Nitrogen mustard compounds
Medchemexpress LLC 2-chloroethyl (2-chloroethyl)phosphonate | 17378-30-2 | MFCD24393365 | >95.0% | 206.99 | C4H9Cl2O3P | 5 MG
2-Chloroethyl (2-chloroethyl)phosphonate is an organophosphorus compound used as an intermediate in organic synthesis. It is a low-molecular-weight phosphonate (C4H9Cl2O3P, MW 206.99) with CAS 17378-30-2, provided with supporting documentation; consult the certificate of analysis for recommended storage and handling.
- Organophosphorus intermediate for organic synthesis.
- Molecular formula C4H9Cl2O3P; molecular weight 206.99.
- CAS number 17378-30-2 for unambiguous identification.
- Purity greater than 95% by HPLC.
- Available in small research quantities, such as 5 mg.
- Supplied with certificate of analysis for storage and handling guidance.
Medchemexpress LLC Gamcemetinib | 1887069-10-4 | 99.1% | C22H20ClN5O3S | 10MG
Gamcemetinib is a covalent, irreversible inhibitor of MAP kinase-activated protein kinase-2 (MK2) used as a research compound for in vitro and preclinical studies. It is characterized by submicromolar activity in biochemical and cell-based assays and is supplied as a solid or as a DMSO solution for laboratory use.
- Potent, covalent MK2 inhibitor with low-nanomolar to submicromolar activity.
- High purity suitable for research use (≈99.1%).
- Available as multiple solid quantities and as a 10 mM solution in DMSO for convenience.
- Soluble in DMSO; enhanced solubility with warming and sonication.
- Defined storage recommendations for powder and solution to preserve stability.
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.
Medchemexpress LLC Rv01 | 1016897-10-1 | 98.1% | 263.29 g/mol | C17H13NO2 | 50MG
RV01 is a resveratrol analogue that inhibits aldehyde dehydrogenase (ALDH) activity and reduces ethanol-induced ALDH2 mRNA expression. Supplied as a solid research compound for in vitro biochemical and cellular studies, it has documented solubility in DMSO and defined storage/stability conditions.
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.
eMolecules Bistrifluoroacetamide | 407-24-9 | MFCD00013564 | 25g
Combi-Blocks, Inc. | Bistrifluoroacetamide | 25g | 586077145 | HA-3249 | 95.000 | 407-24-9 | MFCD00013564 | 209.047 | C4HF6NO2
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eMolecules AstaTech / 4-METHOXYPYRIDINE 1-OXIDE / 5g / 233625492 / 34702 / 95.000 / 1122-96-9 / MFCD00006207 / 125.127 / C6H7NO2
AstaTech / 4-METHOXYPYRIDINE 1-OXIDE / 5g / 233625492 / 34702 / 95.000 / 1122-96-9 / MFCD00006207 / 125.127 / C6H7NO2
Medchemexpress LLC CDC25B-IN-1 | 2374831-10-2 | 98.1% | 321.37 g/mol | C20H19NO3 | 50MG
CDC25B-IN-1 is a small-molecule research inhibitor of the cell division cycle 25B (CDC25B) phosphatase. It has a reported Ki of approximately 8.5 μM, reduces cell proliferation and colony formation, and increases the proportion of cells in the G2/M phase. The compound is supplied at high reported purity and is available in multiple pack sizes, including mg quantities and as a DMSO solution suitable for biochemical and cell-based assays.
- Potent inhibitor of CDC25B phosphatase with reported Ki ≈ 8.5 μM.
- Inhibits cell proliferation and colony formation in cellular assays.
- Causes accumulation of cells in the G2/M phase.
- Supplied with high reported purity for research use.
- Available in multiple pack sizes and as a DMSO solution for convenience.
Chem-Impex International, Inc. N,N-Bis(2-chloroethyl)-p-toluenesulfonamide | MFCD00018944 | 25G
N,N-Bis(2-chloroethyl)-p-toluenesulfonamide, MFCD00018944, 25G
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
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
eMolecules AstaTech / 2-ETHYL-6-METHYLPYRIDINE / 0.25g / 721956956 / S10152 / 97.000 / 1122-69-6 / MFCD00023531 / 121.183 / C8H11N
AstaTech / 2-ETHYL-6-METHYLPYRIDINE / 0.25g / 721956956 / S10152 / 97.000 / 1122-69-6 / MFCD00023531 / 121.183 / C8H11N
Medchemexpress LLC Bis(2-chloroethyl)amine hydrochloride | 821-48-7 | MFCD00012515 | 98.0% | 178.49 g·mol⁻¹ | C4H10Cl3N | 100g
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 Metarrestin | 1443414-10-5 | 99.9% | 50 MG
Metarrestin is a small-molecule perinucleolar compartment inhibitor provided as a high-purity research compound for in vitro and in vivo studies investigating nucleolar structure and metastasis.
- Provides high purity (99.9%).
- Molecular formula C31H30N4O and molecular weight 474.60 g/mol.
- Available in solid and solution formats for flexibility in experiments.
- Suitable for use in biochemical, cell-based, and pharmacokinetic studies.
- Recommended storage: powder at -20°C; in solvent at -80°C.