Hydrochlorides
Chem-Impex International, Inc. 3-Butyn-1-amine hydrochloride | 88211-50-1 | MFCD06658391 | 5G
3-Butyn-1-amine hydrochloride, 88211-50-1, MFCD06658391, 5G
Chem-Impex International, Inc. 3-Butyn-1-amine hydrochloride | 88211-50-1 | MFCD06658391 | 1G
3-Butyn-1-amine hydrochloride, 88211-50-1, MFCD06658391, 1G
Sigma Aldrich Fine Chemicals Biosciences o-Phenylenediamine dihydrochloride | 615-28-1 | MFCD00012966 | 50 tablets
o-Phenylenediamine dihydrochloride | Mol Wt: 181.06 | 615-28-1 | MFCD00012966 | 50 tablets
Medchemexpress LLC DPTN (dihydrochloride) | 325767-87-1 | C22H20Cl2N4OS | 50 MG
DPTN dihydrochloride is a potent and selective antagonist for human, mouse, and rat A3 adenosine receptors. It exhibits Ki values of 1.65 nM for human A3AR, 9.61 nM for mouse A3AR, and 8.53 nM for rat A3AR. While it is weaker at mouse and rat A3AR compared with human A3AR, it also shows reduced selectivity (approximately 20-fold) versus the A2B adenosine receptor.
- Potent and selective A3 adenosine receptor antagonist
- Effective in human, mouse, and rat models
- Solid, light yellow to yellow appearance
- Stable under recommended storage conditions
Medchemexpress LLC Cefotiam hydrochloride | 66309-69-1 | 98.0% | 50 MG
Cefotiam hydrochloride is a parenteral cephalosporin antibiotic known for its broad-spectrum activity against both Gram-positive and Gram-negative bacteria.
- Parenteral cephalosporin antibiotic
- Broad-spectrum activity
- Effective against Gram-positive bacteria
- Effective against Gram-negative bacteria
Medchemexpress LLC Dapoxetine hydrochloride | 129938-20-1 | 99.96% | 50 MG
Dapoxetine hydrochloride is an orally active and selective serotonin reuptake inhibitor (SSRI) used for premature ejaculation (PE) research. It binds to 5-HT, norepinephrine, and dopamine reuptake transporters.
- Inhibits 5-HT, norepinephrine, and dopamine uptake
- Can be used for premature ejaculation (PE) research
- Oral gavage significantly inhibits testosterone-mediated increase in prostate weight in rats
Medchemexpress LLC VU 0364439 | 1246086-78-1 | C18H13Cl2N3O3S | 50 MG
VU 0364439 is a mGlu4 positive allosteric modulator (PAM), with an EC50 of 19.8 nM. Intended for research use only, this solid compound appears white to off-white. While it demonstrates better stability in Human Liver Microsomes, its less than ideal PK properties prevent its use as an in vivo tool.
- Positive allosteric modulator (PAM) for mGlu4
- EC50 of 19.8 nM
- Purity of 99.42%
- Solid appearance, white to off-white color
- Exhibits better stability in HLM (63% remaining) compared to RLM (2% remaining)
- Target: mGluR
Medchemexpress LLC KHK-IN-1 hydrochloride | 1303470-48-5 | 98.0% | 50 MG
KHK-IN-1 hydrochloride is a selective and cell membrane permeable ketohexokinase (KHK) inhibitor. It effectively inhibits the production of F1P in HepG2 cell lysates, demonstrating an IC50 value of 400 nM. This compound holds potential for research related to diabetes and obesity, offering a valuable tool for scientific investigation.
- Demonstrates selectivity as a ketohexokinase inhibitor.
- Is cell membrane permeable, allowing intracellular action.
- Inhibits F1P production in HepG2 cell lysates.
- Possesses potential for studying diabetes and obesity.
- Stable in human and rat liver microsome preparations.
- Does not significantly inhibit cytochrome P450s.
Medchemexpress LLC MK2-IN-1 hydrochloride | 1314118-94-9 | 98.2% | 50 MG
MK2-IN-1 hydrochloride (compound 1) is a potent and selective MAPKAPK2 (MK2) inhibitor. It features an IC50 of 0.11 uM for MK2 and an EC50 of 0.35 uM for pHSP27, and impairs the phosphorylation level of serine residues in the Tfcp2l1 protein.
