Pyrans
Medchemexpress LLC 5-carboxy-2'-deoxyuridine | 14599-46-3 | 272.21 g/mol | C10H12N2O7 | 25 MG
5-Carboxy-2'-deoxyuridine is a deoxyuridine derivative and a metabolite of trifluridine supplied as a solid for research and analytical use. It is a methyl-oxidation product of thymidine and is intended for laboratory and analytical applications only.
- Molecular formula: C10H12N2O7.
- Molecular weight: 272.21 g/mol.
- CAS number: 14599-46-3.
- Physical form: powder for research use.
- Storage: powder -20°C (long term) or 4°C (short term); in solvent -80°C recommended.
- Applications: analytical standard and metabolite studies.
eMolecules D-Glucuronamide | 3789-97-7 | | 1g
Oakwood Chemical | D-Glucuronamide | 1g | 537710227 | 103609 | | 3789-97-7 | | 193.155 | C6H11NO6
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Medchemexpress LLC 5-Carboxy-2′-deoxycytidine | 1210427-59-0 | 98.1% | 271.23 | 25 MG
5-Carboxy-2′-deoxycytidine is a metabolite of Trifluridine. It is for research use only.
- Metabolite of trifluridine
- For research use only
Medchemexpress LLC MF-094 | 2241025-68-1 | 99.8% | 535.70 | 50 MG
MF-094 is a potent and selective USP30 inhibitor, effective at an IC50 of 120 nM. This compound has been shown to increase protein ubiquitination and accelerate mitophagy, making it suitable for biochemical research applications. It exhibits high selectivity, with less than 30% inhibitory activity against a panel of 22 other USPs at 10 μM.
- Potent and selective USP30 inhibitor
- Increases protein ubiquitination
- Accelerates mitophagy
- Minimal inhibitory activity against other USPs
- Stable as powder at -20°C for 3 years
- Stable in solvent at -80°C for 2 years
Medchemexpress LLC Carboxy-PTIO potassium | 148819-94-7 | 99.0% | 315.39 | 50 MG
Carboxy-PTIO potassium is a potent nitric oxide (NO) scavenger that rapidly reacts with NO to produce NO2. It can prevent hypotension and endotoxic shock through its direct NO-scavenging action in a lipopolysaccharide-stimulated rat model. This compound is intended for research use only and is not sold to patients.
- Potent nitric oxide (NO) scavenger
- Reacts quickly with NO to produce NO2
- Can prevent hypotension and endotoxic shock by scavenging NO in LPS-stimulated rat models
- Significantly suppresses stimulation of NO expression induced by Physalin A treatment in vitro
- Reduces Physalin A-induced cleavage of procaspase-3 and PARP, and down-regulates ICAD expression, diminishing DNA fragmentation in nuclei
- Reverses decreased mTOR and p-mTOR levels induced by Physalin A, with concomitant suppression of LC3 I to LC3 II conversions in A375-S2 cells
Medchemexpress LLC (2R)-octyl-α-hydroxyglutarate | 1391194-67-4 | MFCD30735809 | 99.9% | 260.33 g·mol⁻¹ | C13H24O5 | 100 MG
(2R)-Octyl-α-hydroxyglutarate is a cell-permeable, esterified derivative of D-2-hydroxyglutarate used as a research reagent to investigate the biological effects of 2-HG in cellular systems, including effects on histone methylation, DNA damage, and mitochondrial oxidative processes.
- Cell-permeable analogue of D-2-hydroxyglutarate.
- Used to study histone methylation and epigenetic regulation.
- Reported purity approximately 99.9%.
- Molecular weight 260.33 g·mol⁻¹; chemical formula C13H24O5.
- Provided as an analytical/research standard in small pack sizes suitable for cell-based assays.
TARGETMOL CHEMICALS INC MF-438 2MG
Also available in 1 mL, 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. MF-438 is an effective and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor (EC50 2.3 nM for rSCD1). Purity 99.66%
Medchemexpress LLC Progesterone carboxylic acid (Etienic acid) | 302-97-6 | 316.43 | 100 MG
Progesterone carboxylic acid (also known as Etienic acid or Testosterone-17β-carboxylic acid) is an analogue of androstenedione. This compound has the ability to conjugate with 20-mer peptide nucleic acid (PNA), resulting in a conjugate that exhibits superior binding capacity to complementary DNA. It is actively researched for its potential applications in treating cancers and type 2 diabetes (T2D).
- Androstenedione analogue.
- Conjugates with PNA for enhanced DNA binding.
- Used for cancers and type 2 diabetes research.