Benzenoids
Apexbio Technology LLC 2,4,6-Triiodophenol 609-23-4 10mg
2 4 6-Triiodophenol (CAS 609-23-4) is a small molecule inhibitor known to block the biosynthetic pathway of leukotriene B4 (LTB4) thereby modulating the production of pro-inflammatory mediators By targeting LTB4 synthesis it serves as a valuable tool for studying inflammatory processes and related signaling mechanisms Additionally this compound has been reported to induce apoptosis in murine blastocyst-stage cells making it relevant for investigations into early embryonic development embryotoxicity and the regulation of apoptotic pathways
Matrix Scientific 2,3,5,6-TETRAFLUOROBENZYL -25G
2,3,5,6-Tetrafluorobenzyl alcohol, 98%; 25g,C7H4F4O, MFCD00792428, mw 180.10, [4084-38-2]
Medchemexpress LLC (R)-UT-155 | 2031161-54-1 | 98.1% | 405.35 | 50 MG
(R)-UT-155 is a selective androgen receptor degrader (SARD) ligand. It is less active than its S-isomer. This product is for research use only and is not sold to patients.
- Selective androgen receptor degrader (SARD) ligand.
- Antagonist activity at human androgen receptor expressed in HEK293 cells with an IC50 of 0.598 μM, assessed as inhibition of R1881-induced receptor transactivation after 24 hours by luciferase reporter gene assay.
Medchemexpress LLC Tiazotic acid | 64679-65-8 | 95.0% | 173.20 | 25 MG
Tiazotic acid is a metabolic agent with immunomodulatory, anti-inflammatory, antioxidant, anti-ischemic, cardio- and endothelioprotective, antiplatelet, and hepatoprotective activities. It functions by increasing the levels of eNOS and also reduces D-dimer levels in the blood, which can mitigate the risks of heart attacks and strokes in post-COVID syndrome.
- Metabolic agent
- Increases eNOS levels
- Reduces blood D-dimer levels
- Immunomodulatory activity
- Anti-inflammatory activity
- Antioxidant activity
- Anti-ischemic activity
- Cardio- and endothelioprotective activity
- Antiplatelet activity
- Hepatoprotective activity
![Medchemexpress LLC 1,1′,1′′,1′′′-[1,4-Piperazinediylbis(2,1-ethanediylnitrilo)]tetrakis[2-dodecanol] | 1265904-26-4 | 98.0% | 909.54 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000439070-Logo.png-250.jpg){kind=logo}
Medchemexpress LLC 1,1′,1′′,1′′′-[1,4-Piperazinediylbis(2,1-ethanediylnitrilo)]tetrakis[2-dodecanol] | 1265904-26-4 | 98.0% | 909.54 | 25 MG
1,1′,1′′,1′′′-[1,4-Piperazinediylbis(2,1-ethanediylnitrilo)]tetrakis[2-dodecanol] is a lipid/lipidoid used in preparation of lipid-based or lipidoid nanoparticles.
- Purity of 98.0%
- Molecular weight of 909.54
- Appears as a solid
- Color is light yellow to orange
- Ships at room temperature in continental US
- Storage conditions: powder at -20°C for 3 years, 4°C for 2 years; in solvent at -80°C for 6 months, -20°C for 1 month
Selleck Chemical LLC L-Hydroorotic acid
L-Dihydroorotic acid (L-dihydroorotate) is an intermediate in the metabolism of Pyrimidine It is a substrate for Dihydroorotate dehydrogenase (mitochondrial)
Selleck Chemical LLC JNK Inhibitor VIII
JNK Inhibitor VIII (TCS JNK 6o) is an inhibitor of c-Jun N-terminal kinases with IC50 of 45 nM and 160 nM for JNK-1 and JNK-2 respectively JNK Inhibitor VIII (TCS JNK 6o) inihibits JNK-1 JNK-2 and JNK-3 with Ki of 2 nM 4 nM and 52 nM respectively
Apexbio Technology LLC Valaciclovir HCl 124832-27-5 10mM (in 1mL DMSO)
Valaciclovir HCl is an orally bioavailable hydrochloride ester prodrug of the antiviral nucleoside analog acyclovir It is designed to selectively inhibit viral DNA polymerase thereby disrupting herpesvirus DNA synthesis and replication Valaciclovir HCl exerts its biological activity primarily through rapid conversion to acyclovir which is phosphorylated first by viral thymidine kinase and then by cellular kinases to form acyclovir triphosphate This metabolite selectively inhibits viral DNA polymerase Based on these pharmacological properties Valaciclovir HCl holds research potential in exploring antiviral mechanisms and investigating pharmacological pharmacokinetic and resistance aspects associated with herpesvirus infections
Apexbio Technology LLC 8-Bromo-cGMP, sodium salt 51116-01-9 25mg
8-Bromo-cGMP sodium salt (CAS 51116-01-9) is a membrane-permeable analog of cyclic GMP that functions as an activator of protein kinase G (PKG) By mimicking endogenous cGMP it modulates intracellular signaling pathways notably influencing Ca2 channel activity Studies indicate that 8-Bromo-cGMP sodium salt can suppress macroscopic ionic currents and reduce insulin secretion under high K stimulation Due to its role in signal transduction and vascular function this compound is frequently employed in research addressing nociceptive modulation and vascular biology
![Medchemexpress LLC Pyrazolo[1,5-a]pyrimidine-3-carbonitrile, 4,7-dihydro-6-isopropyl-7-oxo-5-phenyl hydrochloride | 2095432-28-1 | 100.0% | 314.77 g/mol | C16H15ClN4O | 1 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000213936.png-250.jpg)
Medchemexpress LLC Pyrazolo[1,5-a]pyrimidine-3-carbonitrile, 4,7-dihydro-6-isopropyl-7-oxo-5-phenyl hydrochloride | 2095432-28-1 | 100.0% | 314.77 g/mol | C16H15ClN4O | 1 MG
CPI-455 hydrochloride is the hydrochloride salt of a potent pan-KDM5 histone demethylase inhibitor with reported low-nanomolar activity against KDM5A. It is intended for research use in epigenetics and cancer biology to elevate H3K4me3 levels and probe mechanisms of drug-tolerant persister cells. Supplied as a high-purity reagent for in vitro studies.
- Potent pan-KDM5 inhibition with low-nanomolar activity against KDM5A.
- Elevates global H3K4me3 levels in cellular assays.
- High purity suitable for research-grade experiments.
- Available in small milligram pack sizes for screening and assays.
- Hydrochloride salt form improves aqueous solubility for formulation.