Thiophenes
eMolecules 6165-68-0 | Thiophen-2-ylboronic acid | Ambeed | MFCD00151850 | 127.950 | C4H5BO2S | 98.000 | OB(O)c1cccs1 | 5g | 552669675
Thiophen-2-ylboronic acid | Ambeed | 6165-68-0 | MFCD00151850 | 127.950 | C4H5BO2S | 98.000 | OB(O)c1cccs1 | 5g | 552669675
Medchemexpress LLC 2-Methylthiophene | 554-14-3 | 99.94% | 98.16 | 5 G
2-Methylthiophene is an intermediate used in the synthesis of aromatic sulfur compounds. It is for research use only and not sold to patients. It appears as a colorless to light yellow liquid.
- Purity: 99.94%
- Available in various sizes
- Documentation includes Data Sheet, COA, SDS, and Handling Instructions
- Soluble in DMSO for in vitro use
- Storage at 4°C under nitrogen
eMolecules 36052-27-4 | 3-Amino-pyridine-2-carboxylic acid methyl ester | J & W PharmLab LLC | MFCD08695602 | 152.153 | C7H8N2O2 | 96.000 | COC(=O)c1ncccc1N | 1g | 525324906
3-Amino-pyridine-2-carboxylic acid methyl ester | J & W PharmLab LLC | 36052-27-4 | MFCD08695602 | 152.153 | C7H8N2O2 | 96.000 | COC(=O)c1ncccc1N | 1g | 525324906
Apexbio Technology LLC Clozapine N-oxide(CNO) dihydrochloride(Synonyms: CNO dihydrochloride, Clozapine N-oxide hydrochloride,Clozapine N-oxide dihydrochloride), 50mg, CAS: 2250025-93-3.
Clozapine N-oxide (CNO) dihydrochloride (CAS 2250025-93-3) is a synthetic metabolite derived from clozapine commonly utilized as an agonist for designer receptors exclusively activated by designer drugs (DREADDs) In neuroscience research CNO selectively binds and activates engineered muscarinic receptors particularly hM3Dq and hM4Di thereby influencing neuronal signaling upon penetrating the blood-brain barrier Due to its specificity CNO dihydrochloride serves as a valuable tool for dissecting neuronal circuits and elucidating their functional roles in behavioral studies
Apexbio Technology LLC Cyclizine 2HCl 5897-18-7 50mg
Cyclizine 2HCl (CAS 5897-18-7) is a synthetic piperazine derivative that functions as an antagonist at histamine H1 receptors By inhibiting H1 receptor-mediated signaling Cyclizine 2HCl effectively suppresses histamine-induced physiological responses including those involved in allergic reactions and motion sickness This compound is widely utilized in biomedical research to investigate histaminergic pathways allergic mechanisms and the pharmacological modulation of H1 receptor activity Its antagonist properties make it valuable for studies examining the mechanistic basis of histamine-mediated processes and for evaluating novel anti-allergic therapeutics
Medchemexpress LLC Ro 10-5824 dihydrochloride | 189744-94-3 | 99.9% | 353.29 g/mol | C17H22Cl2N4 | 25 MG
Ro 10-5824 dihydrochloride is a selective dopamine D4 receptor partial agonist used in pharmacology and neuroscience research. It binds D4 receptors with high affinity and is supplied as a white to off-white solid for laboratory use.
- High purity (99.9%) for research applications.
- Selective D4 receptor partial agonist with Ki ≈ 5.2 nM.
- Molecular formula C17H22Cl2N4 and molecular weight 353.29 g/mol.
- Available in small milligram quantities for experimental studies.
- White to off-white solid suitable for handling and formulation.
Medchemexpress LLC HOIPIN-1 | 2470242-33-0 | 99.6% | 304.28 | 10 MG
HOIPIN-1 (JTP-0819958) is a selective linear ubiquitin chain assembly complex (LUBAC) inhibitor with an IC50 of 2.8 μM. It suppresses LUBAC-mediated NF-κB activation in vitro and is intended for research use only.
- Selectively inhibits LUBAC-mediated ubiquitination
- Suppresses NF-κB activation in vitro
- Exhibits increased inhibitory activity with longer preincubation times
- Inhibits expression of NF-κB target genes
eMolecules 96803-30-4 | 2-(1-benzothiophen-5-yl)ethan-1-ol | MFCD08062283 | 1g
Pharmablock | 2-(1-benzothiophen-5-yl)ethan-1-ol | 1g | 551245950 | PBLJ1804 | 96803-30-4 | MFCD08062283 | 178.250 | C10H10OS
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Medchemexpress LLC Seltorexant | 1293281-49-8 | 99.8% | 407.44 | 10 MG
Seltorexant (JNJ-42847922) is an orally active, high-affinity, and selective orexin-2 receptor (OX2R) antagonist. It crosses the blood-brain barrier and quickly occupies OX2R binding sites in the rat brain.
- Orally active
- High-affinity and selective orexin-2 receptor (OX2R) antagonist
- Crosses the blood-brain barrier
- Quickly occupies OX2R binding sites in the rat brain
- Dose-dependently induces and prolongs sleep in male Sprague-Dawley rats
- Sleep-promoting effects maintained upon 7-day repeated dosing in rats
Aobchem 3 5-Dibromo-2-thiophenecarboxaldehyde | ≥95% | CAS 23688-07-5 | C5H2Br2OS | 250mg
3 5-Dibromo-2-thiophenecarboxaldehyde | ≥95% | CAS 23688-07-5 | C5H2Br2OS | 250mg
Aobchem 3 5-Dibromo-2-thiophenecarboxaldehyde | ≥95% | CAS 23688-07-5 | C5H2Br2OS | 1g
3 5-Dibromo-2-thiophenecarboxaldehyde | ≥95% | CAS 23688-07-5 | C5H2Br2OS | 1g