Nitrogen mustard compounds
Medchemexpress LLC ML-184 50mg | 794572-10-4 | 470.63 g/mol | C25H34N4O3S | 50 MG
ML-184 is a selective GPR55 agonist research compound (CAS 794572-10-4) used to probe GPR55-mediated signaling pathways in vitro and in vivo. It activates ERK1/2 phosphorylation, promotes PKCβII translocation, and has been shown to increase neural stem cell proliferation and differentiation.
- Selective GPR55 agonist with an EC50 of about 250 nM.
- Greater than 100-fold selectivity over GPR35, CB1, and CB2.
- Induces ERK1/2 phosphorylation and PKCβII membrane translocation.
- Demonstrated activity in neural stem cell proliferation and differentiation assays.
- Provided as a high-purity solid and as a DMSO solution for biological assays.
eMolecules AstaTech / PYRIDINE-2356-TETRAAMINE 3HCL / 0.1g / 722706699 / C15643 / 97.000 / 34981-10-7 / MFCD00235198 / 248.540 / C5H12Cl3N5
AstaTech / PYRIDINE-2356-TETRAAMINE 3HCL / 0.1g / 722706699 / C15643 / 97.000 / 34981-10-7 / MFCD00235198 / 248.540 / C5H12Cl3N5
Chem-Impex International, Inc. N,N-Bis(2-chloroethyl)-p-toluenesulfonamide | MFCD00018944 | 25G
N,N-Bis(2-chloroethyl)-p-toluenesulfonamide, MFCD00018944, 25G
![Medchemexpress LLC 4-(5-fluoro-1H-benzo[d]imidazol-2-yl)-N,N-dimethylaniline | 1458664-10-2 | MFCD20720876 | 99.6% | 255.29 | C15H14FN3 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000222052.png-250.jpg)
Medchemexpress LLC 4-(5-fluoro-1H-benzo[d]imidazol-2-yl)-N,N-dimethylaniline | 1458664-10-2 | MFCD20720876 | 99.6% | 255.29 | C15H14FN3 | 5 MG
β-catenin-IN-2 (Compound H1B1) is a small-molecule β-catenin inhibitor for research use, reported as a pink to red solid with high purity. It is characterized by molecular formula C15H14FN3 and a molecular weight of 255.29 g/mol, and is used in studies of colorectal cancer and β-catenin pathway biology.
- Potent β-catenin inhibitor for colorectal cancer research.
- Molecular formula C15H14FN3.
- Molecular weight 255.29 g/mol.
- Appearance: pink to red solid.
- Purity around 99.6% by HPLC.
- Available in small milligram-scale packages for laboratory studies.
- Typically prepared and handled in solution (DMSO) for assays.
Medchemexpress LLC Camonsertib | 2417489-10-0 | MFCD34578462 | 100.0% | C21H26N6O3 | 10MG
Camonsertib is an orally active, selective ATR kinase inhibitor developed for oncology research and clinical investigation. It exhibits low-nanomolar biochemical potency against ATR, reported selectivity versus related kinases, and has shown antitumor activity in preclinical and early clinical studies. The compound is supplied as a high-purity solid for research use only.
- Potent ATR inhibition with low-nanomolar biochemical potency.
- High selectivity versus related kinases, limiting off-target effects.
- Demonstrated antitumor activity in preclinical and early clinical evaluations.
- Provided as a high-purity solid suitable for laboratory research.
- Available in small research-scale quantities for experimental studies.
eMolecules ChemScene / 4-(Cyclopropylsulfonimidoyl)aniline / 100mg / 761283903 / CS-0184344 / 0.000 / 1523618-10-1 / MFCD27987215 / 196.270 / C9H12N2OS
ChemScene / 4-(Cyclopropylsulfonimidoyl)aniline / 100mg / 761283903 / CS-0184344 / 0.000 / 1523618-10-1 / MFCD27987215 / 196.270 / C9H12N2OS
eMolecules Medchem Express / 10-Methoxycamptothecin / 5mg / 532150217 / HY-N0446 / / 19685-10-0 / MFCD11975376 / 378.384 / C21H18N2O5
Medchem Express / 10-Methoxycamptothecin / 5mg / 532150217 / HY-N0446 / / 19685-10-0 / MFCD11975376 / 378.384 / C21H18N2O5
Medchemexpress LLC RV01 | 1016897-10-1 | 98.1% | 263.29 g/mol | C17H13NO2 | 10MG
RV01 is a resveratrol analogue used as a research tool to probe ALDH2-related pathways and oxidative stress. It inhibits DNA damage, reduces ethanol-induced ALDH2 mRNA expression, scavenges hydroxyl radicals, and decreases iNOS expression, indicating anti-neuroinflammatory activity. Supplied as a powder for biochemical and cell-based research applications.
- Inhibits DNA damage and reduces ALDH2 mRNA expression.
- Scavenges hydroxyl radicals, indicating antioxidant activity.
- Decreases iNOS expression and exhibits anti-neuroinflammatory effects.
- Provided as a research-grade powder suitable for biochemical studies.
- High purity for reliable experimental results.
Medchemexpress LLC 1-(2-chloroethyl)-3-((1R,4R)-4-hydroxycyclohexyl)-1-nitrosourea-d4 | 00-00-0 | 99.0% | 253.72 | C9H12D4ClN3O3 | 5 MG
Deuterium-labeled trans-4'-Hydroxy CCNU Lomustine-d4 is a research-grade labeled analogue of trans-4'-Hydroxy lomustine intended for use as a tracer and internal standard in quantitative analytical methods. The product is supplied as a high-purity solid in a 5 MG vial and requires cold storage to maintain stability.
- Deuterium-labeled internal standard for NMR, GC-MS, and LC-MS.
- High purity (99.0%).
- Solid, white to off-white appearance.
- Suitable as a tracer for pharmacokinetic and metabolic studies.
- Powder storage: -20°C for long-term stability; in solvent: -80°C for short-term stability.
- Supplied as a 5 MG vial for laboratory use.
Medchemexpress LLC Bis(2-chloroethyl)amine hydrochloride | 821-48-7 | MFCD00012515 | 98.0% | 178.49 | C4H10Cl3N | 1kg
Bis(2-chloroethyl)amine hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research
Medchemexpress LLC HN37 | 1821222-10-9 | 99.5% | 340.39 g/mol | C20H21FN2O2 | 5 MG
HN37 is a small-molecule research compound that functions as a potent activator of the KCNQ2 potassium channel. It contains an alkyne moiety suitable for click-chemistry derivatization and is intended for in vitro pharmacology and chemical biology applications.
- Potent KCNQ2 activation with EC50 of 37 nM.
- Alkyne functional group suitable for copper-catalyzed azide-alkyne cycloaddition.
- High reported purity for reproducible assay performance.
- Soluble in DMSO at 50 mg/mL for preparation of concentrated stocks.
- Available in multiple milligram quantities for research use.