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Osthenol

Cat. No. M19368
Osthenol Structure
Size Price Availability Quantity
1mg USD 110  USD110 In stock
5mg USD 245  USD245 In stock
10mg USD 365  USD365 In stock
20mg USD 500  USD500 In stock
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Quality Control & Documentation
Biological Activity

Osthenol (Ostenol) is a selective, reversible, and competitive human monoamine oxidase-A (hMAO-A) inhibitor (Ki=0.26 µM). Osthenol potently inhibits recombinant hMAO-A with an IC50 of 0.74 µM and shows a high selectivity index for hMAO-A versus hMAO-B.

Chemical Information
Molecular Weight 230.26
Formula C14H14O3
CAS Number 484-14-0
Form Solid
Solubility (25°C) DMSO 100 mg/mL (ultrasonic)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Jia-Ming Guo, et al. Zhongguo Zhong Yao Za Zhi. [Chemical constituents from Clausena excavata and their inhibitory activities against proliferation of synoviocytes]

[2] Piljoung Cho, et al. Xenobiotica. Characterization of osthenol metabolism in vivo and its pharmacokinetics

[3] Seung Cheol Baek, et al. Bioorg Med Chem Lett. Osthenol, a prenylated coumarin, as a monoamine oxidase A inhibitor with high selectivity

[4] Pil Joung Cho, et al. Pharmaceutics. Characterization of CYPs and UGTs Involved in Human Liver Microsomal Metabolism of Osthenol

[5] X Lv, et al. Xenobiotica. Isolation and identification of metabolites of osthole in rats

Related Monoamine Oxidase Products
Indazole

Indazole, also called isoindazole, a heterocyclic aromatic organic compound.

PF9601N

PF9601N is a monoamine oxidase B (MAO-B) inhibitor with neuroprotective properties in various ex vivo and in vivo models of Parkinson's disease (PD) for the study of excitotoxicity-mediated neurodegenerative diseases. In addition, PF9601N is a click chemistry reagent containing an Alkyne moiety that undergoes a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing an Azide moiety.

Verbasoside

Decaffeoylacteoside is an inhibitor of AChE/BChE/LOX with moderate activity.

ETAP

ETAP is a MAO-A and MAO-B inhibitor.

Rosmarinic acid racemate

Rosmarinic acid racemate is the racemate of Rosmarinic acid.

  Catalog
Abmole Inhibitor Catalog




Keywords: Osthenol supplier, Monoamine Oxidase, inhibitors, activators


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