Rome, Zachary et al. published their patent in 2022 |CAS: 1428327-31-4

The Article related to antipurinergic agent nervous system disorder treatment, Pharmacology: Effects Of Nervous System- and Behavior-Affecting Drugs and Neuromuscular Agents and other aspects.Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide

On April 28, 2022, Rome, Zachary; Derby, Michael published a patent.Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide The title of the patent was Administration of antipurinergic compositions for treating nervous system disorders. And the patent contained the following:

The present invention provides methods and compositions for treating nervous system disorders such as cognitive, social, or behavioral disabilities, and neurodevelopmental disorders. More specifically, the present invention demonstrates that administration of antipurinergic agents such as berberine, emodin, suramin, tangeretin, A-438079, A-839977, A-804598, JNJ-47965567, and KN-62 are effective to ameliorate or provide an improvement in one or more of the symptoms or manifestations associated with these disabilities and disorders. The experimental process involved the reaction of N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide(cas: 1428327-31-4).Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide

The Article related to antipurinergic agent nervous system disorder treatment, Pharmacology: Effects Of Nervous System- and Behavior-Affecting Drugs and Neuromuscular Agents and other aspects.Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Platania, Chiara Bianca Maria et al. published their research in Biochemical Pharmacology (Amsterdam, Netherlands) in 2017 |CAS: 1428327-31-4

The Article related to p2x7 receptor antagonism diabetic retinopathy, diabetic retinopathy, il-1β, inflammation, molecular modeling, p2x7 receptor, pericytes, Pharmacology: Effects Of Agents For Treating Metabolic and Endocrine Disorders and other aspects.COA of Formula: C28H32N4O2S

On August 15, 2017, Platania, Chiara Bianca Maria; Giurdanella, Giovanni; Di Paola, Luisa; Leggio, Gian Marco; Drago, Filippo; Salomone, Salvatore; Bucolo, Claudio published an article.COA of Formula: C28H32N4O2S The title of the article was P2X7 receptor antagonism: Implications in diabetic retinopathy. And the article contained the following:

Diabetic retinopathy (DR) is the most frequent complication of diabetes and one of leading causes of blindness worldwide. Early phases of DR are characterized by retinal pericyte loss mainly related to concurrent inflammatory process. Recently, an important link between P2X7 receptor (P2X7R) and inflammation has been demonstrated indicating this receptor as potential pharmacol. target in DR. Here the authors first carried out an in silico mol. modeling study in order to characterize the allosteric pocket in P2X7R, and identify a suitable P2X7R antagonist through mol. docking. JNJ47965567 was identified as the hit compound in docking calculations, as well as for its absorption, distribution, metabolism and excretion (ADME) profile. As an in vitro model of early diabetic retinopathy, human retinal pericytes were exposed to high glucose (25 mM, 48 h) that caused a significant (p < 0.05) release of IL-1β and LDH. The block of P2X7R by JNJ47965567 significantly (p < 0.05) reverted the damage elicited by high glucose, detected as IL-1β and LDH release. Overall, the findings suggest that the P2X7R represents an attractive pharmacol. target to manage the early phase of diabetic retinopathy, and the compound JNJ47965567 is a good template to discover other P2X7R selective antagonists. The experimental process involved the reaction of N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide(cas: 1428327-31-4).COA of Formula: C28H32N4O2S

The Article related to p2x7 receptor antagonism diabetic retinopathy, diabetic retinopathy, il-1β, inflammation, molecular modeling, p2x7 receptor, pericytes, Pharmacology: Effects Of Agents For Treating Metabolic and Endocrine Disorders and other aspects.COA of Formula: C28H32N4O2S

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Garrosa-Jimenez, Javier et al. published their research in Neuroscience Letters in 2021 |CAS: 1428327-31-4

The Article related to human mdd calcium inflammatory marker purinergic stimulation monocyte, calcium homeostasis, inflammation, major depression disorder, p2x7 receptors, Mammalian Pathological Biochemistry: Nervous System and Psychiatric Diseases and other aspects.Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide

On November 20, 2021, Garrosa-Jimenez, Javier; Sanchez Carro, Yolanda; Ovejero-Benito, Maria C.; del Sastre, Eric; Garcia, Antonio G.; Lopez, Manuela G.; Lopez-Garcia, Pilar; Cano-Abad, Maria F. published an article.Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide The title of the article was Intracellular calcium and inflammatory markers, mediated by purinergic stimulation, are differentially regulated in monocytes of patients with major depressive disorder. And the article contained the following:

