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Filtered Search Results
Alkali Scientific LM Sieve Agarose, 500 G
Low Melting Sieve Agarose is a specialized agarose designed for DNA gel electrophoresis. It has a lower melting point compared to standard agarose, making it ideal for the separation of DNA fragments at lower temperatures. This 500g package is used for preparing gels that are ideal for applications requiring low melting points, such as DNA fragment separation, electrophoresis, and enzymatic reactions. The agarose is pre-formulated for easy use in laboratories that routinely conduct gel electrophoresis for DNA analysis. It offers reliable resolution, sharp band separation, and high sensitivity, ensuring reproducibility in molecular biology and genetic research applications.
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Medchemexpress LLC Chloridazon 25g
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Chloridazon is a herbicide with an LD50 value of 76 6 ppm at genotoxicity assay[1]
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Medchemexpress LLC Propafenone hydrochloride | 34183-22-7 | 98.5% | 377.90 | 500 MG
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Propafenone hydrochloride is an anti-arrhythmic medication used to treat illnesses associated with rapid heartbeats such as atrial and ventricular arrhythmias. It functions by slowing the influx of sodium ions into cardiac muscle cells, which decreases cell excitability. This medication is more selective for cells with a high rate, but also blocks normal cells more than class Ia or Ib antiarrhythmics. It possesses beta-adrenergic blocker activity.
- Treats atrial and ventricular arrhythmias
- Slows influx of sodium ions into cardiac muscle cells
- Decreases cardiac cell excitability
- Exhibits beta-adrenergic blocker activity
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Medchemexpress LLC Minocycline (hydrochloride) | 13614-98-7 | MFCD00078028 | 99.7% | 493.94 | 5 MG
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Minocycline (hydrochloride) | 13614-98-7 | MFCD00078028 | 99.7% | 493.94 | 5 MG
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Medchemexpress LLC Bromperidol hydrochloride | 59453-24-6 | 99.96% | 25 MG
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Bromperidol hydrochloride is an antipsychotic agent that demonstrates high affinity for central dopamine D2 receptors. It also exhibits synergistic mycobacterial killing activity when combined with Spectinomycin.
- Exhibits antipsychotic activity.
- Demonstrates high affinity for central dopamine D2 receptors.
- Can synergistically kill Mycobacteria when combined with Spectinomycin.
- Antagonizes stereotyped behavior and agitation induced by apomorphine or amphetamine.
- Inhibits conditioned reactions and learned intracranial self-stimulation in rats.
- Antagonizes apomorphine-induced emesis and inhibits conditioned avoidance response in dogs.
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Alkali Scientific Doripenem, 1 G
Doripenem is a broad-spectrum antibiotic used in clinical and laboratory research to treat infections caused by Gram-positive and Gram-negative bacteria. The 1g quantity is commonly used in antimicrobial susceptibility testing, bacterial resistance studies, and the development of new antibiotics. Doripenem inhibits bacterial cell wall synthesis and is effective against a wide variety of pathogens. It is especially valuable in studies investigating carbapenem-resistant organisms. This product plays a critical role in exploring bacterial pathogenicity, developing new therapeutic approaches, and understanding the global challenge of antibiotic resistance.
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eMolecules 16415-12-6 | Hexadecyltrimethoxysilane | Combi-Blocks, Inc. | MFCD00069149 | 346.627 | C19H42O3Si | 95.000 | CCCCCCCCCCCCCCCC[Si](OC)(OC)OC | 25g | 586071472
Hexadecyltrimethoxysilane | Combi-Blocks, Inc. | 16415-12-6 | MFCD00069149 | 346.627 | C19H42O3Si | 95.000 | CCCCCCCCCCCCCCCC[Si](OC)(OC)OC | 25g | 586071472
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Medchemexpress LLC Norverapamil (hydrochloride) | 67812-42-4 | MFCD00078605 | 99.8% | 477.04 g·mol⁻¹ | C26H37ClN2O4 | 1 MG
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Norverapamil hydrochloride is the monohydrochloride salt of an N-demethylated metabolite of verapamil. It acts as an L-type calcium channel blocker and an inhibitor of P-glycoprotein (P-gp), and is used in pharmacological and transporter research.
- Acts as an L-type calcium channel blocker.
- Inhibits P-glycoprotein (P-gp) function.
- Suitable for in vitro pharmacology and transporter studies.
- Supplied as a solid or as a DMSO solution for experimental use.
- High reported purity (99.8%).
- Molecular weight 477.04 g·mol⁻¹; formula C26H37ClN2O4.
