Nitrogen mustard compounds
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.
eMolecules Oakwood Chemical 1-Chloroethyl chloroformate 1kg 537678299 019459 0 000 50893-53-3 MFCD00000647 142 960 C3H4Cl2O2
Oakwood Chemical 1-Chloroethyl chloroformate 1kg 537678299 019459 0 000 50893-53-3 MFCD00000647 142 960 C3H4Cl2O2
Selleck Chemical LLC Bendamustine HCl 100mg 3543-75-7 SDX-105 (Cytostasane) HCl
Bendamustine (SDX-105, Cytostasane) HCl is a DNA-damaging agent with IC50 of 50 ?M in cell-free assay. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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 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.
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 JW PharmLab LLC / 2-(Pentafluorosulfur)aniline / 50mg / 722712393 / 20R2505 / 96.000 / 1246998-10-6 / MFCD21362226 / 219.170 / C6H6F5NS
JW PharmLab LLC / 2-(Pentafluorosulfur)aniline / 50mg / 722712393 / 20R2505 / 96.000 / 1246998-10-6 / MFCD21362226 / 219.170 / C6H6F5NS
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
Medchemexpress LLC ML-184 10mg | 794572-10-4 | 470.63 g·mol⁻¹ | C25H34N4O3S | 10 MG
ML-184 is a selective GPR55 agonist research compound supplied for in vitro and preclinical pharmacology studies. It is provided as a solid and as ready-to-use DMSO solutions, and is characterized by molecular formula C25H34N4O3S and molecular weight 470.63 g·mol⁻¹.
- Selective GPR55 agonist (EC50 ≈ 250 nM)
- Suitable for in vitro and preclinical research applications
- Available as a 10 mg solid and as 10 mM solution in DMSO
- High purity (99.57%) as provided by manufacturer
- Store powder at -20°C for long-term stability; store solutions at -80°C for extended storage