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S-Methylisothiourea sulfate

Cat. No. M10926
S-Methylisothiourea sulfate Structure
Synonym:

S-甲基异硫脲半硫酸盐

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25mg USD 50  USD50 In stock
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Quality Control & Documentation
Biological Activity

S-Methylisothiourea sulfate is a highly effective, selective, competitive inducible nitric oxide synthase (iNOS) inhibitor. S-Methylisothiourea sulfate plays a beneficial role in rodent models of septic shock.

Chemical Information
Molecular Weight 139.18
Formula C2H8N2O4S2
CAS Number 867-44-7
Solubility (25°C) Water ≥ 20 mg/mL
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] Caiyang Zhang, et al. Org Biomol Chem. Cesium carbonate-promoted synthesis of aryl methyl sulfides using S-methylisothiourea sulfate under transition-metal-free conditions

[2] Amar S More, et al. Naunyn Schmiedebergs Arch Pharmacol. Effect of S-methylisothiourea in acetaminophen-induced hepatotoxicity in rat

[3] Yuan-Jin Guo, et al. Inflammation. S-methylisothiourea induces apoptosis of herpes simplex virus-1-infected microglial cells

[4] Ahmet Guzel, et al. Int J Pediatr Otorhinolaryngol. Protective effects of S-methylisothiourea sulfate on different aspiration materials-induced lung injury in rats

[5] C Mitaka, et al. Intensive Care Med. S-Methylisothiourea sulfate improves renal, but not hepatic dysfunction in canine endotoxic shock model

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Keywords: S-Methylisothiourea sulfate, S-甲基异硫脲半硫酸盐 supplier, NO Synthase, inhibitors, activators


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