Hydrochlorides
![Medchemexpress LLC 1,1′,1′′,1′′′-[1,4-Piperazinediylbis(2,1-ethanediylnitrilo)]tetrakis[2-dodecanol] | 1265904-26-4 | 98.0% | 909.54 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000437399-Logo.png-250.jpg){kind=logo}
Medchemexpress LLC 1,1′,1′′,1′′′-[1,4-Piperazinediylbis(2,1-ethanediylnitrilo)]tetrakis[2-dodecanol] | 1265904-26-4 | 98.0% | 909.54 | 10 MG
1,1′,1′′,1′′′-[1,4-Piperazinediylbis(2,1-ethanediylnitrilo)]tetrakis[2-dodecanol] is a lipid/lipidoid for the preparation of lipid-based or lipidoid nanoparticles. This product is for research use only and not sold to patients.
- Used in preparation of lipid-based or lipidoid nanoparticles.
- Appearance as a solid, light yellow to orange.
- Recommended storage for powder is -20°C for 3 years, 4°C for 2 years.
- Recommended storage for in solvent is -80°C for 6 months, -20°C for 1 month.
- Soluble in DMSO (25 mg/mL), requiring sonication.
Medchemexpress LLC IACS-9571 hydrochloride | 2319611-93-1 | 98.3% | 679.22 g·mol⁻¹ | C32H43ClN4O8S | 100 MG
IACS-9571 hydrochloride is a potent, selective small-molecule inhibitor of the TRIM24 and BRPF1 bromodomains, used as a research tool in epigenetics and bromodomain biology. It exhibits nanomolar potency and is supplied as a high-purity research chemical with recommended storage guidance.
- Potent dual TRIM24 and BRPF1 bromodomain inhibition (IC50 8 nM; Kd 31 nM and 14 nM).
- High purity suitable for biochemical and cellular assays.
- Available as solid and DMSO solution formats for flexible dosing.
- Multiple pack sizes to support screening and follow-up experiments.
- Recommended sealed storage to maintain stability.
Medchemexpress LLC Ambroxol (hydrochloride) | 23828-92-4 | 100.0% | 10 MM 1 ML
Ambroxol hydrochloride is an active metabolite of Bromhexine with potent expectorant effects. It functions as a glucocerebrosidase (GCase) chaperone, enhancing glucocerebrosidase activity. This compound also induces lung autophagy and is a potential area of research for Parkinson's disease and neuronopathic Gaucher disease.
- Active metabolite of Bromhexine
- Potent expectorant effects
- Acts as a glucocerebrosidase (GCase) chaperone
- Increases glucocerebrosidase activity
- Induces lung autophagy
- Potential for research in Parkinson's disease
- Potential for research in neuronopathic Gaucher disease
- High purity (99.96%)
- White to off-white solid appearance
Medchemexpress LLC Etazolate hydrochloride | 35838-58-5 | MFCD00209848 | 98.0% | 325.79 g/mol | C14H20ClN5O2 | 100 MG
Etazolate hydrochloride is the hydrochloride salt of etazolate, a research compound that selectively inhibits phosphodiesterase-4 (PDE4) and modulates GABAA receptors. It is provided as a solid for preclinical biochemical and neuroscience research, including studies of inflammation and neuroprotection.
- Selective PDE4 inhibitor and GABAA receptor modulator.
- Hydrochloride salt form, solid suitable for laboratory use.
- Purity approximately 98.0%.
- Molecular weight 325.79 g/mol.
- CAS number 35838-58-5.
- Supplied in a 100 mg pack for bench-scale experiments.
eMolecules 21987-29-1 | 4,4-Difluoropiperidine | Combi-Blocks | MFCD03094281 | 121.131 | C5H9F2N | 98.000 | FC1(F)CCNCC1 | 1g | 205391142
4,4-Difluoropiperidine | Combi-Blocks | 21987-29-1 | MFCD03094281 | 121.131 | C5H9F2N | 98.000 | FC1(F)CCNCC1 | 1g | 205391142
Medchemexpress LLC JDTic dihydrochloride | 785835-79-2 | MFCD22419279 | 98.0% | 538.55 g·mol⁻¹ | C28H41Cl2N3O3 | 1 ML
JDTic dihydrochloride is the dihydrochloride salt of JDTic, a selective kappa-opioid receptor (KOR) antagonist used in research to block κ-agonist-induced antinociception. Supplied as a concentrated solution for in vitro pharmacology and receptor signaling studies.
- Selective kappa-opioid receptor antagonist suitable for pharmacology research.
- Provided as a 10 mM solution in a 1 mL vial.
- High purity appropriate for research applications.
- Soluble in DMSO and water for assay preparation.
- Commonly used for receptor antagonism and KOR signaling studies.
Medchemexpress LLC Cefotiam (hydrochloride) | 66309-69-1 | 98.0% | 25 MG
Cefotiam hydrochloride is a parenteral cephalosporin antibiotic that exhibits broad-spectrum activity against both Gram-positive and Gram-negative bacteria. It is highly active against various bacterial strains.