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Cayman Chemical RCS4C4 homolog Analytical Refe
Identical to RCS-4 except the N-1 alkyl chain length has been shortened from C5 to C4; detected in herbal blends
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Medchemexpress LLC Pf-06815345 (hydrochloride) | 2334434-49-8 | 98.15% | 634.49 | 25 MG
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PF-06815345 hydrochloride is an orally active and potent inhibitor of proprotein convertase subtilisin/kexin type 9 (PCSK9) with an IC50 value of 13.4 μM. It significantly decreases the PCSK9 level in vivo in mouse.
- Orally active.
- Potent inhibitor of proprotein convertase subtilisin/kexin type 9 (PCSK9).
- Has an IC50 value of 13.4 μM for PCSK9 inhibition.
- Significantly decreases PCSK9 levels in vivo in mice.
- Lowers plasma PCSK9 to 72% at 500 mg/kg 4 hours after treatment in a humanized PCSK9 mouse model.
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Medchemexpress LLC Drotaverine (hydrochloride) | 985-12-6 | 99.65% | 433.97 | 25 MG
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Drotaverine hydrochloride is a type 4 cyclic nucleotide phosphodiesterase (PDE4) inhibitor and an L-type voltage-dependent calcium channel (L-VDCC) blocker, which blocks the degradation of 3',5'-cyclic adenosine monophosphate. It exhibits in vivo antispasmodic efficacy without anticholinergic effects.
- Type 4 cyclic nucleotide phosphodiesterase (PDE4) inhibitor
- L-type voltage-dependent calcium channel (L-VDCC) blocker
- Blocks the degradation of 3',5'-cyclic adenosine monophosphate
- Exhibits in vivo antispasmodic efficacy without anticholinergic effects
- Relaxant for pre-contracted airways
- Suppresses bronchial contractions in guinea pigs
- Shows higher selectivity for KCl-induced contractions
- Improves cognitive impairment and regulates levels of neurotransmitters in the brain in animal models
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Medchemexpress LLC Pardoprunox hydrochloride | 269718-83-4 | 99.5% | 269.73 | 100 MG
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Pardoprunox hydrochloride is a compound that acts as a partial agonist for both dopamine D2 and D3 receptors, and a full agonist for the serotonin 5-HT1A receptor. This compound is intended for research purposes only.
- Partial dopamine D2 and D3 receptor agonist
- Serotonin 5-HT1A receptor agonist
- Acts as a partial D2 receptor agonist with an efficacy of 50%
- Induces [(35)S]GTPgammaS binding as a partial D3 receptor agonist
- Full 5-HT1A receptor agonist on forskolin induced cAMP accumulation
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Medchemexpress LLC Guretolimod (hydrochloride) | 98.7% | 550.01 | 25 MG
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Guretolimod hydrochloride is a Toll-like receptor 7 (TLR7) agonist. It is used in laboratory settings for research purposes, particularly in the study of immunology and inflammation.
- Toll-like receptor 7 (TLR7) agonist
- Molecular weight of 550.01
- Molecular formula C24H35ClF3N5O4
- Off-white to light yellow solid appearance
- Purity of 98.7% by HPLC
- Soluble in DMSO at 100 mg/mL
- Recommended storage at -20°C in sealed container, away from moisture and light
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Medchemexpress LLC -Coniine hydroch 25mg
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( )-Coniine hydrochloride (2-Propylpiperidine hydrochloride) is a potent nAChR agonist with an EC50 value of 0 3 mM ( )-Coniine hydrochloride shows acute toxicity with an LD50 value of 7 7 mg/kg[1]
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Medchemexpress LLC Benzamide, 2,6-dichloro-4-(cyclopentylamino)-N-[3-(1,1-dimethylethyl)-4-hydroxyphenyl] hydrochloride | 1660153-21-8 | 100.0% | 457.82 g/mol | C22H27Cl3N2O2 | 10 MG
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FXR Antagonist 2 (hydrochloride) is a diarylamide-derived farnesoid X receptor (FXR) antagonist provided as the hydrochloride salt for research use. It is intended for biochemical and cellular studies of FXR-related signaling and metabolic-disease models. The compound is characterized by a molecular formula C22H27Cl3N2O2, molecular weight 457.82 g/mol, and high HPLC purity as reported on the certificate of analysis.
- High purity suitable for research applications.
- Hydrochloride salt form for improved solubility.
- Diarylamide scaffold useful for FXR antagonism studies.
- Supplied with a certificate of analysis including molecular weight and formula.
- Available in small research pack sizes for assay development.
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