Picroside II
Uses- Product Name
- Picroside II
- CAS No.
- 39012-20-9
- Chemical Name
- Picroside II
- Synonyms
- AMPHICOSIDE;PICROSID II;Picroside-2;Picroside Ⅱ;PICROSIDE II;PICROSIDE ò;Picroside a…;Berberine II;AMPHICOSIDE II;Picroside II-RM
- CBNumber
- CB8745879
- Molecular Formula
- C23H28O13
- Formula Weight
- 512.46
- MOL File
- 39012-20-9.mol
Picroside II Property
- Melting point:
- 145 - 155oC
- Boiling point:
- 780.8±60.0 °C(Predicted)
- Density
- 1.66±0.1 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,2-8°C
- solubility
- ethanol: soluble1mg/mL, clear, colorless
- pka
- 8.07±0.20(Predicted)
- form
- Solid
- color
- Pale Yellow
- InChIKey
- AKNILCMFRRDTEY-MRFBWRKESA-N
- SMILES
- C12(CO)OC1C(C1C=COC(O[C@H]3[C@H](O)[C@H]([C@H](O)[C@@H](CO)O3)O)C21)OC(=O)C1=CC=C(O)C(OC)=C1 |&1:12,13,15,16,18,r|
Safety
- Safety Statements
- 24/25
- WGK Germany
- 3
- HS Code
- 29389090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- G0174
- Product name
- Picroside II
- Purity
- ≥98% (HPLC)
- Packaging
- 10mg
- Price
- $362
- Updated
- 2023/06/20
- Product number
- G0174
- Product name
- Picroside II
- Purity
- ≥98% (HPLC)
- Packaging
- 50mg
- Price
- $1170
- Updated
- 2023/06/20
- Product number
- P2594
- Product name
- Picroside II
- Packaging
- 100MG
- Price
- $345
- Updated
- 2025/07/31
- Product number
- 30319
- Product name
- Picroside II
- Packaging
- 10mg
- Price
- $73
- Updated
- 2024/03/01
- Product number
- 30319
- Product name
- Picroside II
- Packaging
- 250mg
- Price
- $717
- Updated
- 2024/03/01
Picroside II Chemical Properties,Usage,Production
Uses
Picroside II similar to Picroside I (P437635), acts as an oxygen free radical scavenger and thus promotes anti-inflammatory activity and may be used in the treatment of arthritis or ischemic injury.
Chemical Properties
Yellow needle-shaped crystals, soluble in methanol, derived from Picrorhizoma Coptidis.
Uses
Picroside II similar to Picroside I (P437635), acts as an oxygen free radical scavenger and thus promotes anti-inflammatory activity and may be used in the treatment of arthritis or ischemic injury.
Definition
ChEBI: Picroside ii is a tannin.
Biological Activity
Picroside II displaysmany anti-cancer properties such as anti-metastatic, anti-angiogenic, and anti-apoptotic activities in both in vitro and in vivo studies.It also exerts antioxidant, anti-inflammatory, and antidiarrheal effectsagainst acute oxidative injuries such as severe acute pancreatitis-inducedintestinal barrier injury. PII has protective effects onischemia/reperfusion (I/R)-induced injury by interacting with differentmechanisms in various in vitro and in vivo models.', 'Phytochemical found in Traditional Chinese Medicine herbal preparations. Picroside II, a glucoside, is reported to have hepatoprotective, cardioprotective, and neuroprotective properties.
in vivo
Picroside II (0-20 mg/kg, i.g., given in two doses) protects liver cells from damage and prevents apoptosis[1].
Picroside II (20 mg/kg, intravenous injection, given in four doses) inhibits the activation of NLRP3 inflammasome and NF-κB pathway in mice, reducing the inflammatory response in sepsis and enhancing immune function[3].
Picroside II (20 mg/kg, intraperitoneal injection, a single dose) protects the blood-brain barrier by inhibiting oxidative signaling pathways in a rat model of ischemia-reperfusion injury[4].
Picroside II (5-20 mg/kg, i.g., once a day for seven days) has anti-lipid peroxidation effects and protects against mitochondrial damage in mice with liver injury[5].
| Animal Model: | DGalN and LPS(HY-D1056)-induced acute liver injury in mice[1] |
| Dosage: | 0, 5, 10, 20 mg/kg; administered 10 min before and 4 h after D-GalN and LPS administration |
| Administration: | i.g. |
| Result: | Reduced the levels of alanine aminotransferase and aspartate aminotransferase in the serum, decreased MDA content, had a dose-dependent effect on hepatocyte apoptosis, and upregulated the expression of the bcl-2 gene. |
| Animal Model: | Sepsis mouse model[3] |
| Dosage: | 20 mg/kg; four times injected (2 h, 14 h, 26 h and 38 h after CLP) |
| Administration: | Intravenous injection (i.v.) |
| Result: | Improved survival, reduced sepsis-related infiltration and attenuated lung injury, enhanced bacterial clearance, reduced IL-6, IL-1β, and TNF-α levels, inhibited splenic lymphocyte apoptosis, reduced p-NF-κB (p65) expression, and reduced IL-1β and caspase-1 levels. |
| Animal Model: | Rats with cerebral ischemia-reperfusion injury[4] |
| Dosage: | 20 mg/kg; single dose |
| Administration: | Intraperitoneal injection (i.p.) |
| Result: | Reduced the nervous system score, neuronal injury, BBB damage, ROS content and NADPH oxidase activity, down-regulated the protein levels of Rac-1, Nox2, ROCK, MLCK and MMP-2, and up-regulated the expression of claudin-5. |
| Animal Model: | Mouse model of liver injury induced by CCl4, D-GalN and AP[5] |
| Dosage: | 5, 10, 20mg/kg; daily; 7 days |
| Administration: | i.g. |
| Result: | Reduced the high levels of ALT and AST in serum caused by CCl4, D-GalN and AP, significantly alleviated liver cell damage, reduced MDA, and increased SOD and GSH-Px content in a dose-dependent manner, inhibited AP-induced liver toxicity in mice, enhanced ATPase activity, and improved mitochondrial swelling. |
Picroside II Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from Picroside II manufacturers
- Product
- Picroside II 39012-20-9
- Price
- US $0.00/mg
- Min. Order
- 5mg
- Purity
- ≥98%(HPLC)
- Supply Ability
- 10 g
- Release date
- 2019-09-20
- Product
- Picroside II 39012-20-9
- Price
- US $3.00/KG
- Min. Order
- 1KG
- Purity
- 98%
- Supply Ability
- 1kg,5kg,50kg
- Release date
- 2020-01-18