Nitrogen mustard compounds
Medchemexpress LLC Bis(2-chloroethyl)amine hydrochloride | 821-48-7 | MFCD00012515 | 98.0% | 178.49 | C4H10Cl3N | 25g
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 Bis(2-chloroethyl)amine hydrochloride | 821-48-7 | MFCD00012515 | ≥98.0% | 178.49 g/mol | C4H10Cl3N | 500g
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 KB-5492 (anhydrous) | 129200-10-8 | 99.5% | 546.57 | 5 MG
KB-5492 anhydrous is a potent and selective inhibitor of the sigma receptor, inhibiting specific [3H]1,3-di(2-tolyl)guanidine (DTG) binding with an IC50 of 3.15 μM. It also functions as an anti-ulcer agent, preventing ethanol- and acidified aspirin-induced increases in 51Cr release from gastric epithelial cells in vitro, and macroscopic lesions in the gastric mucosa in vivo.
- Potent and selective sigma receptor inhibitor
- Inhibits specific DTG binding in a concentration-dependent manner
- Prevents ethanol- and acidified aspirin-induced increases in 51Cr release from gastric epithelial cells
- Prevents macroscopic lesions in the gastric mucosa in animal models
- Suitable for research use only
eMolecules 213211-10-0 | Medchem Express | BIRT 377 | 5mg | 758391260 | HY-110117 | MFCD28166481 | 442.13 | C18H15BrCl2N2O2
Medchem Express | Isoorientin | 1mg | 446275345 | HY-N0767 | 4261-42-1 | MFCD00017433 | 448.380 | C21H20O11
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Medchemexpress LLC Metarrestin | 1443414-10-5 | 99.9% | 100 MG
Metarrestin is a first-in-class small-molecule inhibitor of the perinucleolar compartment (PNC) used in preclinical cancer research to disrupt nucleolar structure and inhibit RNA polymerase I transcription.
- First-in-class perinucleolar compartment inhibitor for preclinical research.
- Disrupts nucleolar structure and inhibits RNA polymerase I transcription.
- Molecular formula C31H30N4O; molecular weight 474.60.
- Purity 99.9% (reported by supplier).
- Available as a 100 MG powder; store powder at -20°C (long term) or 4°C.
- For research use only; not for human or clinical applications.
eMolecules 1801-10-1 | 3-(Trifluoromethyl)benzamide | Ambeed | MFCD00014802 | 189.137 | C8H6F3NO | 98.000 | NC(=O)c1cccc(c1)C(F)(F)F | 1mg | 761204476
3-(Trifluoromethyl)benzamide | Ambeed | 1801-10-1 | MFCD00014802 | 189.137 | C8H6F3NO | 98.000 | NC(=O)c1cccc(c1)C(F)(F)F | 1mg | 761204476
Medchemexpress LLC Beta-catenin-IN-2 | 1458664-10-2 | 99.55% | 255.29 | 100 MG
Beta-catenin-IN-2 (Compound H1B1) is a potent β-catenin inhibitor used for the study of colorectal cancer. It suppresses the transcriptional activity of β-catenin/Tcf-4 in HCT116 cells in a dose-dependent manner at concentrations of 10-40 μM. The product is a solid, pink to red in color. It is soluble in DMSO at 83.33 mg/mL (326.41 mM).
- Potent β-catenin inhibitor
- Suppresses transcriptional activity of β-catenin/Tcf-4
- Used for the study of colorectal cancer
- Solid, pink to red in color
- Soluble in DMSO
eMolecules 2377151-10-3 | Medchem Express | ZL0580 | 5mg | 527574223 | HY-126428 | 532.54 | C25H23F3N4O4S
Medchem Express | Cefuroxime (sodium) | 500mg | 491484622 | HY-B1256 | 56238-63-2 | MFCD09878727 | 446.370 | C16H15N4NaO8S
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Medchemexpress LLC ML-184 25mg | 794572-10-4 | 470.63 g·mol⁻¹ | C25H34N4O3S | 25 MG
ML-184 is a small-molecule research compound described as a GPR55 agonist and used in cell-based and pharmacological studies. It is supplied as a high-purity solid for laboratory research and is identified by CAS 794572-10-4.
- Acts as a GPR55 agonist for pharmacology and cell studies.
- High reported purity suitable for research applications.
- Molecular formula C25H34N4O3S and molecular weight 470.63 g·mol⁻¹.
- Supplied as a solid in a 25 mg package for benchtop use.
- CAS number 794572-10-4 provides an unambiguous chemical identifier.
Medchemexpress LLC ML-184 5mg | 794572-10-4 | 470.63 g/mol | C25H34N4O3S | 5 MG
ML-184 is a selective GPR55 agonist research compound (CAS 794572-10-4) used to investigate GPR55-mediated signaling. It activates GPR55 with an EC50 of approximately 250 nM, induces ERK1/2 phosphorylation and PKCβII translocation, and has been reported to increase neural stem cell proliferation and promote neuronal differentiation. The supplied material is a 5 mg vial with reported purity of 99.57% and molecular weight 470.63 g/mol.
- Selective GPR55 agonist with EC50 ≈ 250 nM.
- Induces ERK1/2 phosphorylation and PKCβII translocation.
- Shown to increase neural stem cell proliferation and promote neuronal differentiation in vitro.
- High reported purity suitable for research use.
- Supplied as a 5 mg vial for small-scale experiments.
Medchemexpress LLC Mizagliflozin (DSP-3235 free base) | 666843-10-3 | 99.2% | 564.67 g/mol | C28H44N4O8 | 10 MG
Mizagliflozin is a potent, orally active, selective SGLT1 inhibitor used in research on postprandial glucose regulation and constipation amelioration. It exhibits a Ki of approximately 27 nM for human SGLT1 and about 303-fold selectivity versus SGLT2.
- Selective SGLT1 inhibition (Ki ≈ 27 nM).
- High purity (99.2%).
- Molecular formula C28H44N4O8; molecular weight 564.67 g/mol.
- Solid, off-white to light yellow appearance.
- Store at 4°C protected from light; in solution store -80°C for long-term.
Medchemexpress LLC Alamandine | 1176306-10-7 | 99.9% | 855.00 | 5 MG
Alamandine | 1176306-10-7 | 99.9% | 855.00 | 5 MG
Medchemexpress LLC Methyl (4-((4-fluorobenzyl)(prop-2-yn-1-yl)amino)-2,6-dimethylphenyl)carbamate | 1821222-10-9 | MFCD34676457 | 99.5% | C20H21FN2O2 | 10MG
HN37 is a small-molecule KCNQ2 (Kv7) activator intended for laboratory research use. It exhibits potent neuronal Kv7 activation with reported antiepileptic activity (EC50 ≈ 37 nM) and contains an alkyne functional group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAC) for bioconjugation and probe synthesis. The compound is provided as a high-purity solid or DMSO solution for experimental use.
- Potent KCNQ2 (Kv7) activator with EC50 ≈ 37 nM.
- Contains an alkyne group for CuAAC click chemistry.
- High purity (99.53%) suitable for research applications.
- Supplied in solid and DMSO solution formats.
- Intended for laboratory research only; not for human use.
eMolecules 75390-44-2 | Ambeed | 4-Phenylthiazole-2-carbaldehyde | 100mg | 595927454 | A503314 | MFCD02665589 | 189.23 | C10H7NOS
Ambeed | 4-Phenylthiazole-2-carbaldehyde | 100mg | 595927454 | A503314 | 75390-44-2 | MFCD02665589 | 189.230 | C10H7NOS