Drug Standards
Medchemexpress LLC Naftifine hydrochloride | 65473-14-5 | 99.7% | 250 MG
Naftifine hydrochloride is an antibiotic with antifungal activity against dermatophytes, aspergilli, Sporothrix schenckii, and yeasts of the genus Candida. It can be used for the research of superficial dermatomycoses inhibition.
- Antifungal activity against dermatophytes, aspergilli, and yeasts
- Used for superficial dermatomycoses inhibition research
Medchemexpress LLC Methylprednisolone | 83-43-2 | 99.8% | 1 G
Methylprednisolone is a synthetic corticosteroid with anti-inflammatory and immunomodulating properties. It improves severe or critical COVID-19 by activating ACE2 and reducing IL-6 levels. This compound is commonly used for anti-inflammatory purposes and can be utilized in the study of bronchial inflammation or acute bronchitis caused by arthritis and various respiratory diseases. It can also improve neurological recovery in acute spinal cord injury.
- Synthetic corticosteroid
- Anti-inflammatory and immunomodulating properties
- Improves severe or critical COVID-19 by activating ACE2 and reducing IL-6 levels
- Commonly used for anti-inflammatory purposes
- Can be used in the study of bronchial inflammation or acute bronchitis
- Can improve neurological recovery in acute spinal cord injury
- Targets glucocorticoid receptor
- Molecular formula: C22H30O5
- Molecular weight: 374.47
Medchemexpress LLC Sarafloxacin hydrochloride | 91296-87-6 | MFCD03427297 | 98.1% | 10 G
Sarafloxacin hydrochloride (A-56620 hydrochloride) is a quinolone antibiotic agent. It is a fluoroquinolone antibiotic registered for use against poultry diseases. It has been shown to be effective in treating E. ictaluri infections in channel catfish in vivo. This product is for research use only.
- Quinolone antibiotic agent
- Fluoroquinolone antibiotic for poultry diseases
- Efficacious in treating E. ictaluri infections in channel catfish
- Demonstrates mineralization in loam, silt loam, and sandy loam soils
- Inhibitory level for tested bacteria is strain dependent
Medchemexpress LLC Nitisinone | 104206-65-7 | 99.93% | 5 MG
Nitisinone is an orally active, competitive, and reversible 4-hydroxyphenylpyruvate dioxygenase (4-HPPD) inhibitor. It promotes tyrosine accumulation in a dose-dependent manner and is utilized in studies of hereditary tyrosinemia type 1 (HT-1) and albinism.
- Orally active 4-HPPD inhibitor
- Promotes tyrosine accumulation
- Used in studies of hereditary tyrosinemia type 1 (HT-1)
- Applicable in albinism research
- Purity of 99.93%
Medchemexpress LLC Nitisinone | 104206-65-7 | 100 MG
Nitisinone is an orally active, competitive, and reversible 4-hydroxyphenylpyruvate dioxygenase (4-HPPD) inhibitor with an IC50 of 173 nM. It promotes tyrosine accumulation in a dose-dependent manner and can be used in studies of hereditary tyrosinemia type 1 (HT-1) and albinism.
- Orally active and competitive 4-HPPD inhibitor
- Promotes tyrosine accumulation
- Useful in studies of hereditary tyrosinemia type 1 (HT-1)
- Applicable in studies of albinism
![Medchemexpress LLC (2-chloro-5-iodophenyl)[4-[[(3S)-tetrahydro-3-furanyl]oxy]phenyl]methanone | 915095-87-3 | MFCD22665921 | 100mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000270120.png-250.jpg)
Medchemexpress LLC (2-chloro-5-iodophenyl)[4-[[(3S)-tetrahydro-3-furanyl]oxy]phenyl]methanone | 915095-87-3 | MFCD22665921 | 100mg
Empagliflozin impurity 108 is an impurity of Empagliflozin (HY-15409)
Medchemexpress LLC Fostamatinib | 901119-35-5 | 99.7% | 1 ML
Fostamatinib (R788) is an orally available proagent of R406, which is a competitive inhibitor of Syk and FLT3. It also demonstrates inhibitory activity against Lyn and Lck.
- Syk/FLT3 inhibitor
- Also inhibits Lyn and Lck
- Active compound R406
- High purity of 99.7%
- Pre-prepared 10 mM solution in DMSO
- Stable under recommended storage conditions
- Used in various clinical trials
Medchemexpress LLC Enalapril | 75847-73-3 | MFCD00865774 | 99.96% | 50 MG
Enalapril (MK-421) is an angiotensin-converting enzyme (ACE) inhibitor commonly used in hypertensive diseases research. It is a solid, white to off-white compound with a high purity of 99.96%.
