Hydrochlorides
Med Vet International Terbinafine Tablets (Lamisil), 250mg, 100ct
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Terbinafine is a generic version of Lamisil. It is an antifungal medication used to fight infections caused by fungus.
Apexbio Technology LLC Tirofiban hydrochloride monohydrate 150915-40-5 25mg
Tirofiban hydrochloride monohydrate (CAS 150915-40-5) is a small-molecule inhibitor targeting platelet glycoprotein IIb/IIIa receptors It is designed to reversibly antagonize the binding of fibrinogen to these receptors thereby inhibiting platelet aggregation and thrombus formation Tirofiban hydrochloride monohydrate exerts its biological activity primarily through selective reversible inhibition of glycoprotein IIb/IIIa-mediated platelet aggregation Based on these pharmacological properties tirofiban hydrochloride monohydrate holds research potential in antithrombotic therapy and the investigation of unstable angina and thrombus-associated cardiovascular conditions
Medchemexpress LLC L-368,899 hydrochloride | 160312-62-9 | 99.97% | 591.23 | 100 MG
L-368,899 hydrochloride is a potent, selective, orally bioavailable, non-peptide oxytocin receptor antagonist. It has IC50s of 8.9 nM for rat uterus and 26 nM for human uterus oxytocin receptor. This compound is used as a tocolytic agent.
- Potent oxytocin receptor antagonist.
- Selective for oxytocin receptor.
- Orally bioavailable.
- Non-peptide structure.
- Used as a tocolytic agent.
- Less active on VP receptor in human liver and kidney, and rat liver and kidney.
- Exhibits similar pharmacokinetics in rats and dogs with a t1/2 of 2 hours after a single IV injection.
- Plasma clearance between 23 and 36 ml/min/kg in rats or dogs.
- Vdss values of 2.0 and 2.6 liters/kg for rats and 3.4 to 4.9 liters/kg for dogs.
- Oral bioavailabilities in rats: 14% (female) and 18% (male) at 5 mg/kg; 17% (female) and 41% (male) at 25 mg/kg.
Medchemexpress LLC Nilotinib hydrochloride dihydrate | 00-00-0 | MFCD09833716 | 99.9% | 602.01 g/mol | C28H27ClF3N7O3 | 100 MG
Nilotinib hydrochloride dihydrate is the hydrochloride salt, dihydrate form of nilotinib, supplied as a white to off-white solid for research use. It functions as a Bcr-Abl tyrosine kinase inhibitor and is intended for biochemical and cell-based studies of Bcr-Abl signaling and leukemia models, provided in laboratory-scale quantities for in vitro and preclinical experiments.
- High purity suitable for research-grade assays.
- Hydrochloride dihydrate salt form for improved handling and reproducibility.
- Soluble in DMSO at high concentrations (≈100 mg/mL) with ultrasonic assistance.
- Stable when stored sealed at 4°C; long-term storage in solvent at -80°C.
- White to off-white powder form for easy weighing and dissolution.
Cayman Chemical Teijin Compound 1 hydrochlor
A CCR2b antagonist (IC50 = 180 nM in a radioligand binding assay); inhibits CCL2-induced chemotaxis in THP-1 cells (EC50 = 24 nM)
Medchemexpress LLC Harmalol hydrochloride | 6028-07-5 | 1 ML
Harmalol hydrochloride is a beta carboline alkaloid found in medicinal plants like *Peganum harmala*. It is a main metabolite of Harmaline and significantly inhibits the dioxin-mediated induction of CYP1A1 at both transcriptional and posttranslational levels. This compound also exhibits antioxidant and hydroxyl radical-scavenging properties.
- Purity: 99.91%
- Inhibits dioxin-mediated induction of CYP1A1
- Possesses antioxidant and hydroxyl radical-scavenging properties
- For research use only
Medchemexpress LLC Kevetrin hydrochloride | 66592-89-0 | 98.0% | 179.67 | 1 ML
Kevetrin hydrochloride is a potent activator of p53, inducing apoptosis in TP53 wild-type and mutant acute myeloid leukemia cells. It exhibits preferential cytotoxic activity against blast cells.
- Potent activator of p53.
- Induces apoptosis in TP53 wild-type and mutant acute myeloid leukemia cells.
- Exhibits preferential cytotoxic activity against blast cells.
Medchemexpress LLC Erlotinib hydrochloride | 183319-69-9 | 99.7% | 5 MG
Erlotinib hydrochloride is the hydrochloride salt of erlotinib, a quinazoline-derived epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor supplied as an analytical standard for research and analytical applications. It is presented in small pack sizes suitable for laboratory assays.
- Analytical standard for EGFR inhibitor studies.
- CAS number 183319-69-9.
- Purity 99.7% (analytical grade).
