Phenylhydrazines
Accela Chembio Inc 4-cyanophenylhydrazine Hydrochloride | 25g | 2863-98-1 | MFCD00673994 | 97+% | Shelf Life: 1800 Days | Moisture Sensitive
4-cyanophenylhydrazine Hydrochloride | 25g | 2863-98-1 | MFCD00673994 | 97+% | Shelf Life: 1800 Days | Moisture Sensitive
eMolecules 6971-45-5 | 2-Methoxyphenylhydrazine hydrochloride | Combi-Blocks | MFCD00035456 | 174.630 | C7H11ClN2O | 97.000 | Cl.COc1ccccc1NN | 5g | 205388128
2-Methoxyphenylhydrazine hydrochloride | Combi-Blocks | 6971-45-5 | MFCD00035456 | 174.630 | C7H11ClN2O | 97.000 | Cl.COc1ccccc1NN | 5g | 205388128
Medchemexpress LLC Proparacaine hydrochloride | 5875-06-9 | 99.9% | C16H27ClN2O3 | 1 ML
Proparacaine hydrochloride, also known as Proxymetacaine hydrochloride, is a derivative of lidocaine. It exhibits immunomodulatory and glucocorticomimetic activity. This product is intended for research use only.
- Exhibits dose- and time-dependent cytotoxicity to HCS cells
- Induces apoptosis of HCS cells
- Induces G1 phase arrest
- Activates caspase-2, -3, and -9
- Modulates Bcl-xL and Bax expression
- Reduces nasal symptoms and inflammation in allergic rhinitis mouse models
Medchemexpress LLC Carnostatine hydrochloride (SAN9812 hydrochloride) | 99.00% | 292.72 | 25 MG
Carnostatine hydrochloride (SAN9812 hydrochloride) | 99.00% | 292.72 | 25 MG
Medchemexpress LLC Fructosamine hydrochloride | 39002-30-7 | MFCD27981318 | >97.0% | 215.63 | C6H14ClNO5 | 100 MG
Fructosamine hydrochloride is the hydrochloride salt of D-isoglucosamine supplied as a white to off-white solid. It serves as a reference standard and reagent in biochemical and analytical research, commonly used in studies of carbohydrate metabolism and glycation.
- White to off-white solid suitable for laboratory use.
- High purity for analytical applications.
- Comes in multiple pack sizes including 100 mg.
- Useful as an analytical reference standard and reagent.
- Molecular formula C6H14ClNO5 and molecular weight 215.63.
Medchemexpress LLC Ampreloxetine hydrochloride | 1227056-87-2 | 99.5% | 357.80 g/mol | C18H19ClF3NO | 100 MG
Ampreloxetine hydrochloride is an orally active, CNS-penetrant inhibitor of norepinephrine and serotonin transporters used as a research compound to investigate monoamine reuptake and central nervous system pharmacology. Supplied as the hydrochloride salt, it is intended for preclinical and biochemical assays and is characterized by high reported purity.
- Orally active, CNS-penetrant norepinephrine and serotonin transporter inhibitor.
- Useful for studies of monoamine reuptake and central nervous system pharmacology.
- Provided as a hydrochloride salt to aid solubility in formulations.
- High reported purity suitable for biochemical and preclinical assays.
- Available in laboratory-scale quantity for research use.
- Molecular weight 357.80 g/mol and formula C18H19ClF3NO.
Medchemexpress LLC Bendamustine hydrochloride | 3543-75-7 | 99.9% | C16H22Cl3N3O2 | 500 MG
Bendamustine hydrochloride is a purine analogue and a DNA cross-linking agent. It activates DNA-damage stress response and apoptosis, demonstrating potent alkylating, anticancer, and antimetabolite properties. This compound has been shown to reduce the viability of multiple myeloma cell lines and to induce specific caspase-dependent cell death.
- Functions as a DNA cross-linking agent
- Activates DNA-damage stress response and apoptosis
- Possesses potent alkylating, anticancer, and antimetabolite properties
- Reduces viability of multiple myeloma cell lines
- Induces specific caspase-dependent cell death
- Causes DNA breaks
- Regulates apoptosis and DNA repair pathways in non-Hodgkin's lymphoma cells
- Blocks mitotic checkpoints and causes mitotic catastrophe
Medchemexpress LLC Itacnosertib (hydrochloride) | 2409543-84-4 | 99.4% | 505.01 | 50 MG
Itacnosertib hydrochloride (TP-0184 hydrochloride) is an inhibitor for FLT3, ACVR1, and JAK2. It exhibits anti-leukemic activity and is intended for research use only. This compound has shown promising results in pre-clinical studies, demonstrating its potential in various biological applications.
- Inhibits FLT3, ACVR1 (ALK2), and JAK2
- Exhibits anti-leukemic activity
- Arrests cell cycle of MOLM-13, MOLM-14, and MV4-11 at G1/G0 phase
- Inhibits proliferation of acute myeloid leukemia (AML) cells
- Inhibits activation of FLT3 and ACVR1 downstream signaling pathways
- Shows antitumor activity in mouse xenograft models