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.
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.
Medchemexpress LLC SKF-96365 hydrochlor 10mg
SKF-96365 hydrochloride is a potent TRP channel blocker and a store-operated Ca2 entry (SOCE) inhibitor SKF-96365 hydrochloride significantly inhibits hERG hKCNQ1/hKCNE1 hKir2 1 and hKv4 3 current and significantly prolongs the QTc interval in isolated guinea pig hearts SKF-96365 hydrochloride exhibits potent anti-neoplastic activity by inducing cell-cycle arrest and apoptosis in colorectal cancer cells1]2]
Medchemexpress LLC Amiloride hydrochloride dihydrate | 17440-83-4 | MFCD00211292 | 99.9% | 1 ML
Amiloride hydrochloride dihydrate is an inhibitor of both epithelial sodium channel (ENaC) and urokinase-type plasminogen activator receptor (uTPA). It also acts as a blocker of polycystin-2 (PC2; TRPP2) channel.
- Inhibits epithelial sodium channel (ENaC)
- Inhibits urokinase-type plasminogen activator receptor (uTPA)
- Blocks polycystin-2 (PC2; TRPP2) channel
Medchemexpress LLC Mafenide hydrochloride | 138-37-4 | 99.97% | 100 MG
Mafenide hydrochloride is an effective sulfonamide-type antimicrobial agent used for burn wounds. It exhibits activity against both Gram-positive and Gram-negative organisms, including Pseudomonas aeruginosa, by inhibiting nucleotide synthesis. It is a white to off-white solid with a purity of 99.97% and a molecular weight of 222.69.
- Effective sulfonamide-type antimicrobial agent
- Active against Gram-positive and Gram-negative organisms
- Inhibits nucleotide synthesis
- Purity of 99.97%
- Soluble in DMSO (125 mg/mL)
- Recommended storage at 4°C in sealed container, away from moisture
Medchemexpress LLC PNU-22394 hydrochloride | 15923-42-9 | 98.8% | 236.74 g/mol | C13H17ClN2 | 5 MG
PNU-22394 hydrochloride is a research-grade small-molecule agonist of serotonin (5-HT) receptors, showing selectivity for 5-HT2C and activity at 5-HT2A. Supplied as a hydrochloride salt, it is intended for in vitro pharmacology and receptor signaling studies.
- Selective agonist at 5-HT2C with Ki = 6.1 nM.
- Also active at 5-HT2A (Ki = 10 nM).
- Assay-dependent EC50: 5-HT2C 7.7 nM (Fluo-4/Ca2+) and 0.12 μM (IP-One); 5-HT2A 23 nM (Fluo-4/Ca2+) and 0.21 μM (IP-One).
- Molecular formula C13H17ClN2; molecular weight 236.74 g/mol.
- High chemical purity (98.8%).
- Available in small milligram quantities for laboratory research.
eMolecules 21987-29-1 | 4,4-Difluoropiperidine | Apollo Scientific | MFCD03094281 | 121.131 | C5H9F2N | 97.000 | FC1(F)CCNCC1 | 1g | 600856207
4,4-Difluoropiperidine | Apollo Scientific | 21987-29-1 | MFCD03094281 | 121.131 | C5H9F2N | 97.000 | FC1(F)CCNCC1 | 1g | 600856207
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%