Drug Standards
Medchemexpress LLC Tosylate-DPA-714 | 958233-17-5 | 97.0% | 10 MG
Tosylate-DPA-714 is the tosylate analog of DPA-714 used as a precursor for synthesizing 18F-labeled DPA-714, a translocator protein (TSPO)-selective ligand for neuroinflammation imaging research. Supplied for research use only in small laboratory quantities.
- Precursor for 18F radiolabeling of DPA-714.
- High purity (HPLC), approximately 97.0%.
- Molecular formula C29H34N4O5S; molecular weight 550.67 g·mol⁻¹.
- Supplied in small quantities suitable for synthesis (e.g., 10 MG).
- Intended for research use only; not for human or clinical use.
Selleck Chemical LLC Osimertinib mesylate S5078-1g
Osimertinib mesylate (AZD9291) is the mesylate form of osimertinib which is an oral third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) drug
Sigma Aldrich Fine Chemicals Biosciences Formoterol for impurity I identification European Pharmacopoeia (EP) Reference Standard | 43229-80-7 |
Formoterol for impurity I identification European Pharmacopoeia (EP) Reference Standard | Mol Wt: 402.44 | 43229-80-7 |
Apexbio Technology LLC Digoxin 10mM (in 1mL DMSO)
B7684 is a small molecule currently investigated in biomedical research for its modulatory effects on cellular signaling pathways It is reported to interact with specific protein targets involved in regulatory mechanisms thereby influencing downstream biological processes relevant to disease models B7684 serves as a chemical tool to probe pathway modulation and target validation in cellular and molecular biology studies Its applications include elucidating target-specific mechanisms and supporting preclinical research into therapeutic strategies
Apexbio Technology LLC Fenoldopam 67227-56-9 10mM (in 1mL DMSO)
Fenoldopam is a small-molecule partial agonist targeting dopamine D1-like receptors It is designed to selectively activate these receptors thereby mediating peripheral vasodilation and modulating vascular resistance Fenoldopam exerts its biological activity primarily through D1-like receptor activation In in vitro studies Fenoldopam demonstrates partial agonist activity with an EC50 value of approximately 57 nM Additionally it exhibits inhibitory activity against 2-adrenoceptors with a reported Ki of 15 25 nM Based on these pharmacological properties Fenoldopam holds research potential in studies of cardiovascular regulation receptor pharmacodynamics and selective receptor ligand profiling
Sigma Aldrich Fine Chemicals Biosciences Ceftizoxime United States Pharmacopeia (USP) Reference Standard | 68401-81-0 | 350MG
Ceftizoxime United States Pharmacopeia (USP) Reference Standard | Mol Wt: 383.4 | 68401-81-0 | 350MG
Selleck Chemical LLC Cefcapene Pivoxil Hydrochloride S4844-25mg
Cefcapene Pivoxil is the pivalate ester prodrug form of cefcapene a semi-synthetic third-generation cephalosporin with antibacterial activity
Medchemexpress LLC Rosuvastatin | 287714-41-4 | 99.7% | 50 MG
Rosuvastatin | 287714-41-4 | 99.7% | 50 MG
Cayman Chemical Flavopiridol hydrochloride
An inhibitor of cyclin-dependent kinases (Cdks; IC50s = ~100, ~100, ~100, and 300 nM for Cdk1, Cdk2, Cdk4, and Cdk7, respectively); inhibits TEFb (Ki = 3 nM); inhibits transcription of a CMV promoter in HeLa nuclear extract (IC50 = 34 nM), Tat-stimulated transcription of an HIV-1 promotor (IC50 = 7 nM), and HIV-1 replication in HEK239T cells (IC50 = <10 nM); induces apoptosis and cyclin D1 depletion and delays tumor growth in an HN-12 head and neck carcinoma mouse xenograft model at 5 mg/kg; suppresses synovial hyperplasia and joint destruction in a mouse model of collagen-induced arthritis
Apexbio Technology LLC Meclizine 2HCl 1104-22-9 5g
Meclizine dihydrochloride (Meclizine 2HCl CAS 1104-22-9) is a small molecule antagonist of histamine H1 receptors commonly investigated for its antiemetic properties In addition to its antihistaminic activity meclizine exhibits antimuscarinic effects and inhibits oxidative phosphorylation It has also been identified as an agonist of the mouse constitutive androstane receptor (mCAR) and demonstrates inverse agonist activity at other signaling pathways These multifunctional pharmacological properties make meclizine 2HCl a useful tool in research exploring receptor-mediated signaling mitochondrial function and metabolism-related diseases
Medchemexpress LLC Androgen receptor antagonist 9 | 915086-32-7 | 99.9% | 405.39 | 10 MM 1 ML
Androgen receptor antagonist 9 (compound 28) is an antagonist of the androgen receptor.
- Antagonist of the androgen receptor.
- Applicable in related screening libraries: Endocrinology Compound Library, Transcription Factor-Targeted Library, Nuclear Receptor Compound Library, Bioactive Compound Library, Max MCE Bioactive Compound Library, Bioactive Compound Library Plus, High-Throughput Bioactive Compound Library.
Selleck Chemical LLC Benztropine mesylate 50mg 132-17-2
Benztropine is a dopamine transporter (DAT) inhibitor with IC50 of 118 nM. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Sigma Aldrich Fine Chemicals Biosciences Repaglinide Related Compound E United States Pharmacopeia (USP) Reference Standard | 147852-26-4 | 20MG
Repaglinide Related Compound E United States Pharmacopeia (USP) Reference Standard | Mol Wt: 452.59 | 147852-26-4 | 20MG
![Medchemexpress LLC L-Glutamic acid, N-[4-[[(2-amino-3,4-dihydro-4-oxo-6-pteridinyl)methyl)amino]benzoyl]- | 59-30-3 | 99.0% | 441.40 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000392393.png-250.jpg)
Medchemexpress LLC L-Glutamic acid, N-[4-[[(2-amino-3,4-dihydro-4-oxo-6-pteridinyl)methyl)amino]benzoyl]- | 59-30-3 | 99.0% | 441.40 | 100 MG
Folic acid (Vitamin B9) is an orally active essential nutrient from the B complex group of vitamins. It demonstrates an antidepressant-like effect and its sodium form can reduce the risk of neonatal neural tube defects. Folic acid is also used in the research of megaloblastic and macrocytic anemias caused by folic deficiency.
- Exhibits an antidepressant-like effect.
- Sodium form reduces the risk of neonatal neural tube defects.
- Used in research of megaloblastic and macrocytic anemias due to folic deficiency.
- Plays a critical role in preventing chromosome breakage and hypomethylation of DNA.
- Can be used to induce acute kidney injury models.
Sigma Aldrich Fine Chemicals Biosciences Desogestrel Related Compound B United States Pharmacopeia (USP) Reference Standard | 70805-85-5 | 25MG
Desogestrel Related Compound B United States Pharmacopeia (USP) Reference Standard | Mol Wt: 326.47 | 70805-85-5 | 25MG