- Increases Tfcp2l1 protein level without changing transcript level within 2 hours
- Induces alkaline phosphatase (AP)-positive colonies in short time
- Soluble in H2O at ≥ 100 mg/mL
- Soluble in DMSO at 100 mg/mL (requires ultrasonication)
- Appearance: Solid
- Color: Light yellow to pink
Medchemexpress LLC SKF89976A hydrochloride | 85375-15-1 | 98.7% | 371.90 | C22H26ClNO2 | 50 MG
SKF89976A hydrochloride is a selective inhibitor of the GABA transporter GAT-1 used in research to probe GABA uptake and transporter pharmacology. It exhibits high potency at GAT-1 with markedly lower potency at GAT-2 and GAT-3, and shows weak activity at monoamine transporters. Supplied as a solid for in vitro and in vivo preclinical studies.
- Selective GAT-1 inhibition with IC50 0.28 μM.
- Lower potency at GAT-2 and GAT-3 (IC50 137.34 μM and 202.8 μM).
- Weak activity at SERT, NET, and DAT consistent with transporter profiling.
- High purity solid suitable for biochemical assays (98.73%).
- Usable in both in vitro transporter assays and preclinical in vivo models.
Medchemexpress LLC 1-(2-Hydroxy-4,6-dimethoxyphenyl)-4-(piperazin-1-yl)butan-1-one dihydrochloride | 99.9% | 381.29 | 50 MG
Y13g dihydrochloride is a chemical compound supplied by MedChemExpress. It has a molecular weight of 381.29 and a purity of 99.89% as determined by LCMS. It appears as an off-white to light yellow solid and is stored at -20°C in sealed conditions away from moisture.
- Appears as an off-white to light yellow solid
- Purity of 99.89% verified by LCMS
- Consistent with ¹H NMR spectrum and LCMS analysis
- Recommended storage at -20°C in sealed conditions away from moisture
Medchemexpress LLC AQ-13 dihydrochloride | 169815-40-1 | 98.1% | 364.74 | C16H24Cl3N3 | 50 MG
AQ-13 dihydrochloride is an aminoquinoline antimalarial research compound reported to be active against drug-resistant strains of Plasmodium falciparum. It is supplied as a solid for laboratory use and should be handled according to safety protocols; not for human or clinical use.
- Aminoquinoline antimalarial agent active against drug-resistant Plasmodium falciparum.
- Solid form suitable for laboratory handling.
- Reported purity approximately 98.1%.
- Molecular weight 364.74 g/mol.
- CAS number 169815-40-1 for unambiguous identification.
- Store sealed, away from moisture; in solvent: -80°C (6 months), -20°C (1 month).
Medchemexpress LLC IACS-9571 hydrochloride | 2319611-93-1 | 98.3% | 679.22 | C32H43ClN4O8S | 50 MG
IACS-9571 hydrochloride is the hydrochloride salt form of a potent, selective inhibitor of the epigenetic readers TRIM24 and BRPF1. It is supplied as a solid for research use and offers improved aqueous solubility and stability versus the free base.
- Potent, selective inhibitor of TRIM24 and BRPF1 (IC50 8 nM; Kd 31 nM and 14 nM).
- High purity suitable for research (98.3%).
- Molecular weight 679.22; formula C32H43ClN4O8S.
- Solid, light brown to brown appearance; sealed storage recommended.
- Supplied with product data sheet and SDS for handling and storage.
Medchemexpress LLC Duloxetine metabolite Para-Naphthol Duloxetine | 949095-98-1 | 297.41 | 50 MG
Duloxetine metabolite Para-Naphthol Duloxetine is a metabolite of Duloxetine, a serotonin-norepinephrine reuptake inhibitor (SNRI). This product is intended for research use only and is not sold to patients.
- Metabolite of Duloxetine
- For research use only
- Molecular formula: C18H19NOS
- Appearance: Solid
- Color: White to off-white
- Store powder at -20°C for 3 years
- Store in solvent at -80°C for 6 months, or -20°C for 1 month
Medchemexpress LLC Roxindole hydrochloride | 108050-82-4 | 99.5% | 382.93 g·mol⁻1 | C23H27ClN2O | 50 MG
Roxindole hydrochloride is a research-grade small molecule used as a pharmacological tool to study serotonin and dopamine receptor activity. It functions as a 5-HT1A agonist and dopaminergic modulator and is provided as a hydrochloride salt for use in in vitro and biochemical assays.
- Used to probe 5-HT1A and dopamine receptor pharmacology
- High purity suitable for research assays (HPLC)
- Molecular weight 382.93 g·mol⁻1
- Chemical formula C23H27ClN2O; CAS 108050-82-4
- Available in small solid quantities for laboratory experiments
- Store solid at -20°C and protect from light