Furans
Sigma Aldrich Fine Chemicals Biosciences Methyl 2-furoate >=98%, FG | 611-13-2 | MFCD00003236 | 5KG
Methyl 2-furoate >=98%, FG | Purity: >=98% | Mol Wt: 126.11 | 611-13-2 | MFCD00003236 | 5KG
Sigma Aldrich Fine Chemicals Biosciences C646 >=98% (HPLC) | 328968-36-1 | MFCD01784780 | 25MG
C646 >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 445.42 | 328968-36-1 | MFCD01784780 | 25MG
Sigma Aldrich Fine Chemicals Biosciences Methyl 2-furoate >=98%, FG | 611-13-2 | MFCD00003236 | 1KG
Methyl 2-furoate >=98%, FG | Purity: >=98% | Mol Wt: 126.11 | 611-13-2 | MFCD00003236 | 1KG
Medchemexpress LLC Sonlicromanol | 1541170-75-5 | 99.8% | 50 MG
Sonlicromanol (KH176) is an orally active reactive oxygen species (ROS) modulator used in preclinical and clinical research to study mitochondrial disease. It is supplied for research use only and is typically provided as a small research pack for laboratory studies.
- Orally active small-molecule ROS modulator
- Modulates reductive and oxidative cellular distress with anti-inflammatory effects
- Used to investigate mitochondrial disease mechanisms and redox biology
- Shown to protect mitochondrial-diseased cells from redox stress in published studies
- Provided as a research reagent, not for therapeutic use
- Molecular formula C19H28N2O3, molecular weight 332.4 g/mol
Medchemexpress LLC 7-tfa-ap-7-deaza-da | 178420-75-2 | 98.8% | C16H16F3N5O4 | 10MG
7-TFA-ap-7-Deaza-dA is a modified deoxynucleoside bearing a trifluoroacetyl-protected alkyne; designed for incorporation into DNA/oligonucleotides and for conjugation via copper-catalyzed azide-alkyne cycloaddition. Supplied as a solid or as a DMSO solution for use in synthetic and analytical workflows requiring a terminal alkyne handle.
- Contains an alkyne functional group for CuAAC click chemistry.
- Suitable for incorporation into deoxyribonucleic acid and oligonucleotide synthesis.
- Available as a solid and as a 10 mM solution in DMSO.
- High purity (~98.8%) suitable for research applications.
- Store solids at 4°C sealed; store solutions at low temperatures to preserve stability.
Medchemexpress LLC CK2 inhibitor 2 | 2641079-92-5 | 98.5% | C21H17ClN4O2 | 10MG
CK2 inhibitor 2 is a potent, selective, orally active small-molecule inhibitor of casein kinase 2 (CK2) with sub-nanomolar enzymatic potency and documented cellular activity. Supplied as a solid for research use, it includes solubility data for DMSO and recommended storage conditions for powder and solutions.
- Potent CK2 inhibition (IC50 0.66 nM) for biochemical assays.
- Selectable kinase profile with measurable activity against Clk2.
- Cellular activity in multiple cancer cell lines at low micromolar concentrations.
- High purity suitable for biochemical and cell-based studies (98.5%).
- Documented solubility in DMSO and example in vivo formulation options.
- Defined storage recommendations for powder and solvent preparations.
Medchemexpress LLC Cobomarsen (MRG-106) | 1848257-52-2 | 4736.00 g/mol | C148H177N52O77P13S13 | 5 MG
Cobomarsen (MRG-106) is a locked nucleic acid-modified oligonucleotide inhibitor of microRNA-155 (miR-155) used in preclinical research to reduce cellular proliferation and survival by modulating multiple signaling pathways. The material is supplied as a solid research-grade compound and should be handled per the manufacturer's storage and handling guidance.
- Inhibits miR-155 to modulate JAK/STAT, MAPK/ERK, and PI3K/AKT signaling.
- Designed as an LNA/modified oligonucleotide for increased affinity and stability.
- Provided as a white to off-white solid suitable for laboratory use.
- CAS 1848257-52-2; molecular weight approximately 4736.00 g/mol.
- Intended for preclinical and mechanistic studies in hematologic and lymphoid disease models.
![Medchemexpress LLC 1-[4-(6-bromo-1,3-benzodioxol-5-yl)-3a,4,5,9b-tetrahydrocyclopenta[c]quinolin-8-yl]ethanone | 881639-98-1 | 99.8% | 412.28 g·mol⁻¹ | C21H18BrNO3 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000239967.png-250.jpg)
Medchemexpress LLC 1-[4-(6-bromo-1,3-benzodioxol-5-yl)-3a,4,5,9b-tetrahydrocyclopenta[c]quinolin-8-yl]ethanone | 881639-98-1 | 99.8% | 412.28 g·mol⁻¹ | C21H18BrNO3 | 50 MG
G-1 is a nonsteroidal, high-affinity, selective agonist of GPR30 (G protein-coupled estrogen receptor) with a reported Ki of 11 nM. It is supplied as a research reagent with formula C21H18BrNO3, molecular weight 412.28 g·mol⁻¹, and high reported purity suitable for in vitro signaling studies.
- Selective GPR30 agonist (Ki = 11 nM).
- High purity (99.76%).
- Molecular formula C21H18BrNO3 and molecular weight 412.28 g·mol⁻¹.
- Soluble in DMSO for assay preparation.
- Intended for research use only; not for human use.
Medchemexpress LLC N-(3-(4-amino-7-(2-deoxy-pentofuranosyl)-prop-2-yn-1-yl)-2,2,2-trifluoroacetamide | 178420-75-2 | MFCD29904589 | 98.8% | 399.32 g·mol⁻¹ | C16H16F3N5O4 | 5 MG
7-TFA-ap-7-Deaza-dA is a modified deoxynucleoside that contains an alkyne functional group for bioorthogonal labeling. It is intended for incorporation into DNA or RNA and for conjugation via copper-catalyzed azide-alkyne cycloaddition (CuAAC), supplied as a well-characterized solid or as a DMSO solution for synthesis and labeling workflows.
- High purity of 98.8% for reliable synthetic use.
- Alkyne handle enables CuAAC click chemistry conjugation.
- Compatible with DNA and RNA synthesis protocols.
- Available as solid or as 10 mM solution in DMSO for convenience.
- Characterized molecular weight and formula for analytical confirmation.
Medchemexpress LLC 1-aminohydantoin hydrochloride | 2827-56-7 | MFCD02181047 | ≥98.0% | 151.55 | C3H6ClN3O2 | 500mg
1-Aminohydantoin hydrochloride (Standard) is the analytical standard of 1-Aminohydantoin hydrochloride (HY-Y0469) This product is intended for research and analytical applications 1-Aminohydantoin hydrochloride is a major metabolite of Nitrofurantoin (HY-A0090) in animal tissues and can be used as a standard for the determination of residues of veterinary agents in meat milk et al 1-Aminohydantoin hydrochloride covalently binds to tissue proteins and is released from the tissues under slightly acidic conditions and derivatized with 2-nitrobenzaldehyde to form nitrophenyl derivatives of 1-Aminohydantoin hydrochloride before detection[1][2]