Hydrochlorides
Medchemexpress LLC Bay-6672 hydrochloride | 2247520-31-4 | 98.0% | C26H28BrCl2N3O3 | 10MG
BAY-6672 hydrochloride is a potent, selective antagonist of the human Prostaglandin F (FP) receptor (reported IC50 ≈ 11 nM). It is used as a research reagent to probe FP receptor signaling and pharmacology and has demonstrated in vivo efficacy in preclinical lung fibrosis models. The compound is supplied as a solid with high reported purity.
- Potent FP receptor antagonism (IC50 ≈ 11 nM).
- Demonstrated in vivo efficacy in preclinical lung fibrosis models.
- Selective for FP over related prostaglandin receptors in published assays.
- High reported purity (~98.0%), suitable for biochemical studies.
- Provided as a solid research reagent for pharmacology and mechanistic assays.
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
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
eMolecules 18413-14-4 | Ethylhydrazine hydrochloride | MFCD01722460 | 1g
Ambeed | 13-Dimesityl-1H-imidazol-3-ium tetrafluoroborate | 250mg | 627733048 | A539978 | 286014-53-7 | MFCD04971186 | 392.250 | C21H25BF4N2
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Medchemexpress LLC Ambroxol hydrochloride | 23828-92-4 | 99.9% | 50 MG
Ambroxol hydrochloride | 23828-92-4 | 99.9% | 50 MG
Medchemexpress LLC Ambroxol (hydrochloride) | 23828-92-4 | 99.96% | 500 MG
Ambroxol hydrochloride, an active metabolite of Bromhexine, possesses potent expectorant effects. It acts as a glucocerebrosidase (GCase) chaperone, increasing glucocerebrosidase activity. This compound also induces lung autophagy and shows potential for research in Parkinson's disease and neuronopathic Gaucher disease.
- Potent expectorant effects
- Increases glucocerebrosidase activity
- Induces lung autophagy
- Potential for research in Parkinson's disease
- Potential for research in neuronopathic Gaucher disease
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
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 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
Medchemexpress LLC Benzamide, 4-butoxy-N-(2,4-difluorophenyl)- | 433967-28-3 | C17H17F2NO2 | 5 MG
VU 0357121 is a positive and highly selective mGlu5R allosteric modulator (PAM) with an EC50 of 33 nM. It is inactive or very weakly antagonizing at other mGlu receptor subtypes, enhancing glutamate sensitivity of mGlu5 likely due to interaction at a site on the receptor distinct from the MPEP binding site.
- Positive and highly selective mGlu5R allosteric modulator
- EC50 of 33 nM for mGlu5 receptor
- Inactive or very weakly antagonizing at other mGlu receptor subtypes
- Enhances glutamate sensitivity of mGlu5
- Does not bind at the MPEP allosteric site of mGlu5
Chem-Impex International, Inc. O-Benzyl-hydroxylamine hydrochloride | 2687-43-6 | MFCD00012952 | 2.5KG
O-Benzyl-hydroxylamine hydrochloride, 2687-43-6, MFCD00012952, 2.5KG
Medchemexpress LLC Benzamide, 4-butoxy-N-(2,4-difluorophenyl)- | 433967-28-3 | C17H17F2NO2 | 50 MG
VU 0357121 is a positive and highly selective mGlu5R allosteric modulator (PAM) with an EC50 of 33 nM. It is inactive or very weakly antagonizing at other mGlu receptor subtypes.
- Positive and highly selective mGlu5R allosteric modulator
- EC50 of 33 nM for mGlu5R
- Inactive or very weakly antagonizing at other mGlu receptor subtypes
- Appearance: solid, white to off-white
- Solubility in DMSO: ≥ 50 mg/mL (163.76 mM)