- Molecular formula C22H24ClN3O4.
- Molecular weight 429.90 g/mol.
- Available in 5 mg pack size for small-scale laboratory use.
- Suitable as a reference standard for analytical assays.
Apexbio Technology LLC RS 127445 HCl 199864-87-4 50mg
RS 127445 HCl (CAS 199864-87-4) is a small-molecule antagonist targeting the serotonin 5-HT2B receptor a member of the G-protein coupled receptor family It is designed to selectively block 5-HT2B receptor activity thereby modulating intracellular signaling pathways such as calcium elevation and inositol phosphate production RS 127445 HCl exerts its biological activity primarily through selective antagonism of the 5-HT2B receptor In isolated tissue preparations such as rat stomach fundus and jugular vein RS 127445 HCl inhibits serotonin-induced contraction Based on these pharmacological properties RS 127445 HCl holds research potential in studies of 5-HT2B receptor function and related physiological processes
![Medchemexpress LLC N-[3-oxo-3-(4-pyridin-4-ylpiperazin-1-yl)propyl]-2,1,3-benzothiadiazole-4-sulfonamide | 1135243-19-4 | MFCD18086889 | 99.8% | 432.52 | C18H20N6O3S2 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000242004.png-250.jpg)
Medchemexpress LLC N-[3-oxo-3-(4-pyridin-4-ylpiperazin-1-yl)propyl]-2,1,3-benzothiadiazole-4-sulfonamide | 1135243-19-4 | MFCD18086889 | 99.8% | 432.52 | C18H20N6O3S2 | 10 MG
VU 0255035 is a selective, competitive antagonist of the M1 muscarinic acetylcholine receptor used in preclinical research on central nervous system disorders. The compound (CAS 1135243-19-4) has molecular formula C18H20N6O3S2 and is supplied as a high-purity research-grade material for in vitro and in vivo pharmacology.
- Selective M1 receptor antagonism for pharmacological and mechanistic studies.
- High chemical purity suitable for analytical and biological assays.
- Available in multiple small-quantity formats for flexibility in dosing and screening.
- Suitable for both in vitro and in vivo experimental applications.
- Stable when stored under recommended conditions for research use.
Medchemexpress LLC 1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol hydrochloride | 62717-42-4 | MFCD00069248 | 99.5% | 291.77 g/mol | C16H18ClNO2 | 500MG
SKF 38393 hydrochloride is a selective agonist of the dopamine D1 receptor used as a research reagent to study D1-mediated signaling. It is supplied as a solid (also available as a 10 mM solution in DMSO) with analytical-grade purity and intended for research use only.
- CAS number 62717-42-4.
- Chemical formula C16H18ClNO2.
- Molecular weight 291.77 g/mol.
- D1 receptor IC50 ~110 nM.
- Purity approximately 99.5%.
- Available as solid quantities including 500 mg and larger sizes.
- Provided for research use only; not for human or clinical use.
Medchemexpress LLC Co 101244 hydrochloride (PD 174494) | 193356-17-1 | 99.9% | 377.90 | C21H28ClNO3 | 50 MG
Co 101244 hydrochloride is the hydrochloride salt of a small-molecule NR2B-containing NMDA receptor antagonist supplied for research use. It is a light yellow to yellow solid with high purity and characterized molecular properties and storage/solubility data for in vitro and in vivo applications.
- Selective NR2B NMDA receptor antagonist useful for neuroscience research.
- High purity suitable for analytical and biological assays.
- Well-characterized solubility in DMSO for solution preparation.
- Stable when stored sealed at recommended temperatures.
- Available in multiple small-scale quantities for laboratory use.
Medchemexpress LLC Piperoxan hydrochloride | 135-87-5 | MFCD00079224 | 99.7% | 269.77 g/mol | C14H20ClNO2 | 50 MG
Piperoxan hydrochloride is a small-molecule research reagent that functions as an α2 adrenoceptor antagonist and an early-generation antihistamine. Supplied as the hydrochloride salt in high purity, it is used in receptor pharmacology, GPCR studies, and biochemical assays, and is commonly provided as small solid quantities or prepared DMSO stock solutions.
- α2 adrenoceptor antagonist activity suitable for receptor pharmacology studies.
- First-generation antihistamine properties for comparative pharmacology.
- High purity (manufacturer-reported ~99.7%) appropriate for biochemical assays.
- Available as small solid quantities and as prepared DMSO solutions for convenience.
- Molecular formula C14H20ClNO2 and molecular weight 269.77 g/mol.
- Safety and quality documents available, including SDS and COA.
Med Vet International Terbinafine Hydrochloride, 250mg Tablets, 30 Count
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Terbinafine Hydrochloride, 250mg Tablets, 30 Count