Drug Standards
Apexbio Technology LLC Streptozocin, 18883-66-4, MFCD00006607, 100 mg
MF: C8H15N3O7, MW: 265.22, Solubility: 10.3mg/mL in DMSO, 53.2mg/mL in H2O, 26.5mg/mL in EtOH with gentle warming. Antibiotic and antitumor agent. Alkylates DNA and induces diabetes mellitus via reduction of nicotinamide adenine dinucleotide in pancreatic beta-cells in vivo.
Medchemexpress LLC Metoprolol (succinate) (standard) | 98418-47-4 | 99.9% | 652.82 | 25 MG
Metoprolol succinate (Standard) is the analytical standard of Metoprolol succinate, intended for research and analytical applications. It is an orally active, selective β1-adrenoceptor antagonist that exhibits anti-inflammation, antitumor, and anti-angiogenic properties.
- Used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS
- Orally active, selective β1-adrenoceptor antagonist
- Exhibits anti-inflammation, antitumor, and anti-angiogenic properties
![Medchemexpress LLC 2-Propanol, 1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]- | 51384-51-1 | 99.9% | 267.36 | 10 MM / 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000387184-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 2-Propanol, 1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]- | 51384-51-1 | 99.9% | 267.36 | 10 MM / 1 ML
Metoprolol is an orally active, selective β1-adrenoceptor antagonist. It exhibits anti-inflammatory, antitumor, and anti-angiogenic properties.
- Orally active
- Functions as a selective β1-adrenoceptor antagonist
- Shows anti-inflammatory effects
- Exhibits antitumor properties
- Demonstrates anti-angiogenic characteristics
Selleck Chemical LLC Cabozantinib malate S4001-50mg
Cabozantinib malate (XL184) is the malate of Cabozantinib a potent VEGFR2 inhibitor with IC50 of 0 035 nM and also inhibits c-Met Ret (c-Ret) Kit (c-Kit) Flt-1/3/4 Tie2 and AXL with IC50 of 1 3 nM 4 nM 4 6 nM 12 nM/11 3 nM/6 nM 14 3 nM and 7 nM in cell-free assays respectively Cabozantinib malate (XL184) induces apoptosis
Sigma Aldrich Fine Chemicals Biosciences Ritonavir European Pharmacopoeia (EP) Reference Standard | 155213-67-5 |
Ritonavir European Pharmacopoeia (EP) Reference Standard | Mol Wt: 720.94 | 155213-67-5 |
Medchemexpress LLC Octyl gallate | 1034-01-1 | MFCD00002197 | 282.33 | 25 MG
Octyl gallate, also known as Progallin O, is a derivative of gallic acid recognized for its diverse biological activities. It is frequently employed as a food additive due to its potent antioxidant and antimicrobial properties. Research indicates its promising effectiveness against a broad spectrum of microorganisms, including both Gram-positive and Gram-negative bacteria. Furthermore, it has demonstrated significant antiviral effects against viruses such as HSV-1, vesicular stomatitis virus (VSV), and poliovirus, as well as notable antifungal activity.
- Acts as a powerful antioxidant.
- Exhibits broad-spectrum antibacterial activity.
- Shows selective antiviral properties.
- Possesses antifungal effects.
- Commonly used as a food additive.
![Medchemexpress LLC 2-[(3-chlorobenzoyl)amino]-3-(2-oxo-1H-quinolin-4-yl)propanoic acid | 90098-05-8 | MFCD30748222 | 250mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000267438.png-250.jpg)
Medchemexpress LLC 2-[(3-chlorobenzoyl)amino]-3-(2-oxo-1H-quinolin-4-yl)propanoic acid | 90098-05-8 | MFCD30748222 | 250mg
Rebamipide impurity 1 is an impurity of Rebamipide (HY-B0360)
![Medchemexpress LLC 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-3H-2-benzofuran-5-carboxamide | 64372-56-1 | MFCD24857372 | 10mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000269462.png-250.jpg)
Medchemexpress LLC 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-3H-2-benzofuran-5-carboxamide | 64372-56-1 | MFCD24857372 | 10mg
Citalopram impurity-1 (Compound iv) is an amide impurity generated during the synthesis of Citalopram (HY-121203)[1]
Selleck Chemical LLC Buparlisib (BKM120) 10mM/1mL 944396-07-0 NVP-BKM120
Buparlisib (BKM120, NVP-BKM120) is a selective PI3K inhibitor of p110?/?/?/? with IC50 of 52 nM/166 nM/116 nM/262 nM in cell-free assays, respectively. Reduced potency against VPS34, mTOR, DNAPK, with little activity to PI4K?. Buparlisib induces apoptosis. Phase 2. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Sigma Aldrich Fine Chemicals Biosciences Choline chloride United States Pharmacopeia (USP) Reference Standard | 67-48-1 | MFCD00011721 | 500MG
Choline chloride United States Pharmacopeia (USP) Reference Standard | Mol Wt: 139.62 | 67-48-1 | MFCD00011721 | 500MG
Selleck Chemical LLC Betahistine mesylate
Betahistine mesylate is the mesylate salt form of Betahistine a histamine analog and H3 receptor agonist that serves as a vasodilator
Medchemexpress LLC Fexofenadine | 83799-24-0 | 99.8% | 1 ML
Fexofenadine is an orally active and nonsedative H1 receptor antagonist, suitable for research into allergic rhinitis and chronic idiopathic urticarial. It is provided as a 10 mM solution in DMSO.
- Active and nonsedative H1 receptor antagonist
- Can be used in allergic rhinitis research
- Can be used in chronic idiopathic urticarial research
- Purity of 99.8%
Medchemexpress LLC Loxapine (succinate) | 27833-64-3 | 98.8% | 445.90 | 10 MM 1 ML
Loxapine succinate is an orally active dopamine inhibitor, 5-HT receptor antagonist, and a dibenzoxazepine anti-psychotic agent. It can also suppress bacterial efflux pump activity and inhibit intracellular multiple-antibiotic-resistant *Salmonella enterica* serovar Typhimurium in macrophages.
- Orally active dopamine inhibitor
- 5-HT receptor antagonist
- Dibenzoxazepine anti-psychotic agent
- Suppresses bacterial efflux pump activity
- Inhibits intracellular multiple-antibiotic-resistant Salmonella enterica serovar Typhimurium in macrophages