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Chemical Structure| 4261-42-1 Chemical Structure| 4261-42-1

Structure of Isoorientin
CAS No.: 4261-42-1

Chemical Structure| 4261-42-1

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Isoorientin is a natural product isolated and purified from the herbs of Polygonum orientale Linn. with antioxidant activity.

Synonyms: Homoorientin; Lespecapitioside; Lutonaretin

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Product Details of Isoorientin

CAS No. :4261-42-1
Formula : C21H20O11
M.W : 448.38
SMILES Code : O=C1C=C(C2=CC=C(O)C(O)=C2)OC3=C1C(O)=C([C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O4)C(O)=C3
Synonyms :
Homoorientin; Lespecapitioside; Lutonaretin
MDL No. :MFCD00017433
InChI Key :ODBRNZZJSYPIDI-VJXVFPJBSA-N
Pubchem ID :114776

Safety of Isoorientin

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

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Plasmodium falciparum W2 0.8-100 μg/mL 48 h Evaluate anti-plasmodial activity, results showed no activity at concentrations of 50 μg/mL or below PMC6523950
Plasmodium falciparum 3D7 0.8-100 μg/mL 48 h Evaluate anti-plasmodial activity, results showed no activity at concentrations of 50 μg/mL or below PMC6523950
WI-38 2-100 μg/mL 48 h Evaluate cytotoxicity, results showed no cellular toxicity at concentrations of 100 μg/mL or below PMC6523950
A549 2-100 μg/mL 48 h Evaluate cytotoxicity, results showed no cellular toxicity at concentrations of 100 μg/mL or below PMC6523950
HeLa 2-100 μg/mL 48 h Evaluate cytotoxicity, results showed no cellular toxicity at concentrations of 100 μg/mL or below PMC6523950
Human hepatocyte HL-7702 cells 25, 50, 100, 200 μg/mL 12 h To evaluate cell viability and antioxidant capacity, results showed that Zein/GA-Iso nanoparticles significantly increased the survival rate of HL-7702 cells. PMC11268198
Human colorectal adenocarcinoma Caco-2 cells 25, 50, 100, 200 μg/mL 12 h To evaluate cell viability and antioxidant capacity, results showed that Zein/GA-Iso nanoparticles significantly increased the survival rate of Caco-2 cells. PMC11268198
T lymphocytes 40 μM 96 h Inhibited T lymphocyte proliferation, reducing CD4+ T cell proliferation to 57.07±6.4%, but no significant effect on CD8+ T cells PMC9405454
HL-7702 liver cells 5 μM 24 h Isoorientin attenuated BaP-induced pyroptotic hepatocyte damage by inhibiting the ROS/NF-κB/NLRP3/Caspase-1 signaling pathway PMC8389279
Primary colon epithelial cells 10 μM 48 h To compare the effects of four main BLF components on inflammatory cytokines and oxidative markers in primary colon epithelial cells of AD mice, Isoorientin showed the strongest bioactivity. PMC10853884
Primary neuronal cells 10 μM 48 h To compare the effects of four main BLF components on inflammatory cytokines and oxidative markers in primary neuronal cells of AD mice, Isoorientin showed the strongest bioactivity. PMC10853884

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Zebrafish Zebrafish larvae Water solution 0.1-100 μg/mL Once daily for 72 hours Evaluate whole organism toxicity, results showed no toxicity at tested concentrations PMC6523950
APP/PS1 transgenic mice Alzheimer's disease (AD) mouse model Oral gavage 2 mg/kg Once daily for 4 weeks To evaluate the therapeutic effects of BLF on ulcerative colitis in AD mice, BLF significantly alleviated colitis injury and possessed neuroprotective properties. PMC10853884
ICR male mice Acetic acid-writhing, hot plate and formalin-induced nociception models Intraperitoneal injection 7.5, 15, 30 mg/kg Single administration, evaluated 1 hour later Assessed the antinociceptive and anti-inflammatory activities of isoorientin. Results showed that isoorientin at 30 mg/kg significantly inhibited acetic acid-induced writhing (86.2% inhibition) and formalin-induced licking time (73.9% in the first phase and 48.3% in the second phase), with effects superior to clinical drugs like rotundine and aspirin. Additionally, isoorientin suppressed TRPV1 and GluN2B protein expression in the spinal dorsal horn and modulated inflammatory cytokines (TNF-α, IL-1β, IL-10) and oxidative stress markers (GSH, MDA, SOD, VC). PMC7060329

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.23mL

0.45mL

0.22mL

11.15mL

2.23mL

1.12mL

22.30mL

4.46mL

2.23mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

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
Protocol 2

References

 

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