Chromatography Standards
Apexbio Technology LLC Enoxaparin 25mg
Enoxaparin (CAS 679809-58-6) is a low molecular weight heparin derivative that acts by potentiating the inhibitory activity of antithrombin III leading to the inhibition of coagulation factors such as thrombin (factor IIa) Through this mechanism Enoxaparin demonstrates anticoagulant properties Experimental studies indicate that it confers neuroprotection in rat hippocampus following traumatic brain injury via antioxidative and anti-inflammatory pathways Enoxaparin is widely used in research investigating deep vein thrombosis pulmonary embolism traumatic brain injury and thrombotic complications associated with COVID-19
![Medchemexpress LLC A-[(3-chlorobenzoyl)amino]-1,2-dihydro-2-oxo-4-quinolinepropanoic acid | 90098-05-8 | MFCD30748222 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Medchemexpress LLC A-[(3-chlorobenzoyl)amino]-1,2-dihydro-2-oxo-4-quinolinepropanoic acid | 90098-05-8 | MFCD30748222 | 1g
Rebamipide impurity 1 is an impurity of Rebamipide (HY-B0360)
Medchemexpress LLC Flutrimazole | 119006-77-8 | 99.3% | 50 MG
Flutrimazole is an imidazole antifungal with dual anti-inflammatory and antifungal activity. It shows scarce transdermal penetration and is advantageous in the research of topical fungal infections with an inflammatory component.
- Imidazole antifungal
- Dual anti-inflammatory and antifungal activity
- Scarce transdermal penetration
- Suitable for research into topical fungal infections with an inflammatory component
Apexbio Technology LLC Betamethasone 378-44-9 10mM (in 1mL DMSO)
Betamethasone is a synthetic corticosteroid functioning primarily as a glucocorticoid receptor agonist Mechanistically it modulates gene expression through binding glucocorticoid receptors regulating transcription factors and subsequently affecting protein synthesis Betamethasone influences inflammatory pathways by inhibiting key enzyme expressions such as phospholipase A2 cyclooxygenase-2 (COX-2) and nitric oxide synthase (NOS) resulting in decreased synthesis of inflammatory mediators like prostaglandins leukotrienes and nitric oxide Additionally it has been reported to suppress keratinocyte proliferation Due to its glucocorticoid-modulating properties and anti-inflammatory effects betamethasone is commonly employed in biomedical research involving inflammatory signaling pathways dermatological models and gene expression studies
U.S. Pharmacopeia Ketorolac Related Compound C, 113502-52-6, MFCD22048820, 20 mg
Empirical Formula (Hill Notation): C14H11NO2, Molecular Weight: 225.24, Synonym: 5-Benzoyl-2,3-dihydro-1H-pyrrolizin-1-one.
Sigma Aldrich Fine Chemicals Biosciences Enalaprilat dihydrate >=98% (HPLC) | 84680-54-6 | MFCD00941393 | 5MG
Enalaprilat dihydrate >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 384.42 | 84680-54-6 | MFCD00941393 | 5MG
Medchemexpress LLC Flunixin (meglumine) | 42461-84-7 | 99.65% | 1 ML
Flunixin meglumine is a cyclooxygenase (COX) inhibitor exhibiting anti-inflammatory effects. It inhibits lipopolysaccharide-induced inducible nitric oxide synthase (iNOS) activity and nuclear factor kappa B (NfκB) activation in RAW 264.7 murine macrophages. In vivo, it inhibits carrageenan-induced exudate PGE2 and serum TXB2 generation.
Sigma Aldrich Fine Chemicals Biosciences Vinpocetine United States Pharmacopeia (USP) Reference Standard | 42971-09-5 | MFCD00211233 | 100MG
Vinpocetine United States Pharmacopeia (USP) Reference Standard | Mol Wt: 350.45 | 42971-09-5 | MFCD00211233 | 100MG
Selleck Chemical LLC Ivermectin 50mg 70288-86-7 MK933
Ivermectin (MK-933, IVM) is a glutamate-gated chloride channel (GluCls) activator, used as a broad-spectrum antiparasitic drug. Ivermectin (MK-933, IVM) is a specific positive allosteric effector of P2X4 and ?7 nicotinic acetylcholine receptors (nAChRs). Ivermectin has potent antiviral activity towards both HIV-1 and dengue virus. Ivermectin induces autophagy through the AKT/mTOR signaling pathway and mitophagy. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC Aminopterin | 54-62-6 | 98.7% | C19H20N8O5 | 50 MG
Aminopterin, also known as 4-Aminofolic acid, is a powerful folic acid antagonist. It operates by catalyzing the reduction of folic acid to tetrahydrofolic acid and competitively inhibits dihydrofolate reductase (DHFR) with a high affinity (Ki of 3.7 pM). This compound is recognized for its significant anticancer and immunosuppressive activities, making it a valuable agent in medical applications, particularly in the treatment of pediatric leukemia.
- Acts as a folic acid antagonist
- Competitively inhibits dihydrofolate reductase (DHFR)
- Exhibits anticancer properties
- Possesses immunosuppressive activities
- Used in the treatment of pediatric leukemia
Medchemexpress LLC Diphenhydramine (Standard) | 58-73-1 | MFCD00274173 | 98.7% | 100 MG
Diphenhydramine (Standard) is an analytical standard intended for research and analytical applications. It is a first-generation histamine H1-receptor antagonist with an anti-cholinergic effect and can cross the ovine blood-brain barrier (BBB). This compound is supplied as a reference standard assay and is commonly used in qualitative, quantitative, and methodological research experiments.
- First-generation histamine H1-receptor antagonist
- Anti-cholinergic effect
- Can cross the ovine blood-brain barrier (BBB)
- Used in HPLC, GC, and MS experiments
- Molecular weight: 255.35
- Formula: C17H21NO
- Appearance: liquid
- Color: colorless to light yellow
- Classified as an alkaloid
- Initial source: endogenous metabolite
- For research use only
Medchemexpress LLC Felodipine | 72509-76-3 | 99.83% | 5 MG
Felodipine is a potent, vasoselective dihydropyridine calcium channel antagonist. It lowers blood pressure by selectively acting on vascular smooth muscle, particularly in the resistance vessels. This anti-hypertensive agent also induces autophagy and can cross the blood-brain barrier. It is intended for research use only and not for sale to patients.
- Potent, vasoselective calcium channel antagonist
- Lowers blood pressure by acting on vascular smooth muscle
- Induces autophagy
- Can cross the blood-brain barrier
Sigma Aldrich Fine Chemicals Biosciences Tinidazole Related Compound A United States Pharmacopeia (USP) Reference Standard | 696-23-1 | MFCD00151322 | 100MG
Tinidazole Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 127.1 | 696-23-1 | MFCD00151322 | 100MG
Apexbio Technology LLC Manidipine 89226-50-6 200mg
Manidipine (CAS 89226-50-6) is a dihydropyridine derivative functioning as a calcium channel blocker This compound specifically inhibits voltage-dependent calcium channels impairing calcium influx into vascular smooth muscle cells resulting in systemic arterial vasodilation Due to this mechanism manidipine is used mainly in research involving cardiovascular regulation hypertension models and investigations into calcium-mediated smooth muscle signaling pathways