Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Warfarin British Pharmacopoeia (BP) Reference Standard | 81-81-2 | MFCD00006854 |
Warfarin British Pharmacopoeia (BP) Reference Standard | Mol Wt: 308.33 | 81-81-2 | MFCD00006854 |
Selleck Chemical LLC Fluconazole S1331-1g
Fluconazole is a fungal lanosterol 14 alpha-demethylase inhibitor which thereby prevents the formation of ergosterol used in the treatment and prevention of superficial and systemic fungal infections
Chem-Impex International, Inc. Norfloxacin | 70458-96-7 | MFCD00079532 | 5G
Norfloxacin, 70458-96-7, MFCD00079532, 5G
Chem-Impex International, Inc. Cefonicid Sodium | 61270-78-8 | MFCD00941437 | 1G
Cefonicid Sodium, 61270-78-8, MFCD00941437, 1G
Medchemexpress LLC Afatinib impurity 32 | 2223677-62-9 | 25mg
Afatinib impurity 32 is an impurity of Afatinib (HY-10261)
U.S. Pharmacopeia Ketorolac Related Compound D, 113502-55-9, MFCD27965995, 20 mg
Empirical Formula (Hill Notation): C14H13NO, Molecular Weight: 211.26, Synonym: 5-Benzoyl-2,3-dihydro-1H-pyrrolizine.
Selleck Chemical LLC Tyloxapol S4578-1g
Tyloxapol (Triton WR1339) is a nonionic liquid polymer of the alkyl aryl polyether alcohol type used as a surfactant to aid liquefaction removal of mucopurulent and bronchopulmonary secretions It also blocks plasma lipolytic activity and thus the breakdown of triglyceride-rich lipoproteins Tyloxapol can be used to induce animal models of Hyperlipidemia Atherosclerosis
Selleck Chemical LLC Dolutegravir (GSK1349572) 5mg 1051375-16-6 S/GSK1349572
Dolutegravir (GSK1349572, S/GSK1349572) is a two-metal-binding HIV integrase inhibitor with IC50 of 2.7 nM in a cell-free assay, modest activity against raltegravir-resistant signature mutants Y143R, Q148K, N155H, and G140S/Q148H. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC Gabapentin | 60142-96-3 | 98.0% | 171.24 | 10 MG
Gabapentin is a potent, orally active P/Q type Ca2+ channel blocker. It inhibits neuronal Ca2+ influx and reduces neurotransmitter release. As a GABA analog, it can be used to relieve neuropathic pain.
- Inhibits neuronal Ca2+ influx
- Reduces neurotransmitter release
- Alleviates neuropathic pain
- Inhibits K+-induced [Ca2+]i increase in synaptosomes
- Decreases K+-evoked release of endogenous aspartate and glutamate in neocortical slices
- Reduces K+-evoked [3H]-noradrenaline release in neocortical slices
U.S. Pharmacopeia acetazolamide | 59-66-5 | 222.3 g/mol | 2G
acetazolamide | 59-66-5 | 222.3 g/mol | 2G
Medchemexpress LLC Sulfamerazine (Standard) | 127-79-7 | 99.7% | 25 MG
Sulfamerazine (Standard) is the analytical standard for Sulfamerazine. It is intended for research and analytical applications, serving as a reference standard for assays.
- Used in qualitative research experiments
- Used in quantitative research experiments
- Used in methodological research experiments
- Compatible with techniques such as HPLC, GC, and MS
Medchemexpress LLC Citalopram (hydrobromide) | 59729-32-7 | 1 ML
Citalopram hydrobromide is a selective serotonin reuptake inhibitor (SSRI) with blood-brain barrier permeability. It inhibits 5-HT uptake into synaptosomes and rabbit blood platelets, demonstrating an antidepressant effect. It also exhibits concentration-dependent cytotoxicity on various neuroblastoma cell lines and human primary Schwann cells in vitro.
- Selective serotonin reuptake inhibitor (SSRI)
- Blood-brain barrier permeability
- Inhibits 5-HT uptake into synaptosomes with an IC50 of 1.8 nM
- Inhibits 5-HT uptake in rabbit blood platelets with an IC50 of 14 nM
- Exhibits concentration-dependent cytotoxicity on various neuroblastoma cell lines and human primary Schwann cells in vitro
TARGETMOL CHEMICALS INC MOGROSIDE V 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Mogroside V is a widely used sweetener has in vitro AMPK activating effect it also has anti-inflammatory potential in murine macrophages and a murine ear edema model and has the potential to protect against LPS-induced airway inflammation in a model of ALI. Mogroside V has antioxidant properties and possesses tumor growth inhibitory activity in pancreatic cancer models. purity: 98%
Cayman Chemical S S-hydroxy Bupropion hydroc
An active metabolite of bupropion; inhibits dopamine and norepinephrine but not 5-HT reuptake in HEK293 cells expressing the human transporters (IC50s = 0.63, 0.241, and >100 µM, respectively); an antagonist of α3β4-, α4β2-, α4β4-, and α1β1 subunit-containing nAChRs (IC50s = 11, 3.3, 30, and 28 µM, respectively); inhibits nicotine-induced analgesia in the tail-flick and hot plate tests, hyperlocomotion, and hypothermia in mice (ED50s = 0.2, 1, 0.9, and 1.5 mg/kg, respectively); substitutes for (+)-amphetamine in rats in a two-lever drug discrimination test (ED50 = 4.4 mg/kg)
Cayman Chemical N-NItroso Metoprolol 10mg
A genotoxic derivative of metoprolol; induces DNA fragmentation in rat hepatocytes from 0.1-1 mM; induces micronucleation of rat hepatocytes in vivo at 1,000 mg/kg