Biochemical Reagents
Medchemexpress LLC Estradiol benzoate-d3 | 1192354-74-7 | 99.0% | 1 MG
Estradiol benzoate-d3 is the deuterium labeled Estradiol benzoate. It is a proagent of estradiol that acts as a steroid sex hormone. This compound exhibits mild anabolic and metabolic properties, and increases blood coagulability. It is for research use only.
- This compound can be used as a tracer.
- This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Medchemexpress LLC Estradiol benzoate | 50-50-0 | 1 G
Estradiol benzoate (β-Estradiol 3-benzoate) is an HBx protein inhibitor that inhibits androgen and hepatitis B virus (HBV) transcription and replication. It also shows antifertility effects, anti-Toxoplasma gondii activity, and can improve memory behavior in Ovariectomy (Ovx) female mice.
- Inhibits HBx protein.
- Suppresses androgen and hepatitis B virus (HBV) transcription and replication.
- Exhibits antifertility effects.
- Shows anti-Toxoplasma gondii activity.
- Improves memory behavior in ovariectomy (Ovx) female mice.
- Reverses lowered uterine weight in Ovx mice.
- Increases number and density of synaptic vesicles.
Medchemexpress LLC Estradiol benzoate | 50-50-0 | 99.9% | 25 MG
Estradiol benzoate is an HBx protein inhibitor that inhibits androgen and hepatitis B virus (HBV) transcription and replication. It demonstrates antifertility effects and anti-Toxoplasma gondii activity.
- Improves memory behavior in ovariectomy (Ovx) female mice
- Appearance: solid, white to off-white
- For research use only
Medchemexpress LLC U-73343 | 142878-12-4 | 99.4% | 466.66 | 10 MG
U-73343, which works as a protonophore, is an inactive analog of U-73122 and can be used as a negative control. It dose-dependently inhibits acid secretion irrespective of the stimulant. U-73122 is a phospholipase C (PLC) and 5-LO (5-lipoxygenase) inhibitor with an IC50 of 1-2.1 μM for PLC.
- Functions as a protonophore
- Can be used as a negative control
- Inhibits acid secretion dose-dependently
Medchemexpress LLC Cagrilintide acetate | 1415456-99-3 | CB712152538 | 99.96% | 4409.01 | 5 MG
Cagrilintide acetate is a non-selective AMYR/CTR agonist and a long-acting acylated amylase analogue. It reduces food intake and causes significant weight loss in a dose-dependent manner, making it suitable for obesity studies.
- Non-selective AMYR/CTR agonist
- Long-acting acylated amylase analogue
- Reduces food intake
- Causes significant weight loss in a dose-dependent manner
- Suitable for obesity studies
- For research use only
Medchemexpress LLC Retinol, acetate, 9-cis- | 29584-22-3 | 85.0% | 328.49 | 1 MG
9-cis-Retinol acetate is a retinal derivative developed for research applications. This compound is presented as a solid, typically white to off-white in appearance, with a molecular weight of 328.49. Its purity is 85.0%, making it suitable for various scientific investigations.
- Retinal derivative.
- Intended for research use only.
- Molecular formula C22H32O2.
- Appearance is solid, white to off-white.
- Recommended storage for powder: -20°C for 3 years, 4°C for 2 years.
- Recommended storage in solvent: -80°C for 6 months, -20°C for 1 month.
Medchemexpress LLC Resolvin D2 | 810668-37-2 | 99.9% | 376.49 | 25 UG
Resolvin D2 is a metabolite derived from docosahexaenoic acid (DHA) that exhibits anti-inflammatory and anti-infective properties. It acts as a potent regulator of leukocytes and is effective in controlling microbial sepsis. This compound also functions as a remarkably potent inhibitor of TRPV1 (IC50 = 0.1 nM) and TRPA1 (IC50 = 2 nM) in primary sensory neurons.
- Anti-inflammatory activities
- Anti-infective activities
- Leukocyte regulation
- Control of microbial sepsis
- TRPV1 and TRPA1 inhibition
- Resolution of inflammation and tissue regeneration
- Decreases leukocyte:endothelial interactions
- Inhibits inflammatory pain
Medchemexpress LLC Hexanoylglycine-d2 | 1256842-52-0 | 175.22 | 100 MG
Hexanoylglycine-d2 | 1256842-52-0 | 175.22 | 100 MG
Medchemexpress LLC Thymidine-d3 | 74848-84-3 | 245.25 | 5 MG
Thymidine-d3 | 74848-84-3 | 245.25 | 5 MG
Medchemexpress LLC Alogliptin-d3 | 1133421-35-8 | 99.6% | C18H18D3N5O2 | 5 MG
Alogliptin-d3 is the deuterium labeled Alogliptin, a potent, selective, and orally active inhibitor of DPP-4 with an IC50 of <10 nM. It exhibits greater than 10,000-fold selectivity over DPP-8 and DPP-9 and can be used for the research of type 2 diabetes. Stable heavy isotopes, like deuterium, are incorporated into drug molecules for quantitation during drug development and can influence pharmacokinetic and metabolic profiles.
- Deuterium labeled Alogliptin.
- Potent, selective, and orally active inhibitor of DPP-4.
- Exhibits greater than 10,000-fold selectivity over DPP-8 and DPP-9.
- Suitable for research of type 2 diabetes.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Cayman Chemical 5 6-trns-VItamIn D3 5mg
An isomer of vitamin D3; increases tibia ash weight and bone mineralization in vitamin D-deficient chicks at 1, 3, and 10 UG/day; induces intestinal calcium transport and bone calcium mobilization in anephric rats fed a low-calcium and vitamin D-deficient diet at 25 UG/animal