The P2X7 receptor (P2X7R) is a ligand-gated ion channel that is being recognized as a major player in neuropsychiatric disorders such as Major Depressive Disorder (MDD). P2X7R activation is triggered by high extracellular ATP concentrations, leading to channel opening and inducing an increase in cytosolic calcium concentration ([Ca2+]c), that activates the inflammatory pathway. Those receptors are expressed not only in CNS cells but also in peripheral blood cells, where they are activated in response to inflammatory mols. such as bacterial lipopolysaccharide (LPS). LPS induced-tissue damage promotes an elevation of extracellular ATP, triggering the NRLP3-inflammasome assembly and activation that, sequentially, induces caspase-1 cleavage and IL-1β processing and secretion. In this context, we attempt to understand the role of P2X7R in [Ca2+]c homeostasis regulation, inflammasome expression and its pharmacol. modulation in MDD. For this purpose, monocytes were isolated from peripheral blood of MDD patients and [Ca2+]c was monitored with the intracellular probe Fura-2. Our results point out to P2X7R as the responsible of the Ca2+ imbalance, as well as TNF-α-dependent activation of caspase-1 in MDD patients. In addition, P2X7R blockade with its specific antagonist, JNJ-47965567, reduces the Ca2+ entry upon Bz-ATP exposure. Altogether, our results point that MDD patients have both, Ca2+ homeostasis alteration and an inflammatory status, which promote an independent-inflammasome activation of caspase-1. Therefore, we propose the pharmacol. modulation of P2X7R as a therapeutic approach against MDD symptoms. The experimental process involved the reaction of N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide(cas: 1428327-31-4).Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide

The Article related to human mdd calcium inflammatory marker purinergic stimulation monocyte, calcium homeostasis, inflammation, major depression disorder, p2x7 receptors, Mammalian Pathological Biochemistry: Nervous System and Psychiatric Diseases and other aspects.Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Zhao, Ya-Fei et al. published their research in International Journal of Molecular Sciences in 2022 |CAS: 1428327-31-4

The Article related to acute stress depression astrocyte microglia receptor rodent hippocampus, p2x7 receptor, extracellular atp, hippocampus, major depression, mouse, rat, Mammalian Pathological Biochemistry: Nervous System and Psychiatric Diseases and other aspects.Electric Literature of 1428327-31-4

Zhao, Ya-Fei; Ren, Wen-Jing; Zhang, Ying; He, Jin-Rong; Yin, Hai-Yan; Liao, Yang; Rubini, Patrizia; Deussing, Jan M.; Verkhratsky, Alexei; Yuan, Zeng-Qiang; Illes, Peter; Tang, Yong published an article in 2022, the title of the article was High, in Contrast to Low Levels of Acute Stress Induce Depressive-like Behavior by Involving Astrocytic, in Addition to Microglial P2X7 Receptors in the Rodent Hippocampus.Electric Literature of 1428327-31-4 And the article contains the following content:

Extracellular ATP (ATP) in the brain is suggested to be an etiol. factor of major depressive disorder (MDD). It has been assumed that stress-released ATP stimulates P2X7 receptors (Rs) at the microglia, thereby causing neuroinflammation; however, other central nervous system (CNS) cell types such as astrocytes also possess P2X7Rs. In order to elucidate the possible involvement of the MDD-relevant hippocampal astrocytes in the development of a depressive-like state, we used various behavioral tests (tail suspension test [TST], forced swim test [FST], restraint stress, inescapable foot shock, unpredictable chronic mild stress [UCMS]), as well as fluorescence immunohistochem., and patch-clamp electrophysiol. in wild-type (WT) and genetically manipulated rodents. The TST and FST resulted in learned helplessness manifested as a prolongation of the immobility time, while inescapable foot shock caused lower sucrose consumption as a sign of anhedonia. We confirmed the participation of P2X7Rs in the development of the depressive-like behaviors in all forms of acute (TST, FST, foot shock) and chronic stress (UCMS) in the rodent models used. Further, pharmacol. agonists and antagonists acted in a different manner in rats and mice due to their diverse potencies at the resp. receptor orthologs. In hippocampal slices of mice and rats, only foot shock increased the current responses to locally applied dibenzoyl-ATP (Bz-ATP) in CA1 astrocytes; in contrast, TST and restraint depressed these responses. Following stressful stimuli, immunohistochem. demonstrated an increased co-localization of P2X7Rs with a microglial marker, but no change in co-localization with an astroglial marker. Pharmacol. damage to the microglia and astroglia has proven the significance of the microglia for mediating all types of depression-like behavioral reactions, while the astroglia participated only in reactions induced by strong stressors, such as foot shock. Because, in addition to acute stressors, their chronic counterparts induce a depressive-like state in rodents via P2X7R activation, we suggest that our data may have relevance for the etiol. of MDD in humans. The experimental process involved the reaction of N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide(cas: 1428327-31-4).Electric Literature of 1428327-31-4

