Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Follitropin European Pharmacopoeia (EP) Reference Standard | 146479-72-3 |
Follitropin European Pharmacopoeia (EP) Reference Standard | 146479-72-3 |
Selleck Chemical LLC Tenofovir alafenamide fumarate S4428-5mg
Tenofovir alafenamide (TAF GS-7340) fumarate is a prodrug of tenofovir but results in significantly higher intracellular tenofovir concentrations and lower serum levels Tenofovir alafenamide is a novel nucleotide reverse transcriptase inhibitor for the treatment of HIV-1 infection
Sigma Aldrich Fine Chemicals Biosciences Azelastine impurity D European Pharmacopoeia (EP) Reference Standard | 53242-88-9 |
Azelastine impurity D European Pharmacopoeia (EP) Reference Standard | Mol Wt: 270.71 | 53242-88-9 |
Medchemexpress LLC Stearyl arachidate 100mg
Stearyl arachidate is a biochemical reagent that can be used as a biological material or organic compound for life science related research
Apexbio Technology LLC Ranitidine 66357-59-3 100mg
Ranitidine (CAS 66357-59-3) is a small-molecule antagonist targeting histamine H2 receptors It is designed to competitively inhibit histamine binding to H2 receptors on gastric parietal cells thereby reducing gastric acid secretion Ranitidine exerts its biological activity primarily through blockade of histamine H2 receptors In experimental pharmacological assays ranitidine demonstrates antagonist activity with an IC50 value of approximately 3 3 1 4 M Based on these pharmacological properties ranitidine holds research potential in studies of gastric acid-related physiology gastrointestinal ulcer models and pharmacological interventions involving histaminergic pathways
Medchemexpress LLC Meclizine dihydrochloride | 1104-22-9 | 99.95% | 1 ML
Meclizine dihydrochloride is an antihistamine that reversibly inhibits the interaction of histamine at the H1 receptors. As a member of the piperazine class of H1 antagonists, it serves as an effective anti-motion sickness agent. This compound can cross the blood-brain barrier, making it suitable for research into polyQ toxicity disorders such as Huntington's disease. It acts as an agonist ligand for mouse constitutive androstane receptor (CAR) and an inverse agonist for Human CAR. When stored as a solution, it should be kept at -80°C for up to 6 months or -20°C for up to 1 month, under sealed conditions and away from moisture.
- Reversibly inhibits histamine at H1 receptors
- Effective anti-motion sickness agent
- Crosses the blood-brain barrier
- Used for research of polyQ toxicity disorders
- Agonist for mouse CAR and inverse agonist for human CAR
Medchemexpress LLC Meloxicam (Standard) | 71125-38-7 | 99.89% | 25 MG
Meloxicam (Standard) is the analytical standard of Meloxicam, a non-steroidal anti-inflammatory agent that inhibits COX activity. It is intended for research and analytical applications, commonly used as a reference standard in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
- Inhibits COX activity with IC50s of 0.49 μM for COX-2 and 36.6 μM for COX-1.
- Used as a reference standard in qualitative, quantitative, and methodological research experiments.
- Suitable for use in HPLC, GC, and MS.
- Has a molecular weight of 351.40.
- Chemical formula is C14H13N3O4S2.
- Appearance is a solid, light yellow to green yellow in color.
- Purity is 99.89%.
Apexbio Technology LLC Citalopram hydrobromide 59729-32-7 50mg
Citalopram hydrobromide (CAS 59729-32-7) is a selective serotonin reuptake inhibitor (SSRI) that functions by specifically blocking the reuptake of 5-hydroxytryptamine (5-HT) at presynaptic neuronal membranes thereby increasing 5-HT concentrations in the synaptic cleft In vitro studies demonstrate that citalopram hydrobromide exhibits potent nanomolar-level inhibition of 5-HT reuptake in synaptosomal preparations as well as low nanomolar inhibition in rabbit platelet assays This compound is widely utilized in research exploring serotonergic signaling neurotransmission processes and experimental models of depression
Selleck Chemical LLC Idoxuridine S1883-1g
Idoxuridine (NSC 39661 SKF 14287 5-Iodo-2 -deoxyuridine 5-IUdR IdUrd) is an antiviral agent for feline herpesvirus type-1 with IC50 of 4 3 M
Apexbio Technology LLC Econazole nitrate 24169-02-6 10mM (in 1mL DMSO)
Econazole nitrate (24169-02-6) is a small-molecule inhibitor targeting the enzyme 14 -demethylase It is designed to disrupt ergosterol synthesis in fungal membrane sterol biosynthesis thereby decreasing membrane integrity altering permeability and attenuating fungal cellular growth Econazole nitrate exerts its biological activity primarily through inhibition of 14 -demethylase In vitro studies demonstrate antifungal activity with reported IC50 values against various fungal isolates typically ranging from approximately 0 05 to 1 g/mL depending on experimental parameters and organism specificity Based on these pharmacological properties econazole nitrate holds research potential in antifungal susceptibility testing exploration of drug resistance mechanisms in fungal strains characterization of dermatopathogenic microorganisms and drug target identification studies
Medchemexpress LLC (R)-2-(Methoxymethyl)oxirane | 64491-70-9 | MFCD00273372 | 500mg
Rivaroxaban impurity 6 is an impurity of Rivaroxaban (HY-50903)
Sigma Aldrich Fine Chemicals Biosciences Captopril impurity B European Pharmacopoeia (EP) Reference Standard | 80629-35-2 |
Captopril impurity B European Pharmacopoeia (EP) Reference Standard | Mol Wt: 264.12 | 80629-35-2 |
Medchemexpress LLC Dabigatran impurity 14 hydrochloride | 1422435-39-9 | 25mg
Dabigatran Impurity 14 hydrochloride is an impurity of Dabigatran (HY-10163)