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  1. General Info
  2. Source Info
  3. Effects Info
  4. Reference
Phytochemical Details
01. General Information
Name Hispidulin
PubChem CID 5281628
Molecular Weight 300.26g/mol
Synonyms

4',5,7-trihydroxy-6-methoxy-flavone, 4',5,7-trihydroxy-6-methoxyflavone, dinatin, hispidulin

Formula C₁₆H₁₂O₆
SMILES COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O
InChI 1S/C16H12O6/c1-21-16-11(19)7-13-14(15(16)20)10(18)6-12(22-13)8-2-4-9(17)5-3-8/h2-7,17,19-20H,1H3
InChIKey IHFBPDAQLQOCBX-UHFFFAOYSA-N
CAS Number 1447-88-7
ChEMBL ID CHEMBL293776
ChEBI ID CHEBI:75902
Herb ID HBIN029430
Drug Bank ID DB14008
KEGG ID C10058
Structure 2D-img
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2D MOL 3D MOL
02. Source Information of Phytochemical
Stevia rebaudiana Even
Chineses Pinyin TianYeJu
Use Part Leaf
Species
>Kingdom: Viridiplantae
 -->Phylum: Streptophyta
  -->Class: Equisetopsida
   -->Order: Asterales
    -->Family: Asteraceae
     -->Genus: Stevia
      -->Species: Stevia rebaudiana
03. Combinatorial Therapeutic Effect(s)
Synergistic Effect
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Drug(s) whose efficacy can be enhanced by this phytochemical
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Combination Pair ID: 108
Pair Name Hispidulin, Temozolomide
Partner Name Temozolomide
Disease Info [ICD-11: 2A00] Glioblastoma multiforme Investigative
Biological Phenomena Inhibition-->Autophagy
Gene Regulation Up-regulation Expression BAX hsa581
Down-regulation Expression BCL2 hsa596
Up-regulation Cleavage CASP3 hsa836
Up-regulation Cleavage CASP9 hsa842
Down-regulation Expression MAP1LC3A hsa84557
Up-regulation Expression MAP1LC3B hsa81631
In Vitro Model U-87MG ATCC Glioblastoma Homo sapiens (Human) CVCL_0022
Result These results collectively suggested that the combination of hispidulin and TMZ could improve the antitumor efficiency of TMZ against malignant gliomas.
04. Reference
No. Title Href
1 Hispidulin Enhances Temozolomide (TMZ)-Induced Cytotoxicity against Malignant Glioma Cells In Vitro by Inhibiting Autophagy. Comput Intell Neurosci. 2022 Jun 28;2022:5266770. doi: 10.1155/2022/5266770. Click
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