Chromatography Standards
Sigma Aldrich Fine Chemicals Biosciences Betamethasone dipropionate
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.for further information and support please go to the website of the issuing Pharmacopoeia.
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
Medchemexpress LLC Doxycycline hyclate | 24390-14-5 | 512.94 | 50 G
Doxycycline hyclate is an orally active, broad-spectrum antibiotic and metalloproteinase (MMP) inhibitor. It exhibits antibacterial activity and anti-cancer cell proliferation activity. This compound can also be utilized in constructing gene expression regulation models.
- Orally active and broad-spectrum metalloproteinase (MMP) inhibitor.
- Shows antibacterial activity.
- Exhibits anti-cancer cell proliferation activity.
- Can be used to construct gene expression regulation models.
- Longer activity compared to Tetracycline, allowing for once or twice daily administration.
- Shorter time to reach peak concentration and significantly longer half-life compared to Tetracycline.
Medchemexpress LLC Itacitinib | 1334298-90-6 | 100.0% | 553.51 | 5 MG
Itacitinib (INCB039110) is an orally active and selective inhibitor of JAK1, exhibiting significant selectivity over JAK2, JAK3, and TYK2. It is primarily used in the research of myelofibrosis. This product is for research purposes only and has not been fully validated for medical applications.
- Orally active and selective JAK1 inhibitor
- IC50 of 2 nM for human JAK1
- Over 20-fold selectivity for JAK1 over JAK2
- Over 100-fold selectivity over JAK3 and TYK2
- Used in myelofibrosis research
- For research purposes only
Medchemexpress LLC Keto-itraconazole | 112560-33-5 | MFCD08063772 | 98.4% | 719.62 g·mol^-1 | C35H36Cl2N8O5 | 5 MG
Keto-itraconazole is the primary human metabolite of itraconazole used in research as a potent cytochrome P450 3A (CYP3A) inhibitor. It is supplied as a high-purity solid for in vitro pharmacology, metabolism, and drug-drug interaction studies. Typical small pack sizes are provided for lab-scale experiments.
- Potent CYP3A inhibitor (unbound IC50 ≈ 4.6 nM in human liver microsomes with midazolam).
- High purity solid suitable for in vitro assays (reported purity 98.4%).
- Molecular formula C35H36Cl2N8O5 and molecular weight 719.62 g·mol^-1.
- Suitable for liver microsome incubations and drug-drug interaction studies.
- Available in small quantities for research use.
Medchemexpress LLC Atazanavir (sulfate) | 229975-97-7 | 99.7% | 802.93 | 50 MG
Atazanavir sulfate is a highly selective and orally active HIV-1 protease inhibitor with blood-brain barrier permeability. It functions as both a substrate and inhibitor of CYP3A4, and also inhibits P-glycoprotein (P-gp). Additionally, it is a SARS-CoV 3CLpro inhibitor with an IC50 of 3.49 μM. This compound has demonstrated the ability to inhibit cardiac fibrosis and hyperlipidemia, and induce malignant glioma cell death.
- Highly selective and orally active
- HIV-1 protease inhibitor
- Crosses the blood-brain barrier
- Inhibitor and substrate of CYP3A4
- Inhibits P-glycoprotein (P-gp)
- SARS-CoV 3CLpro inhibitor (IC50 of 3.49 μM)
- Inhibits cardiac fibrosis
- Inhibits hyperlipidemia
- Induces malignant glioma cell death
Selleck Chemical LLC Decitabine 10mM/1mL 2353-33-5 Deoxycytidine, Dacogen, 5-aza-2'-deoxycytidine, 5-AZA-dC, 5-aza-CdR
Decitabine (Deoxycytidine, Dacogen, 5-aza-2-deoxycytidine, 5-AZA-dC, 5-aza-CdR) is a DNA methyltransferase inhibitor, incorporating into DNA and resulting in hypomethylation of DNA and intra-S-phase arrest of DNA replication. It is used to treat myelodysplastic syndrome (MDS). Decitabine induces cell cycle arrest and apoptosis in various cancer cell lines. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC Metoprolol | 51384-51-1 | MFCD00599534 | 100.0% | 267.36 g·mol-1 | C15H25NO3 | 10 MG
Metoprolol analytical standard intended for research and analytical applications. Supplied as a 10 mg vial, this reference material supports assay development, method validation, and compound identification; it is intended for laboratory use only and not for human or clinical use.
- Analytical reference standard for assay development and method validation.
- High purity (>99.9%) suitable for chromatographic analysis.
- Molecular formula C15H25NO3; molecular weight 267.36 g·mol-1.
- Provided in small research packaging for laboratory use only.
- Not for human or clinical use.
![eMolecules 1184-88-9 | Sodium pivalate | Oakwood Chemical | MFCD00064202 | 124.115 | C5H9NaO2 | 95.000 | [Na+].CC(C)(C)C([O-])=O | 250mg | 853685506](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000126929.jpg-250.jpg)
eMolecules 1184-88-9 | Sodium pivalate | Oakwood Chemical | MFCD00064202 | 124.115 | C5H9NaO2 | 95.000 | [Na+].CC(C)(C)C([O-])=O | 250mg | 853685506
Sodium pivalate | Oakwood Chemical | 1184-88-9 | MFCD00064202 | 124.115 | C5H9NaO2 | 95.000 | [Na+].CC(C)(C)C([O-])=O | 250mg | 853685506
Cambridge Isotope Laboratories gamma-HCH (gamma-BHC) (lindane) (13C6 99%) 100 ug/mL in nonane 1 2 mL
gamma-HCH (gamma-BHC) (lindane) (13C6 99%) 100 ug/mL in nonane 1 2 mL
Medchemexpress LLC N-(3-Acetyl-4-(2-hydroxy-3-(isopropylamino)propoxy-1,1,2,3,3-d5)phenyl)butyramide | 1189500-68-2 | 897231 | 99.7% | 341.46 | 1 MG
Acebutolol-d5 is the deuterium labeled Acebutolol. This compound can be used as a tracer and as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs.
- 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 Palbociclib impurity 20 | 1774898-55-3 | MFCD28013894 | 308.33 | C14H20N4O4 | 10 MG
Palbociclib impurity 20 is an identified impurity of the CDK4/6 inhibitor palbociclib supplied as a small-scale research reference standard for analytical characterization. It is provided as a powder intended for laboratory research use under controlled storage conditions.
- Intended for analytical and research use as a reference impurity.
- Suitable for LC/MS, HPLC, and NMR verification.
- Powder form with recommended cold storage for stability.
- Available in small quantities for analytical workflows (e.g. 5-100 mg).
AdipoGen Cisplatin, 15663-27-1, MFCD00011623, 250 mg
MF: Cl2H6N2Pt, MW: 300.0, ≥98%, Appearance: Yellow solid. Potent platinum-based antineoplastic agent, Anticancer compound, Forms inter- and intrastrand DNA adducts/crosslinks, consequently blocking DNA replication and transcription and inducing cell death, Nephrotoxic when used in vivo, and potent chemoimmunotherapeutic. Stimulates the immune responses by activating macrophages and other cells of the immune system.