Organic sulfuric acids and derivatives
Sigma Aldrich Fine Chemicals Biosciences CobaltII sulfate heptahydr1KG
CobaltII sulfate heptahydr1KG
Medchemexpress LLC Chondroitin sulfate methacryloyl | 99.5% | 10 MG
Chondroitin sulfate methacryloyl (CSMA) is a methacrylated derivative of chondroitin sulfate developed for photocrosslinkable hydrogel formation and 3D bioprinting. It is biocompatible, forms fibrous hydrogels under photoinitiation, and the degree of methacrylation enables tuning of mechanical strength, swelling behavior, and enzymatic degradability. Supplied as a white to off-white powder; soluble in water (≈20 mg/mL with sonication). Store powder at -20 °C.
- Biocompatible methacrylated polysaccharide suitable for hydrogel scaffolds.
- Photocrosslinkable for rapid curing with appropriate photoinitiators.
- Degree of methacrylation tunable to adjust mechanics and degradation.
- Soluble in water with sonication for solution preparation.
- Stable as a powder at -20 °C for long-term storage.
Matrix Scientific N,N-DIMETHYLSULFAMIDEN,N-DIM-1
N,n-dimethylsulfamide Mf C2h8n2o2s Mw 124.16 Cas 3984-14-3 Mdl MFCD01861286
Selleck Chemical LLC Sulfamide
Sulfamide (Sulfuric diamide) is used in organic chemistry for synthesis
Selleck Chemical LLC Cystamine dihydrochloride S3695-1g
Cystamine dihydrochloride (Decarboxycystine 2-Aminoethyl disulfide 2 2 -Dithiobisethanamine) acts as an anti-infective agent which is used in the treatment of urinary tract infections and also as a radiation-protective agent that interferes with sulfhydryl enzymes
Medchemexpress LLC Cystamine | 51-85-4 | MFCD01002952 | 96.6% | 152.28 g/mol | C4H12N2S2 | 100MG
Cystamine is a low-molecular-weight disulfide compound used in biochemical and pharmacological research, commonly applied as a transglutaminase inhibitor and in studies of apoptosis and neurodegenerative disease models. The supplied research-grade material is typically provided in a small pack for preclinical use and includes supporting documentation.
Medchemexpress LLC Cystamine | 51-85-4 | 96.6% | 152.28 g/mol | C4H12N2S2 | 50MG
Cystamine is the disulfide form of cysteamine and functions as an orally active transglutaminase (Tgase) inhibitor used in biochemical and neuroprotection research. The compound is supplied for research use and is offered in multiple pack sizes and solution formulations to support in vitro assays and in vivo studies.
- Acts as a transglutaminase inhibitor.
- Available in multiple pack sizes and solution formulations.
- Suitable for biochemical assays and neuroprotection research.
- Molecular weight 152.28 g/mol and formula C4H12N2S2.
- Reported purity approximately 96.6% (verify with supplier documentation).
Medchemexpress LLC Sodium laureth sulfate | 9004-82-4 | 70% | (C2H4O)nC12H26O4S.Na | 100 G
Sodium laureth sulfate (70% in water) is an anionic active agent known for its excellent decontamination, emulsification, dispersion, wetting, and antifungal properties. This product is intended for research use only and is not sold to patients.
- Possesses excellent decontamination properties
- Offers emulsification and dispersion capabilities
- Provides effective wetting and antifungal action
- Enhances inactivation efficiency against S. cerevisiae cells when combined with plasma-activated water
- Disrupts membrane integrity and increases cell membrane permeability in S. cerevisiae cells
- Generates reactive oxygen species (ROS) in S. cerevisiae cells
- Elevates activities of various lysosomal enzymes in animal models
Medchemexpress LLC Lobeglitazone (sulfate) | 763108-62-9 | 99.6% | 578.61 | 5 MG
Lobeglitazone sulfate is a novel thiazolidinedione, functioning as an orally active agonist for PPAR with EC50 values of 137.4 nM for PPARγ and 546.3 nM for PPARα. It acts as an inhibitor for the ERK/JNK/Smad/NF-κB signaling pathway, demonstrating anti-inflammatory, anti-diabetic, anti-fibrotic, and anti-atherosclerotic properties.
- Functions as an orally active agonist for PPAR
- Inhibits ERK/JNK/Smad/NF-κB signaling pathway
- Exhibits anti-inflammatory properties
- Exhibits anti-diabetic properties
- Exhibits anti-fibrotic properties
- Exhibits anti-atherosclerotic properties
- Increases glucose uptake in 3T3-L1 adipocytes and L6 muscle cells
- Inhibits NO generation and pro-inflammatory cytokine expression
Medchemexpress LLC Sodium laureth sulfate | 9004-82-4 | 70% | (C2H4O)nC12H26O4S.Na | 25 G
Sodium laureth sulfate (70% in water) is an anionic active agent that exhibits excellent decontamination, emulsification, dispersion, wetting, and antifungal properties. It is intended for research use only.
- Anionic active agent
- Exhibits decontamination properties
- Exhibits emulsification properties
- Exhibits dispersion properties
- Exhibits wetting properties
- Provides antifungal properties
- Enhances inactivation efficiency against *S. cerevisiae* cells
- Disrupts membrane integrity in *S. cerevisiae* cells
- Increases cell membrane permeability in *S. cerevisiae* cells
- Elevates lysosomal enzyme activities in guinea pigs
![Alkali Scientific 3 Indoxyl β D Glucoside [IBDG] [3 Indoxyl β D Glucopyranoside], 10 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000659598.jpg-250.jpg)
Alkali Scientific 3 Indoxyl β D Glucoside [IBDG] [3 Indoxyl β D Glucopyranoside], 10 G
3-Indoxyl β-D-Glucoside (IBDG) is a highly sensitive chromogenic substrate used for the detection of β-glucosidase activity in biochemical assays. The hydrolysis of IBDG by β-glucosidase results in the production of an indigo-colored compound, providing a visual indicator of enzyme activity. The 10g quantity is ideal for large-scale experiments or long-term studies. IBDG is commonly used in molecular biology, microbiology, and biochemical research to detect and quantify β-glucosidase activity in various organisms and samples. This reagent offers a convenient, easy-to-interpret method for screening enzyme activity, studying gene expression systems, and analyzing enzymatic reactions in a wide range of applications.
Medchemexpress LLC S-Methylisothiourea sulfate | 867-44-7 | 99.9% | C2H6N2S·1/2H2O4S | 50 MG
S-Methylisothiourea sulfate | 867-44-7 | 99.9% | C2H6N2S·1/2H2O4S | 50 MG
Medchemexpress LLC S-Methylisothiourea sulfate | 867-44-7 | MFCD00013055 | 99.9% | C2H6N2S.1/2H2O4S | 100 MG
S-Methylisothiourea sulfate is a potent, selective, and competitive inhibitor of inducible nitric oxide synthase (iNOS). It has shown beneficial effects in rodent models of septic shock.
- Acts as a competitive inhibitor of iNOS activity at the L-arginine site.
- Prevents NO-mediated cytotoxic effects of LPS in cultured macrophages.
- Inhibits LPS-induced nitrite production in macrophages and rat aortic vascular muscle cells.
- Reverses hypotension and vascular hyporeactivity caused by endotoxin LPS in anesthetized rats.
- Attenuates increases in plasma aminotransferases, bilirubin, and creatinine.
- Improves survival rates in mice treated with high doses of LPS.
- Restores blood pressure and inhibits iNOS activity in lung homogenates of LPS-treated rats.