Hydrochlorides
Medchemexpress LLC YM-298198 hydrochloride | 1216398-09-2 | MFCD08703122 | ≥99.0% | 378.92 | C18H23ClN4OS | 10 MG
YM-298198 hydrochloride is the hydrochloride salt of a selective, high-affinity, non-competitive antagonist of metabotropic glutamate receptor 1 (mGluR1) supplied for research use in small quantities.
- Selective mGluR1 antagonist with Ki = 19 nM and IC50 = 16 nM in functional assays.
- High reported purity (≥99.0% for latest batches).
- Molecular formula C18H23ClN4OS and molecular weight 378.92.
- CAS number 1216398-09-2 for substance identification.
- Available in small pack sizes such as 10 mg for research applications.
- Recommended storage: -20°C sealed; in solvent: -80°C up to 6 months or -20°C up to 1 month, protected from moisture.
Apexbio Technology LLC Dapoxetine HCl 129938-20-1 100mg
Dapoxetine hydrochloride (CAS 129938-20-1) is a short-acting selective serotonin reuptake inhibitor (SSRI) It exerts its pharmacological effect by inhibiting the reuptake of serotonin (5-HT) at the presynaptic membrane thereby increasing serotonin activity in the synaptic cleft This modulation of serotonergic neurotransmission has been shown to delay ejaculation latency making dapoxetine hydrochloride an established model compound for investigating serotonergic regulation of ejaculatory control It is widely used in research on the neurobiology and therapeutic approaches to premature ejaculation and related disorders
Apexbio Technology LLC Dapoxetine HCl 129938-20-1 50mg
Dapoxetine hydrochloride (CAS 129938-20-1) is a short-acting selective serotonin reuptake inhibitor (SSRI) It exerts its pharmacological effect by inhibiting the reuptake of serotonin (5-HT) at the presynaptic membrane thereby increasing serotonin activity in the synaptic cleft This modulation of serotonergic neurotransmission has been shown to delay ejaculation latency making dapoxetine hydrochloride an established model compound for investigating serotonergic regulation of ejaculatory control It is widely used in research on the neurobiology and therapeutic approaches to premature ejaculation and related disorders
Medchemexpress LLC KHK-IN-1 hydrochloride | 1303470-48-5 | 98.47% | 10 MG
KHK-IN-1 hydrochloride is a selective and cell membrane permeable ketohexokinase (KHK) inhibitor with an IC50 of 12 nM. It inhibits the production of F1P in HepG2 cell lysates with an IC50 of 400 nM and has potential for the study of diabetes and obesity.
- Selective and cell membrane permeable KHK inhibitor
- Inhibits F1P production in HepG2 cell lysates
- Potential for diabetes and obesity research
- Stable in human and rat liver microsome preparations
- Does not significantly inhibit cytochrome P450s
Medchemexpress LLC UPSEM792 hydrochloride | 2341841-08-3 | 99.9% | 277.75 | 25 MG
uPSEM792 hydrochloride is a PSAM4-GlyR agonist.
- Purity: 99.94%
- Molecular weight: 277.75
- CAS number: 2341841-08-3
- Formula: C14H16ClN3O
- Appearance: Solid
- Color: White to light yellow
- Shipping: Room temperature in continental US
- Storage: 4°C, sealed, away from moisture and light (solid)
- Storage in solvent: -80°C for 6 months; -20°C for 1 month (sealed, away from moisture and light)
Medchemexpress LLC 2,4-dichloro-5-(((2-((dimethylamino)methyl)phenyl)methoxy)methyl)pyrimidine hydrochloride | 2289726-31-2 | 99.9% | 375.72 | 50 MG
DCPT1061 hydrochloride is a potent inhibitor of histone methyltransferases, specifically targeting PRMT1, PRMT6, and PRMT8 in vitro. It exhibits weak inhibitory effects on other epigenetic enzymes like PRMT3, PRMT4, and PRMT5. This compound has demonstrated antitumor effects, making it a promising agent for cancer research.
- Strong inhibitory effect on PRMT1, PRMT6, and PRMT8.
- Minimal inhibition of PRMT3, PRMT4, and PRMT5.
- Exhibits antitumor properties.
- Suitable for research applications.
Medchemexpress LLC DPTN dihydrochloride | 325767-87-1 | C22H20Cl2N4OS | 5 MG
DPTN dihydrochloride is a potent and selective human, mouse, and rat A3AR antagonist. It exhibits Ki values of 1.65 nM for human A3AR, 9.61 nM for mouse A3AR, and 8.53 nM for rat A3AR. This product is for research use only.
