Free shipping on all orders over $ 500

Zaprinast

Cat. No. M30017
Zaprinast Structure
Synonym:

M&B 22948

Size Price Availability Quantity
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

Zaprinast (M&B 22948) is an inhibitor of cGMP-selective Phosphodiesterases(PDEs). Zaprinast is a G protein-coupled receptor (GPR) 35 agonist which activates rat GPR35 strongly and activates human GPR35 moderately. Zaprinast reduces vessel remodeling through antiproliferative and proapoptotic effects.

Chemical Information
Molecular Weight 271.27
Formula C13H13N5O2
CAS Number 37762-06-4
Form Solid
Solubility (25°C) DMSO 62.5 mg/mL (ultrasonic)
Storage -20°C, protect from light, sealed
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] Zübeyir Huyut, et al. Arch Physiol Biochem. Zaprinast and avanafil increase the vascular endothelial growth factor, vitamin D3, bone morphogenic proteins 4 and 7 levels in the kidney tissue of male rats applied the glucocorticoid

[2] Zübeyir Huyut, et al. Arch Physiol Biochem. Can zaprinast and avanafil induce the levels of angiogenesis, bone morphogenic protein 2, 4 and 7 in kidney of ovariectomised rats?

[3] Mauro Giorgi, et al. Behav Brain Res. Zaprinast impairs spatial memory by increasing PDE5 expression in the rat hippocampus

[4] Heung-Soon Lee, et al. Int Immunopharmacol. Zaprinast activates MAPKs, NFκB, and Akt and induces the expressions of inflammatory genes in microglia

[5] A Gibson. Eur J Pharmacol. Phosphodiesterase 5 inhibitors and nitrergic transmission-from zaprinast to sildenafil

Related PDE Products
ME-3183

ME-3183 is an oral selective PDE4 inhibitor with anti-inflammatory activity for studies related to plaque psoriasis.

ART-648

ART-648 is a PDE4 inhibitor that may be used in studies related to non-alcoholic steatohepatitis.

(E/Z)-HA155

(E/Z)-HA155 is a potent Autotaxin (ATX) type I inhibitor for studies related to cancer, fibrous disorders, inflammation, pain and angiogenesis.

Autotaxin-IN-3

Autotaxin-IN-3 is an Autotaxin(ATX) inhibitor with an IC50 value of 2.4 nM.

HA155

HA155 is a potent and selective ATX inhibitor with an IC50 value of 5.7 nM.

  Catalog
Abmole Inhibitor Catalog




Keywords: Zaprinast, M&B 22948 supplier, PDE, inhibitors, activators


Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2023 AbMole BioScience. All Rights Reserved.