswell No. 744A / N,N-dimethyl-formamide / 4 h / 80 °C 5.1: triphenylphosphine / water monomer; toluene / 3 h / 70 °C 5.2: 1 h / 25 °C 6.1: trifluoroacetic acid / dichloromethane / 1 h / 25 °C 7.1: Red-Al / toluene / 10 h / 0 - 110 °C / Inert atmosphere 8.1: glacial acetic acid / water monomer / 48 h / 110 °C / Inert atmosphere
Multi-step reaction with 8 steps 1.1: sodium hydride / tetrahydrofuran / 0.5 h 1.2: 1 h / 0 - 25 °C 2.1: glacial acetic acid; zinc powder / 1 h / 25 °C 3.1: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1S)-(6-methoxyquinolin-4-yl)(5-vinylquinuclidin-2-yl)methyl)thiourea / acetonitrile / 0.08 h / 25 °C 3.2: 72 h / 25 °C 4.1: Caswell No. 744A / N,N-dimethyl-formamide / 4 h / 80 °C 5.1: triphenylphosphine / water monomer; toluene / 3 h / 70 °C 5.2: 1 h / 25 °C 6.1: trifluoroacetic acid / dichloromethane / 1 h / 25 °C 7.1: Red-Al / toluene / 10 h / 0 - 110 °C / Inert atmosphere 8.1: glacial acetic acid / water monomer / 48 h / 110 °C / Inert atmosphere
 

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