Aralkylamines
C1CCOCC1 | 1g | 592889575](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502146881.JPG-250.jpg)
eMolecules 871261-12-0 | (R)-Amino-(tetrahydro-pyran-4-yl)-acetic acid methyl ester hydrochloride | J&W PharmLab LLC | MFCD09997723 | 209.670 | C8H16ClNO3 | 96.000 | Cl.COC(=O)[C@H](N)C1CCOCC1 | 1g | 592889575
(R)-Amino-(tetrahydro-pyran-4-yl)-acetic acid methyl ester hydrochloride | J&W PharmLab LLC | 871261-12-0 | MFCD09997723 | 209.670 | C8H16ClNO3 | 96.000 | Cl.COC(=O)[C@H](N)C1CCOCC1 | 1g | 592889575
Medchemexpress LLC (±)-Stylopine hydrochloride | 96087-21-7 | 359.8 | 5 MG
(±)-Stylopine (Tetrahydrocoptisine) hydrochloride is an alkaloid compound originally isolated from Corydalis tubers. This compound exhibits anti-inflammatory and anti-parasitic activities.
- Exhibits anti-inflammatory activity.
- Exhibits anti-parasitic activity.
eMolecules 351534-35-5 | 4-(3-Bromo-phenyl)-piperidine-2,6-dione | J & W PharmLab LLC | MFCD06796573 | 268.110 | C11H10BrNO2 | 96.000 | Brc1cccc(c1)C1CC(=O)NC(=O)C1 | 5g | 289353707
4-(3-Bromo-phenyl)-piperidine-2,6-dione | J & W PharmLab LLC | 351534-35-5 | MFCD06796573 | 268.110 | C11H10BrNO2 | 96.000 | Brc1cccc(c1)C1CC(=O)NC(=O)C1 | 5g | 289353707
Medchemexpress LLC Teneligliptin hydrobromide | 906093-29-6 | MFCD20279612 | ≥98.0% | 628.86 | 25 MG
Teneligliptin hydrobromide is an orally active, potent, and highly selective dipeptidyl peptidase-4 (DPP-4) inhibitor. It improves blood glucose levels and is utilized in research related to type 2 diabetes mellitus. The compound exhibits a unique 'J-shaped' structure, enabling it to bind to four subsites of DPP-4.
- Orally active and selective dipeptidyl peptidase-4 (DPP-4) inhibitor.
- Improves blood glucose levels.
- Used in research for type 2 diabetes mellitus.
- Exhibits a unique 'J-shaped' structure for effective DPP-4 binding.
- Prevents activation of the NLRP3 inflammasome and injury by increasing AMPK phosphorylation.
- Protects against hypoxia/reoxygenation-induced endothelial cell injury.
- Inhibits lipopolysaccharide-induced cytotoxicity and inflammation.
- Prevents high glucose and H2O2 induced USP22-SIRT1 downregulation.
Medchemexpress LLC Grepafloxacin hydrochloride | 161967-81-3 | 99.6% | C19H23ClFN3O3 | 5 MG
Grepafloxacin hydrochloride (OPC-17116) is an orally active fluoroquinolone antibiotic. It exhibits potent activity against community-acquired respiratory pathogens, including *Streptococcus pneumonia*. This compound is characterized by its high tissue penetration and a promising pharmacodynamic profile, making it suitable for various research applications.
- Oral active fluoroquinolone antibiotic
- Potent against *Streptococcus pneumonia*
- High tissue penetration
- Promising pharmacodynamic profile
Medchemexpress LLC Etelcalcetide (hydrochloride) | 1334237-71-6 | 87645 | 99.3% | 1353.33 | 25 MG
Etelcalcetide hydrochloride is a synthetic calcimimetic that acts as an activator of the calcium sensing receptor (CaSR). It is effective in lowering parathyroid hormone (PTH) concentrations in dialysis patients with secondary hyperparathyroidism undergoing hemodialysis, showing promise for research in secondary hyperparathyroidism and chronic kidney disease.
- Activates the calcium sensing receptor (CaSR)
- Lowers parathyroid hormone (PTH) concentrations
- Effective for secondary hyperparathyroidism in dialysis patients
- Useful for research in secondary hyperparathyroidism and chronic kidney disease
- Reduces parathyroid hormone (PTH) levels in human parathyroid cells in vitro
- Significantly reduces plasma parathyroid hormone (PTH) concentrations in vivo
eMolecules 84570-49-0 | (S)-2-AMINO-2-PHENYLPROPANOIC ACID HCL | MFCD12759015 | 1g
AstaTech | (S)-2-AMINO-2-PHENYLPROPANOIC ACID HCL | 1g | 233629596 | 75105 | 95.000 | 84570-49-0 | MFCD12759015 | 201.650 | C9H12ClNO2
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Medchemexpress LLC (S)-Tomoxetine hydrochloride | 82857-39-4 | MFCD11035876 | 99.8% | 291.82 g/mol | C17H22ClNO | 5 MG
(S)-Tomoxetine hydrochloride is the S-enantiomer of tomoxetine, a norepinephrine reuptake inhibitor used as a research reagent to study norepinephrine transport and related pharmacology. It is supplied as a high-purity hydrochloride salt in small, pre-weighed pack sizes for laboratory use; not for human or veterinary use.