- Parenteral cephalosporin antibiotic
- Broad-spectrum activity against Gram-positive and Gram-negative bacteria
- Exhibits antibacterial activity against P. mirabilis IFO 3849
- Highly active against Staph. aureus and Staph. albus
- Active against haemolytic streptococci, pneumococci, and Streptococcus viridans
- Can cure urinary tract infection with P. mirabilis in mice
Medchemexpress LLC Naloxone hydrochloride (Standard) | 357-08-4 | 99.7% | 363.84 | 25 MG
Naloxone hydrochloride (Standard) | 357-08-4 | 99.7% | 363.84 | 25 MG
Medchemexpress LLC Itopride hydrochloride | 122892-31-3 | 99.8% | 500 MG
Itopride (HSR803) hydrochloride is identified as a potent dopamine-2 antagonist and an acetylcholine esterase (AChE) inhibitor. It functions as a gastrointestinal prokinetic agent by enhancing gastric motility through both antidopaminergic and anti-acetylcholinesterasic actions. This compound is also suitable for research related to gastro-esophageal reflux disease (GERD).
- Potent dopamine-2 antagonist.
- Acetylcholine esterase (AChE) inhibitor.
- Enhances gastric motility through antidopaminergic and anti-acetylcholinesterasic actions.
- Can be utilized as a gastrointestinal prokinetic agent.
- Suitable for researching gastro-esophageal reflux disease (GERD).
- Prokinetic effects on both the ileum and colon (in vitro studies).
- Significantly accelerates gastric emptying (in vivo studies).
eMolecules 1803587-72-5 | 5-HYDRAZINYLPYRIMIDINE DIHYDROCHLORIDE | MFCD28383958 | 1g
Ambeed | (S)-2-Aminopropan-1-ol | 10g | 552641488 | A201243 | 2749-11-3 | MFCD00064412 | 75.111 | C3H9NO
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Medchemexpress LLC Gaboxadol hydrochloride | 85118-33-8 | MFCD00055180 | 99.9% | 176.60 g/mol | C6H9ClN2O2 | 1 ML
Gaboxadol hydrochloride is the hydrochloride salt of gaboxadol, a GABAA receptor agonist used as a research reagent. This item is supplied as a ready-to-use 10 mM stock solution (1 mL) in DMSO for in vitro research applications.
- Ready-to-use 10 mM stock solution in DMSO.
- High purity, 99.85%.
- Hydrochloride salt; molecular formula C6H9ClN2O2 and molecular weight 176.60 g/mol.
- Store stock solution at -80°C for long-term storage or -20°C for short-term use.
- Intended for research use only; not for human or veterinary use.
![Medchemexpress LLC 1-([1,1'-biphenyl]-4-ylmethyl)-5-(trifluoromethoxy)indoline-2,3-dione | 1208222-39-2 | MFCD22683818 | 99.4% | 397.35 g·mol^-1 | C22H14F3NO3 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000242026.png-250.jpg)
Medchemexpress LLC 1-([1,1'-biphenyl]-4-ylmethyl)-5-(trifluoromethoxy)indoline-2,3-dione | 1208222-39-2 | MFCD22683818 | 99.4% | 397.35 g·mol^-1 | C22H14F3NO3 | 10 MG
VU 0365114 is a selective muscarinic acetylcholine receptor (mAChR) M5 positive allosteric modulator used in research to potentiate M5-mediated signaling. It displays an EC50 of 2.7 μM for M5 with minimal activity at M1-M4 and has been reported to increase acetylcholine-stimulated insulin secretion in human β-cells.
- Selective mAChR M5 positive allosteric modulator.
- Potentiates M5 responses with EC50 of 2.7 μM.
- Minimal activity at M1-M4 receptors (EC50 > 30 μM).
- High purity solid with light yellow to orange appearance.
- Chemical formula C22H14F3NO3; molecular weight 397.35 g·mol⁻¹.
- Intended for biochemical and pharmacological research applications.
TARGETMOL CHEMICALS INC DULOXETINE 50MG
Also available in 5 mg 10 mg 25 mg 100 mg and bulk. Please contact Fisher for quotes. Duloxetine is an inhibitor of serotonin-norepinephrine reuptake(Ki of 4.6 nM)with treatment of major depressive disorder and generalized anxiety disorder. purity: 99%
Medchemexpress LLC PS372424 (hydrochloride) | 1596362-29-6 | ≥98.0% | 625.20 | 25 MG
PS372424 hydrochloride, a three amino-acid fragment of CXCL10, is a specific human CXCR3 agonist with anti-inflammatory activity. It prevents human T-cell migration in a humanized model of arthritic inflammation.
- Specific human CXCR3 agonist with anti-inflammatory activity.
- Prevents human T-cell migration in a humanized model of arthritic inflammation.
Medchemexpress LLC MK2-IN-1 (hydrochloride) | 1314118-94-9 | 98.4% | 1 ML
MK2-IN-1 hydrochloride (compound 1) is a potent and selective MAPKAPK2 (MK2) inhibitor with an IC50 of 0.11 μM for MK2 and an EC50 of 0.35 μM for pHSP27. It impairs the phosphorylation level of serine residues in the Tfcp2l1 protein. This product is for research use only and not sold to patients.
- Potent and selective MAPKAPK2 (MK2) inhibitor
- Gradually increases Tfcp2l1 protein level without a change in transcript level within 2 hours
- Induces more alkaline phosphatase (AP)-positive colonies
- Molecular weight of 509.43
- Chemical formula C27H26Cl2N4O2
- Appears as a light yellow to pink solid
- Highly soluble in H2O and DMSO