The Article related to acute stress depression astrocyte microglia receptor rodent hippocampus, p2x7 receptor, extracellular atp, hippocampus, major depression, mouse, rat, Mammalian Pathological Biochemistry: Nervous System and Psychiatric Diseases and other aspects.Electric Literature of 1428327-31-4

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Fischer, Wolfgang et al. published their research in PLoS One in 2016 |CAS: 1428327-31-4

The Article related to seizure p2x7 receptor antagonist afc5128 jnj47965567, Pharmacology: Effects Of Nervous System- and Behavior-Affecting Drugs and Neuromuscular Agents and other aspects.Electric Literature of 1428327-31-4

Fischer, Wolfgang; Franke, Heike; Kruegel, Ute; Mueller, Heiko; Dinkel, Klaus; Lord, Brian; Letavic, Michael A.; Henshall, David C.; Engel, Tobias published an article in 2016, the title of the article was Critical evaluation of p2x7 receptor antagonists in selected seizure models.Electric Literature of 1428327-31-4 And the article contains the following content:

The ATP-gated P2X7 receptor (P2X7R) is a non-selective cation channel which senses high extracellular ATP concentrations and has been suggested as a target for the treatment of neuroinflammation and neurodegenerative diseases. The use of P2X7R antagonists may therefore be a viable approach for treating CNS pathologies, including epileptic disorders. Recent studies showed anticonvulsant potential of P2X7R antagonists in certain animal models. To extend this work, we tested three CNS-permeable P2X7R blocker (Brilliant Blue G, AFC-5128, JNJ-47965567) and a natural compound derivative (tanshinone IIA sulfonate) in four well-characterized animal seizure models. In the maximal electroshock seizure threshold test and the pentylenetetrazol (PTZ) seizure threshold test in mice, none of the four compounds demonstrated anticonvulsant effects when given alone. Notably, in combination with carbamazepine, both AFC-5128 and JNJ-47965567 increased the threshold in the maximal electroshock seizure test. In the PTZ-kindling model in rats, useful for testing antiepileptogenic activities, Brilliant Blue G and tanshinone exhibited a moderate retarding effect, whereas the potent P2X7R blocker AFC-5128 and JNJ-47965567 showed a significant and long-lasting delay in kindling development. In fully kindled rats, the investigated compounds revealed modest effects to reduce the mean seizure stage. Furthermore, AFC- 5128- and JNJ-47965567-treated animals displayed strongly reduced Iba 1 and GFAP immunoreactivity in the hippocampal CA3 region. In summary, our results show that P2X7R antagonists possess no remarkable anticonvulsant effects in the used acute screening tests, but can attenuate chem.-induced kindling. Further studies would be of interest to support the concept that P2X7R signalling plays a crucial role in the pathogenesis of epileptic disorders. The experimental process involved the reaction of N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide(cas: 1428327-31-4).Electric Literature of 1428327-31-4

The Article related to seizure p2x7 receptor antagonist afc5128 jnj47965567, Pharmacology: Effects Of Nervous System- and Behavior-Affecting Drugs and Neuromuscular Agents and other aspects.Electric Literature of 1428327-31-4

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Rome, Zachary et al. published their patent in 2022 |CAS: 1428327-31-4

The Article related to antipurinergic agent nervous system disorder treatment, Pharmacology: Effects Of Nervous System- and Behavior-Affecting Drugs and Neuromuscular Agents and other aspects.Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide

On April 28, 2022, Rome, Zachary; Derby, Michael published a patent.Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide The title of the patent was Administration of antipurinergic compositions for treating nervous system disorders. And the patent contained the following:

