Drug Standards
Medchemexpress LLC Triamcinolone | 124-94-7 | 99.8% | 5 G
Triamcinolone is a long-acting corticosteroid that exhibits anti-inflammatory, anti-oedematous, anti-proliferative, anti-angiogenetic, immunomodulatory, and neuroprotective effects by binding to glucocorticoid receptors. It is used to alleviate several dermatitis, immune diseases, and ocular diseases.
- Long-acting corticosteroid.
- Exhibits anti-inflammatory, anti-oedematous, anti-proliferative, anti-angiogenetic, immunomodulatory, and neuroprotective effects.
- Binds to glucocorticoid receptors.
- Used to alleviate dermatitis, immune diseases, and ocular diseases.
- Demonstrates dose-dependent inhibition of bovine retinal endothelial cell proliferation.
- Lowers neovascular cell count in retinopathy of prematurity animal models.
- Investigated in numerous clinical trials.
Apexbio Technology LLC Salinomycin 53003-10-4 10mg
Salinomycin is a polyether ionophore antibiotic derived from Streptomyces albus with demonstrated antitumor activities against various cancer cell types It is proposed to function by disrupting multiple signaling pathways including Wnt/ -catenin signaling and interference with ABC drug transport proteins In vitro research on human hepatocellular carcinoma (HCC) cell lines HepG2 SMMC-7721 and BEL-7402 indicates antiproliferative effects with IC50 values of 7 7 M 13 7 M and 10 4 M respectively after 24-hour treatment Studies show that salinomycin induces cell cycle arrest apoptosis via increased Bax/Bcl-2 ratio reduces -catenin expression and elevates intracellular calcium concentrations In vivo assays using orthotopic liver cancer models corroborate its antiproliferative and pro-apoptotic activities suggesting utility in oncology research
Medchemexpress LLC Ticagrelor impurity 10 | 98.5% | 562.63 g·mol⁻¹ | C26H32F2N6O4S | 10 MG
Ticagrelor impurity 10 is a research-grade impurity of the antiplatelet agent ticagrelor, supplied for analytical reference, impurity profiling, and method development. The material is provided at high stated purity (98.51%) and is characterized by a molecular weight of 562.63 g·mol⁻¹. Small-mass packages are offered for laboratory use, and accompanying documentation (SDS, COA) is available.
- Research-grade impurity for analytical and QC applications.
- High stated purity (98.51%) for reliable reference standards.
- Available in small milligram quantities suitable for method development.
- Characterized molecular weight for analytical confirmation.
- SDS and COA available to support safe handling and verification.
Cayman Chemical VorIconazole-d3 N-oxIde 100ug
An internal standard for the quantification of voriconazole N-oxide by GC- or LC-MS
Medchemexpress LLC Apixaban impurity 2 | 2187409-01-2 | 96.7% | 476.53 | C25H28N6O4 | 10 MG
Apixaban impurity 2 is an analytical reference impurity of the anticoagulant apixaban intended for research and analytical applications. The substance is supplied as a solid reference standard with a reported purity of 96.7% and CAS number 2187409-01-2; a certificate of analysis and safety data sheet are provided for handling and quality information.
- Analytical reference for impurity profiling and method development.
- Reported purity 96.7% suitable for use as a standard.
- Supplied with COA and SDS for lot-specific data and safe handling.
- Available in small analytical sizes, including 10 MG, to support laboratory testing.
