Other Solvents
Medchemexpress LLC 20:0-20:1-20:0 TG-d5 | 958764-14-2 | 99.9% | 978.65 | 1 MG
20:0-20:1-20:0 TG-d5 is deuterium labeled 20:0-20:1-20:0 TG. 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.
Sigma Aldrich Fine Chemicals Biosciences Deuterium oxide | 7789-20-0 | MFCD00044636 | 100mL
Deuterium oxide | 99.9 atom % D, contains 0.05 wt. % 3-(trimethylsilyl)propionic-2,2,3,3-d4 acid, sodium salt | MW:20.03 | 7789-20-0 | MFCD00044636 | 100mL
Cambridge Isotope Laboratories Deuterium Oxide (D, 99.9%), 10 G, 7789-20-0
This item has a minimum order quantity of 4 per supplier requirements
Deuterium Oxide (D, 99.9%), 4 G, 7789-20-0
Medchemexpress LLC Darolutamide-d4 | 2484757-20-0 | 98.6% | 402.87 | 1 MG
Darolutamide-d4 | 2484757-20-0 | 98.6% | 402.87 | 1 MG
Cambridge Isotope Laboratories DEUTERIUM OXIDE (D, 99.9%), 50 G, 7789-20-0
This item has a minimum order quantity of 2 per supplier requirements
DEUTERIUM OXIDE (D, 99.9%), 50 G, 7789-20-0
Medchemexpress LLC (Rac)-Rotigotine-d3 hydrochloride | 1215846-20-0 | C19H23D3ClNOS | 1 MG
(Rac)-Rotigotine-d3 hydrochloride is a deuterium labeled (Rac)-Rotigotine (hydrochloride), which is a racemate of Rotigotine. Rotigotine acts as a full agonist of the dopamine receptor, a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor, with Ki values for the dopamine D3 receptor and D2, D5, D4 receptors, and dopamine D1 receptor ranging from 0.71 nM to 83 nM.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Functions as a full agonist of dopamine receptors.
- Acts as a partial agonist of the 5-HT1A receptor.
- Antagonizes the α2B-adrenergic receptor.
Medchemexpress LLC Darolutamide-d4 | 2484757-20-0 | 98.6% | 402.87 | 500 UG
Darolutamide-d4 is a deuterium-labeled version of Darolutamide. It is an orally active, competitive androgen receptor (AR) antagonist that inhibits testosterone-induced AR nuclear translocation and transcriptional activation. This compound selectively affects AR-positive cells by inhibiting AR-dependent signaling pathways, and its active metabolite maintains full antagonistic activity against AR mutants. It can be used for research on prostate cancer, including androgen receptor-dependent prostate cancer.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Sigma Aldrich Fine Chemicals Biosciences Deuterium oxide 99.9 atom D, 7789-20-0, MFCD00044636
Deuterium oxide 99.9 atom D
Cambridge Isotope Laboratories LYSO-PC 20:0 (EICOSANOYL-12,12,13,13-D4, 98, 1 MG
LYSO-PC 20:0 (EICOSANOYL-12,12,13,13-D4, 98, 1 MG
Cambridge Isotope Laboratories LYSO-PC 20:0 (EICOSANOYL-12,12,13,13-D4, 98, 5 MG
LYSO-PC 20:0 (EICOSANOYL-12,12,13,13-D4, 98, 5 MG
Cambridge Isotope Laboratories Deuterium Oxide (D, 99.9%) | 7789-20-0 | 10 x 0.7ml
This item has a minimum order quantity of 4 per supplier requirements
Deuterium Oxide (D, 99.9%) | 7789-20-0 | 4 x 0.7ml
Cambridge Isotope Laboratories Deuterium Oxide (D, 99.9%), 10 X 1 Ml, 7789-20-0
This item has a minimum order quantity of 3 per supplier requirements
Deuterium Oxide (D, 99.9%), 10 X 1 Ml, 7789-20-0
Medchemexpress LLC Donepezil-d7 hydrochloride | 1261394-20-0 | 420782 | 99.0% | C24H23D7ClNO3 | 2.5 MG
Donepezil-d7 (hydrochloride) is the deuterium labeled Donepezil. Donepezil (E2020 free base) is a specific and potent AChE inhibitor with IC50s of 8.12 nM and 11.6 nM for bovine AChE and human AChE, respectively. It is 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 Darolutamide-d4 | 2484757-20-0 | 98.6% | 402.87 g/mol | C19H15D4ClN6O2 | 10 MG
Darolutamide-d4 is a deuterium-labeled analogue of the androgen receptor antagonist darolutamide supplied as a solid for research use. It is used as a tracer or internal standard in quantitative analytical methods such as NMR, GC-MS, and LC-MS and reflects the parent compound's AR antagonist profile.
- Deuterium-labeled internal standard for analytical assays.
- Intended for research use only; not for human or clinical use.
- High purity (≈98.6%).
- Soluble in DMSO at 100 mg/mL; sonication recommended.
- Powder storage: -20°C (multi-year stability); in solution: -80°C for long-term storage.
- White to off-white solid; molecular weight ~402.87 g/mol.
Medchemexpress LLC Darolutamide-d4 (ODM-201-d4) | 2484757-20-0 | 98.6% | 402.87 | 5 MG
Darolutamide-d4 (ODM-201-d4) is a deuterium-labeled version of Darolutamide (HY-16985). Darolutamide (ODM-201) is an orally active, competitive androgen receptor (AR) antagonist, with a Ki of 11 nM for rat wild-type AR (wtAR) and an IC50 of 26 nM for human wild-type AR (hAR)-mediated transcriptional activation. It inhibits testosterone-induced AR nuclear translocation and transcriptional activation and is used in research for prostate cancer.
- Can be used as a tracer
- Can serve as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Selectively affects AR-positive cells
- Maintains full antagonistic activity against AR mutants