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Chemical Structure| 568-72-9 Chemical Structure| 568-72-9

Structure of Tanshinone IIA
CAS No.: 568-72-9

Chemical Structure| 568-72-9

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Tanshinone IIA (Tan IIA) is a major component of the root of Salvia miltiorrhiza, inhibiting angiogenesis by targeting the kinase domain of VEGF/VEGFR2.

Synonyms: Dan Shen ketone; NSC 686518; TSA

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Product Citations

Product Citations

Şumnulu, Deniz ;

Abstract: Background: The study demonstrated that 89.72 µg/mL Theranekron D6 (TD6), 62.46 µM Tanshinone IIA (Tansh), and both Tansh-TD6 (Mix) exhibited selective apoptotic mechanisms on HEL299, A549, and Hep3B cells. Materials and methods: Application doses were determined by MTT assays. Apoptotic and ROS-affected cells were assessed via flow cytometry, gene expression changes by qRT-PCR, and mitochondrial membrane potential alterations through fluorescence microscopy. Results: Tansh reduced cell viability in all three cell lines, whereas the application of Mix increased cell viability in HEL299 cells, had no effect on A549 cells, and significantly decreased viability in Hep3B cells. This situation has also shown similarities in studies on ROS, mitochondrial membrane potential, and apoptosis. qRT-PCR analysis showed that in HEL299, Tansh, TD6, and Mix upregulated XIAP (2.42-fold, 1.4-fold, and 1.72-fold) and c-IAP1(2.97-fold, 1.44-fold, and 1.67-fold), whereas SMAC induction by Tansh was attenuated in the Mix (2.49-fold to 1.45-fold). In A549, Tansh strongly upregulated XIAP (3.86-fold), c-IAP1 (5.14-fold), and SMAC (5.02-fold), while TD6 downregulated them (0.4-fold, 0.68-fold, and 0.58-fold). In Hep3B, XIAP (0.63-fold, 0.61-fold, and 0.29-fold) and c-IAP1 (0.3-fold, 0.36-fold, and 0.08-fold) were consistently downregulated with all appplication, while SMAC expression was markedly elevated with Tansh (5.23-fold), TD6 (3.46-fold), and Mix (8.59-fold) applications. Apoptosis increased in HEL299 with Tansh (59.62%) but decreased with Mix (17.56%), whereas in Hep3B it rose with Mix (50.76% to 59.75%). Conclusion: TD6 enhances or sustains anticancer activity in malignant cells, suggesting therapeutic potential in combination strategies for many types of cancers.

Keywords: ROS ; SMAC ; Tanshinone IIA ; Theranekron D6

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Product Details of Tanshinone IIA

CAS No. :568-72-9
Formula : C19H18O3
M.W : 294.34
SMILES Code : CC1=COC(C2=C(C3=O)C(CCCC(C)4C)=C4C=C2)=C1C3=O
Synonyms :
Dan Shen ketone; NSC 686518; TSA
MDL No. :MFCD00238692
InChI Key :HYXITZLLTYIPOF-UHFFFAOYSA-N
Pubchem ID :164676

Safety of Tanshinone IIA

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of Tanshinone IIA

pyroptosis

Isoform Comparison

Biological Activity

Target
  • Lipase

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.40mL

0.68mL

0.34mL

16.99mL

3.40mL

1.70mL

33.97mL

6.79mL

3.40mL

Dissolving Methods
The prepared working fluid is recommended to be prepared now and used up as soon as possible in a short period of time. The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1

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