Structure of Polyphyllin I
CAS No.: 50773-41-6
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Polyphyllin D, a natural product isolated and purified from the rhizomes of Paris yunnanensis Franch. with anti-angiongenic, toxic and anti-cancer effects, induces apoptosis via the mitochondrial apoptotic pathway as evidenced by decreased Bcl-2 expression levels, disruption of MMP and increased Bax, cytochrome C and cleaved-caspase-3 levels.
Synonyms: (+)-Polyphyllin D
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Batch number can be found on the product's label following the word 'Batch'.
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Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
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Batch number can be found on the product's label following the word 'Batch'.
CAS No. : | 50773-41-6 |
Formula : | C44H70O16 |
M.W : | 855.02 |
SMILES Code : | C[C@@]12[C@@]3([C@]([H])(C[C@]1([C@]4([C@]([H])(CC2)[C@]5(C)C(C[C@H](CC5)O[C@]6([C@H](O[C@]7([C@H](O)[C@H](O)[C@H]([C@@H](O7)C)O)[H])[C@@H](O)[C@@H]([C@H](O6)CO)O[C@@]8(O[C@H]([C@@H]([C@H]8O)O)CO)[H])[H])=CC4)[H])[H])O[C@@]9([C@H]3C)CC[C@H](CO9)C)[H] |
Synonyms : |
(+)-Polyphyllin D
|
MDL No. : | MFCD12407435 |
GHS Pictogram: |
![]() |
Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
Non-small cell lung cancer cells PC9 | 0.8-1.2 μM | 72 h | PPI significantly inhibited the growth of PC9 cells and induced cell cycle arrest at G0/G1 phase. | PMC4947306 |
Non-small cell lung cancer cells A549 | 0.8-1.2 μM | 72 h | PPI significantly inhibited the growth of A549 cells and induced cell cycle arrest at G0/G1 phase. | PMC4947306 |
PLC | 0.1, 0.3, 1 µM | 48 h | PPI inhibited the transcriptional activity of Twist1 and reduced the expression of VE-cadherin, thereby suppressing VM formation. | PMC6125388 |
SMMC7721 | 0.1, 0.3, 1 µM | 48 h | PPI significantly inhibited the migration and invasion ability of HCC cells and reduced the formation of tube-like structures. | PMC6125388 |
L-02 cells | 0.66, 0.88, 1.1 mg/mL | 24 h | To evaluate the cytotoxicity and hepatotoxicity of PPI on L-02 cells, the results showed that PPI dose-dependently decreased cell viability and induced apoptosis and liver dysfunction. | PMC9937801 |
Primary microglia | 1 μM and 2 μM | 72 h | PPI promoted M1 to M2 microglia polarization, reduced the secretion of pro-inflammatory cytokines (TNF-α, IL-1β, IL-6), and increased the secretion of anti-inflammatory cytokines (IL-4, IL-13, TGF-β). | PMC11094947 |
Peritoneal elucidated macrophages (PEMs) | 1 µM | 3 h | PPI significantly reduced the mRNA expression of IL-1β, IL-6, and iNOS induced by LPS/IFN-γ. | PMC6170622 |
Bone marrow-derived macrophages (BMMs) | 0.5 µM, 1 µM | 3 h | PPI significantly reduced the mRNA expression of IL-1β, TNF-α, IL-6, and iNOS induced by LPS/IFN-γ, and decreased the production of these inflammatory cytokines. | PMC6170622 |
Hep3B 2.1–7 | 2.5 μg/mL and 5 μg/mL | 24 h | PPI significantly inhibited the proliferation and migration of Hep3B cells and induced apoptosis | PMC11344421 |
HaCaT keratinocytes | 0.3, 0.6, 0.9 μg/ml | 8 h | PPI significantly reduced TLR2 mRNA and protein expression in a concentration-dependent manner, and downregulated the mRNA and protein expression of IL-1α and K16. | PMC6394558 |
HaCaT keratinocytes | 0.3, 0.6, 0.9 μg/ml | 24 h | PPI significantly suppressed the secretion of inflammatory cytokines, including IL-6, IL-8, and TNF-α, and the expression of TLR2 in P. acnes-treated cells. | PMC6394558 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Nude mice | Non-small cell lung cancer xenograft model | Intraperitoneal injection | 1 mg/kg and 3 mg/kg | Once daily for 27 days | PPI significantly inhibited tumor growth, reduced protein expression levels of p65, DNMT1 and EZH2, and increased phosphorylation of SAPK/JNK. | PMC4947306 |
BALB/c nude mice | HCC xenograft model | Oral | 10 mg/kg | Once daily for 25 days | PPI significantly inhibited tumor growth and lung metastasis, and prolonged the survival time of nude mice. | PMC6125388 |
C57BL/6 mice | Middle cerebral artery occlusion (MCAO) model | Intraperitoneal injection | 2 mg/kg and 5 mg/kg | Once daily for one week | PPI alleviated cerebral ischemia-reperfusion injury and neuroinflammation, improved functional recovery in MCAO mice, and promoted M1 to M2 microglial polarization. | PMC11094947 |
DBA/1J mice | Collagen-induced arthritis (CIA) model | Intragastric | 1 mg/kg | Once daily for 7 weeks | PPI significantly alleviated arthritis symptoms in CIA mice, reduced joint inflammation and bone erosion, and decreased infiltration of M1-like macrophages. | PMC6170622 |
Zebrafish | Hep3B cell xenograft model | Culture medium | 0.3 μg/mL and 0.6 μg/mL | 48 hours | PPI significantly inhibited tumor growth of Hep3B cells in the zebrafish model | PMC11344421 |
Bio Calculators | ||||
Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.17mL 0.23mL 0.12mL |
5.85mL 1.17mL 0.58mL |
11.70mL 2.34mL 1.17mL |
Tags: Polyphyllin I | JNK | mTOR | Akt | PDK-1 | Autophagy | Apoptosis | c-Jun N-terminal kinase | Mammalian target of Rapamycin | JNK signaling | PDK1/Akt/mTOR inhibition | G2/M phase arrest | Protein kinase B | 3-Phosphoinositide-dependent protein kinase 1 | Paris polyphylla | anti-tumor | PDK1/Akt/mTOR signaling | G2/M phase | 50773-41-6
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