Hydrochlorides
Sigma Aldrich Fine Chemicals Biosciences Tirofiban hydrochloride monohydrate >=98% (HPLC) | 150915-40-5 | MFCD07368623 | 50MG
Tirofiban hydrochloride monohydrate >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 495.07 | 150915-40-5 | MFCD07368623 | 50MG
Apexbio Technology LLC VU 0364439 1246086-78-1 100mg
VU 0364439 (CAS 1246086-78-1) is a positive allosteric modulator (PAM) of the metabotropic glutamate receptor 4 (mGluR4) a member of the class C G protein-coupled receptor (GPCR) family involved in regulating glutamatergic neurotransmission In vitro studies have demonstrated that VU 0364439 enhances mGluR4 activity with an EC50 of 19 8 nM exhibiting greater maximal response and potency compared to the partially selective PAM ()-PHCCC Although its pharmacokinetic properties limit in vivo applications VU 0364439 serves as a valuable tool compound for investigating mGluR4 function and modulation in cellular assays
Medchemexpress LLC RS-102221 hydrochloride | 187397-18-8 | 98.0% | 649.08 g/mol | C27H32ClF3N4O7S | 50 MG
RS-102221 hydrochloride is a selective 5-HT2C receptor antagonist used in preclinical research to probe serotonin 5-HT2C-mediated signaling. It exhibits high affinity (Ki ≈ 10 nM) and strong selectivity versus related receptor subtypes and is supplied as a white to off-white solid for laboratory use.
- Selective 5-HT2C receptor antagonist with high affinity.
- Approximately 100-fold selectivity over 5-HT2A and 5-HT2B receptors.
- Supplied as a white to off-white solid suitable for research.
- Available in multiple small-scale sizes for laboratory experiments.
- Stable when stored under recommended conditions for powder and solutions.
Medchemexpress LLC (±)-1-(3,4-dichlorophenyl)acetyl-2-(1-pyrrolidinyl)methylpiperidine hydrochloride | 112282-24-3 | MFCD00672679 | >98.0% | 391.76 g·mol⁻¹ | C18H25Cl3N2O | 50 MG
BRL 52537 hydrochloride is a selective kappa-opioid receptor (KOR) agonist used in preclinical research. It exhibits potent KOR activity and has been reported to reduce ischemia-evoked nitric oxide production and attenuate early stroke-related damage. The compound is supplied as a solid for laboratory use and should be stored sealed and protected from moisture at recommended temperatures.
- Selective kappa-opioid receptor agonist.
- Potent KOR affinity with low nanomolar activity.
- Demonstrated neuroprotective effects in preclinical studies.
- Suitable for in vitro and in vivo research applications.
- Store sealed and protected from moisture under recommended conditions.
Medchemexpress LLC (R)-VU 6008667 | 2097818-14-7 | 99.8% | 438.85 | C24H17ClF2N2O2 | 1 ML
(R)-VU 6008667 is the (R)-enantiomer of VU 6008667 supplied for research use. It is described as the less active enantiomer and lacks M5 negative allosteric modulator activity (IC50 > 10 μM). Available as a solid or as a 10 mM solution in DMSO, the product includes purity, molecular, and storage information for laboratory applications.
- High purity (99.8%).
- Available as solid or 10 mM solution in DMSO.
- White to off-white solid appearance.
- Molecular weight 438.85 and formula C24H17ClF2N2O2.
- Storage: solid at 4°C under nitrogen; in solvent at -80°C (6 months) or -20°C (1 month).
- Intended for research use only; not for human or clinical use.
Medchemexpress LLC Piperoxan hydrochloride | 135-87-5 | 99.7% | 269.77 g·mol^-1 | C14H20ClNO2 | 100 MG
Piperoxan hydrochloride is a research chemical described as an α2 adrenoceptor antagonist and a first-generation antihistamine, provided for laboratory pharmacology and biochemical studies. Consult the product datasheet and safety data sheet for handling, storage, and purity specifications.
- High reported purity (about 99.7%).
- Available as a solid and as a 10 mM solution in DMSO.
- Suitable for pharmacology and biochemical research applications.
- CAS number provided for unambiguous identification.
- Manufacturer datasheet and SDS available for safety and handling.
