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Filtered Search Results
eMolecules 88491-61-6 | 3-Bromopyridazine | Combi-Blocks | MFCD10688587 | 158.986 | C4H3BrN2 | 98.000 | Brc1cccnn1 | 25g | 335354101
3-Bromopyridazine | Combi-Blocks | 88491-61-6 | MFCD10688587 | 158.986 | C4H3BrN2 | 98.000 | Brc1cccnn1 | 25g | 335354101
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eMolecules 791061-00-2 | 3,3-Difluorocyclobutanamine | Combi-Blocks | MFCD11869718 | 107.104 | C4H7F2N | 98.000 | NC1CC(F)(F)C1 | 10g | 482935004
3,3-Difluorocyclobutanamine | Combi-Blocks | 791061-00-2 | MFCD11869718 | 107.104 | C4H7F2N | 98.000 | NC1CC(F)(F)C1 | 10g | 482935004
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eMolecules 288315-03-7 | 3,3-difluoroazetidine hydrochloride | Pharmablock | MFCD05663714 | 129.530 | C3H6ClF2N | 97.000 | Cl.FC1(F)CNC1 | 5g | 551053262
3,3-difluoroazetidine hydrochloride | Pharmablock | 288315-03-7 | MFCD05663714 | 129.530 | C3H6ClF2N | 97.000 | Cl.FC1(F)CNC1 | 5g | 551053262
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Medchemexpress LLC 3-Aminoisonicotinic acid | 7579-20-6 | 97.5% | C6H6N2O2 | 10 G
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3-Aminoisonicotinic acid is a biochemical reagent that functions as a biological material or organic compound. It is suitable for various life science related research applications and is provided as a solid.
- Molecular weight of 138.12
- Purity of 99.73%
- Light yellow to brown appearance
- Store at 4°C, protected from light
- In solvent, store at -80°C for 6 months or -20°C for 1 month, protected from light
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Medchemexpress LLC Pat1inh-b01 hydrochloride | C22H19BrClF3N6O2 | 5 MG
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PAT1inh-B01 hydrochloride is a selective SLC26A6 inhibitor that blocks fluid absorption in the small intestine. It can be used for research into small intestinal hyposecretory disorders. For research use only, not for sale to patients.
- Inhibits PAT1 (a Cl-/HCO3- exchanger)-mediated anion exchange with an IC50 of 350 nM
- Blocks fluid absorption in the small intestine
- Suitable for research of small intestinal hyposecretory disorders
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Medchemexpress LLC Icapamespib hydrochloride | 2267287-26-1 | 98.7% | 599.32 | 50 MG
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Icapamespib hydrochloride | 2267287-26-1 | 98.7% | 599.32 | 50 MG
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Medchemexpress LLC Ticlopidine hydrochloride | 53885-35-1 | 99.99% | 1 ML
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Ticlopidine hydrochloride is an antithrombotic proagent that acts as an allosteric, noncompetitive inhibitor of CD39. It also blocks several NTPDase isoenzymes and inhibits human liver cytochromes CYP2C19, CYP2C9, and CYP3A4.
- Acts as an allosteric, noncompetitive inhibitor of CD39 (IC50 of 81.7 μM)
- Blocks NTPDase isoenzymes, including NTPDase2 and NTPDase3
- Inhibits CYP2C19 human liver cytochrome
- Inhibits CYP2C9 (IC50 of 26.0 μM)
- Inhibits CYP3A4 (IC50 of 32.3 μM)
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Medchemexpress LLC Epetraborole hydrochloride | 1234563-16-6 | 99.6% | 273.52 | C11H17BClNO4 | 10MM 1ML
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Epetraborole hydrochloride is a small-molecule leucyl-tRNA synthetase (LeuRS) inhibitor used in antibacterial research to block bacterial protein synthesis. Supplied as a concentrated solution (10 mM, 1 mL) for research use, it has formula C11H17BClNO4, molecular weight 273.52, and CAS 1234563-16-6.
- Inhibits leucyl-tRNA synthetase, blocking protein synthesis.
- Suitable for in vitro antibacterial assays and mechanism studies.
- Provided as a concentrated solution for immediate use in assays.
- High purity suitable for research applications.
- Includes chemical identifiers for traceability and documentation.
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Medchemexpress LLC Atomoxetine hydrochloride | 82248-59-7 | 99.9% | 291.82 | 500 MG
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Atomoxetine hydrochloride is a selective noradrenaline reuptake inhibitor that can be used for attention-deficit hyperactivity disorder (ADHD) research. It acts as a potent Na+ channels (VGSCs) blocker and interacts with the human heart muscle sodium channel (hNav1.5).