The present invention provides methods and compositions for treating nervous system disorders such as cognitive, social, or behavioral disabilities, and neurodevelopmental disorders. More specifically, the present invention demonstrates that administration of antipurinergic agents such as berberine, emodin, suramin, tangeretin, A-438079, A-839977, A-804598, JNJ-47965567, and KN-62 are effective to ameliorate or provide an improvement in one or more of the symptoms or manifestations associated with these disabilities and disorders. The experimental process involved the reaction of N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide(cas: 1428327-31-4).Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide

The Article related to antipurinergic agent nervous system disorder treatment, Pharmacology: Effects Of Nervous System- and Behavior-Affecting Drugs and Neuromuscular Agents and other aspects.Recommanded Product: N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Goldman, Steven A. et al. published their patent in 2019 |CAS: 1428327-31-4

The Article related to neuroprotectant antihuntington drug huntington disease treatment, Pharmacology: Effects Of Nervous System- and Behavior-Affecting Drugs and Neuromuscular Agents and other aspects.Category: piperazines

On December 26, 2019, Goldman, Steven A.; Osipovitch, Mikhail published a patent.Category: piperazines The title of the patent was Methods of treating or inhibiting onset of Huntington’s disease with gene modulatory compounds. And the patent contained the following:

The disclosure herein relates generally to a method of treating or inhibiting onset of Huntington’s disease. This method involves selecting a subject having or at risk of having Huntington’s disease and administering to the subject one or modulators of one or more genes as described herein, or proteins encoded therefrom, under conditions effective to treat or inhibit onset of Huntington’s disease in the subject. The exemplary compounds of the invention include e.g. 2-amino-4-(3,4-(methylenedioxy)benzylamino)-6-(3-methoxyphenyl)pyrimidine (2-AMBMP), curcumin, simvastatin, opicinumab, GSK-249320, sodium lauryl sulfate, repaglinide, altiratinib. The experimental process involved the reaction of N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide(cas: 1428327-31-4).Category: piperazines

The Article related to neuroprotectant antihuntington drug huntington disease treatment, Pharmacology: Effects Of Nervous System- and Behavior-Affecting Drugs and Neuromuscular Agents and other aspects.Category: piperazines

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Hopper, Allen T. et al. published their research in Journal of Medicinal Chemistry in 2021 |CAS: 1428327-31-4

The Article related to orally bioavailable cns penetrant p2x7 receptor antagonist probe, Pharmacology: Effects Of Nervous System- and Behavior-Affecting Drugs and Neuromuscular Agents and other aspects.Related Products of 1428327-31-4

On April 22, 2021, Hopper, Allen T.; Juhl, Martin; Hornberg, Jorrit; Badolo, Lassina; Kilburn, John Paul; Thougaard, Annemette; Smagin, Gennady; Song, Dekun; Calice, Londye; Menon, Veena; Dale, Elena; Zhang, Hong; Cajina, Manuel; Nattini, Megan E.; Gandhi, Adarsh; Grenon, Michel; Jones, Ken; Khayrullina, Tanzilya; Chandrasena, Gamini; Thomsen, Christian; Zorn, Stevin H.; Brodbeck, Robb; Poda, Suresh Babu; Staal, Roland; Moller, Thomas published an article.Related Products of 1428327-31-4 The title of the article was Synthesis and Characterization of the Novel Rodent-Active and CNS-Penetrant P2X7 Receptor Antagonist Lu AF27139. And the article contained the following:

There remains an insufficient number of P2X7 receptor antagonists with adequate rodent potency, CNS permeability, and pharmacokinetic properties from which to evaluate CNS disease hypotheses preclinically. Herein, we describe the mol. pharmacol., safety, pharmacokinetics, and functional CNS target engagement of Lu AF27139, a novel rodent-active and CNS-penetrant P2X7 receptor antagonist. Lu AF27139 is highly selective and potent against rat, mouse, and human forms of the receptors. The rat pharmacokinetic profile is favorable with high oral bioavailability, modest clearance (0.79 L/(h kg)), and good CNS permeability. In vivo mouse CNS microdialysis studies of lipopolysaccharide (LPS)-primed and 2′(3′)-O-(benzoylbenzoyl)adenosine-5′-triphosphate (BzATP)-induced IL-1β release demonstrate functional CNS target engagement. Importantly, Lu AF27139 was without effect in standard in vitro and in vivo toxicity studies. Based on these properties, we believe Lu AF27139 will be a valuable tool for probing the role of the P2X7 receptor in rodent models of CNS diseases. The experimental process involved the reaction of N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide(cas: 1428327-31-4).Related Products of 1428327-31-4

