Lipids and Lipid Derivatives
Medchemexpress LLC Medroxyprogesterone acetate-d3 | 71-58-9 | 98.1% | 1 MG
Medroxyprogesterone acetate-d3 is a deuterium labeled version of Medroxyprogesterone acetate, a synthetic steroid known for its interaction with progesterone, androgen, and glucocorticoid receptors. This product is intended for research use only.
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
Medchemexpress LLC Paramethasone acetate | 1597-82-6 | MFCD00200359 | 98.0% | 434.50 g·mol⁻¹ | C24H31FO6 | 5 MG
Paramethasone acetate is a synthetic glucocorticoid acetate ester supplied for research use. It shows anti-inflammatory and immunosuppressant activity and is provided as a solid reagent for laboratory and analytical applications. Safety data and handling information are available in the SDS and supporting documentation.
- Exhibits anti-inflammatory and immunosuppressant activity.
- Acetate ester form suitable for standard biochemical assays.
- High purity (98.0%) for reproducible research results.
- Solid, white to light yellow appearance simplifies storage and handling.
- Available in small research quantities (e.g., 5 mg).
- SDS and safety documentation available for laboratory compliance.
Medchemexpress LLC Eptifibatide acetate | 881997-86-0 | 99.67% | 5 MG
Eptifibatide acetate is a cyclic heptapeptide that functions as a competitive antagonist for the activated platelet glycoprotein IIb/IIIa receptor, exhibiting anti-platelet activity. It is intended for research use only.
- Cyclic heptapeptide
- Competitive antagonist for activated platelet glycoprotein IIb/IIIa receptor
- Anti-platelet activity
Medchemexpress LLC Bazedoxifene (acetate) | 198481-33-3 | 99.9% | C32H38N2O5 | 25 MG
Bazedoxifene acetate is an oral, nonsteroidal selective estrogen receptor modulator (SERM) that acts as an inhibitor of IL-6/GP130 protein-protein interactions. It is used in research for osteoporosis and pancreatic cancer.
- Small molecular GP130 inhibitor
- Inhibits STAT3 phosphorylation induced by IL-6 and IL-11
- Induces apoptosis in human pancreatic cancer cells
- Inhibits STAT3 nuclear translocation induced by IL-6
- Blocks cell migration in pancreatic cancer cells by inhibiting GP130
- Inhibits Capan-1 tumor growth in mouse models
Medchemexpress LLC Velmupressin acetate | 1647120-04-4 | 1006.64 g/mol | 1 MG
Velmupressin acetate is a potent, selective, and short-acting peptidic V2 receptor (V2R) agonist. It exhibits EC50 values of 0.07 nM for human V2R (hV2R) and 0.02 nM for rat V2R (rV2R). This product is stable under recommended storage conditions and is not classified as a hazardous substance or mixture according to safety data.
- Potent, selective, and short-acting peptidic V2 receptor (V2R) agonist
- EC50 values of 0.07 nM for human V2R (hV2R)
- EC50 values of 0.02 nM for rat V2R (rV2R)
- Stable under recommended storage conditions
- Not a hazardous substance or mixture
- For research use only
Sigma Aldrich Fine Chemicals Biosciences Ethisterone >=99% (HPLC) | 434-03-7 | MFCD00003656 | 100G
Ethisterone >=99% (HPLC) | Purity: >=99% (HPLC) | Mol Wt: 312.45 | 434-03-7 | MFCD00003656 | 100G
Sigma Aldrich Fine Chemicals Biosciences Desoxycortone acetate European Pharmacopoeia (EP) Reference Standard | 56-47-3 | MFCD00003660 |
Desoxycortone acetate European Pharmacopoeia (EP) Reference Standard | Mol Wt: 372.5 | 56-47-3 | MFCD00003660 |
Selleck Chemical LLC U18666A-5mg
U18666A (U18) is an inhibitor of intra-cellular cholesterol transport that inhibits dengue virus entry and replication.
Sigma Aldrich Fine Chemicals Biosciences U 18666A powder | 3039-71-2 | MFCD00210908 | 25MG
U 18666A powder | Purity: >=98% (HPLC) | Mol Wt: 424.06 | 3039-71-2 | MFCD00210908 | 25MG
Aobchem Mandelonitrile benzoate | 95% | CAS 4242-46-0 | C15H11NO2 | 1g
Mandelonitrile benzoate | 95% | CAS 4242-46-0 | C15H11NO2 | 1g
Medchemexpress LLC Skatole-d3 | 111399-60-1 | 134.19 | 10 MG
Skatole-d3 is a deuterium labeled form of Skatole. Skatole is produced by intestinal bacteria and regulates intestinal epithelial cellular functions by activating aryl hydrocarbon receptors and p38. This compound can be used as a tracer or as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS. It is identified for use as a laboratory chemical and in the manufacture of substances.
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Laboratory chemical
- Used in the manufacture of substances
AdipoGen Rubiginone D2
Chemical. CAS 274913-71-2. Formula C20H16O6. MW 352.3. Isolated from Streptomyces sp. strain Gö N1/5. Antibiotic. Antibacterial. Antitumor compound.
Apexbio Technology LLC PYRAZINAMIDE-D3-1MG
Pyrazinamide-d3 (CAS No 1432059-16-9) is a deuterium-labeled derivative used in biomedical research as a stable isotope for various studies Originating from antimicrobial research it is primarily utilized to investigate Mycobacterium tuberculosis the causative agent of tuberculosis Pyrazinamide-d3 acts by disrupting the bacterial membrane potential and interfering with fatty acid synthase I which is critical for the bacterium s survival and replication In vitro studies frequently demonstrate its activity in the nanomolar to low micromolar range making it effective for precise quantitative analysis This compound is commonly applied in cell models animal studies and drug screening assays to measure drug metabolism and pharmacokinetics Experimental concentrations typically depend on the specific research design allowing for flexibility across various experimental frameworks ultimately aiding in the development of novel therapeutics against bacterial infections