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Allisartan isoproxil

Cat. No. M41781
Allisartan isoproxil Structure
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Biological Activity

Allisartan isoproxil (ALS-3) is an orally potent, selective, non-peptide inhibitor of Angiotensin II Type 1.

Chemical Information
Molecular Weight 553.01
Formula C27H29ClN6O5
CAS Number 947331-05-7
Form Solid
Solubility (25°C) DMSO 90 mg/mL (ultrasonic and warming)
Storage 4°C, protect from light
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] Y Xiao et al. Bull Exp Biol Med. Allisartan Isoproxil Promotes Uric Acid Excretion by Interacting with Intestinal Urate Transporters in Hyperuricemic Zebrafish (Danio rerio)

[2] Hongyi Wang et al. Am J Hypertens. Efficacy of Allisartan Isoproxil in the Treatment of Mild-to-Moderate Essential Hypertension

[3] Qi-Sheng Ling et al. Acta Pharmacol Sin. Allisartan isoproxil reduces mortality of stroke-prone rats and protects against cerebrovascular, cardiac, and aortic damage

[4] Qinyang Jin et al. Mol Med Rep. Allisartan isoproxil attenuates oxidative stress and inflammation through the SIRT1/Nrf2/NF‑κB signalling pathway in diabetic cardiomyopathy rats

[5] Gaoxing Zhang et al. Adv Ther. Allisartan Isoproxil Improves Endothelial Function and Vascular Damage in Patients with Essential Hypertension: A Single-Center, Open-Label, Randomized Controlled Trial

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