Nitrogen mustard compounds
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.
Chemscene ChemScene | 4,7-Dibromoisoquinoline | 250MG | CS-0139734 | 0.97 | 223671-10-1| MFCD13191776 | 286.95
ChemScene | 4,7-Dibromoisoquinoline | 250MG | CS-0139734 | 0.97 | 223671-10-1| MFCD13191776 | 286.95
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.
Sigma Aldrich Fine Chemicals Biosciences Bis(2-chloroethyl)amine hydrochloride 98% | 821-48-7 | MFCD00012515 | 250G
Bis(2-chloroethyl)amine hydrochloride 98% | Purity: 98% | Mol Wt: 178.49 | 821-48-7 | MFCD00012515 | 250G
Selleck Chemical LLC Camonsertib-E1108-5MG
Camonsertib is a highly potent and selective inhibitor of ATR kinase with an IC50 of 1 nM
Sigma Aldrich Fine Chemicals Biosciences Bis(2-chloroethyl)amine hydrochloride 98% | 821-48-7 | MFCD00012515 | 100G
Bis(2-chloroethyl)amine hydrochloride 98% | Purity: 98% | Mol Wt: 178.49 | 821-48-7 | MFCD00012515 | 100G
Medchemexpress LLC Flesinoxan | 98206-10-1 | 99.9% | 50 MG
Flesinoxan is a selective 5-HT1A receptor agonist research compound intended for laboratory research use. It is supplied as an off-white to light yellow solid with demonstrated potency at the 5-HT1A receptor and standard handling and storage recommendations for small-molecule research chemicals.
- Selective 5-HT1A receptor agonist (EC50 24 nM).
- High reported purity: 99.9%.
- Off-white to light yellow solid appearance.
- Soluble in DMSO (31.25 mg/mL); in vivo formulations reported at ≥2.08 mg/mL.
- Storage: powder stable at -20°C (3 years) and 4°C (2 years).
- For research use only; not for human consumption or clinical use.
Medchemexpress LLC Mizagliflozin | 666843-10-3 | 99.2% | 564.67 | 50 MG
Mizagliflozin (DSP-3235 free base) is a potent, orally active, and selective SGLT1 inhibitor, with a Ki of 27 nM for human SGLT1. It displays 303-fold selectivity over SGLT2. This compound functions as an antidiabetic agent capable of modifying postprandial blood glucose excursion and also shows potential in the amelioration of chronic constipation. In vivo, the compound at doses of 3-30 mg/kg orally has a laxative effect, increasing fecal wet weight in a rat model of low-fiber-diet-induced constipation. The compound has a short half-life, with 0.23 h after intravenous administration and 1.14 h after oral administration.
- Highly selective SGLT1 inhibitor
- Helps manage postprandial blood glucose levels
- Potential to treat chronic constipation
- Orally active for convenient administration
Medchemexpress LLC Metarrestin | 1443414-10-5 | 99.9% | 25MG
Metarrestin | 1443414-10-5 | 99.9% | 25MG
Medchemexpress LLC Gamcemetinib (CC-99677) | 1887069-10-4 | 99.1% | 469.94 | 50 MG
Gamcemetinib (CC-99677) is a potent, covalent, and irreversible inhibitor of the mitogen-activated protein (MAP) kinase-activated protein kinase-2 (MK2) pathway. It exhibits an IC50 of 156.3 nM in biochemical assays and an EC50 of 89 nM in cell-based assays.
- Potent, covalent, and irreversible MK2 inhibitor
- Exhibits IC50 of 156.3 nM in biochemical assays and EC50 of 89 nM in cell-based assays
- Extracted from patent WO2020236636, compound 1
- Available in solid and solution forms
- Appearance: Solid, light yellow to yellow color
- Useful for research purposes
- Offers high purity of 99.1%
Medchemexpress LLC Iriflophenone | 52591-10-3 | MFCD20260852 | 98.1% | 246.22 g/mol | C13H10O5 | 10 MG
Iriflophenone is a plant-derived phenolic compound (C13H10O5, MW 246.22) isolated from Aquilaria sinensis and provided for laboratory research; it has been reported to stimulate proliferation of MCF-7 and T-47D human breast cancer cell lines.
- Plant-derived phenolic compound isolated from Aquilaria sinensis.
- Reported to stimulate proliferation of MCF-7 and T-47D human breast cancer cells.
- High purity suitable for in vitro research (reported purity ~98.1%).
- Available as solid or as ready-to-use DMSO solution for cell-based assays.
- Characterized chemical profile with CAS 52591-10-3 and formula C13H10O5.