Furans
Medchemexpress LLC 3-Furaldehyde | 498-60-2 | 99.9% | C5H4O2 | 1 G
3-Furaldehyde is a furan aldehyde used in the synthesis of the neoclerodane diterpene Salvinorin A. It is also recognized as an atmospheric pollutant, predominantly resulting from biomass burning, and is known to undergo photoisomerization and photolysis reactions under ultraviolet light.
- Used in the synthesis of Salvinorin A
- Recognized as an atmospheric pollutant
- Undergoes photoisomerization and photolysis under UV light
- Appears as a colorless to light yellow liquid
- Purity is 99.9%
- Soluble in DMSO at 100 mg/mL
Medchemexpress LLC WST-1 | 150849-52-8 | 97.3% | 651.34 | 50 MG
WST-1 is a water-soluble tetrazolium salt that induces intracellular mitochondrial dehydrogenase to conduct an NADH-dependent enzyme digestion reaction, releasing a water-soluble methyl benzene product. It can be used for the detection of cell proliferation and cytotoxicity by determining the light absorption value at 450 nm. This product is for research use only.
- Water-soluble tetrazolium salt
- Induces intracellular mitochondrial dehydrogenase activity
- Releases a water-soluble methyl benzene product
- Suitable for detection of cell proliferation
- Suitable for cytotoxicity analysis
- Determines light absorption value at 450 nm
- Used in cell staining analysis
- Relevant for cell function analysis
- Considered a cell viability dye
Medchemexpress LLC Nitrofurazone (Nitrofural) | 59-87-0 | MFCD00003225 | 99.96% | 1 G
Nitrofurazone (Nitrofural) is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. It is a nitrofuran antibiotic primarily used topically for various bacterial skin infections, burns, ulcers, and wounds. It retains its antibacterial activity in blood, serum, and pus, and does not interfere with healing.
- Broad spectrum antibiotic
- Active against Gram-positive and Gram-negative bacteria
- Used for bacterial skin infections, burns, ulcers, and wounds
- Maintains antibacterial activity in biological fluids
- Does not inhibit phagocytosis
- Does not interfere with healing
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]
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.
Sigma Aldrich Fine Chemicals Biosciences Nitrofurantoin 98.0-102.0% (EP, UV) | 67-20-9 | MFCD00003224 | 25G
Nitrofurantoin 98.0-102.0% (EP, UV) | Purity: 98.0-102.0% (EP, UV) | Mol Wt: 238.16 | 67-20-9 | MFCD00003224 | 25G
Medchemexpress LLC PAR-2-IN-1 | 1690176-75-0 | 98.9% | 267.71 | 50 MG
PAR-2-IN-1 is a protease-activated receptor-2 (PAR2) signaling pathway inhibitor. It demonstrates anti-inflammatory and anticancer effects.
- Protease-activated receptor-2 (PAR2) signaling pathway inhibitor
- Exhibits anti-inflammatory effects
- Demonstrates anticancer effects
- Related to cancer targeted therapy and cancer metabolism
- Acts on GPCR/G protein and protease activated receptor (PAR) pathways
![Medchemexpress LLC Methyl 8-(tert-butyl)-6-chloroimidazo[1,2-b]pyridazine-2-carboxylate | 1690176-75-0 | MFCD28144723 | 99.8% | C12H14ClN3O2 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000260296.png-250.jpg)
Medchemexpress LLC Methyl 8-(tert-butyl)-6-chloroimidazo[1,2-b]pyridazine-2-carboxylate | 1690176-75-0 | MFCD28144723 | 99.8% | C12H14ClN3O2 | 10MG
PAR-2-IN-1 is a small-molecule inhibitor of protease-activated receptor 2 (PAR2) signaling with reported anti-inflammatory and anticancer effects. The compound is supplied as a solid research reagent with defined solubility in DMSO and formulation examples for in vivo studies.
- Selective PAR2 pathway inhibitor.
