Drug Standards
Medchemexpress LLC Methylprednisolone-d7 | 83-43-2 | 99.7% | 1 MG
Methylprednisolone-d7 is a deuterium-labeled version of Methylprednisolone. Methylprednisolone is a synthetic corticosteroid with anti-inflammatory and immunomodulating properties.
- Anti-inflammatory properties
- Immunomodulating properties
- Can improve severe or critical COVID-19 by activating ACE2 and reducing IL-6 levels
Medchemexpress LLC Norfloxacin | 70458-96-7 | MFCD00079532 | 98.3% | 319.33 | 500 MG
Norfloxacin (MK-0366) is a broad-spectrum antibiotic active against both Gram-positive and Gram-negative bacteria, functioning by inhibiting DNA gyrase. It is a synthetic chemotherapeutic antibacterial agent sometimes used for common and complicated urinary tract infections.
- Broad-spectrum antibiotic
- Active against Gram-positive bacteria
- Active against Gram-negative bacteria
- Inhibits DNA gyrase
- Synthetic chemotherapeutic antibacterial agent
- Used for urinary tract infections
Selleck Chemical LLC Thioguanine 50mg 154-42-7
Thioguanine, a purine antimetabolite, inhibits DNMT1 activity through ubiquitin-targeted degradation, used in the treatment of acute lymphoblastic leukemia, autoimmune disorders (e.g., Crohn's disease, rheumatoid arthritis) and organ transplant recipients. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Selleck Chemical LLC Efavirenz 20mg 154598-52-4 Sustiva, Stocrin, DMP-266, DMP 266
Efavirenz (Sustiva, Stocrin, DMP-266) is a synthetic non-nucleoside reverse transcriptase (RT) inhibitor with antiviral activity. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Selleck Chemical LLC Mifepristone 50mg 84371-65-3 RU486, C-1073
Mifepristone (RU486, C-1073) is a remarkably active antagonist of progesterone receptor and glucocorticoid receptor with IC50 of 0.2 nM and 2.6 nM, respectively. Mifepristone promotes cell autophagy and apoptosis, decreases Bcl-2 level and increases Beclin1 level, accompanied by weakened interaction between Bcl-2 and Beclin1. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Selleck Chemical LLC Tenofovir Alafenamide
Tenofovir Alafenamide is a prodrug of tenofovir which is a reverse transcriptase inhibitor used to treat HIV and Hepatitis B
Selleck Chemical LLC Plerixafor (AMD3100) 10mg 110078-46-1 JM 3100
Plerixafor (AMD3100, JM 3100) is a chemokine receptor antagonist for CXCR4 and CXCL12-mediated chemotaxis with IC50 of 44 nM and 5.7 nM in cell-free assays, respectively. Plerixafor inhibits human immunodeficiency virus (HIV) replication. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Selleck Chemical LLC Netarsudil (AR-13324) 2HCl 2mg 1253952-02-1
Netarsudil (a.k.a. AR-13324) is ROCK inhibitor with Ki value of 0.2-10.3 nM. It is currently in clinical trials for the treatment of glaucoma and ocular hypertension. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Apexbio Technology LLC Norfloxacin hydrochloride 104142-93-0 10mg
Norfloxacin hydrochloride is a small-molecule inhibitor targeting bacterial DNA gyrase It is designed to inhibit DNA gyrase an enzyme essential for the supercoiling and replication of bacterial DNA thereby disrupting bacterial DNA synthesis and interfering with bacterial replication and growth Norfloxacin hydrochloride exerts its biological activity primarily through the inhibition of DNA gyrase by binding within the enzyme s active site impeding its catalytic activity Based on these pharmacological properties Norfloxacin hydrochloride holds research potential in the study of bacterial resistance mechanisms bacterial enzyme inhibition assays antimicrobial susceptibility testing and therapeutic research on antibacterial treatment strategies against Gram-positive and Gram-negative bacteria
Medchemexpress LLC Sofosbuvir impurity A | 1496552-16-9 | 529.45 | 5 MG
Sofosbuvir impurity A is a diastereoisomer of Sofosbuvir, which is an inhibitor of HCV RNA replication demonstrating potent anti-hepatitis C virus activity. This product is intended for research and analytical applications.
