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  1. General Info
  2. Effects Info
  3. Reference
Drug Interaction Details
01. General Information
Pair Name Oridonin, Venetoclax
Phytochemical Name Oridonin (PubChem CID: 5321010 )
Anticancer drug Name Venetoclax (PubChem CID: 49846579 )
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: 1009
Pair Name Oridonin, Venetoclax
Disease Info [ICD-11: 2A60.Z] Acute myeloid leukemia Investigative
Biological Phenomena Induction-->Apoptosis
Gene Regulation Down-regulation Phosphorylation AKT1 hsa207
Down-regulation Expression BAD hsa572
Up-regulation Expression BAX hsa581
Down-regulation Expression BCL-xL hsa598
Up-regulation Expression BIM hsa10018
Up-regulation Cleavage CASP3 hsa836
Down-regulation Expression CCND1 hsa595
Down-regulation Phosphorylation CDK2 hsa1017
Up-regulation Expression CDKN1A hsa1026
Down-regulation Phosphorylation GSK3B hsa2932
Up-regulation Expression H2AX hsa3014
Down-regulation Expression MCL1 hsa4170
Down-regulation Expression MDM2 hsa4193
Down-regulation Expression MYC hsa4609
Up-regulation Cleavage PARP1 hsa142
Up-regulation Expression TP53 hsa7157
In Vitro Model MOLM-13 Adult acute myeloid leukemia Homo sapiens (Human) CVCL_2119
OCI-AML-3 Adult acute myeloid leukemia Homo sapiens (Human) CVCL_1844
U-937 Adult acute monocytic leukemia Homo sapiens (Human) CVCL_0007
THP-1 Childhood acute monocytic leukemia Homo sapiens (Human) CVCL_0006
In Vivo Model 5×10⁶ OCI-AML3 cells stably expressing luciferase were injected into the tail vein of NTG mice, and in vivo imaging was performed on the fourth day to confirm successful establishment of the AML xenografts.
Result Oridonin and venetoclax synergistically promote AML cell apoptosis by inhibiting AKT signaling.
03. Reference
No. Title Href
1 Oridonin Synergistically Enhances the Pro-Apoptotic Effect of Venetoclax on Acute Myeloid Leukemia Cells by Inhibiting AKT Signaling. Front Biosci (Landmark Ed). 2023 Sep 6;28(9):195. doi: 10.31083/j.fbl2809195. Click
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