- Demonstrated anti-inflammatory and anticancer activity in preclinical studies.
- High purity (99.8%).
- Soluble in DMSO (~83.33 mg/mL) and formulatable for in vivo use.
- Supplied as a stable powder with recommended storage at -20°C.
- Available in multiple research quantities.
Medchemexpress LLC Opiranserin hydrochloride | 1440796-75-7 | MFCD34676620 | 99.6% | 430.97 g/mol | C21H35ClN2O5 | 5 MG
Opiranserin hydrochloride is a research-stage, non-opioid analgesic candidate that acts as a dual antagonist of glycine transporter 2 (GlyT2) and the serotonin 2A receptor (5-HT2A). Supplied as the hydrochloride salt, it is used in preclinical pharmacology and mechanism-of-action studies.
- Dual antagonist activity at GlyT2 and 5-HT2A demonstrated in vitro.
- Non-opioid, non-NSAID analgesic candidate suitable for postoperative pain research.
- Available in solid and DMSO solution formats for flexible dosing and formulation.
- High reported purity (99.6%) appropriate for preclinical experiments.
- Supplied in small pack sizes compatible with early-stage studies.
Medchemexpress LLC Mk2-in-1 hydrochloride | 1314118-94-9 | 98.4% | 509.43 g/mol | C27H26Cl2N4O2 | 5 MG
MK2-IN-1 hydrochloride is the hydrochloride salt of a small-molecule MAPKAPK2 (MK2) inhibitor intended for biochemical and cell-based research. It provides potent biochemical activity with high solubility and is supplied as a solid for laboratory use.
- Potent and selective MAPKAPK2 (MK2) inhibitor (IC50 = 0.11 μM; EC50 = 0.35 μM).
- High purity (98.36%).
- Molecular formula C27H26Cl2N4O2; molecular weight 509.43 g/mol.
- Solid, light yellow to pink appearance suitable for handling and storage.
- High solubility in water and DMSO (water ≥ 100 mg/mL; DMSO 100 mg/mL).
- Includes recommended in vivo formulation options for dosing studies.
Apexbio Technology LLC DANTROLENE-5MG
Dantrolene (CAS No 7261-97-4) is a hydantoin derivative primarily used in the research category of muscle relaxants originating from its unique ability to interfere with excitation-contraction coupling in skeletal muscle Its mechanism of action involves blocking the ryanodine receptor (RyR1) calcium channels in the sarcoplasmic reticulum reducing calcium release and subsequent muscle contraction In vitro it exhibits activity in the nanomolar to low micromolar range Dantrolene is frequently applied in studies utilizing cell models to investigate calcium dynamics and neuroprotection as well as in animal studies exploring its potential in treating conditions such as malignant hyperthermia and muscular dystrophies It is also used in drug screening for therapeutic agents targeting calcium-related disorders Experimental concentrations typically depend on the specific research design
Apexbio Technology LLC DANTROLENE-50MG
Dantrolene (CAS No 7261-97-4) is a hydantoin derivative primarily used in the research category of muscle relaxants originating from its unique ability to interfere with excitation-contraction coupling in skeletal muscle Its mechanism of action involves blocking the ryanodine receptor (RyR1) calcium channels in the sarcoplasmic reticulum reducing calcium release and subsequent muscle contraction In vitro it exhibits activity in the nanomolar to low micromolar range Dantrolene is frequently applied in studies utilizing cell models to investigate calcium dynamics and neuroprotection as well as in animal studies exploring its potential in treating conditions such as malignant hyperthermia and muscular dystrophies It is also used in drug screening for therapeutic agents targeting calcium-related disorders Experimental concentrations typically depend on the specific research design
Medchemexpress LLC HY-18600A 5mg Medchemexpress, Azimilide (Dihydrochloride) CAS:149888-94-8 Purity:>98%
Medchemexpress, HY-18600A 5mg Azimilide (Dihydrochloride) CAS:149888-94-8 Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.