- Selective noradrenaline reuptake inhibitor
- Potent Na+ channels (VGSCs) blocker
- Suitable for ADHD research
- Interacts with human heart muscle sodium channel
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Medchemexpress LLC Desmethyl-VS-5584 hydrochloride | 98.6% | 413.30 g/mol | C16H22Cl2N8O | 25 MG
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Desmethyl-VS-5584 hydrochloride is a dimethyl analog of VS-5584 that functions as a potent and selective dual inhibitor of mTOR and PI3K, intended for research use. It contains a pyrido[2,3-d]pyrimidine core and is supplied as a light yellow solid with high reported purity.
- Potent, selective mTOR and PI3K dual inhibitor.
- High purity (98.6%) suitable for research applications.
- Molecular weight 413.30 g/mol and formula C16H22Cl2N8O.
- Solid, light yellow to yellow appearance.
- Available in small lab-scale quantities (e.g., 25 mg).
- Storage: store sealed, away from moisture; in solvent: -80°C for 6 months, -20°C for 1 month.
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eMolecules 109-78-4 | 3-Hydroxypropionitrile | Combi-Blocks | MFCD00002826 | 71.079 | C3H5NO | 96.000 | OCCC#N | 500g | 335346494
3-Hydroxypropionitrile | Combi-Blocks | 109-78-4 | MFCD00002826 | 71.079 | C3H5NO | 96.000 | OCCC#N | 500g | 335346494
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Medchemexpress LLC Pilocarpine hydrochloride | 54-71-7 | 99.98% | 5 G
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Pilocarpine Hydrochloride is a potent M3-type muscarinic acetylcholine receptor (M3 muscarinic receptor) agonist. It is intended for research use only.
- Potent M3-type muscarinic acetylcholine receptor agonist
- Unstable in solutions, freshly prepared is recommended
- Suitable for laboratory centrifugation and storage
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Medchemexpress LLC Cyclobenzaprine hydrochloride | 6202-23-9 | MFCD00079039 | 99.95% | 1 ML
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Cyclobenzaprine hydrochloride is an orally active 5-HT2 receptor antagonist. It acts centrally to provide skeletal muscle relaxation, alleviate muscle spasms, and reduce pain. It also possesses antiparasitic activity and holds promise for research in acute, painful skeletal muscle disorders and infectious diseases.
- Orally active 5-HT2 receptor antagonist
- Provides skeletal muscle relaxation
- Alleviates muscle spasms
- Reduces pain
- Possesses antiparasitic activity
- Potential for research in acute, painful skeletal muscle disorders
- Potential for research in infectious diseases
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Medchemexpress LLC Propafenone hydrochloride | 34183-22-7 | 98.5% | 1 G
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Propafenone hydrochloride is a class of anti-arrhythmic medication used to treat illnesses associated with rapid heartbeats, such as atrial and ventricular arrhythmias. It works by slowing the influx of sodium ions into cardiac muscle cells, which decreases the excitability of these cells. This compound is more selective for cells with a high rate of activity but also affects normal cells more than Class Ia or Ib antiarrhythmics. It also possesses beta-adrenergic blocking activity, which can lead to bradycardia and bronchospasm.
- Treats atrial and ventricular arrhythmias
- Slows influx of sodium ions into cardiac muscle cells
- Decreases excitability of cardiac cells
- More selective for cells with a high rate of activity
- Possesses beta-adrenergic blocking activity
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Medchemexpress LLC Cefotiam hexetil hydrochloride | 95789-30-3 | MFCD00897074 | 95.1% | 768.76 | C27H39Cl2N9O7S3 | 10 MG
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Cefotiam hexetil hydrochloride is the hydrochloride salt of cefotiam hexetil, an oral prodrug of the third-generation cephalosporin cefotiam. Intended for research and analytical use, the compound is used in prodrug, formulation, and pharmacology studies and is inactive as an antibacterial until converted to cefotiam.
- Hydrochloride salt with reported purity 95.1%
- Molecular formula C27H39Cl2N9O7S3 and molecular weight 768.76
- Soluble in DMSO (250 mg/mL); ultrasonic agitation recommended
- Appearance: solid, off-white to light yellow
- Storage: store sealed at 4°C, protect from moisture and light
- Supplied in small research sizes such as 10 mg
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