Hydrochlorides
Medchemexpress LLC Anabasine ((S)-Anabasine) | 494-52-0 | MFCD00006370 | 99.0% | 50 MG
Anabasine is an alkaloid found as a minor component in tobacco (Nicotiana). It is a botanical pesticide that acts as a full agonist of nicotinic acetylcholine receptors (nAChRs). Anabasine induces depolarization of TE671 cells endogenously expressing human fetal muscle-type nAChRs (EC50=0.7 μM).
- Found in tobacco (Nicotiana)
- Acts as a full agonist of nicotinic acetylcholine receptors
- Induces depolarization of TE671 cells
- Molecular weight: 162.24
- Formula: C10H14N2
- Appearance: Liquid (Density: 1.0455 g/cm3)
- Colorless to light yellow liquid
- Storage: 4°C, protect from light
Medchemexpress LLC GSK-LSD1 dihydrochloride | 2102933-95-7 | 99.5% | 289.24 g·mol⁻1 | C14H22Cl2N2 | 50 MG
This dihydrochloride salt is a potent, selective, and irreversible inhibitor of lysine-specific demethylase 1 (LSD1), used as a research probe for epigenetic regulation and metabolic studies. It exhibits an IC50 of 16 nM and is supplied with high reported purity.
- Potent LSD1 inhibition with IC50 of 16 nM.
- High purity (≈99.5%).
- Supplied as a dihydrochloride salt in solid and DMSO solution formats.
- Suitable for epigenetic and metabolic research applications.
- Available in small research pack sizes including 50 MG.
Medchemexpress LLC Tirofiban (hydrochloride monohydrate) | 150915-40-5 | 99.9% | 495.07 | 1 ML
Tirofiban (hydrochloride monohydrate) | 150915-40-5 | 99.9% | 495.07 | 1 ML
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.
Medchemexpress LLC Rs-127445 hydrochloride | 199864-86-3 | 99.8% | 317.79 g·mol⁻¹ | C17H17ClFN3 | 10 MG
RS-127445 hydrochloride is a selective, high-affinity 5-HT2B receptor antagonist (pKi ≈ 9.5) provided as a research-grade chemical. It shows approximately 1,000-fold selectivity versus other receptors and is supplied as a solid (powder) or as a ready-to-use 10 mM solution in DMSO. Intended for research use only.
Medchemexpress LLC BAY-6672 hydrochloride | 2247520-31-4 | 98.0% | C26H28BrCl2N3O3 | 25 MG
BAY-6672 hydrochloride is a potent and selective human Prostaglandin F (FP) receptor antagonist with an IC50 value of 11 nM. It is suitable for use as a laboratory chemical for the manufacture of substances.
- Potent and selective human Prostaglandin F (FP) receptor antagonist
- IC50 value of 11 nM
- Stable under recommended storage conditions
- Appears as a white to off-white solid
- Identified for laboratory chemical use
Medchemexpress LLC Niraparib hydrochlor 25mg | 1038915-64-8 | 25MG
Niraparib hydrochloride (MK-4827 hydrochloride) is a highly potent and orally bioavailable PARP1 and PARP2 inhibitor with IC50s of 3 8 and 2 1 nM respectively Niraparib hydrochloride leads to inhibition of repair of DNA damage activates apoptosis and shows anti-tumor activity[1 [2 [3
Medchemexpress LLC Piperoxan hydrochloride | 135-87-5 | MFCD00079224 | ≥98% | 269.77 g/mol | C14H20ClNO2 | 1 ML
Piperoxan hydrochloride is an α2 adrenoceptor antagonist and first-generation antihistamine supplied as a 10 mM solution in DMSO (1 mL) for research use. It is identified by CAS 135-87-5 and has a molecular weight of 269.77 g/mol. The ready-to-use format is intended for in vitro receptor pharmacology and small-scale assay applications.
- Ready-to-use 10 mM solution in DMSO.
- Suitable for adrenergic receptor and antihistamine research.
- Supplied at 1 mL volume for small-scale assays.
- Molecular weight 269.77 g/mol; CAS 135-87-5.
- Reported high purity (≥98%) in supplier documentation.