- Diastereoisomer of Sofosbuvir
- Inhibits HCV RNA replication
- Potent anti-hepatitis C virus activity
- Targeted for HCV
- Solid appearance
- White to yellow color
Medchemexpress LLC Latanoprost lactone diol | 145667-75-0 | MFCD05865275 | 99.9% | 304.38 g·mol⁻¹ | C18H24O4 | 25MG
Latanoprost lactone diol is a high-purity chemical intermediate used in the synthesis of latanoprost and for related research applications. The material is provided as solid quantities and as a DMSO solution, and is intended for synthetic workflows, analytical method development, and laboratory research requiring an intermediate of the prostaglandin F2α family.
- High purity: 99.86% reported
- Chemical formula: C18H24O4
- Molecular weight: 304.38 g·mol⁻¹
- Available sizes include 5 mg, 10 mg, 25 mg, 50 mg, and 100 mg
- Also available as a 10 mM solution in DMSO (1 mL)
- Intended use as a synthesis intermediate and research reagent
Medchemexpress LLC Ticagrelor impurity 27 | 2096989-55-6 | 98.9% | 522.57 g/mol | C23H28F2N6O4S | 10 MG
Ticagrelor impurity 27 is an analytical standard and characterized drug intermediate supplied for research and analytical testing related to ticagrelor. The material is provided as a high-purity solid with documented molecular formula C23H28F2N6O4S and molecular weight 522.57 g/mol; accompanying safety and quality documents are available.
- High purity: 98.9%.
- Molecular formula C23H28F2N6O4S.
- Molecular weight 522.57 g/mol.
- Available in small pack sizes including 1 mg, 5 mg, 10 mg, 50 mg, and 100 mg.
- Intended for research and analytical use only; not for human consumption.
- Comes with COA and SDS for quality and safety information.
![eMolecules 184475-35-2 | 4-[(3-Chloro-4-fluorophenyl)amino]-7-methoxy-6-(3-morpholinopropoxy)quinazoline | Accela ChemBio (ASD) | MFCD04307832 | 446.910 | C22H24ClFN4O3 | 98.000 | COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCCN1CCOCC1 | 10g | 349007343](https://assets.fishersci.com/TFS-Assets/CCG/product-images/NC2045968.JPG-250.jpg)
eMolecules 184475-35-2 | 4-[(3-Chloro-4-fluorophenyl)amino]-7-methoxy-6-(3-morpholinopropoxy)quinazoline | Accela ChemBio (ASD) | MFCD04307832 | 446.910 | C22H24ClFN4O3 | 98.000 | COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCCN1CCOCC1 | 10g | 349007343
4-[(3-Chloro-4-fluorophenyl)amino]-7-methoxy-6-(3-morpholinopropoxy)quinazoline | Accela ChemBio (ASD) | 184475-35-2 | MFCD04307832 | 446.910 | C22H24ClFN4O3 | 98.000 | COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCCN1CCOCC1 | 10g | 349007343
Apexbio Technology LLC Cefditoren Pivoxil 117467-28-4 10mg
Cefditoren pivoxil is a small-molecule prodrug antibiotic targeting penicillin-binding proteins It is designed to inhibit these proteins thereby disrupting peptidoglycan cross-linking essential for bacterial cell wall integrity Cefditoren pivoxil exerts its biological activity primarily through inhibition of bacterial cell wall synthesis This mechanism confers bactericidal activity against a broad range of Gram-positive and Gram-negative organisms Based on these pharmacological properties cefditoren pivoxil holds research potential in studying bacterial susceptibility profiles characterizing resistance mechanisms in pathogens and evaluating pharmacokinetic-pharmacodynamic relationships associated with cephalosporins