Hydrochlorides
eMolecules 1080640-91-0 | 8-(TRIFLUOROMETHYL)QUINOLIN-6-AMINE | AstaTech | MFCD11052592 | 212.175 | C10H7F3N2 | 95.000 | Nc1cc(c2ncccc2c1)C(F)(F)F | 1g | 410713139
8-(TRIFLUOROMETHYL)QUINOLIN-6-AMINE | AstaTech | 1080640-91-0 | MFCD11052592 | 212.175 | C10H7F3N2 | 95.000 | Nc1cc(c2ncccc2c1)C(F)(F)F | 1g | 410713139
TARGETMOL CHEMICALS INC TIROFIBAN HYDROCHLORIDE 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 200 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Tirofiban hydrochloride monohydrate (MK-383 Hydrochloride) is a potent non-peptide glycoprotein IIb/IIIa (integrins alphaIIbbetaIII) antagonist. purity: 99%
Medchemexpress LLC PXS-4787 hydrochloride | 2409964-40-3 | C10H13ClFNO2S | 10 MM * 1 ML
PXS-4787 hydrochloride is a specific and effective pan-LOX (lysyl oxidase) inhibitor that abolishes lysyl oxidase activity. It inhibits LOX with IC50s of 2 μM (Bovine LOX), 3.2 μM (rh LOXL1), 0.6 μM (rh LOXL2), 1.4 μM (rh LOXL3), and 0.2 μM (rh LOXL4). This compound also reduces the deposition and crosslinking of collagen I secreted by human fibroblasts. It is for research use only and not sold to patients.
- Specific and effective pan-LOX inhibitor
- Abolishes lysyl oxidase activity
- Inhibits LOX with IC50s of 2 μM (Bovine LOX), 3.2 μM (rh LOXL1), 0.6 μM (rh LOXL2), 1.4 μM (rh LOXL3), and 0.2 μM (rh LOXL4)
- Reduces deposition and crosslinking of collagen I secreted by human fibroblasts
- For research use only
Medchemexpress LLC OPC-14523 hydrochlor 10mM 1mL | 145969-31-9 | 450.40 g/mol | C23H29Cl2N3O2 | 1 ML
OPC-14523 hydrochloride is a sigma and 5-HT1A receptor agonist supplied as a hydrochloride salt for research use. It is available as a lyophilized solid and as a ready-to-use 10 mM solution in DMSO, with documented solubility and storage recommendations for in vitro and in vivo studies.
- Hydrochloride salt form for improved stability and handling.
- High purity (99.95%) suitable for pharmacology studies.
- Chemical formula C23H29Cl2N3O2; molecular weight 450.40 g/mol.
- Available as solid in multiple mg sizes and as a 10 mM, 1 mL solution in DMSO.
- Soluble in DMSO (~83.3 mg/mL) and moderately soluble in water with warming.
- Recommended storage: sealed, away from moisture; in solvent: -20°C short term, -80°C long term.
![Medchemexpress LLC 3(2H)-pyridazinone, 4,5-dihydro-6-[4-(4-pyridinylamino)phenyl]-, hydrochloride | 98326-33-1 | 99.8% | 302.76 g/mol | C15H15ClN4O | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000247664.png-250.jpg)
Medchemexpress LLC 3(2H)-pyridazinone, 4,5-dihydro-6-[4-(4-pyridinylamino)phenyl]-, hydrochloride | 98326-33-1 | 99.8% | 302.76 g/mol | C15H15ClN4O | 1 ML
Senazodan hydrochloride is the monohydrochloride salt of Senazodan (MCI 154), a Ca2+ sensitiser that also exhibits inhibitory activity against phosphodiesterase III (PDE III). It is provided for research use in biochemical and pharmacological studies and is supplied in solid and solution formats for assay applications.
- High purity (99.84%) as verified by certificate of analysis.
- Exact chemical identity: C15H15ClN4O, MW 302.76 g/mol, CAS 98326-33-1.
- Suitable for biochemical and pharmacological assays involving Ca2+ sensitization and PDE III modulation.
- Available as solid powder and as concentrated solution formats for convenient dosing.
- COA available for batch-specific quality and analytical data.
Medchemexpress LLC Mafenide hydrochloride | 138-37-4 | MFCD00013005 | 99.97% | 50 MG
Mafenide hydrochloride is an effective sulfonamide-type antimicrobial agent used for burn wounds. It shows activity against both Gram-positive and Gram-negative organisms, including Pseudomonas aeruginosa, via inhibition of nucleotide synthesis.
- Effective sulfonamide-type antimicrobial agent
- Used for burn wounds
- Active against Gram-positive organisms
- Active against Gram-negative organisms
- Effective against Pseudomonas aeruginosa
- Inhibits nucleotide synthesis
- Regulatory Status: RUO
- Ships at room temperature
- Store at 4°C, sealed, and away from moisture
Sigma Aldrich Fine Chemicals Biosciences Cysteamine hydrochloride BioXtra | 156-57-0 | MFCD00012904 | 25g
Cysteamine hydrochloride BioXtra | Mol Wt: 113.61 | 156-57-0 | MFCD00012904 | 25g
Medchemexpress LLC Erlotinib hydrochloride | 183319-69-9 | >99.0% | 10 G
Erlotinib hydrochloride is the hydrochloride salt of erlotinib, a potent epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor used as a research reagent. It inhibits purified EGFR kinase (IC50 ≈ 2 nM) and shows anti-tumor activity in preclinical studies. For research use only.