Medchemexpress LLC Niraparib (hydrochloride) | 1038915-64-8 | 99.4% | 356.85 g/mol | C19H21ClN4O | 50 MG
Niraparib hydrochloride is the hydrochloride salt of niraparib, a potent, orally bioavailable inhibitor of poly(ADP-ribose) polymerase 1 and 2 (PARP1/2). It inhibits DNA damage repair and induces apoptosis, making it useful for preclinical studies of DNA repair pathways and anti-tumor activity. Supplied as a solid 50 mg package for research use.
- Potent PARP1 and PARP2 inhibition at nanomolar potency.
- Effective tool for studying DNA damage repair and apoptosis.
- Suitable for in vitro and in vivo preclinical assays.
- Hydrochloride salt form improves handling and solubility.
- Available as a 50 MG solid for small-scale experiments.
Medchemexpress LLC Cyclopentanecarboxamide, N-[(1S)-4-[(aminoiminomethyl)amino]-1-[2-(2,3,5,6-tetrafluorophenoxy)acetyl]bu | 2097865-47-7 | 97.2% | 25 MG
Kgp-IN-1 hydrochloride is an arginine-specific gingipain (Rgp) inhibitor, identified as compound 13-R from patent WO2017201322A1. This product is intended for research use only.
- Arginine-specific gingipain (Rgp) inhibitor
- Targets cathepsin
- Pathway: metabolic enzyme/protease
- White to off-white solid
- Store at 4°C, sealed, away from moisture
eMolecules 912999-79-2 | 5-Chloroisoindoline hydrochloride | Ambeed | MFCD11223562 | 190.07 | C8H9Cl2N | 98 | Cl.Clc1ccc2CNCc2c1 | 5g | 552537975
5-Chloroisoindoline hydrochloride | Ambeed | 912999-79-2 | MFCD11223562 | 190.070 | C8H9Cl2N | 98.000 | Cl.Clc1ccc2CNCc2c1 | 5g | 552537975
Medchemexpress LLC Doxapram hydrochloride hydrate | 7081-53-0 | MFCD09954698 | 99.3% | 432.98 g/mol | C24H33ClN2O3 | 10 MG
Doxapram hydrochloride hydrate is a small-molecule respiratory stimulant and TASK-1 potassium channel inhibitor supplied as a solid hydrate for research use. It is provided with high purity and is available in small solid quantities and pre-made DMSO solutions for assay work.
- High purity (99.3%).
- Molecular weight 432.98 g/mol.
- Supplied as a solid hydrate; white to off-white appearance.
- Available in small pack sizes suitable for assay development.
- Offered in solution formats (10 mM in DMSO) for immediate use.
Medchemexpress LLC PNU-22394 hydrochloride | 15923-42-9 | 98.8% | 236.74 | C13H17ClN2 | 10 MG
PNU-22394 hydrochloride is a research-grade small molecule agonist of serotonin (5-HT) receptors, reported as a 5-HT2C agonist and partial 5-HT2A/2B agonist. Supplied as the hydrochloride salt and provided at high purity for pharmacology and receptor biology studies in vitro and in vivo.
- Potent 5-HT2C agonist with reported Ki ≈ 6.1 nM and 5-HT2A activity ≈ 10 nM.
- Hydrochloride salt, suitable for dissolution in common assay solvents.
- Molecular formula C13H17ClN2 and molecular weight 236.74 g/mol.
- High purity (>98.7%), appropriate for research applications.
- Intended for pharmacological research and receptor characterization studies.
Medchemexpress LLC Etazolate hydrochloride | 35838-58-5 | MFCD00209848 | 98.0% | 325.79 | C14H20ClN5O2 | 5 MG
Etazolate hydrochloride is a pyrazolopyridine research compound that functions as a selective phosphodiesterase-4 (PDE4) inhibitor, a GABAA receptor regulator, and an α-secretase activator. It is used in neuropharmacology and inflammation studies to probe cAMP signaling, amyloid precursor protein processing, and behavioral pharmacology.
Medchemexpress LLC d,l-SKF89976A hydrochloride | 85375-15-1 | 98.7% | 371.90 | C22H26ClNO2 | 100 MG
SKF89976A hydrochloride is a research reagent that selectively inhibits the GABA transporter GAT-1 and is used in preclinical studies to probe GABA uptake and transporter pharmacology. Reported data in CHO cells show submicromolar potency at GAT-1 and substantially weaker activity at other GAT subtypes.