- Potent and selective A3AR antagonist
- High purity (98.47%)
- Solid appearance
- Light yellow to yellow color
- Store at -20°C, sealed, away from moisture
- Shipped at room temperature in continental US
Medchemexpress LLC Queuine dihydrochloride | 86496-18-6 | 350.20 | 5 MG
Queuine dihydrochloride | 86496-18-6 | 350.20 | 5 MG
Medchemexpress LLC Verubulin hydrochloride | 917369-31-4 | 98.7% | 1 ML
Verubulin hydrochloride is the hydrochloride salt of verubulin (MPC-6827), a microtubule/tubulin inhibitor used in preclinical research. It is supplied as a ready-to-use 10 mM solution in DMSO and is also available as solid quantities for custom preparation. Intended for research use only.
- Highly pure product (98.7% typical).
- Provided as 10 mM, 1 mL solution in DMSO for ready-to-use applications.
- Available as solid in multiple masses (mg scale) for flexible dosing.
- Molecular weight 315.8 g/mol; formula C17H18ClN3O.
- Suitable for in vitro and in vivo preclinical research; not for human use.
Medchemexpress LLC Epertinib hydrochloride | 2071195-74-7 | >98.0% | 596.48 g/mol | C30H28Cl2FN5O3 | 1 ML
Epertinib hydrochloride is the hydrochloride salt of epertinib, a reversible and selective tyrosine kinase inhibitor of EGFR, HER2, and HER4 used in oncology research. The product is supplied as a 10 mM solution in DMSO (1 mL) and as solid powders; consult the datasheet and safety information for handling and purity details.
- Potent, reversible inhibitor of EGFR, HER2, and HER4.
- Suitable for in vitro and in vivo oncology research.
- Available as a 10 mM DMSO solution for ready-to-use assays.
- Also available as solid for formulation or long-term storage.
- Molecular weight 596.48 g/mol and CAS number 2071195-74-7.
Medchemexpress LLC SB 202190 hydrochloride | 350228-36-3 | MFCD28391789 | 99.7% | 367.80 g·mol⁻¹ | C20H15ClF3NO | 1 ML
SB 202190 hydrochloride is a selective p38 MAP kinase inhibitor used in cell signaling and pharmacology research. It is commonly supplied in concentrated stock formats for convenient preparation of working solutions.
- Selective p38 MAPK inhibitor; p38α IC50 ≈ 50 nM, p38β2 IC50 ≈ 100 nM.
- Supplied in a 10 mM solution format (1 mL) for ready stock preparation.
- Molecular weight 367.80 g·mol⁻¹; formula C20H15ClF3NO.
- DMSO-soluble; may require sonication and warming (up to 60°C) for full dissolution.
- Storage in solvent: -80°C (up to 6 months) or -20°C (up to 1 month); keep sealed and dry.
- High purity (manufacturer reported ~99.7%) suitable for research applications.
eMolecules 57754-86-6 | Medchem Express | Nisoxetine (hydrochloride) | 5mg | 533802639 | HY-B1704A | MFCD00153850 | 307.82 | C17H22ClNO2
Medchem Express | Nisoxetine (hydrochloride) | 5mg | 533802639 | HY-B1704A | 57754-86-6 | MFCD00153850 | 307.820 | C17H22ClNO2
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 2-Buten-1-amine, 3-fluoro-4-(phenylsulfonyl)-, hydrochloride (1:1), (2Z)- | 2409964-40-3 | C10H13ClFNO2S | 25 MG
PXS-4787 hydrochloride is a specific and effective pan-LOX (lysyl oxidase) inhibitor, abolishing lysyl oxidase activity. It inhibits LOX with IC50s ranging from 0.2 μM to 3.2 μM across various LOX isoforms, and also reduces deposition and crosslinking of collagen I secreted by human fibroblasts.
- Purity of 99.71%
- Solid, white to off-white appearance
- Molecular weight of 265.73
- Storage conditions: 4°C sealed for solid; -80°C for 6 months or -20°C for 1 month in solvent
- Soluble in DMSO at 100 mg/mL
- Inhibits LOX isoforms including Bovine LOX, rh LOXL1, rh LOXL2, rh LOXL3, and rh LOXL4
- Reduces collagen I deposition and crosslinking