- Angiotensin-converting enzyme (ACE) inhibitor
- Suitable for hypertensive diseases research
- High purity of 99.96%
- Solid, white to off-white appearance
- Soluble in DMSO and water
- Melting point of 142-147 °C
- Store under inert gas (nitrogen or argon) at 2-8 °C
Medchemexpress LLC Amoxicillin trihydrate | 61336-70-7 | 99.8% | 1 ML
Amoxicillin trihydrate is an antibiotic exhibiting good oral absorption and broad-spectrum antimicrobial activity. It functions by inhibiting the biosynthesis of polypeptides in the bacterial cell wall, thereby inhibiting cell growth.
- Good oral absorption
- Broad-spectrum antimicrobial activity
- Inhibits biosynthesis of polypeptides in the cell wall
- Inhibits cell growth
- Suitable for in vitro studies
- Effective in in vivo models against various infections
Medchemexpress LLC Hydrochlorothiazide (Standard) | 58-93-5 | MFCD00049453 | 99.6% | 100 MG
Hydrochlorothiazide (Standard) is an analytical standard of Hydrochlorothiazide, an orally active diuretic agent of the thiazide class. It is intended for research and analytical applications, including qualitative, quantitative, and methodological research experiments such as HPLC, GC, and MS.
- Inhibits the transforming TGF-β/Smad signaling pathway.
- Exhibits direct vascular relaxant effects by opening the calcium-activated potassium (KCA) channel.
- Improves cardiac function.
- Reduces fibrosis.
- Has an antihypertensive effect.
Medchemexpress LLC Fluticasone propionate-d5 | 1093258-28-6 | 91.7% | 1 MG
Fluticasone propionate-d5 is a deuterium labeled form of Fluticasone propionate. It is a potent topical anti-inflammatory corticosteroid and a selective glucocorticoid receptor agonist with an absolute affinity (KD) of 0.5 nM. It exhibits little to no activity at other steroid receptors and possesses anti-viral activity.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Medchemexpress LLC Cefaclor | 53994-73-3 | 98.5% | 1 ML
Cefaclor is a well-absorbed orally active cephalosporin antibiotic that specifically binds to penicillin-binding protein 3 (PBP3). It is used in research for various bacterial infections, including respiratory tract infections, bacterial bronchitis, pharyngitis, and skin infections, and also for depression studies.
- Specifically binds to penicillin-binding protein 3 (PBP3)
- Used for research on depression
- Active against various bacterial infections, such as respiratory tract infections, bacterial bronchitis, pharyngitis, and skin infections
- Well-absorbed orally active cephalosporin antibiotic
Medchemexpress LLC Amoxicillin | 26787-78-0 | 99.9% | 1 ML
Amoxicillin is an antibiotic characterized by good oral absorption and broad-spectrum antimicrobial activity. It functions by inhibiting the biosynthesis of polypeptides in the cell wall, which in turn inhibits cell growth. This product is intended for research use only.
- Antibiotic with good oral absorption
- Broad-spectrum antimicrobial activity
- Inhibits biosynthesis of polypeptides in the cell wall
- Inhibits cell growth
- For research use only
Medchemexpress LLC Niclosamide (olamine) | 1420-04-8 | 98.66% | 10 G
Niclosamide olamine is an orally active antihelminthic agent used in parasitic infection research. It acts as a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells. This compound demonstrates biological activities against cancer and inhibits DNA replication in Vero E6 cells.
- Orally active antihelminthic agent
- Used in parasitic infection research
- STAT3 inhibitor
- Demonstrates biological activities against cancer
- Inhibits DNA replication in Vero E6 cells
- Inhibits adrenocortical carcinoma cellular proliferation
- Suppresses colony formation and reduces invasive properties of endometrial cancer cells
- Inhibits tumor growth in vivo
Medchemexpress LLC Spironolactone | 52-01-7 | 99.8% | 5 G
Spironolactone is a high-purity chemical compound, with 99.8% purity, primarily acting as an aldosterone antagonist and also demonstrating antagonist activity at the androgen receptor. This compound is offered in solid form, soluble at 10 mM in DMSO, and is notable for its involvement in podocyte autophagy and pain regulation, alongside its multifaceted antihypertensive effects.
- Improves hypertension-related vascular hypertrophy and remodeling.
- Reduces aldosterone-induced vascular and soft tissue calcification.
- Alleviates vascular dysfunction in type II diabetic mice.
- Promotes podocyte autophagy and regulates pain.
- Acts as an androgen receptor antagonist for hormonal regulation.