Apexbio Technology LLC VU 0361737 1161205-04-4 100mg
VU 0361737 (CAS 1161205-04-4) is a selective brain-penetrant positive allosteric modulator of the metabotropic glutamate receptor 4 (mGluR4) It demonstrates high selectivity for mGluR4 over other mGluR subtypes with EC50 values of 240 nM for human and 110 nM for rat mGluR4 and shows minimal to no activity at mGluR1 mGluR2 mGluR3 mGluR6 and mGluR7 while exhibiting weak activity at mGluR5 and mGluR8 VU 0361737 crosses the blood-brain barrier and achieves significant brain exposure (brain plasma ratio of 4 1) with a short half-life (T1/2 20 min) following administration in rats This compound is utilized in studies exploring the modulation of basal ganglia neurotransmission and the pathophysiology of Parkinson s disease
Medchemexpress LLC TG 100572 hydrochloride | 867331-64-4 | 98.8% | 512.43 g/mol | C26H27Cl2N5O2 | 25 MG
TG 100572 Hydrochloride is the hydrochloride salt of TG 100572, a multi-targeted kinase inhibitor that potently inhibits several receptor tyrosine kinases and Src family kinases. Supplied as a pink-red solid for research use, the material is provided at high purity with specified storage recommendations to maintain stability and activity.
- Multi-targeted kinase inhibitor activity.
- Inhibits receptor tyrosine kinases and Src family kinases.
- High purity for research applications.
- Pink to red solid appearance.
- Stable when stored sealed and protected from moisture.
- Available as solid quantities and as a DMSO solution.
![Medchemexpress LLC 1H-indol-5-ol, 3-[4-(3,6-dihydro-4-phenyl-1(2H)-pyridinyl)butyl] hydrochloride | 108050-82-4 | 99.0% | 382.93 g/mol | C23H27ClN2O | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000243157.png-250.jpg)
Medchemexpress LLC 1H-indol-5-ol, 3-[4-(3,6-dihydro-4-phenyl-1(2H)-pyridinyl)butyl] hydrochloride | 108050-82-4 | 99.0% | 382.93 g/mol | C23H27ClN2O | 100 MG
Roxindole hydrochloride is the hydrochloride salt of roxindole (EMD 38362), a research tool compound investigated as a dopamine autoreceptor (D2-like) agonist and a 5-HT1A agonist that also inhibits serotonin uptake. It is used in vitro and in vivo to study dopaminergic and serotonergic signaling and to model psychiatric disorder pharmacology.
- High purity (99.0%) suitable for analytical and research use.
- Molecular weight 382.93 g/mol for accurate dosing calculations.
- Hydrochloride salt form to improve solubility in polar solvents.
- Appropriate for in vitro and in vivo pharmacology studies.
- Provided in milligram quantities to support small-scale experiments.
Medchemexpress LLC Zt 52656a hydrochloride | 115730-24-0 | MFCD00673899 | 100.0% | 390.87 g·mol⁻¹ | C19H26ClF3N2O | 100 MG
ZT 52656A hydrochloride is the hydrochloride salt of a selective kappa opioid receptor agonist used in research to investigate kappa-mediated analgesia and the prevention or alleviation of ocular pain. Supplied as a white to off-white solid for laboratory applications, it is intended for research use only and not for clinical or human use.
- Selective kappa opioid receptor agonist.
- High reported purity (99.98%).
- Molecular weight 390.87 g·mol⁻¹.
- White to off-white solid suitable for analytical and in vivo studies.
- Recommended storage: 4°C sealed; in solvent: -80°C up to 6 months, -20°C up to 1 month.
- Available in multiple package sizes, including 100 mg.
Medchemexpress LLC IACS-9571 hydrochloride | 2319611-93-1 | 98.3% | 679.22 g/mol | C32H43ClN4O8S | 1 ML
IACS-9571 hydrochloride is a potent, selective small-molecule inhibitor of the bromodomain proteins TRIM24 and BRPF1. It is used in biochemical and cellular research to probe bromodomain function, assess target engagement, and study downstream epigenetic regulation in vitro and in cells.
- Potent TRIM24 inhibition (IC50 = 8 nM) and strong BRPF1 binding (Kd = 14 nM).
- Demonstrates cellular activity (EC50 ≈ 50 nM).
- High purity suitable for research applications (>98% reported by supplier).
- Available as a 10 mM solution in DMSO (1 mL) and as solid quantities for custom preparation.
- Molecular formula C32H43ClN4O8S; molecular weight 679.22 g/mol.
Medchemexpress LLC CP 93129 dihydrochloride | 879089-64-2 | MFCD16875420 | 99.0% | 288.17 g/mol | C12H15Cl2N3O | 5 MG
CP 93129 dihydrochloride is the dihydrochloride salt of a potent and selective 5-HT1B receptor agonist used as a research reagent in neuroscience, including Parkinson's disease models. Supplied as an off-white to light yellow solid, it is intended for research and analytical applications.
- Potent, selective 5-HT1B receptor agonist for pharmacological studies.
- High purity (≈99.0%) suitable for analytical and in vitro work.
- CAS number 879089-64-2 for unambiguous identification.
- Molecular formula C12H15Cl2N3O; molecular weight ~288.17 g/mol.
- Recommended storage: 4°C; in solvent keep at -80°C (6 months) or -20°C (1 month).