- Inhibits EGFR kinase (IC50 ≈ 2 nM).
- Molecular weight 429.90 g/mol.
- Chemical formula C22H24ClN3O4.
- Purity >99% (manufacturer claim).
- Supplied as an off-white powder; store at -20°C.
Medchemexpress LLC Zk756326 dihydrochloride | 1780259-94-0 | MFCD09038571 | 99.9% | 429.38 | C21H30Cl2N2O3 | 1 ML
ZK756326 dihydrochloride is a small-molecule, nonpeptide agonist of the CC chemokine receptor CCR8 supplied for research use in biochemical and cell-based assays. It is available as a 10 mM solution in DMSO (1 mL) and as crystalline solids, and is provided with analytical documentation to verify identity and purity.
- Nonpeptide CCR8 agonist suitable for receptor pharmacology studies.
- Offered as 10 mM solution in DMSO (1 mL) and in multiple solid quantities for assay flexibility.
- High purity (99.87%) supporting reproducible experimental results.
- Comes with analytical documentation: COA, HNMR, LCMS, and SDS.
- Storage guidance for stability: sealed storage; in solvent, -80°C (6 months) or -20°C (1 month).
Medchemexpress LLC PD 128907 hydrochloride | 112960-16-4 | 99.5% | 285.77 g/mol | C14H20ClNO3 | 50 MG
PD 128907 hydrochloride is a selective dopamine D3 receptor agonist used as a biochemical reagent for life-science research. It exhibits sub-nanomolar potency at D3 receptors (EC50 ~0.64 nM) and substantial selectivity over D2 receptors, and is supplied as a high-purity solid for in vitro pharmacology and receptor-binding studies.
- Potent D3 receptor agonist with EC50 ~0.64 nM.
- High selectivity over D2 receptors (≈53-fold).
- Reported high purity suitable for research use.
- Available in small package sizes for experimental workflows.
- Applicable to dopaminergic signaling and receptor pharmacology studies.
Medchemexpress LLC Azvudine hydrochloride | 1333126-31-0 | 99.2% | 322.68 | 1 ML
Azvudine hydrochloride | 1333126-31-0 | 99.2% | 322.68 | 1 ML
[C@H]1CC[C@@H](CC1)C(=O)Nc1ccncc1 | 100mg | 874279628](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000128392.jpg-250.jpg)
eMolecules 129830-38-2 | Y-27632 (dihydrochloride) (Standard) | Medchem Express (US) | MFCD03490488 | 320.260 | C14H23Cl2N3O | 98.000 | Cl.Cl.C[C@@H](N)[C@H]1CC[C@@H](CC1)C(=O)Nc1ccncc1 | 100mg | 874279628
Y-27632 (dihydrochloride) (Standard) | Medchem Express (US) | 129830-38-2 | MFCD03490488 | 320.260 | C14H23Cl2N3O | 98.000 | Cl.Cl.C[C@@H](N)[C@H]1CC[C@@H](CC1)C(=O)Nc1ccncc1 | 100mg | 874279628
Medchemexpress LLC Etazolate hydrochloride | 35838-58-5 | MFCD00209848 | 98.0% | 325.79 | C14H20ClN5O2 | 5 MG
Etazolate hydrochloride is a pyrazolopyridine research compound that functions as a selective phosphodiesterase-4 (PDE4) inhibitor, a GABAA receptor regulator, and an α-secretase activator. It is used in neuropharmacology and inflammation studies to probe cAMP signaling, amyloid precursor protein processing, and behavioral pharmacology.
Medchemexpress LLC Aq-13 dihydrochloride | 169815-40-1 | MFCD01938526 | 98.1% | 364.74 | C16H24Cl3N3 | 100 MG
AQ-13 dihydrochloride is an aminoquinoline antimalarial compound active against drug-resistant strains of Plasmodium falciparum, provided for research use. It is supplied as a light yellow solid and in solution formats, with molecular formula C16H24Cl3N3 and molecular weight 364.74.
- Active against drug-resistant Plasmodium falciparum.
- High purity (98.08%) appropriate for research applications.
- Available as a light yellow solid and in solution formats.
- Soluble in DMSO and water; may require ultrasonic agitation.
- Stable when stored sealed away from moisture; in solvent, -80°C (6 months) or -20°C (1 month).
- Molecular formula C16H24Cl3N3; molecular weight 364.74.
Medchemexpress LLC Ly2365109 hydrochloride | 1779796-27-8 | MFCD12828768 | 98.7% | 421.91 | C22H28ClNO5 | 1 ML
LY2365109 hydrochloride is a potent, selective glycine transporter 1 (GlyT1) inhibitor intended for laboratory research use. It inhibits glycine uptake in cells over-expressing hGlyT1a with an IC50 of 15.8 nM and is supplied with high purity for biochemical and pharmacological assays.
- Potent GlyT1 inhibition (IC50 15.8 nM).
- High purity suitable for research (≈98.7%).
- Available as solid or 10 mM solution in DMSO.
- White to off-white solid appearance.
- Suitable for in vitro pharmacology and uptake assays.