Nitrogen mustard compounds
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 N-Methylmoranoline | 69567-10-8 | 177.20 | 5 MG
N-Methylmoranoline is a chemical substance identified by CAS No. 69567-10-8, with a molecular formula of C7H15NO4 and a molecular weight of 177.20. It appears as a white to off-white solid with a purity of 99.0% (HPLC). This product is stable under recommended storage conditions and is intended for laboratory research use.
- White to off-white solid appearance
- Purity of 99.0% by HPLC
- Molecular formula of C7H15NO4
- Molecular weight of 177.20
- Stable under recommended storage conditions
- Powder storage at -20°C for 3 years
- Solution storage at -80°C for 6 months or -20°C for 1 month
- Identified by CAS No. 69567-10-8
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
eMolecules 50893-53-3 | 1-Chloroethyl chloroformate | Apollo Scientific US - Building Blocks | MFCD00000647 | 142.960 | C3H4Cl2O2 | 98.000 | CC(Cl)OC(Cl)=O | 500g | 448253967
1-Chloroethyl chloroformate | Apollo Scientific US - Building Blocks | 50893-53-3 | MFCD00000647 | 142.960 | C3H4Cl2O2 | 98.000 | CC(Cl)OC(Cl)=O | 500g | 448253967
Medchemexpress LLC ZL0580 | 2377151-10-3 | 99.4% | 532.53 | 10 MG
ZL0580, an analog of ZL0590, epigenetically suppresses HIV by binding to the BD1 domain of BRD4. It inhibits Tat transactivation and transcription elongation, and also induces a repressive chromatin structure at the HIV promoter.
- Induces HIV transcriptional suppression.
- Exhibits low toxicity.
- Suppresses both PMA-stimulated and basal HIV transcription.
- Does not cause significant cell death at concentrations below 40 μM.
- Suppresses HIV in primary CD4+ T cells.
Medchemexpress LLC ZL0580 | 2377151-10-3 | 99.4% | 532.53 | 50 MG
ZL0580 is a structurally similar analog of ZL0590. It induces epigenetic suppression of HIV by selectively binding to the BD1 domain of BRD4. This compound suppresses HIV by inhibiting Tat transactivation and transcription elongation, and by inducing repressive chromatin structure at the HIV promoter. It is intended for research use only.
- Induces epigenetic suppression of HIV
- Selectively binds to BD1 domain of BRD4
- Inhibits Tat transactivation and transcription elongation
- Induces repressive chromatin structure at the HIV promoter
- Demonstrates low toxicity at effective concentrations (e.g., 8 μM in PBMCs)
- Suppresses both PMA-stimulated and basal HIV transcription
- Shows almost complete loss of productive HIV infection in CD4+ T cells at 8 μM
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 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