Drug Standards
Medchemexpress LLC Diclofenac epolamine | 119623-66-4 | 100.0% | 411.32 | 50 MG
Diclofenac epolamine is a non-steroidal anti-inflammatory drug (NSAID) used for relieving arthritis pain, acute pain, osteoarthritis, and actinic keratosis. It demonstrates good skin absorption characteristics without local adverse reactions or allergies.
- Relieves arthritis pain, acute pain, osteoarthritis, and actinic keratosis.
- Demonstrates good skin absorption characteristics.
- Does not cause local adverse reactions or allergies.
- Effective in treating inflammatory conditions.
- Increases partitioning into the skin.
- Enhances and sustains drug transport through the skin.
Medchemexpress LLC TMPyP4 tosylate | 36951-72-1 | 98.0% | 1363.60 | 50 MG
TMPyP4 tosylate (TMP 1363) is identified as a quadruplex-specific ligand. It functions by inhibiting the interaction between G-quadruplexes and IGF-1. This compound also acts as a telomerase inhibitor, which in turn inhibits the proliferation of cancer cells. Furthermore, TMPyP4 tosylate serves as a stabilizer of nucleic acid secondary structure and an acetylcholinesterase inhibitor. It has also demonstrated antiviral activity against SARS-CoV-2.
- Quadruplex-specific ligand.
- Inhibits the interaction between G-quadruplexes and IGF-1.
- Telomerase inhibitor.
- Inhibits cancer cell proliferation.
- Stabilizes nucleic acid secondary structure.
- Acts as an acetylcholinesterase inhibitor.
- Possesses antiviral activity against SARS-CoV-2.
TARGETMOL CHEMICALS INC ENALAPRILAT DIHYDRATE 200MG
Also available in 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Enalaprilat Dihydrate (MK-422 Dihydrate) （IC50=1.94 nM） is a potent angiotensin-converting enzyme (ACE) inhibitor. purity: 99%
TARGETMOL CHEMICALS INC THEAFLAVIN-3-GALLATE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg and bulk. Please contact Fisher for quotes. Theaflavin-3'-Gallate (Theaflavin 2B) usually comes from the leaves of Camellia sinensis (L.) O. Kuntze. Theaflavin-3'-gallate act as prooxidants and induce oxidative stress with carcinoma cells more sensitive than normal fibroblasts. purity: 99%
U.S. Pharmacopeia Mesalamine, 89-57-6, MFCD00007877, 200 mg
Linear Formula: H2NC6H3-2-(OH)CO2H, Molecular Weight: 153.14, mp: 275-280 °C, Synonym: 5-Amino-2-hydroxybenzoic acid, 5-AS, 5-Aminosalicylic acid, Mesalamine.
Medchemexpress LLC Oxibendazole | 20559-55-1 | MFCD00133728 | 99.6% | 50 MG
Oxibendazole is an effective benzimidazole anthelmintic against nematode infections. It induces apoptosis and has anti-cancer and anti-inflammation activities. For research use only; not sold to patients.
- Molecular weight: 249.27
- Formula: C12H15N3O3
- Appearance: Solid
- Color: White to yellow
- Shipping: Room temperature in continental US; may vary elsewhere
- Storage: Powder: -20°C for 3 years, 4°C for 2 years; In solvent: -80°C for 6 months, -20°C for 1 month
- Solubility (In Vitro): DMSO: 5 mg/mL (20.06 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Apexbio Technology LLC Bromhexine HCl 611-75-6 10mM (in 1mL DMSO)
Bromhexine Hydrochloride is an expectorant compound utilized frequently in respiratory research to examine mucolytic mechanisms It functions primarily by disrupting acidic polysaccharide fibers within bronchial mucus reducing mucus viscosity and facilitating mucociliary clearance The compound is routinely employed in in vitro studies involving respiratory epithelial cells and ex vivo respiratory tract tissues to investigate its pharmacological influence on mucus production and secretion Reported IC50 values for Bromhexine Hydrochloride in mucolytic assays typically range between 30-50 M under standard experimental conditions Its applications extend to the study of respiratory disorders associated with abnormal mucus secretion enabling researchers to better characterize molecular pathways involved in mucus regulation and investigate potential therapeutic targets
SIGMA ALDRICH FINE CHEMICALS BIOSCIENCES CYSTINE CRS EP REF STND 100MG
NC3362773 CYSTINE CRS EP REF STND 100MG
U.S. Pharmacopeia Salicylic Acid, 69-72-7, MFCD00002439, 125mg
Molecular formula C7H6O3, Molecular weight 138.12, Melting point 314.6 - 321.8 °F (157 - 161 °C) ; 76 ° C (sublimes), Boiling point 411.8 °F (211 °C) at 20 mm Hg, Flash point 315.00 °F (157.22 °C) Closed Cup
Medchemexpress LLC Doxazosin | 74191-85-8 | 99.9% | C23H25N5O5 | 25 MG
Doxazosin is a quinazoline-derivative that selectively antagonizes postsynaptic α1-adrenergic receptors. It is a long-lasting inhibitor of α1-adrenoceptors used to treat benign prostatic hyperplasia and lower urinary tract symptoms.
- Selectively antagonizes postsynaptic α1-adrenergic receptors.
- Long-lasting inhibitor of α1-adrenoceptors.
- Used to treat benign prostatic hyperplasia.
- Used to treat lower urinary tract symptoms.
- May inhibit cholesterol synthesis and reduce LDL cholesterol.
Medchemexpress LLC Lenalidomide 4'-PEG2-amine dihydrochloride | 2624336-88-3 | 99.0% | 463.36 g/mol | C19H28Cl2N4O5 | 10 MG
Lenalidomide 4'-PEG2-amine dihydrochloride is a lenalidomide-derived Cereblon (CRBN) ligand functionalized with a PEG2-amine linker, supplied as the dihydrochloride salt for use in targeted protein degradation research. It is intended for conjugation to target ligands to construct PROTACs and other E3 ligase-recruiting molecules.
- Lenalidomide-derived CRBN ligand functionalized with a PEG2-amine linker.
- Designed for conjugation to target-binding ligands to enable PROTAC synthesis.
- Dihydrochloride salt for improved handling in research workflows.
- Molecular weight 463.36 g/mol and formula C19H28Cl2N4O5.
- High purity (98.96%), suitable for research applications.
- Available in mg-scale packages for lab-scale synthesis and screening.
U.S. Pharmacopeia meso-Zeaxanthin | 31272-50-1 | MFCD28579804 | 5 x 30 mg
meso-Zeaxanthin | Mol Wt: 568.88 | 31272-50-1 | MFCD28579804 | 5 x 30 mg
Selleck Chemical LLC Pirfenidone 10mg 53179-13-8 S-7701,AMR-69
Pirfenidone (S-7701, AMR-69) is an inhibitor for TGF-? production and TGF-? stimulated collagen production, reduces production of TNF-? and IL-1?, and also has anti-fibrotic and anti-inflammatory properties. Pirfenidone attenuates chemokine (CC motif) ligand-2 (CCL2) and CCL12 production with anti-fibrotic activity. Phase 3. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC Iluoridine impurity 9 | 191604-81-6 | 1g
Iluoridine Impurity 9 is an impurity of Iluoridine
Medchemexpress LLC Afatinib impurity 90 | 2803420-62-2 | 5mg
Afatinib impurity 90 is an impurity of Afatinib (HY-10261)