- High purity suitable for analytical and preclinical research.
- Reported Ki of 16.8 nM for norepinephrine reuptake.
- Molecular weight 291.82 g/mol; formula C17H22ClNO.
- Provided with purity specification and batch traceability.
- Available in small milligram pack sizes for assay work.
- Intended for laboratory research use only.
Medchemexpress LLC Navlimetostat hydrochloride | 2630904-45-7 | MFCD34604075 | 99.61% | 501.34 | 50 MG
Navlimetostat hydrochloride, also known as MRTX-1719 hydrochloride, is a potent, orally active, selective PRMT5-MTA complex inhibitor (IC50 values of 3.6 nM for PRMT5-MTA and 20.5 nM for PRMT5). It binds strongly to the PRMT5-MTA complex (KD of 0.14 pM) and demonstrates antineoplastic activity in vitro and in vivo, making it suitable for cancer research.
- In vitro activity: Inhibits PRMT5 activity (IC50 8 nM) and viability (IC50 12 nM) in MTAP-deleted HCT116 cells.
- In vivo activity: Significantly reduces tumor growth in Lu-99 orthotopic xenograft models (12.5-100 mg/kg/day, oral, 21 days).
- Pharmacokinetics: High bioavailability in CD-1 mice (80% at 30 mg/kg p.o.) and Beagle dogs (59% at 10 mg/kg p.o.).
eMolecules 2096338-01-9 | 1-(2,6-Dichlorophenyl)pyrazole-4-boronic acid, pinacol ester | Combi-Blocks | MFCD19981556 | 339.020 | C15H17BCl2N2O2 | 95.000 | CC1(C)OB(OC1(C)C)c1cnn(c1)-c1c(Cl)cccc1Cl | 1g | 117545847
1-(2,6-Dichlorophenyl)pyrazole-4-boronic acid, pinacol ester | Combi-Blocks | 2096338-01-9 | MFCD19981556 | 339.020 | C15H17BCl2N2O2 | 95.000 | CC1(C)OB(OC1(C)C)c1cnn(c1)-c1c(Cl)cccc1Cl | 1g | 117545847
eMolecules 958334-24-2 | Methyl 7-bromo-1,5-naphthyridine-3-carboxylate | MFCD11518964 | 1g
Ambeed | Methyl 7-bromo-1,5-naphthyridine-3-carboxylate | 1g | 600847140 | A754093 | 958334-24-2 | MFCD11518964 | 267.082 | C10H7BrN2O2
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![eMolecules 32166-04-4 | trans-2,6-Dimethyl-piperidine hydrochloride | J&W PharmLab LLC299.320 | C14H32Cl2N2 | 96.000 | Cl.Cl.C[C@H]1CCC[C@H](C)N1.C[C@@H]1CCC[C@@H](C)N1 | 1g | 592897674](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502147000.JPG-250.jpg)
eMolecules 32166-04-4 | trans-2,6-Dimethyl-piperidine hydrochloride | J&W PharmLab LLC299.320 | C14H32Cl2N2 | 96.000 | Cl.Cl.C[C@H]1CCC[C@H](C)N1.C[C@@H]1CCC[C@@H](C)N1 | 1g | 592897674
trans-2,6-Dimethyl-piperidine hydrochloride | J&W PharmLab LLC | 32166-04-4299.320 | C14H32Cl2N2 | 96.000 | Cl.Cl.C[C@H]1CCC[C@H](C)N1.C[C@@H]1CCC[C@@H](C)N1 | 1g | 592897674
Apexbio Technology LLC Fingolimod (FTY720), 100mg. Cas: 162359-56-0 MFCD: MFCD00939512. S1P receptors agonist
Fingolimod is Src-bcr-Abl Inhibitor & S1P receptor agonist with IC50 of 0.137, 10.98 nM for (S)- and (R)- FTY720-phosphate. 162359-56-0. MFCD00939512
Medchemexpress LLC (-)-GSK598809 hydrochloride | 863766-31-8 | 517.97 | 50 MG
(-)-GSK598809 is an isomer of GSK598809. GSK598809 is a potent and selective dopamine D3 Receptor (DRD3) antagonist.
- Potent and selective dopamine D3 receptor (DRD3) antagonist
- Target: D3 Receptor
- Store at 4°C, sealed, away from moisture
- In solvent, store at -80°C for 6 months or -20°C for 1 month (sealed, away from moisture)
eMolecules 221095-80-3 | AZETIDIN-3-YLMETHANAMINE 2HCL | AstaTech | MFCD10565803 | 159.050 | C4H12Cl2N2 | 95.000 | Cl.Cl.NCC1CNC1 | 0.25g | 233621883
AZETIDIN-3-YLMETHANAMINE 2HCL | AstaTech | 221095-80-3 | MFCD10565803 | 159.050 | C4H12Cl2N2 | 95.000 | Cl.Cl.NCC1CNC1 | 0.25g | 233621883