1. Anti-infection
  2. Fungal
  3. (±)-Pinoresinol

(±)-Pinoresinol is a potent antifungal agent. (±)-Pinoresinol shows antifungal activity.

For research use only. We do not sell to patients.

(±)-Pinoresinol

(±)-Pinoresinol Chemical Structure

CAS No. : 4263-88-1

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Other Forms of (±)-Pinoresinol:

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Description

(±)-Pinoresinol is a potent antifungal agent. (±)-Pinoresinol shows antifungal activity[1].

Cellular Effect
Cell Line Type Value Description References
BV-2 IC50
31.1 μM
Compound: 9; Pinoresinol
Antineuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess assay
Antineuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess assay
[PMID: 26774654]
BV-2 IC50
76.19 μM
Compound: 20
Antineuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced NO production after 24 hrs in presence of LPS by Griess reaction based assay
Antineuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced NO production after 24 hrs in presence of LPS by Griess reaction based assay
[PMID: 28911817]
HepG2 IC50
51 nM
Compound: 47
Antiproliferative activity against human HepG2 cells assessed as inhibition of cell growth incubated for 48 hrs by MTT assay
Antiproliferative activity against human HepG2 cells assessed as inhibition of cell growth incubated for 48 hrs by MTT assay
[PMID: 37847948]
Neutrophil IC50
1.3 μg/mL
Compound: 20
Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced superoxide anion generation by measuring superoxide dismutase SOD-inhibitable ferricytochrome c reduction incubated for 5 mins before fMLP/CB stimulation for 3 mins by spectrophotometry
Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced superoxide anion generation by measuring superoxide dismutase SOD-inhibitable ferricytochrome c reduction incubated for 5 mins before fMLP/CB stimulation for 3 mins by spectrophotometry
[PMID: 28218000]
Neutrophil IC50
> 10 μg/mL
Compound: 20
Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release pre-incubated for 5 mins before fMLP/CB stimulation using MeO-Suc-Ala-Ala-Pro-Val-pnitroanilide as substrate
Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release pre-incubated for 5 mins before fMLP/CB stimulation using MeO-Suc-Ala-Ala-Pro-Val-pnitroanilide as substrate
[PMID: 28218000]
PANC-1 IC50
37.5 μM
Compound: 7
Cytotoxicity against human PANC1 cells after 72 hrs by WST8 assay
Cytotoxicity against human PANC1 cells after 72 hrs by WST8 assay
[PMID: 28495081]
In Vitro

(±)-Pinoresinol shows antifungal activity with a MIC value of 1.0 mg/mL for Fusarium verticillioides[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

358.39

Formula

C20H22O6

CAS No.
SMILES

COC1=C(O)C=CC([C@@H]2[C@]3([H])[C@@](CO2)([H])[C@@H](C4=CC(OC)=C(C=C4)O)OC3)=C1

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
(±)-Pinoresinol
Cat. No.:
HY-N0957
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