Piperazines
TARGETMOL CHEMICALS INC Cetirizine dihydrochloride
Also available in 1 mL, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. Cetirizine dihydrochloride (UCB P071) is an effective second-generation histamine H1 antagonist that is potent in the therapy of allergic rhinitis, confirmed urticaria, and pollen-induced asthma. Unlike other conventional antihistamines, it does not cause side effects of drowsiness or anticholinergic. Purity 100%
Apexbio Technology LLC GW 583340 dihydrochloride 50mg
GW 583340 dihydrochloride (CAS 1173023-85-2) is a small molecule inhibitor targeting the tyrosine kinase activity of both EGFR and ErbB2 exhibiting potent inhibitory effects with IC50 values of 0 01 M and 0 014 M respectively In addition to suppressing these receptor-mediated signaling pathways GW 583340 dihydrochloride has been shown to inhibit ABC transporters including ABCG2 and ABCB1 thereby reversing transporter-associated multidrug resistance This compound is utilized in tumor biology research to investigate the modulation of oncogenic signaling mechanisms underlying drug resistance and to explore potential therapeutic strategies
eMolecules 2-Phenylpiperazine | 5271-26-1 | MFCD01871362 | 5g
Apollo Scientific | 2-Phenylpiperazine | 5g | 562441185 | OR0220 | 97.000 | 5271-26-1 | MFCD01871362 | 162.236 | C10H14N2
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Apexbio Technology LLC Dexrazoxane HCl (ICRF-187, ADR-529) 149003-01-0 50mg
Dexrazoxane HCl (ICRF-187 ADR-529) is a small-molecule inhibitor targeting topoisomerase II It is designed to inhibit topoisomerase II activity and sequester intracellular iron thereby reducing DNA strand cleavage and mitigating iron-dependent oxidative stress Dexrazoxane HCl exerts its biological activity primarily through intracellular iron chelation and inhibition of topoisomerase II which attenuates reactive oxygen species formation and stabilizes DNA structure Based on these pharmacological properties Dexrazoxane HCl holds research potential in investigating cardioprotective strategies particularly against anthracycline-induced cardiotoxicity
Medchemexpress LLC N-(Benzyloxycarbonyloxy)succinimide | 13139-17-8 | 99.97% | C12H11NO5 | 1 KG
N-(Benzyloxycarbonyloxy)succinimide is an effective amino-protecting reagent for organic synthesis. It also functions as a neutral ionophore, which significantly improves the performance of erbium ion (Er3+) sensors, offering a practical tool for rapid detection of erbium ions in environmental and water quality analysis.
- Efficient amino-protecting reagent
- Improves erbium ion (Er3+) sensor performance
- Practical tool for rapid erbium ion detection
ALADDIN SCIENTIFIC CORPORATION 2-Hydroxy-4-2-hydroxyethoxy-2-, 25g
2-Hydroxy-4 -(2-hydroxyethoxy)-2-methylpropiophenone 98%(HPLC)Cas-106797-53-9
Medchemexpress LLC 3'-O-(2-Methoxyethyl)adenosine | 303197-30-0 | C13H19N5O5 | 50 MG
3'-O-(2-Methoxyethyl)adenosine is an adenosine analogue that functions as a smooth muscle vasodilator and has been shown to inhibit cancer progression. This product is for research use only.
- Adenosine analogue
- Smooth muscle vasodilator
- Inhibits cancer progression
- For research use only
Medchemexpress LLC H-9 dihydrochloride | 116700-36-8 | MFCD00069286 | 99.0% | 324.23 g/mol | C11H15Cl2N3O2S | 5 MG
H-9 dihydrochloride is the dihydrochloride salt of H-9, a small-molecule protein kinase A (PKA) inhibitor used in biochemical and cellular research to block PKA-mediated phosphorylation. Supplied as a dry solid, it has a molecular weight of 324.23 g/mol and is commonly prepared as DMSO stock solutions for in vitro and in vivo applications.
- Inhibits protein kinase A activity in biochemical and cellular assays.
- Applicable to studies of serotonin (5-HT) receptor and EGFR signaling pathways.
- High purity suitable for research-grade experiments (≈99%).
- Soluble in DMSO and compatible with common in vivo vehicles.
- Store sealed and away from moisture to preserve stability.
Medchemexpress LLC H-9 dihydrochloride | 116700-36-8 | MFCD00069286 | 99.0% | 324.23 g·mol⁻¹ | C11H15Cl2N3O2S | 50 MG
H-9 dihydrochloride is a cell-permeable small-molecule inhibitor of protein kinase A (PKA) supplied as a research reagent for in vitro biochemical and cellular studies. It is used to probe PKA-dependent signaling pathways and phosphorylation-dependent processes, and is provided with high reported purity suitable for assay applications.
- Potent PKA inhibition for signaling studies.
- High reported purity suitable for biochemical assays.
- Available in small quantities for dose-response and optimization.
- Stable solid form for convenient storage and handling.
- Applicable to in vitro kinase assays and cellular experiments.
Apexbio Technology LLC KX2-391 dihydrochloride 1038395-65-1 5mg
KX2-391 dihydrochloride (CAS 1038395-65-1) is an orally bioavailable small molecule that inhibits Src tyrosine kinase through selective interaction with the peptide substrate binding site rather than the ATP-binding site By blocking this non-catalytic domain KX2-391 disrupts Src kinase-mediated signaling pathways involved in tumor cell proliferation and metastatic processes Src kinases are frequently upregulated in various malignancies underscoring their importance in cancer biology KX2-391 is widely utilized in preclinical studies investigating Src-driven mechanisms of oncogenesis and tumor progression
Apexbio Technology LLC KX2-391 dihydrochloride 1038395-65-1 250mg
KX2-391 dihydrochloride (CAS 1038395-65-1) is an orally bioavailable small molecule that inhibits Src tyrosine kinase through selective interaction with the peptide substrate binding site rather than the ATP-binding site By blocking this non-catalytic domain KX2-391 disrupts Src kinase-mediated signaling pathways involved in tumor cell proliferation and metastatic processes Src kinases are frequently upregulated in various malignancies underscoring their importance in cancer biology KX2-391 is widely utilized in preclinical studies investigating Src-driven mechanisms of oncogenesis and tumor progression
TARGETMOL CHEMICALS INC Sultosilic acid piperazine
Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Sultosilic acid piperazine salt (A-585) is a novel lipid-lowering compound that can be used to study type IIb familial combined hyperlipidemia. Purity 99.1%