Hydrochlorides
Medchemexpress LLC SKF-96365 hydrochlor 50mg
SKF-96365 hydrochloride is a potent TRP channel blocker and a store-operated Ca2 entry (SOCE) inhibitor SKF-96365 hydrochloride significantly inhibits hERG hKCNQ1/hKCNE1 hKir2 1 and hKv4 3 current and significantly prolongs the QTc interval in isolated guinea pig hearts SKF-96365 hydrochloride exhibits potent anti-neoplastic activity by inducing cell-cycle arrest and apoptosis in colorectal cancer cells1]2]
Medchemexpress LLC SKF-96365 hydrochlor 100mg
SKF-96365 hydrochloride is a potent TRP channel blocker and a store-operated Ca2 entry (SOCE) inhibitor SKF-96365 hydrochloride significantly inhibits hERG hKCNQ1/hKCNE1 hKir2 1 and hKv4 3 current and significantly prolongs the QTc interval in isolated guinea pig hearts SKF-96365 hydrochloride exhibits potent anti-neoplastic activity by inducing cell-cycle arrest and apoptosis in colorectal cancer cells1]2]
Medchemexpress LLC SKF-96365 hydrochlor 10mg
SKF-96365 hydrochloride is a potent TRP channel blocker and a store-operated Ca2 entry (SOCE) inhibitor SKF-96365 hydrochloride significantly inhibits hERG hKCNQ1/hKCNE1 hKir2 1 and hKv4 3 current and significantly prolongs the QTc interval in isolated guinea pig hearts SKF-96365 hydrochloride exhibits potent anti-neoplastic activity by inducing cell-cycle arrest and apoptosis in colorectal cancer cells1]2]
Medchemexpress LLC PD 128907 hydrochloride | 112960-16-4 | MFCD01529976 | 99.5% | 285.77 | C14H20ClNO3 | 25 MG
PD 128907 hydrochloride is a potent and selective dopamine D3 receptor agonist supplied as a solid biochemical reagent for life-science research. It is used in pharmacology and neurobiology to probe D3-mediated signaling and dopaminergic mechanisms, and is provided at high purity in small pack sizes for laboratory experiments.
- Potent D3 receptor agonist with low-nanomolar activity.
- High selectivity over D2 receptors for receptor-specific studies.
- High purity suitable for research applications.
- Solid form with white to light yellow appearance.
- Available in multiple small pack sizes for dosing flexibility.
- Recommended sealed storage away from moisture to preserve stability.
Matrix Scientific 3,3-DIFLUOROPIPERIDINE H-250MG
3,3-Difluoropiperidine hydrochloride, 99%; 250mg,C5H10ClF2N, MFCD03452800, mw 157.59, [496807-97-7]
Medchemexpress LLC PD 128907 hydrochloride | 112960-16-4 | 99.5% | 285.77 g/mol | C14H20ClNO3 | 50 MG
PD 128907 hydrochloride is a selective dopamine D3 receptor agonist used as a biochemical reagent for life-science research. It exhibits sub-nanomolar potency at D3 receptors (EC50 ~0.64 nM) and substantial selectivity over D2 receptors, and is supplied as a high-purity solid for in vitro pharmacology and receptor-binding studies.
- Potent D3 receptor agonist with EC50 ~0.64 nM.
- High selectivity over D2 receptors (≈53-fold).
- Reported high purity suitable for research use.
- Available in small package sizes for experimental workflows.
- Applicable to dopaminergic signaling and receptor pharmacology studies.
Medchemexpress LLC Ly-2365109 hydrochloride | 1779796-27-8 | 98.7% | 421.91 g·mol^-1 | C22H28ClNO5 | 100 MG
LY2365109 hydrochloride is a research-grade small molecule and selective inhibitor of the glycine transporter 1 (GlyT1). Supplied as the hydrochloride salt for laboratory research use, it has been characterized in cell-based glycine uptake assays and is intended for in vitro pharmacology and transporter studies.
- Potent, selective GlyT1 inhibition (IC50 15.8 nM).
- High purity suitable for research (≈98.7%).
- Hydrochloride salt form for improved handling and solubility.
- Molecular weight consistent with salt form (≈421.9 g·mol⁻¹).
- Suitable for in vitro pharmacology and transporter profiling.
Medchemexpress LLC SB-399885 hydrochloride | 402713-81-9 | 98.3% | 482.81 g/mol | C18H22Cl3N3O4S | 1 ML
SB-399885 hydrochloride is a research reagent that acts as a selective 5-HT6 (serotonin 6) receptor antagonist. Supplied as the hydrochloride salt, it is suitable for in vitro and in vivo pharmacology studies and is available as solid material or as a ready-to-use 10 mM solution in DMSO.
- Selective 5-HT6 receptor antagonist for research applications.
- Available as solid and as a 10 mM solution in DMSO.
- High purity (98.3%).
- Molecular weight 482.81 g/mol; molecular formula C18H22Cl3N3O4S.
- CAS number 402713-81-9; supplied as the hydrochloride salt.
Medchemexpress LLC UAMC-3203 hydrochloride | 2271358-65-5 | 98.8% | 508.12 | 1 ML
UAMC-3203 hydrochloride is a potent and selective Ferroptosis inhibitor with an IC50 of 12 nM. No toxicity was observed in mice after repeated intraperitoneal injections (20 μmol/kg daily, over a period of 4 weeks).
- Potent and selective ferroptosis inhibitor.
- Has an IC50 of 12 nM for ferroptosis.
- No observed toxicity in mice at 20 μmol/kg daily for 4 weeks.
- Available in solid form (white to off-white).
- High purity: 98.82%.
Medchemexpress LLC Vu0134992 hydrochloride | 1052515-91-9 | 98.5% | 1 ML
VU0134992 hydrochloride is a selective Kir4.1 inward-rectifier potassium channel blocker provided as the hydrochloride salt. Supplied as a 10 mM solution in DMSO or as a solid, it is used as a research tool to inhibit Kir4.1-mediated currents in electrophysiology and cell-based assays.
- Selective Kir4.1 blocker (IC50 = 0.97 μM).
- Supplied as hydrochloride salt for improved solubility.
- Available as 10 mM solution in DMSO or in solid form.
- Suitable for electrophysiology and cell-based assays.
- High purity suitable for research applications.
Medchemexpress LLC Vu 0255035 | 1135243-19-4 | 99.8% | 432.52 g·mol⁻¹ | C18H20N6O3S2 | 1 ML
VU 0255035 is a selective, competitive antagonist of the muscarinic M1 receptor supplied for research use. It is available as a high-purity solid and as a ready-to-use 10 mM solution in DMSO, supporting receptor pharmacology experiments, selectivity profiling, and dose-response studies.