Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Hydrocortisone British Pharmacopoeia (BP) Assay Standard | 50-23-7 | MFCD00011654 |
Hydrocortisone British Pharmacopoeia (BP) Assay Standard | Mol Wt: 362.46 | 50-23-7 | MFCD00011654 |
Selleck Chemical LLC Raltitrexed 100mg 112887-68-0 ZD-1694
Raltitrexed (ZD-1694) is a thymidylate synthase inhibitor with an IC50 of 9 nM for the inhibition of L1210 cell growth. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
![Medchemexpress LLC 2-butenamide, n-[4-[(4-chloro-3-fluorophenyl)amino]-7-[(3S)-tetrahydro-3-furanyloxy]-6-quinazolinyl] | 2475094-87-0 | 5mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000267580.png-250.jpg)
Medchemexpress LLC 2-butenamide, n-[4-[(4-chloro-3-fluorophenyl)amino]-7-[(3S)-tetrahydro-3-furanyloxy]-6-quinazolinyl] | 2475094-87-0 | 5mg
Afatinib impurity 33 is an impurity of Afatinib (HY-10261)
Medchemexpress LLC 2,3,4,6-tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide | 81058-27-7 | MFCD08275217 | 50g
Empagliflozin impurity 15 is an impurity of Empagliflozin (HY-15409)
Selleck Chemical LLC Granisetron HCl 25mg 107007-99-8
Granisetron is a serotonin 5-HT3 receptor antagonist,used to treat chemotherapy-induced nausea and vomiting. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC Temozolomide acid | 113942-30-6 | MFCD12032160 | 99.7% | 195.14 g/mol | C6H5N5O3 | 100 MG
Temozolomide acid is a carboxylic acid derivative of temozolomide used as a research anticancer agent. It functions as a DNA alkylating agent that can induce DNA strand breaks, cell cycle arrest, and cell death, and is commonly used in glioblastoma and brain cancer research.
- Carboxylic acid derivative of temozolomide.
- Acts as a DNA alkylating agent causing DNA breaks and cell cycle arrest.
- Relevant for glioblastoma and brain cancer research.
- Molecular weight 195.14 g/mol.
- Chemical formula C6H5N5O3.
- High purity per manufacturer specifications.
- Supplied as a solid research material, commonly in 100 mg packs.
- Storage: powder -20°C (long term) or 4°C (short term).
Apexbio Technology LLC Montelukast Sodium 151767-02-1 10mM (in 1mL DMSO)
Montelukast Sodium (CAS 151767-02-1) is a selective reversible antagonist targeting the leukotriene D4 (LTD4) receptor It inhibits LTD4 receptor binding with Ki values of 0 52 nM in U937 cells 0 18 nM in guinea pig lung and 4 nM in sheep lung In U937 and THP-1 cell membranes Montelukast Sodium has IC50 values of 10 mM and 40 mM respectively against leukotrienes C3 and B4 In animal studies oral administration inhibits LTD4-induced bronchoconstriction with an ED50 of 0 03 mg/kg in conscious squirrel monkeys It is widely utilized in biomedical research investigating leukotriene-mediated inflammatory pathways and respiratory disorders
Medchemexpress LLC ARQ 621 | 1095253-39-6 | ≥99.0% | 552.43 | 25 MG
ARQ 621 is an allosteric, potent, and selective inhibitor of Eg5, a microtubule-based ATPase motor protein involved in cell division. It exhibits anti-tumor activity and is a kinesin inhibitor. Additionally, ARQ 621 is a click chemistry reagent containing an Alkyne group, capable of undergoing copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Allosteric, potent, and selective inhibitor of Eg5
- Microtubule-based ATPase motor protein inhibitor
- Involved in cell division
- Anti-tumor activity
- Kinesin inhibitor
- Click chemistry reagent with an alkyne group
- Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide groups
Medchemexpress LLC Cannabidiol-C4 | 60113-11-3 | 99.5% | 300.44 | 1 MG
Cannabidiol-C4 (CBD-C4) is an impurity in cannabidiol. It is for research use only and not sold to patients.
- Cytotoxicity against mouse BV-2 cells assessed as reduction in cell viability by crystal violet staining based assay (IC50: 11.1 μM for Compound: 12c)
- Anti-neuroinflammatory activity in mouse BV-2 cells assessed as inhibition of LPS-induced NO production incubated for 24 hrs by microplate reader analysis (IC50: 5 μM for Compound: 12c)
Selleck Chemical LLC Topiramate 100mg 97240-79-4 MCN 4853, RWJ 17021
Topiramate (MCN 4853, RWJ 17021) is a mutil-targeted inhibitor, including voltage-gated sodium channel and calcium channel, AMPA/kainate receptor and carbonic anhydrase, used to treat epilepsy. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Sigma Aldrich Fine Chemicals Biosciences Ganciclovir European Pharmacopoeia (EP) Reference Standard | 82410-32-0 | MFCD00870588 |
Ganciclovir European Pharmacopoeia (EP) Reference Standard | Mol Wt: 255.23 | 82410-32-0 | MFCD00870588 |
Medchemexpress LLC Pth-related protein (1-34) (human,mouse,rat) | 112540-82-6 | 98.7% | 4018.00 | 1 MG
Pth-related protein (1-34) (human, mouse, rat) is a fragment of parathyroid hormone-related protein. It acts as an anabolic agent and is utilized in studies related to postmenopausal osteoporosis. This product is intended for research purposes only and is not for direct patient use.
- Fragment of parathyroid hormone-related protein
- Anabolic agent
- Used for postmenopausal osteoporosis study
- For research use only
Medchemexpress LLC FOSTAMATINIB (R788) 5MG
Fostamatinib (R788), a prodrug of the active metabolite R406, is a potent Syk inhibitor with IC50 of 41 nM 99.20% CAS#901119-35-5 C₂₃H₂₆FN₆O₉P
Medchemexpress LLC Edoxaban impurity 59 | 228.63 g/mol | 50mg
Edoxaban Impurity 59 is an impurity of Edoxaban (HY-10264)