Drug Standards
TARGETMOL CHEMICALS INC Pantoprazole Sodium Hydrate
Also available in 1 mL, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. Pantoprazole Sodium Hydrate (BY1023 (sodium hydrate)) is a proton pump inhibitor drug, used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease. Purity 98.32%
U.S. Pharmacopeia Ethosuximide, 77-67-8, MFCD00072123, 500mg
Molecular formula C7-H11-N-O2, Molecular weight 141.17 g/mol, Melting point/freezing point 116.6 - 125.6 °F (47 - 52 °C), Synonyms: 2-Ethyl-2-Methylsuccinimide
Medchemexpress LLC Moxifloxacin (BAY 12-8039 free base) | 151096-09-2 | 99.8% | 1 G
Moxifloxacin is an orally active 8-methoxyquinolone antimicrobial.
- Used to treat acute bacterial sinusitis
- Used to treat acute bacterial exacerbations of chronic bronchitis
- Used to treat community-acquired pneumonia
Selleck Chemical LLC Pimecrolimus 10mg 137071-32-0 ASM 981
Pimecrolimus (ASM 981) is an immunophilin ligand, which binds specifically to the cytosolic receptor, immunophilin macrophilin-12 (FKBP-12); a calcineurin inhibitor. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC Manidipine dihydrochloride | 89226-75-5 | 99.8% | 683.62 | 100 MG
Manidipine dihydrochloride | 89226-75-5 | 99.8% | 683.62 | 100 MG
Medchemexpress LLC Fenticonazole Nitrate | 73151-29-8 | 98.9% | 1 ML
Fenticonazole Nitrate is an antifungal imidazole ring derivative. It functions by hindering ergosterol integration, which in turn destructs the cytoplasmatic outer membrane. Fenticonazole Nitrate is effective against Gram-positive bacteria, mycoses, and vaginal candidiasis.
- Antifungal imidazole ring derivative
- Hinders ergosterol integration
- Destroys the cytoplasmatic outer membrane
- Effective against Gram-positive bacteria
- Effective against mycoses
- Effective against vaginal candidiasis
Apexbio Technology LLC Acebutolol HCl 34381-68-5 200mg
Acebutolol hydrochloride (CAS 34381-68-5) is a selective 1-adrenergic receptor antagonist By competitively inhibiting the binding of catecholamines to 1-adrenergic receptors acebutolol modulates sympathetic nervous system activity resulting in decreased heart rate and myocardial contractility This pharmacological profile underlies its utility in preclinical studies on cardiovascular regulation including models of hypertension angina pectoris and cardiac arrhythmias Acebutolol HCl is widely used in biomedical research to investigate -adrenergic signaling pathways and to evaluate therapeutic approaches targeting cardiac function and blood pressure control
Medchemexpress LLC Sarafloxacin hydrochloride | 91296-87-6 | 98.13% | 5 G
Sarafloxacin hydrochloride is a quinolone antibiotic agent, effective against poultry diseases and *Edwardsiella ictaluri* infections in channel catfish. Its inhibitory levels vary by bacterial strain, with *Escherichia coli* isolates showing higher sensitivity in broth culture compared to simulated gut models, suggesting potential absorption to organic matter. In field trials, administration to catfish infected with *E. ictaluri* significantly improved survival rates.
- Quinolone antibiotic agent
- Effective against poultry diseases
- Successfully treated *Edwardsiella ictaluri* infections in channel catfish
- Demonstrated varying inhibitory levels for tested bacteria
- Improved survival rates in field trials for infected catfish
Apexbio Technology LLC BROMFENAC SODIUM HYDRATE50MG
BROMFENAC SODIUM HYDRATE50MG APEXBIO TECHNOLOGIES
Medchemexpress LLC Fluvoxamine maleate | 61718-82-9 | 99.8% | C19H25F3N2O6 | 5 MG
Fluvoxamine maleate is an antidepressant that operates pharmacologically as a selective serotonin reuptake inhibitor. It is effective in inhibiting 5-HT uptake by blood platelets and brain synaptosomes, and it has been studied for its potential in treating various conditions, including depressive disorder, obsessive-compulsive disorder, and post-traumatic stress disorder.
- Functions as an antidepressant.
- Acts as a selective serotonin reuptake inhibitor.
- Inhibits serotonin uptake by blood platelets and brain synaptosomes.
- Demonstrates spermicidal activity against human spermatozoa.
- Shown in studies to improve PTSD symptoms.
- Has been investigated for treating depressive and obsessive-compulsive disorders.
Apexbio Technology LLC (+)-Ketoconazole 142128-59-4 10mg
( )-Ketoconazole (CAS 142128-59-4) is a small-molecule inhibitor targeting cytochrome P450 enzymes primarily CYP3A4 and P450c17 (CYP17A1) It is designed to inhibit these enzymes thereby blocking steroidogenesis pathways and reducing androgen biosynthesis ( )-Ketoconazole exerts its biological activity primarily through inhibition of CYP3A4 and CYP17A1 In in vitro studies ( )-Ketoconazole demonstrates inhibitory activity with reported IC50 values in the low nanomolar to submicromolar range Based on these pharmacological properties ( )-Ketoconazole holds research potential in studying steroid hormone biosynthesis pathways and the biological functions regulated by cytochrome P450 enzyme activity particularly in investigations involving androgen-dependent cell models and related endocrine mechanisms
Cayman Chemical TemozolomIde-d3 1mg
An internal standard for the quantification of temozolomide by GC- or LC-MS
Medchemexpress LLC Chitosan | 9012-76-4 | 90.0% | 10 G
Chitosan (MW 30000) is a polycationic linear polysaccharide derived from chitin with an average molecular weight of 30000. It is a versatile biomaterial, recognized for its non-toxicity, low allergenicity, biocompatibility, and biodegradability. This compound also demonstrates antitumor, antibacterial, antifungal, and antioxidant activities.
- Reduces growth potential and induces pro-apoptotic effects in certain melanoma cells.
- Low molecular weight forms inhibit bacterial DNA transcription and mRNA synthesis.
- High molecular weight forms alter bacterial cell wall permeability.
- Used in water treatment, wound healing, drug delivery, obesity research, and tissue engineering.
- Reduces aberrant crypt foci formation in colonic precancerous lesions in mice.