Phenols
Sigma Aldrich Fine Chemicals Biosciences 4-Chloro-3-methylphenol 99% | 59-50-7 | MFCD00002323 | 5G
4-Chloro-3-methylphenol 99% | Purity: 99% | Mol Wt: 142.58 | 59-50-7 | MFCD00002323 | 5G
Sigma Aldrich Fine Chemicals Biosciences Acetaminophen BioXtra, >=99.0% | 103-90-2 | MFCD00002328 | 1KG
Acetaminophen BioXtra, >=99.0% | Purity: >=99.0% | Mol Wt: 151.16 | 103-90-2 | MFCD00002328 | 1KG
AURUM PHARMATECH INC 4 BROMO 2 METHYLPYRIDIN3 250MG
4-bromo-2-methylpyridin-3-ol, 250mg, 1227570-80-0
Medchemexpress LLC 2,4,6-Trihydroxybenzaldehyde | 487-70-7 | MFCD00003329 | 154.12 | 10 G
2,4,6-Trihydroxybenzaldehyde is an orally active inhibitor demonstrating diverse biological activities. It has shown anti-tumor, anti-cancer cell proliferative, and anti-obesity properties. In vitro, it inhibits adipocyte differentiation and lipid accumulation by down-regulating specific protein expression levels. In vivo, oral administration has been observed to reduce high-fat diet-induced weight gain and lower serum glucose, triglycerides, and total cholesterol levels.
- Functions as an orally active inhibitor.
- Demonstrates anti-tumor and anti-cancer cell proliferative activities.
- Exhibits anti-obesity activity.
- Inhibits adipocyte differentiation and lipid accumulation in cells.
- Reduces high-fat diet-induced weight gain and serum glucose, triglycerides, and total cholesterol levels in vivo.
- Product boasts a high purity of 99.93%.
Apexbio Technology LLC Amorolfine HCl 78613-38-4 10mM (in 1mL DMSO)
Amorolfine hydrochloride (78613-38-4) is a small-molecule inhibitor targeting 14-reductase and 7 8-isomerase enzymes essential for fungal ergosterol synthesis It is designed to disrupt fungal sterol biosynthesis thereby impairing membrane stability and fungal cell viability Amorolfine hydrochloride exerts its biological activity primarily through inhibition of 14-reductase and 7 8-isomerase In in vitro studies Amorolfine hydrochloride demonstrates antifungal activity with IC50 values ranging from approximately 0 02 to 0 5 g/mL depending on fungal species and experimental conditions Based on these pharmacological properties Amorolfine hydrochloride holds research potential in investigating antifungal activity against fungal pathogens including models of human nail infection
Cayman Chemical EA4 Fatty Acids and Derivative
An inhibitor of PLA2 from red blood cells (Ki = 130 µM); inhibits the ionophore-induced arachidonic acid release from human and bovine RBCs; induces mRNA expression and increases protein levels of CYP1A1 in murine hepatoma Hepa-1c1c7 cells; modulates CYP1A1 and CYP1B1 expression in MCF-7, Hep-G2, and HL-60 cells
Medchemexpress LLC Guanoxabenz hydrochloride | 23256-40-8 | 283.54 | 1 ML
Guanoxabenz hydrochloride is an α2 adrenergic receptor agonist supplied as a 10 mM solution in 1 mL of DMSO, primarily used for research purposes.
- Functions as an α2 adrenergic receptor agonist.
- Suitable for in vitro and in vivo research.
- Provided as a 10 mM solution in DMSO.
- Purity greater than 99.7%.
- High-affinity binding inhibited by N-hydroxyguanidine analogs and metabolic inhibitors.
- Known as a centrally active antihypertensive drug.
- Causes dose-related reduction in locomotor activity.
Medchemexpress LLC P-CAB agent 2 (hydrochloride) | 2209911-80-6 | C22H26ClFN2O4S | 50 MG
P-CAB agent 2 hydrochloride is a potent and orally active potassium-competitive acid blocker and a gastric acid secretion inhibitor. It inhibits H+/K+-ATPase activity with an IC50 value of <100 nM and the hERG potassium channel with an IC50 value of 18.69 μM. This compound shows no acute toxicity and inhibits histamine-induced gastric acid secretion.
- Potent and orally active potassium-competitive acid blocker
- Gastric acid secretion inhibitor
- Inhibits H+/K+-ATPase activity with an IC50 value of <100 nM
- Inhibits hERG potassium channel with an IC50 value of 18.69 μM
- Shows no acute toxicity
- Inhibits histamine-induced gastric acid secretion
Medchemexpress LLC Benzoic acid, 3-amino-4-hydroxy-, methyl ester | 536-25-4 | 167.16 | 25 G
Orthocaine is a local agent that can suppress or relieve pain. It features:
- Molecular formula: C8H9NO3
- Appearance: Solid
- Color: Light brown to brown
- Storage: 4°C, protect from light. In solvent: -80°C for 6 months; -20°C for 1 month (protect from light)
- Solubility in DMSO: 100 mg/mL (598.23 mM), requires ultrasonic
- Local anesthetic
Medchemexpress LLC NS-3-008 hydrochloride | 1172854-54-4 | 99.7% | 1 ML
NS-3-008 hydrochloride is a small-molecule transcriptional inhibitor of G0/G1 switch 2 (G0s2) with a reported IC50 of 2.25 μM. It is supplied as a concentrate solution for research use and as solids for analytical or in vivo studies. Typical applications include biochemical assays and disease-model investigations such as chronic kidney disease research.
- Transcriptional inhibitor of G0s2 with IC50 ≈ 2.25 μM.
- Available as 10 mM solution in DMSO (1 mL) and as solid packs for flexibility in workflows.
- High purity (99.7%) suitable for biochemical, cellular, and in vivo studies.
- Off-white to light yellow solid with molecular formula C14H24ClN3 and MW 269.81 g·mol⁻¹.
- Supplied with characterization data to support reproducibility in research.
eMolecules AstaTech / (R)-1-(35-DICHLOROPHENYL)ETHYLAMINE / 0.25g / 200619803 / SC1347 / 95.000 / 617710-53-9 / MFCD07772552 / 190.070 / C8H9Cl2N
AstaTech / (R)-1-(35-DICHLOROPHENYL)ETHYLAMINE / 0.25g / 200619803 / SC1347 / 95.000 / 617710-53-9 / MFCD07772552 / 190.070 / C8H9Cl2N
eMolecules 4-BROMO-2-ETHOXYPHENOL | 211495-66-8 | MFCD09907051 | 1g
AstaTech | 4-BROMO-2-ETHOXYPHENOL | 1g | 493153552 | W18481 | 95.000 | 211495-66-8 | MFCD09907051 | 217.062 | C8H9BrO2
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Cambridge Isotope Laboratories Warfarin (phenyl-D5 98%) 100 ug/mL in MTBE 1 2 mL
Warfarin (phenyl-D5 98%) 100 ug/mL in MTBE 1 2 mL