Thiophenes

Aobchem 5-(1-Naphthalenyl)-2-thiophenecarboxylic acid | ≥95% | CAS 58256-10-3 | C15H10O2S | 250mg

5-(1-Naphthalenyl)-2-thiophenecarboxylic acid | ≥95% | CAS 58256-10-3 | C15H10O2S | 250mg

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Aobchem (2-Bromo-6-chloro-3-(methylthio)phenyl)boronic acid | 95% | C7H7BBrClO2S | 250mg

(2-Bromo-6-chloro-3-(methylthio)phenyl)boronic acid | 95% | C7H7BBrClO2S | 250mg

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Aobchem 4-Butyl-2-(methylthio)thiophene | 95% | C9H14S2 | 250mg

4-Butyl-2-(methylthio)thiophene | 95% | C9H14S2 | 250mg

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Aobchem 4-Chloro-3-fluoro-2-(methylthio)pyridine | 95% | C6H5ClFNS | 250mg

4-Chloro-3-fluoro-2-(methylthio)pyridine | 95% | C6H5ClFNS | 250mg

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Aobchem (4-Bromo-2-fluoro-3-(methylthio)phenyl)boronic acid | 97% | C7H7BBrFO2S | 250mg

(4-Bromo-2-fluoro-3-(methylthio)phenyl)boronic acid | 97% | C7H7BBrFO2S | 250mg

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Aobchem 2-Fluoro-4-formyl-3-(methylthio)benzoic acid | 97% | CAS 2755723-96-5 | C9H7FO3S | 500mg

2-Fluoro-4-formyl-3-(methylthio)benzoic acid | 97% | CAS 2755723-96-5 | C9H7FO3S | 500mg

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Aobchem (4-Chlorophenyl)(thiophen-2-yl)methanol | 97% | CAS 40310-35-8 | C11H9ClOS | 1g

(4-Chlorophenyl)(thiophen-2-yl)methanol | 97% | CAS 40310-35-8 | C11H9ClOS | 1g

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Aobchem 3-Chloro-4-methyl-2-(methylthio)benzoic acid | 97% | CAS 2764729-27-1 | C9H9ClO2S | 1g

3-Chloro-4-methyl-2-(methylthio)benzoic acid | 97% | CAS 2764729-27-1 | C9H9ClO2S | 1g

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Aobchem 1-(5-(Pyridin-2-yl)thiophen-2-yl)propan-1-one | 95% | C12H11NOS | 1g

1-(5-(Pyridin-2-yl)thiophen-2-yl)propan-1-one | 95% | C12H11NOS | 1g

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Aobchem 4-Ethoxy-3-fluoro-2-(methylthio)benzaldehyde | 97% | CAS 2901066-85-9 | C10H11FO2S | 1g

4-Ethoxy-3-fluoro-2-(methylthio)benzaldehyde | 97% | CAS 2901066-85-9 | C10H11FO2S | 1g

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Aobchem Ethyl 2-(2-fluoro-5-(methylthio)-3-(trifluoromethyl)phenyl)-2-oxoacetate | 95% | C12H10F4O3S | 250mg

Ethyl 2-(2-fluoro-5-(methylthio)-3-(trifluoromethyl)phenyl)-2-oxoacetate | 95% | C12H10F4O3S | 250mg

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Apexbio Technology LLC 4-Methylhistamine dihydrochloride 36376-47-3 5mg

4-Methylhistamine dihydrochloride (CAS 36376-47-3) is a selective agonist for the histamine H4 receptor (H4R) displaying a pEC50 of 7 4 0 1 at human H4R It exhibits over 100-fold selectivity for H4R relative to H3R and H2R and over 100 000-fold compared to H1R While affinity for human H4R is moderate it binds rat and mouse H4R with higher affinity (Ki values of 73 nM and 55 nM respectively) In in vivo models 4-Methylhistamine dihydrochloride modulates inflammatory signaling elevating TNF- and NF- B expression via JAK/STAT pathways in response to LPS-induced joint inflammation It serves as a valuable tool in studies of H4R-mediated immune regulation and inflammatory mechanisms

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Medchemexpress LLC Vofopitant dihydrochloride | 168266-51-1 | 99.6% | 1 ML

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Vofopitant dihydrochloride is a selective tachykinin neurokinin 1 (NK1) receptor antagonist supplied as a research reagent. It is available as a solid or as a 10 mM solution in DMSO for in vitro pharmacology and biochemical assays. Not for human or diagnostic use.

• Selective NK1 receptor antagonist for receptor binding and functional assays.
• Available as solid or 10 mM solution in DMSO for convenient dosing.
• High chemical purity suitable for preclinical research.
• Storable at 4°C (solid) or long-term frozen in solvent to preserve stability.

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Medchemexpress LLC 1,4-pentanediamine, N4-(6-chloro-2-methoxy-9-acridinyl)-N1,N1-diethyl-, dihydrochloride | 56100-42-6 | 98.4% | 472.88 | 1 ML

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l-Atabrine dihydrochloride is a less active enantiomer of quinacrine that displays antiprion activity. It is a light yellow to yellow solid with a purity of 98.35%.

• Displays antiprion activity.
• Intended for research use only.
• Soluble in H₂O and DMSO.
• Ships at room temperature.
• Store at 4°C, sealed, away from moisture.
• When in solvent, store at -80°C for 6 months or -20°C for 1 month.

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Apexbio Technology LLC Pramipexole dihydrochloride 104632-25-9 20mg

Pramipexole dihydrochloride is a small-molecule agonist targeting dopamine receptors exhibiting selective affinity toward the D3 dopamine receptor subtype and lower affinity for the D2L D2S and D4 subtypes It is designed to stimulate dopamine receptor-mediated signaling thereby modulating dopaminergic pathways involved in motor function Pramipexole dihydrochloride exerts its biological activity primarily through dopamine receptor agonism and also demonstrates receptor-independent neuroprotective effects by attenuating mitochondrial reactive oxygen species (ROS) production and decreasing apoptosis-related signaling cascades Based on these pharmacological properties pramipexole dihydrochloride holds research potential in exploring dopaminergic system involvement and neuroprotective mechanisms relevant to neurodegenerative conditions such as Parkinson s disease and restless legs syndrome

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