Thiophenes
eMolecules 6-bromo-1-benzothiophen-2-amine | 739362-50-6 | MFCD17016086 | 1g
Pharmablock | 6-bromo-1-benzothiophen-2-amine | 1g | 551201457 | PB03430 | | 739362-50-6 | MFCD17016086 | 228.110 | C8H6BrNS
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eMolecules 2-Amino-pyridine-3-sulfonyl fluoride | 2091139-50-1 | MFCD30662950 | 1g
J & W PharmLab LLC | 2-Amino-pyridine-3-sulfonyl fluoride | 1g | 499972517 | 69R1393 | 96.000 | 2091139-50-1 | MFCD30662950 | 176.170 | C5H5FN2O2S
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Medchemexpress LLC Zastaprazan | 2133852-18-1 | 100.0% | 362.47 | 50 MG
Zastaprazan (JP-1366) is a proton pump inhibitor and a potent potassium-competitive acid blocker. It is suitable for use in the research of gastrointestinal inflammatory diseases or gastric acid-related conditions such as gastroesophageal reflux disease. This product is for research use only.
- Proton pump inhibitor
- Potent potassium-competitive acid blocker
- Used in gastrointestinal inflammatory disease research
- Used in gastric acid-related disease research
- For research use only
Medchemexpress LLC 3-Bromothiophene | 872-31-1 | 99.8% | C4H3BrS | 50 G
3-Bromothiophene is a 3-halogenated thiophene with a bromine atom at the 3-position. Its polymers are conductive and show potential for optoelectronic applications. It also serves as a crucial intermediate in the creation of various pharmaceuticals, agrochemicals, and cosmetic products. This compound can be used in the synthesis of chalcones and their derivatives.
- Polymers show potential for optoelectronic applications
- Key intermediate for pharmaceuticals, agrochemicals, and cosmetics
- Can be used in the synthesis of chalcones and their derivatives
- Some derivatives show anti-inflammatory, analgesic, and antibacterial activities
Medchemexpress LLC Acetyl-CoA Carboxylase-IN-1 | 179343-23-8 | C13H9Br2N5 | 50 MG
Acetyl-CoA Carboxylase-IN-1 is a potent inhibitor of acetyl-CoA carboxylase (ACC), demonstrating an IC50 value of less than 5 nM. This compound also exhibits significant antibacterial activity, with in vitro studies on *E. coli* showing minimum inhibitory concentration (MIC) values ranging from 0.1 μM to over 25 μM depending on the bacterial strain.
- Potent acetyl-CoA carboxylase (ACC) inhibitor
- Exhibits antibacterial activity against *E. coli*
- High purity of 99.18%
- Available as an off-white to light yellow solid
- Long-term stability as a powder at -20°C for up to 3 years
- Stable in solvent at -80°C for 6 months
Sigma Aldrich 1-Boc-hexahydro-1,4-diazepine
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
TARGETMOL CHEMICALS INC Lanepitant 2HCl 1MG
Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Lanepitant 2HCl is a non-peptide neurokinin-1 receptor antagonist with analgesic and anti-inflammatory activity.Lanepitant 2HCl inhibits the binding of Substance P to the neurokinin-1 receptor, inhibits neurogenic inflammation and pain transmission, and can be used in the study of painful neuropathic disorders, such as migraines. Purity 98.89%
Medchemexpress LLC Chroman 1 dihydrochloride | C24H30Cl2N4O4 | 5 MG
Chroman 1 dihydrochloride is a highly potent and selective ROCK inhibitor, showing more potency against ROCK2 (IC50=1 pM) than ROCK1 (IC50=52 pM). It also exhibits inhibitory activity against MRCK, with an IC50 of 150 nM. In vitro studies indicate that Chroman 1 (50 nM, 24 h) inhibits caspase-3/7 activation and reduces apoptosis in human pluripotent stem cells.
- Highly potent and selective ROCK inhibitor
- More potent against ROCK2 (IC50=1 pM) than ROCK1 (IC50=52 pM)
- Inhibits MRCK (IC50=150 nM)
- Inhibits caspase-3/7 activation
- Reduces apoptosis in human pluripotent stem cells
Medchemexpress LLC Chroman 1 dihydrochloride | 1273579-40-0 | C24H30Cl2N4O4 | 1 ML
Chroman 1 dihydrochloride is a highly potent and selective ROCK inhibitor, demonstrating greater potency against ROCK2 (IC50=1 pM) compared to ROCK1 (IC50=52 pM). It also exhibits inhibitory activity against MRCK, with an IC50 of 150 nM. Research indicates that Chroman 1, at 50 nM over 24 hours, inhibits caspase-3/7 activation and reduces apoptosis in human pluripotent stem cells.
- Highly potent and selective ROCK inhibitor
- More potent against ROCK2 (IC50=1 pM) than ROCK1 (IC50=52 pM)
- Exhibits inhibitory activity against MRCK (IC50=150 nM)
- Inhibits caspase-3/7 activation
- Reduces apoptosis in human pluripotent stem cells
- Formulated as a 10 mM solution in DMSO
Medchemexpress LLC 5-Methyl-2-thiophenecarboxaldehyde | 13679-70-4 | 99.9% | 126.18 | 25 G
5-Methyl-2-thiophenecarboxaldehyde is a chemical compound acting as a candidate for microscopic third-order non-linear optical (NLO) material. This compound is typically found as a yellow to brown liquid and is designated for research purposes only.
- Candidate for microscopic third-order non-linear optical (NLO) material
- High purity: 99.87%
- Molecular weight: 126.18
- Chemical formula: C6H6OS
- Appearance: liquid
- Color: yellow to brown
- Originates from plants, Gramineae, Hordeum vulgare L.
- Stable in pure form for up to 3 years at -20°C or 2 years at 4°C
- Stable in solvent for up to 6 months at -80°C or 1 month at -20°C
- Soluble in DMSO at 50 mg/mL
- Intended for research use only