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  1. General Info
  2. Effects Info
  3. Reference
Drug Interaction Details
01. General Information
Pair Name Glucosinalbate, Doxorubicin
Phytochemical Name Glucosinalbate (PubChem CID: 145925702 )
Anticancer drug Name Doxorubicin (PubChem CID: 31703 )
Structure of
Phytochemical
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2D MOL 3D MOL
Structure of
Anticancer Drug
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2D MOL 3D MOL
02. Combinatorial Therapeutic Effect(s)
Synergistic Effect
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Enhancing Drug Efficacy
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Combination Pair ID: 507
Pair Name Glucosinalbate, Doxorubicin
Disease Info [ICD-11: 2C90] Ehrlich ascites carcinoma Investigative
Biological Phenomena Inhibition-->Angiogenesis
Gene Regulation Up-regulation Expression APAF1 hsa317
Up-regulation Expression BAX hsa581
Down-regulation Expression BCL2 hsa596
Up-regulation Cleavage CASP3 hsa836
Up-regulation Expression CASP9 hsa842
Up-regulation Expression CYCS hsa54205
Up-regulation Expression GSTP1 hsa2950
Up-regulation Expression HMOX1 hsa3162
Down-regulation Expression IL6 hsa3569
Down-regulation Expression KEAP1 hsa9817
Up-regulation Expression LBR hsa3930
Down-regulation Expression MMP9 hsa4318
Up-regulation Expression NFE2L2 hsa4780
Up-regulation Expression NFKBIA hsa4792
Down-regulation Expression NOS2 hsa4843
Up-regulation Expression NQO1 hsa1728
Up-regulation Cleavage PARP1 hsa142
Down-regulation Expression PTGS2 hsa5743
Down-regulation Expression RELA hsa5970
Down-regulation Expression VEGFA hsa7422
In Vivo Model Ehrlich ascites carcinoma cell was maintained in Swiss albino mice by weekly intraperitoneal transplantation of 1×10⁶ viable tumor cells suspended in isotonic phosphate-buffered solution (PBS).
Result The present study clearly suggested therapeutic benefit of I3C in combination with DOX by augmenting anticancer efficacy and diminishing toxicity to the host.
03. Reference
No. Title Href
1 Indole-3-Carbinol (I3C) enhances the sensitivity of murine breast adenocarcinoma cells to doxorubicin (DOX) through inhibition of NF-κβ, blocking angiogenesis and regulation of mitochondrial apoptotic pathway. Chem Biol Interact. 2018 Jun 25;290:19-36. doi: 10.1016/j.cbi.2018.05.005. Click
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