Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Drospirenone United States Pharmacopeia (USP) Reference Standard | 67392-87-4 | MFCD00867350 | 200MG
Drospirenone United States Pharmacopeia (USP) Reference Standard | Mol Wt: 366.49 | 67392-87-4 | MFCD00867350 | 200MG
Sigma Aldrich Fine Chemicals Biosciences Sodium salicylate European Pharmacopoeia (EP) Reference Standard | 54-21-7 | MFCD00002440 |
Sodium salicylate European Pharmacopoeia (EP) Reference Standard | Mol Wt: 160.1 | 54-21-7 | MFCD00002440 |
Sigma Aldrich Fine Chemicals Biosciences Lamotrigine Related Compound B United States Pharmacopeia (USP) Reference Standard | 50-45-3 | MFCD00002413 | 20MG
Lamotrigine Related Compound B United States Pharmacopeia (USP) Reference Standard | Mol Wt: 191.01 | 50-45-3 | MFCD00002413 | 20MG
eMolecules Medchem Express / Flutrimazole / 10mg / 705860563 / HY-129060 / / 119006-77-8 / MFCD00865591 / 346.381 / C22H16F2N2
Medchem Express / Flutrimazole / 10mg / 705860563 / HY-129060 / / 119006-77-8 / MFCD00865591 / 346.381 / C22H16F2N2
TARGETMOL CHEMICALS INC Azithromycin hydrate 200MG
Also available in 1 mL, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Azithromycin hydrate (CP-62993 dihydrate) is a semi-synthetic macrolide antibiotic structurally related to ERYTHROMYCIN. It has been used in the treatment of Mycobacterium avium intracellulare infections, toxoplasmosis, and cryptosporidiosis. Purity 99.9%
Selleck Chemical LLC Enzalutamide (MDV3100) 50mg 915087-33-1
Enzalutamide (MDV3100) is an androgen-receptor (AR) antagonist with IC50 of 36 nM in LNCaP cells. Enzalutamide is shown to increase autophagy. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Sigma Aldrich Fine Chemicals Biosciences Sodium stearyl fumarate European Pharmacopoeia (EP) Reference Standard | 4070-80-8 |
Sodium stearyl fumarate European Pharmacopoeia (EP) Reference Standard | Mol Wt: 390.53 | 4070-80-8 |
Medchemexpress LLC Bedaquinoline impurity 1 | 1972612-60-4 | 555.50 g/mol | C32H31BrN2O2 | 10 MG
Bedaquinoline impurity 1 is an identified impurity of the anti-tuberculosis agent bedaquiline, provided as an analytical reference for research and impurity profiling. The compound has molecular formula C32H31BrN2O2 and molecular weight 555.50 g/mol. It is supplied in small milligram quantities for laboratory analytical use.
- Analytical reference for impurity identification and method development.
- Useful for chromatographic and mass spectrometric characterization.
- Supplied in small, defined quantities suitable for lab-scale analysis.
- Chemical identity documented with CAS number and molecular formula for traceability.
Medchemexpress LLC Risperidone | 106266-06-2 | 99.9% | 410.48 | 50 MG
Risperidone | 106266-06-2 | 99.9% | 410.48 | 50 MG
Medchemexpress LLC Butylated hydroxytoluene-d3 | 86819-59-2 | 99.2% | 223.37 | C15H21D3O | 10mg
Butylated hydroxytoluene-d3 is the deuterium labeled Butylated hydroxytoluene[1] Butylated hydroxytoluene is an antioxidant widely used in foods and in food-related products[2] Butylated hydroxytoluene is a Ferroptosis inhibitor[3]
Medchemexpress LLC Suplatast (Tosilate) | 94055-76-2 | 499.64 | 50 MG
Suplatast Tosilate (IPD 1151T) is an orally active Th2 cytokine inhibitor that inhibits both IL-4 and IL-5 production from Th2 cells and suppresses IgE synthesis. It is an anti-allergic agent with antiasthmatic, anti-inflammatory, and antifibrotic activity.
- Orally active Th2 cytokine inhibitor
- Inhibits IL-4 and IL-5 production
- Suppresses IgE synthesis
- Anti-allergic agent
- Antiasthmatic activity
- Anti-inflammatory activity
- Antifibrotic activity
Medchemexpress LLC ARQ 621 | 1095253-39-6 | ≥99.0% | 552.43 | 5 MG
ARQ 621 is an allosteric, potent, and selective inhibitor of Eg5, which is a microtubule-based ATPase motor protein involved in cell division. It exhibits anti-tumor activity and acts as a kinesin inhibitor. Additionally, ARQ 621 is a click chemistry reagent containing an Alkyne group, allowing it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules that contain Azide groups.
- Allosteric, potent and selective inhibitor of Eg5
- Exhibits anti-tumor activity
- Functions as a kinesin inhibitor
- Click chemistry reagent with an Alkyne group
- Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc) with Azide groups
Medchemexpress LLC ARQ 621 | 1095253-39-6 | ≥99.0% | 552.43 | 50 MG
ARQ 621 is an allosteric, potent and selective inhibitor of Eg5, a microtubule-based ATPase motor protein involved in cell division. Anti-tumor activity. ARQ 621 is a kinesin inhibitor. ARQ 621 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. For research use only. We do not sell to patients.
- ARQ 621 is an allosteric, potent and selective inhibitor of Eg5, a microtubule-based ATPase motor protein involved in cell division. It shows anti-tumor activity.
- It is a kinesin inhibitor.
- It is a click chemistry reagent, containing an Alkyne group, and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Selleck Chemical LLC Fasudil (HA-1077) HCl 500mg 105628-07-7
Fasudil(HA-1077), a potent and selective inhibitor of Rho kinase, displays less potent inhibiton over PKA, PKG, PKC and MLCK with Ki of 1.6, 1.6, 3.3, and 36 ?M in cell-free assays, respectively. Fasudil is also a calcium channel blocker. *For Research & Development use only. Product is not intended for drug, household, or human consumption.