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Filtered Search Results
Aobchem 2-Iodo-3-methoxynaphthalene | ≥97% | CAS 795278-91-0 | C11H9IO | 10g
2-Iodo-3-methoxynaphthalene | ≥97% | CAS 795278-91-0 | C11H9IO | 10g
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Medchemexpress LLC Rotigotine Hydrochloride | 125572-93-2 | 99.45% | C19H26ClNOS | 500 MG
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Rotigotine Hydrochloride is a full agonist of the dopamine receptor, a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor. It is suitable for research use only.
- Full agonist of dopamine receptor
- Partial agonist of the 5-HT1A receptor
- Antagonist of the α2B-adrenergic receptor
- Ki values of 0.71 nM for the dopamine D3 receptor
- Ki values of 4-15 nM for D2, D5, and D4 receptors
- Ki value of 83 nM for the dopamine D1 receptor
- White to off-white solid appearance
- Suitable for research use only
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Medchemexpress LLC Rotigotine Hydrochloride | 125572-93-2 | 99.5% | C19H26ClNOS | 1 ML
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Rotigotine Hydrochloride (N-0923 Hydrochloride) is a full agonist of the dopamine receptor, a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor. It has a Ki of 0.71 nM for the dopamine D3 receptor, 4-15 nM for the D2, D5, and D4 receptors, and 83 nM for the dopamine D1 receptor. It is intended for research use only.
- Full agonist of dopamine receptor
- Partial agonist of 5-HT1A receptor
- Antagonist of α2B-adrenergic receptor
- Ki of 0.71 nM for dopamine D3 receptor
- Ki of 4-15 nM for D2, D5, and D4 receptors
- Ki of 83 nM for dopamine D1 receptor
- For research use only
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Medchemexpress LLC Tolazoline hydrochloride | 59-97-2 | 99.93% | C10H13ClN2 | 1 G
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Tolazoline hydrochloride, also known as Imidaline hydrochloride, is an alpha-adrenergic receptor antagonist. It inhibits noradrenaline-induced cell contraction, modulates vascular resistance, increases arterial pressure, and reverses bradycardia and tachypnea. This compound is utilized in research for conditions such as erectile dysfunction, alpha2-adrenergic receptor agonist-related poisoning, and skin vascular diseases.
- Inhibits noradrenaline-induced cell contraction
- Modulates vascular resistance
- Increases arterial pressure
- Reverses bradycardia and tachypnea
- Supports research on erectile dysfunction
- Supports research on alpha2-adrenergic receptor agonist-related poisoning
- Supports research on skin vascular diseases
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Medchemexpress LLC (R)-1-(Naphthalen-1-yl)ethanamine Hydrochloride | 82572-04-1 | 99.8% | C₁₂H₁₄ClN | 10 G
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(R)-1-(Naphthalen-1-yl)ethanamine hydrochloride is a chemical compound commonly used as an intermediate in drug synthesis. It typically presents as a white to off-white solid and is available in high purity for various research and development applications.
