Organosulfur Compounds
eMolecules 62-56-6 | Thiourea | Chem-Impex | MFCD00008067 | 76.120 | CH4N2S | 99.000 | NC(N)=S | 2.5kg | 386903163
Thiourea | Chem-Impex | 62-56-6 | MFCD00008067 | 76.120 | CH4N2S | 99.000 | NC(N)=S | 2.5kg | 386903163
eMolecules 62-56-6 | Thiourea | Oakwood Chemicals | MFCD00008067 | 76.120 | CH4N2S | 99.000 | NC(N)=S | 25kg | 480131784
Thiourea | Oakwood Chemicals | 62-56-6 | MFCD00008067 | 76.120 | CH4N2S | 99.000 | NC(N)=S | 25kg | 480131784
Aobchem 1-Isopropyl-5-(methylthio)-1H-pyrazole | ≥97% | CAS 2734774-81-1 | C7H12N2S | 5g
1-Isopropyl-5-(methylthio)-1H-pyrazole | ≥97% | CAS 2734774-81-1 | C7H12N2S | 5g
Medchemexpress LLC (Bromomethyl)cyclopropane | 7051-34-5 | MFCD00001306 | 99.2% | 135.00 | C4H7Br | 1mL
Cyclopropylmethyl bromide is an intermediate Cyclopropylmethyl bromide can be used in the preparation of Firocoxib (HY-14670) Firocoxib (ML 1785713) is a potent selective orally active COX-2 inhibitor[1]
eMolecules 3326-32-7 | Fluorescein isothiocyanate isomer I | Chem-Impex | MFCD00005063 | 389.380 | C21H11NO5S | 96.000 | Oc1ccc2c(Oc3cc(O)ccc3C22OC(=O)c3cc(ccc23)N=C=S)c1 | 250mg | 112440714
Fluorescein isothiocyanate isomer I | Chem-Impex | 3326-32-7 | MFCD00005063 | 389.380 | C21H11NO5S | 96.000 | Oc1ccc2c(Oc3cc(O)ccc3C22OC(=O)c3cc(ccc23)N=C=S)c1 | 250mg | 112440714
Medchemexpress LLC Diphenyl disulfide | 882-33-7 | MFCD00003065 | 100.0% | 218.35 g/mol | C12H10S2 | 1mL
Diphenyl disulfide is an endogenous metabolite Diphenyl disulfide is a pharmaceutical intermediate Diphenyl disulfide can be coupled with aryl iodide to synthesize asymmetric aryl sulfide[1][2]
Aobchem 3-(Phenylsulfonyl)thiazolidine | 95% | CAS 17418-62-1 | C9H11NO2S2 | 250mg
3-(Phenylsulfonyl)thiazolidine | 95% | CAS 17418-62-1 | C9H11NO2S2 | 250mg
Aobchem N-(Cyclopropylmethyl)benzeneacetamide | 95% | CAS 1363776-59-3 | C12H15NO | 250mg
N-(Cyclopropylmethyl)benzeneacetamide | 95% | CAS 1363776-59-3 | C12H15NO | 250mg
![Medchemexpress LLC Urea, N-[2-(dimethylamino)ethyl]-N'-(7-methylbenzo[1,2-d:3,4-d']bisthiazol-2-yl)- | 1428729-63-8 | 99.5% | 335.45 | C14H17N5OS2 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000241973.png-250.jpg)
Medchemexpress LLC Urea, N-[2-(dimethylamino)ethyl]-N'-(7-methylbenzo[1,2-d:3,4-d']bisthiazol-2-yl)- | 1428729-63-8 | 99.5% | 335.45 | C14H17N5OS2 | 50 MG
RIG-1 modulator 1 is a small-molecule antiviral research compound described as "Compound of claim 13" with reported activity against influenza virus, hepatitis B virus (HBV), hepatitis C virus (HCV), and human immunodeficiency virus (HIV). It is supplied as a solid (white to light yellow) with molecular formula C14H17N5OS2 and molecular weight 335.45 g/mol for preclinical research use.
- High purity suitable for research (≈99.5%).
- Solid form, white to light yellow.
- Molecular weight 335.45 g/mol.
- CAS number 1428729-63-8.
- Reported antiviral activity against influenza, HBV, HCV, and HIV.
- Available in research sizes, 5 mg-500 mg.
Medchemexpress LLC Kv3 modulator 2 | 2101321-76-8 | 99.9% | 379.41 g·mol⁻¹ | C21H21N3O4 | 5 MG
Kv3 modulator 2 is a small-molecule modulator of Kv3 voltage-gated potassium channels with reported analgesic activity. It is provided for laboratory research use and is characterized by a defined molecular formula and molecular weight, and high purity suitable for preclinical studies.
- High purity (99.9%).
- Available in small research quantities (example: 5 mg).
- Molecular formula C21H21N3O4; molecular weight 379.41 g·mol⁻¹.
- Reported Kv3 channel modulatory activity with analgesic effects.
- For research use only; not for human or clinical use.
Medchemexpress LLC Thioacetamide | 62-55-5 | MFCD00008070 | 98.0% | 75.13 | C2H5NS | 500mg
Thioacetamide (TAA) is an indirect hepatotoxin and causes parenchymal cell necrosis Thioacetamide requires metabolic activation by microsomal CYP2E1 to thioacetamide-S-oxide initially and then to thioacetamide-S-dioxide which is a highly reactive metabolite and its reactive metabolites covalently bind to proteins and lipids thereby causing oxidative stress and centrilobular necrosis Thioacetamide can induce chronic liver fibrosis encephalopathy and other events model[1][2][3][4]
Aobchem (4-Methoxyphenyl)-3-thiazolidinylmethanone | 95% | CAS 2329600-35-1 | C11H13NO2S | 5g
(4-Methoxyphenyl)-3-thiazolidinylmethanone | 95% | CAS 2329600-35-1 | C11H13NO2S | 5g
Aobchem (4-Methoxyphenyl)-3-thiazolidinylmethanone | 95% | CAS 2329600-35-1 | C11H13NO2S | 250mg
(4-Methoxyphenyl)-3-thiazolidinylmethanone | 95% | CAS 2329600-35-1 | C11H13NO2S | 250mg
Apexbio Technology LLC Sulfathiazole 72-14-0 10mM (in 1mL DMSO)
Sulfathiazole (CAS 72-14-0) is a small-molecule inhibitor targeting dihydropteroate synthase (DHPS) It is designed to competitively inhibit bacterial folic acid synthesis thereby disrupting the folate pathway and impeding microbial growth Sulfathiazole exerts its biological activity primarily through inhibition of DHPS In in vitro studies sulfathiazole demonstrates bacteriostatic inhibition with IC50 values ranging from low to medium micromolar concentrations depending on specific bacterial strains and experimental conditions Based on these pharmacological properties sulfathiazole holds research potential in investigating antibacterial resistance metabolic pathways of pathogens and enzyme-substrate interactions in microbiological and biochemical research
Apexbio Technology LLC Sulindac 38194-50-2 10mM (in 1mL DMSO)
Sulindac (CAS 38194-50-2) is a nonsteroidal anti-inflammatory drug that functions as a prodrug and is metabolized in vivo to pharmacologically active sulindac sulfide and sulindac sulfone Sulindac sulfide acts as a cyclooxygenase inhibitor and modulates intracellular signaling pathways including the repression of ras activity Sulindac sulfone possesses antitumor properties independent of cyclooxygenase inhibition Due to these distinct metabolites and their activities sulindac is utilized in biomedical research for studying inflammatory processes cyclooxygenase-mediated pathways and the chemopreventive mechanisms involved in tumorigenesis