Drug Standards
Medchemexpress LLC Ciclopirox | 29342-05-0 | 98.3% | 1 ML
Ciclopirox is a synthetic, orally active antifungal agent used in research for superficial mycoses. It demonstrates broad-spectrum activity against dermatophytes, yeasts, molds, and various pathogenic bacteria, and also exhibits anticancer and anti-inflammatory effects.
- Synthetic, orally active antifungal agent
- Used for superficial mycoses research
- Exhibits broad-spectrum activity against dermatophytes, yeasts, molds, and pathogenic bacteria
- Demonstrates anticancer and anti-inflammatory effects
- Available as a 10 mM x 1 mL solution in DMSO
- Shipped at room temperature
- Powder storage: -20°C for 3 years or 4°C for 2 years
- In-solvent storage: -80°C for 2 years or -20°C for 1 year
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
![Medchemexpress LLC β-Alanine, n-[[2-[[[4-(aminocarbonyl)phenyl]amino]methyl]-1-methyl-1h-benzimidazol-5-yl]carb... | 1422435-41-3 | MFCD27996084 | 50mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000267059.png-250.jpg)
Medchemexpress LLC β-Alanine, n-[[2-[[[4-(aminocarbonyl)phenyl]amino]methyl]-1-methyl-1h-benzimidazol-5-yl]carb... | 1422435-41-3 | MFCD27996084 | 50mg
Dabigatran impurity 16 is an impurity of Dabigatran (HY-10163)
Sigma Aldrich Fine Chemicals Biosciences Moricizine hydrochloride United States Pharmacopeia (USP) Reference Standard | 29560-58-5 | 250MG
Moricizine hydrochloride United States Pharmacopeia (USP) Reference Standard | Mol Wt: 463.98 | 29560-58-5 | 250MG
Sigma Aldrich Fine Chemicals Biosciences Terbinafine Related Compound A United States Pharmacopeia (USP) Reference Standard | 65473-13-4 | MFCD00012555 | 25MG
Terbinafine Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 207.7 | 65473-13-4 | MFCD00012555 | 25MG
Sigma Aldrich Fine Chemicals Biosciences Dantrolene Related Compound A United States Pharmacopeia (USP) Reference Standard | 301359-05-7 | 50MG
Dantrolene Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 430.37 | 301359-05-7 | 50MG
Cayman Chemical 2 5dimethyl Celecoxib
An anticancer celecoxib derivative; does not inhibit COX-2 (IC50 = >100 µM); inhibits mPGES-1 in HeLa cells (IC50 = 15.6 µM); reduces PGE2 production in HeLa, A549, and HCA-7 cells (IC50s = 0.64, 0.83, and 3.08 µM, respectively); inhibits proliferation of drug-sensitive RPMI8226 and multidrug-resistant 8226/Dox40 multiple myeloma cells; increases the rate of apoptosis in RPMI8226 and 8226/Dox40 cells at 20 and 30 µM; the antiproliferative effect of 2,5-dimethyl celecoxib is independent of mPGES-1 inhibition
Apexbio Technology LLC Bupivacaine HCl, 50mg. Cas: 18010-40-7 MFCD: MFCD00078956. Anaesthetic drug
Bupivacaine HCl is a local anaesthetic drug belonging to the amino amide group. 18010-40-7. MFCD00078956
Sigma Aldrich Fine Chemicals Biosciences Prednicarbate for system suitability A European Pharmacopoeia (EP) Reference Standard | 73771-04-7 |
Prednicarbate for system suitability A European Pharmacopoeia (EP) Reference Standard | Mol Wt: 488.57 | 73771-04-7 |
Medchemexpress LLC Betamethasone valerate | 2152-44-5 | 99.8% | 25 MG
Betamethasone valerate, also known as Betamethasone 17-valerate, is the 17-valerate ester of Betamethasone. It functions as a topical corticosteroid with anti-inflammatory activity and is used in the treatment of recurrent aphthous stomatitis. It inhibits the binding of radiolabeled glucocorticoid dexamethasone to human epidermis and mouse skin with IC50s of 5 and 6 nM, respectively.
- Topical corticosteroid with anti-inflammatory properties
- Used for recurrent aphthous stomatitis treatment
- Inhibits radiolabeled glucocorticoid binding
- For research use only
Medchemexpress LLC Latanoprost acid | 41639-83-2 | 95.1% | 390.51 | 25 MG
Latanoprost acid is an analog of prostaglandin (PG) F2α and a selective prostanoid receptor (FP) agonist that activates the FP-PG receptor. It inhibits RANKL-induced osteoclastogenesis and function by inhibiting the ERK, AKT, JNK, and p38 cascade, following the c-fos/NFATc1 pathway. This medication is used to lower pressure inside the eyes and is for research use only.
- Selective prostanoid receptor (FP) agonist
- Activates the FP-PG receptor
- Inhibits RANKL-induced osteoclastogenesis and function
- Inhibits ERK, AKT, JNK, and p38 cascade
- Soluble in DMSO at 100 mg/mL
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%.
Medchemexpress LLC Linagliptin impurity 14 | 25mg
Linagliptin impurity 14 is an impurity of Linagliptin (HY-10284)