- High purity: >99.8%
- Appearance: White to off-white solid
- Molecular formula: C₁₂H₁₄ClN
- Molecular weight: 207.70
- Recommended storage: 4°C, stored under nitrogen
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Medchemexpress LLC Etilefrine hydrochloride | 943-17-9 | 99.90% | C10H16ClNO2 | 1 G
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Etilefrine hydrochloride | 943-17-9 | 99.90% | C10H16ClNO2 | 1 G
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Medchemexpress LLC BI-4732 1 mg
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BI-4732 1MG
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Ambeed AMBEED
5000847976 5 7-DICHLORO-1 6-NAPHTH 100MG
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Ambeed AMBEED
5000848529 6-METHOXY-2-NAPHTHOIC A 10G
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![Medchemexpress LLC 1-(4-fluorophenyl)-N-[1-(2-methylsulfonylpyridin-4-yl)cyclopropyl]pyrazolo[3,4-c]pyridine-4-carboxamid | 1295298-26-8 | 98.9% | 10MM 1ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000232721.png-250.jpg)
Medchemexpress LLC 1-(4-fluorophenyl)-N-[1-(2-methylsulfonylpyridin-4-yl)cyclopropyl]pyrazolo[3,4-c]pyridine-4-carboxamid | 1295298-26-8 | 98.9% | 10MM 1ML
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1-(4-fluorophenyl)-N-[1-(2-methylsulfonylpyridin-4-yl)cyclopropyl]pyrazolo[3,4-c]pyridine-4-carboxamid | 1295298-26-8 | 98.9% | 10MM 1ML
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Medchemexpress LLC C13H9N5O5S2 | 883065-90-5 | MFCD01313575 | 99.9% | 379.37 g/mol | C13H9N5O5S2 | 100 MG
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BI-78D3 is a small-molecule substrate-competitive inhibitor of c-Jun N-terminal kinases (JNK) used as a research tool to probe JNK-dependent signaling. It inhibits JNK kinase activity with a reported IC50 of 280 nM and is supplied for in vitro research use only.
- Substrate-competitive JNK inhibitor (IC50 = 280 nM).
- Molecular formula C13H9N5O5S2; molecular weight 379.37 g/mol.
- High purity (99.85%) suitable for biochemical and cell-based assays.
- Soluble in DMSO; handle using standard laboratory safety procedures.
- For research use only; not for human or veterinary applications.
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Medchemexpress LLC Cloricromen hydrochl 10mM 1mL | 74697-28-2 | 1 ML
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Cloricromen hydrochloride is a small-molecule platelet aggregation inhibitor supplied as a solid or as a ready-to-use solution in DMSO. It is used in in vitro platelet aggregation assays and experimental thrombosis models for research applications.
- Platelet aggregation inhibitor for research use.
- Available as solid and as 10 mM, 1 mL solution in DMSO.
- High reported purity (99.8%).
- Soluble in DMSO at 100 mg/mL; may require ultrasonic treatment.
- Store powder at 4 °C (up to 2 years) or -20 °C (up to 3 years); store solutions at -20 °C (1 month) or -80 °C (6 months).
- Molecular weight 432.34 g/mol; formula C20H27Cl2NO5.
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Medchemexpress LLC Cloricromen hydrochl 100mg | 74697-28-2 | 100 MG
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Cloricromen hydrochloride is the hydrochloride salt of cloricromen, a platelet aggregation inhibitor used in research to inhibit platelet aggregation in humans and in experimental thrombosis.
- Platelet aggregation inhibitor used in thrombosis research.
- Reported purity 99.82%.
- Molecular formula C20H27Cl2NO5; molecular weight 432.34.
- White to off-white solid appearance.
- Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
- Available in multiple quantities including 100 MG for dosing flexibility.
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Aobchem 1-(4-(Methoxymethyl)naphthalen-1-yl)ethanone | 95% | CAS 79996-79-5 | C14H14O2 | 1g
1-(4-(Methoxymethyl)naphthalen-1-yl)ethanone | 95% | CAS 79996-79-5 | C14H14O2 | 1g
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Medchemexpress LLC Fananserin | 127625-29-0 | MFCD00866648 | 100.0% | 425.52 g·mol⁻¹ | C23H24FN3O2S | 100 MG
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Fananserin is a potent, selective antagonist of 5-hydroxytryptamine 2 (5-HT2) receptors used as a research tool in pharmacology. It is reported to be orally bioavailable and is supplied as solid material or as a DMSO solution for flexible experimental use.
- Selective 5-HT2 receptor antagonist.
- Suitable for in vitro and in vivo pharmacology studies.
- High reported purity for analytical applications.
- Available in multiple pack sizes, including a 100 mg solid pack.
- Molecular formula C23H24FN3O2S and molecular weight 425.52 g·mol⁻¹.
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