The Article related to orally bioavailable cns penetrant p2x7 receptor antagonist probe, Pharmacology: Effects Of Nervous System- and Behavior-Affecting Drugs and Neuromuscular Agents and other aspects.Related Products of 1428327-31-4

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Letavic, Michael A. et al. published their research in ACS Medicinal Chemistry Letters in 2013 |CAS: 1428327-31-4

The Article related to brain penetrating p2x7 antagonist nicotinamide isoquinolinecarboxamide derivative, p2x7, depression, neuro-inflammation, Heterocyclic Compounds (More Than One Hetero Atom): Pyrazines and Quinoxalines (Including Piperazines) and other aspects.Related Products of 1428327-31-4

On April 11, 2013, Letavic, Michael A.; Lord, Brian; Bischoff, Francois; Hawryluk, Natalie A.; Pieters, Serge; Rech, Jason C.; Sales, Zachary; Velter, Adriana I.; Ao, Hong; Bonaventure, Pascal; Contreras, Victor; Jiang, Xiaohui; Morton, Kirsten L.; Scott, Brian; Wang, Qi; Wickenden, Alan D.; Carruthers, Nicholas I.; Bhattacharya, Anindya published an article.Related Products of 1428327-31-4 The title of the article was Synthesis and Pharmacological Characterization of Two Novel, Brain Penetrating P2X7 Antagonists. And the article contained the following:

The synthesis and preclin. characterization of two novel, brain penetrating P2X7 compounds will be described. Both compounds are shown to be high potency P2X7 antagonists in human, rat, and mouse cell lines and both were shown to have high brain concentrations and robust receptor occupancy in rat. Compound I is of particular interest as a probe compound for the preclin. assessment of P2X7 blockade in animal models of neuro-inflammation. The experimental process involved the reaction of N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide(cas: 1428327-31-4).Related Products of 1428327-31-4

The Article related to brain penetrating p2x7 antagonist nicotinamide isoquinolinecarboxamide derivative, p2x7, depression, neuro-inflammation, Heterocyclic Compounds (More Than One Hetero Atom): Pyrazines and Quinoxalines (Including Piperazines) and other aspects.Related Products of 1428327-31-4

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Letavic, Michael A. et al. published their research in ACS Medicinal Chemistry Letters in 2013 |CAS: 1428327-31-4

The Article related to brain penetrating p2x7 antagonist nicotinamide isoquinolinecarboxamide derivative, p2x7, depression, neuro-inflammation, Heterocyclic Compounds (More Than One Hetero Atom): Pyrazines and Quinoxalines (Including Piperazines) and other aspects.Related Products of 1428327-31-4

On April 11, 2013, Letavic, Michael A.; Lord, Brian; Bischoff, Francois; Hawryluk, Natalie A.; Pieters, Serge; Rech, Jason C.; Sales, Zachary; Velter, Adriana I.; Ao, Hong; Bonaventure, Pascal; Contreras, Victor; Jiang, Xiaohui; Morton, Kirsten L.; Scott, Brian; Wang, Qi; Wickenden, Alan D.; Carruthers, Nicholas I.; Bhattacharya, Anindya published an article.Related Products of 1428327-31-4 The title of the article was Synthesis and Pharmacological Characterization of Two Novel, Brain Penetrating P2X7 Antagonists. And the article contained the following:

The synthesis and preclin. characterization of two novel, brain penetrating P2X7 compounds will be described. Both compounds are shown to be high potency P2X7 antagonists in human, rat, and mouse cell lines and both were shown to have high brain concentrations and robust receptor occupancy in rat. Compound I is of particular interest as a probe compound for the preclin. assessment of P2X7 blockade in animal models of neuro-inflammation. The experimental process involved the reaction of N-((4-(4-Phenylpiperazin-1-yl)tetrahydro-2H-pyran-4-yl)methyl)-2-(phenylthio)nicotinamide(cas: 1428327-31-4).Related Products of 1428327-31-4

The Article related to brain penetrating p2x7 antagonist nicotinamide isoquinolinecarboxamide derivative, p2x7, depression, neuro-inflammation, Heterocyclic Compounds (More Than One Hetero Atom): Pyrazines and Quinoxalines (Including Piperazines) and other aspects.Related Products of 1428327-31-4

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics