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Chemical Structure| 867-44-7 Chemical Structure| 867-44-7

Structure of S-Methylisothiourea sulfate
CAS No.: 867-44-7

Chemical Structure| 867-44-7

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(S)-Methylisothiourea Sulfate is a highly selective, potent and competitive inhibitor of iNOS.

Synonyms: S-methyl Isothiourea (hemisulfate); (S)-Methylisothiourea sulfate; SMIT

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Product Details of S-Methylisothiourea sulfate

CAS No. :867-44-7
Formula : C4H14N4O4S3
M.W : 278.37
SMILES Code : N=C(N)SC.N=C(N)SC.O=S(O)(O)=O
Synonyms :
S-methyl Isothiourea (hemisulfate); (S)-Methylisothiourea sulfate; SMIT
MDL No. :MFCD00013055
InChI Key :BZZXQZOBAUXLHZ-UHFFFAOYSA-N
Pubchem ID :13347

Safety of S-Methylisothiourea sulfate

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
J774.2 macrophages 6 µM 24 hours To evaluate the inhibitory effect of SMT on LPS-induced NO production. Results showed SMT is a potent inhibitor of iNOS with an EC50 of 6 μM. Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12472-6.
HL-1 cells 10 µM 24 hours To investigate the inhibitory effect of SMT on iNOS protein expression in PA-induced HL-1 cells Int J Mol Sci. 2023 Jan 3;24(1):858.
Rat aortic smooth muscle cells 2 µM 48 hours To evaluate the inhibitory effect of SMT on LPS and IFN-γ-induced NO production. Results showed SMT is a potent inhibitor of iNOS with an EC50 of 2 μM. Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12472-6.
FHM cells 0, 1 µM, 10 µM, 0.1 mM, 1 mM 48 hours To investigate the inhibitory effect of SMT on GCRV-induced apoptosis. Results showed that as SMT concentration increased, cytopathic effects were attenuated and apoptosis rate decreased. Int J Mol Sci. 2019 Dec 16;20(24):6335.

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Wistar rats Endotoxic shock model Intravenous injection 0.01-3 mg/kg Single dose To evaluate the effect of SMT on blood pressure in endotoxic shock rats. Results showed SMT dose-dependently reversed LPS-induced hypotension and vascular hyporeactivity. Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12472-6.
Sprague-Dawley rats Pulmonary granulomatous inflammation model Intraperitoneal injection 10 mg Once daily for 3 consecutive days Inhibited NO production, significantly reduced monocyte/macrophage infiltration and inhibited induction of monocyte chemoattractant protein-1 Am J Pathol. 1996 Dec;149(6):2005-22
Rare minnow GCRV infection model Intraperitoneal injection 100 mg/kg Single dose, observed until hemorrhage developed To investigate the inhibitory effect of SMT on GCRV-induced hemorrhage. Results showed that SMT significantly reduced NO content, caspase activities, and hemorrhage symptoms. Int J Mol Sci. 2019 Dec 16;20(24):6335.
Sprague-Dawley rats Hemorrhagic shock model Perfusate 100 μM Single dose, measurements taken 10 min post-administration To investigate the effect of S-methylisothiourea sulfate on hepatic microcirculatory function after hemorrhagic shock, showing no significant effect on sinusoidal flow, hepatic redox state, or function J Clin Invest. 1998 Sep 15;102(6):1220-8

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.59mL

0.72mL

0.36mL

17.96mL

3.59mL

1.80mL

35.92mL

7.18mL

3.59mL

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