Apexbio Technology LLC Atazanavir 198904-31-3 10mM (in 1mL DMSO)
Atazanavir (CAS 198904-31-3) is a small-molecule inhibitor targeting HIV-1 protease It is designed to block protease-mediated cleavage of viral gag and gag-pol polyproteins thereby preventing the maturation of infectious viral particles Atazanavir exerts its biological activity primarily through direct binding to the active site of HIV-1 protease inhibiting polyprotein cleavage In in vitro studies atazanavir demonstrates inhibition of HIV-1 replication with reported EC50 values ranging from 2 6 to 5 3 nmol/L and a protease-inhibition constant (Ki) of approximately 66 nmol/L Based on these pharmacological properties atazanavir holds research potential in anti-retroviral assays and studies involving HIV drug resistance and protease inhibition profiling
eMolecules 65-45-2 | 2-Hydroxybenzamide | Oakwood Chemical137.138 | C7H7NO2 | 99.000 | NC(=O)c1ccccc1O | 1g | 537701996
2-Hydroxybenzamide | Oakwood Chemical | 65-45-2137.138 | C7H7NO2 | 99.000 | NC(=O)c1ccccc1O | 1g | 537701996
![Medchemexpress LLC Methanesulfonamide, n-methyl-n-[5-(bromomethyl)-4-(4-fluorophenyl)-2-pyrimidinyl] | 799842-07-2 | MFCD08694308 | 5g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000267250.png-250.jpg)
Medchemexpress LLC Methanesulfonamide, n-methyl-n-[5-(bromomethyl)-4-(4-fluorophenyl)-2-pyrimidinyl] | 799842-07-2 | MFCD08694308 | 5g
Rosuvastatin impurity 54 is an impurity of Rosuvastatin (HY-17504A)
Med Vet International Levofloxacin Tablets (levaquin) 750mg 20ct
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Levofloxacin Tablets (levaquin) 750mg 20ct
![eMolecules 58207-97-9 | Tributyl[(1E)-2-(trimethylsilyl)ethenyl]stannane | Synthonix - Stock389.286 | C17H38SiSn | 97.000 | CCCC[Sn](CCCC)(CCCC)\C=C\[Si](C)(C)C | 1g | 525923828](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696588.jpg-250.jpg)
eMolecules 58207-97-9 | Tributyl[(1E)-2-(trimethylsilyl)ethenyl]stannane | Synthonix - Stock389.286 | C17H38SiSn | 97.000 | CCCC[Sn](CCCC)(CCCC)\C=C\[Si](C)(C)C | 1g | 525923828
Tributyl[(1E)-2-(trimethylsilyl)ethenyl]stannane | Synthonix - Stock | 58207-97-9389.286 | C17H38SiSn | 97.000 | CCCC[Sn](CCCC)(CCCC)\C=C\[Si](C)(C)C | 1g | 525923828
Sigma Aldrich Fine Chemicals Biosciences Quinine sulfate United States Pharmacopeia (USP) Reference Standard | 207671-44-1 | MFCD00150790 | 500MG
Quinine sulfate United States Pharmacopeia (USP) Reference Standard | Mol Wt: 391.47 | 207671-44-1 | MFCD00150790 | 500MG
Medchemexpress LLC 2-Butenamide, N-[4-[(3-chloro-4-fluorophenyl)amino]-7-[[(3S)-tetrahydro-3-furanyl]oxy]-6-quin azolinyl], | 2223677-64-1 | 50mg
Afatinib impurity 34 is an impurity of Afatinib (HY-10261)
Apexbio Technology LLC Potent Abl and Src kinases inhibitor 302962-49-8. MFCD11046566
Potent Abl and Src kinases inhibitor 302962-49-8. MFCD11046566
Apexbio Technology LLC Famciclovir 104227-87-4 10mM (in 1mL DMSO)
Famciclovir (104227-87-4) is an orally available small-molecule prodrug of penciclovir targeting viral DNA polymerase It is designed to enhance the bioavailability of penciclovir thereby improving inhibition of herpesvirus replication Famciclovir exerts its biological activity primarily through selective inhibition of herpes simplex virus (HSV) DNA polymerase by penciclovir which competes with natural nucleotides In cell-based assays famciclovir-generated penciclovir demonstrates potent antiviral activity with reported IC50 values ranging from 0 1 to 0 8 g/mL Based on these pharmacological properties famciclovir holds research potential in studies of HSV and varicella-zoster virus (VZV) infections
Medchemexpress LLC 1'-epi Gemcitabine hydrochloride | 122111-05-1 | C9H12ClF2N3O4 | 5 MG
1'-epi Gemcitabine hydrochloride is an isomer of Gemcitabine hydrochloride and can be used as an experimental control. It is a pyrimidine nucleoside analog antimetabolite and an antineoplastic agent that inhibits DNA synthesis and repair, resulting in autophagy and apoptosis.
- Isomer of Gemcitabine hydrochloride
- Can be used as an experimental control
- Pyrimidine nucleoside analog antimetabolite
- Antineoplastic agent
- Inhibits DNA synthesis and repair
- Results in autophagy and apoptosis
- For research use only