Toxins
American Radiolabeled Chemicals Inc Tetrodotoxin Citrate, 18660-81-6, MFCD00210218, 1mg
Molecular Formula: C11H17N3O8, Molecular Weight: 319.27, Synonym: TTX citrate
Medchemexpress LLC HY-B0015 100mg Medchemexpress, Paclitaxel CAS:33069-62-4 Purity:>98%
Medchemexpress, HY-B0015 100mg Paclitaxel CAS:33069-62-4 Paclitaxel (Taxol) is a naturally occurring antineoplastic agent and stabilizes tubulin polymerization. Paclitaxel can cause both mitotic arrest and apoptotic cell death. Paclitaxel also induces autophagy[2]. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Biotium Tetrodotoxin, Citrate Free, 1 mg
Tetrodotoxin (TTX) reversibly blocks excitable sodium channels and has been a widely used tool for studies of excitable membranes of nerve, skeletal muscle and cardiac muscle cells. Biotium offers high quality tetrodotoxin with or without citrate, at a competitive price. Tetrodotoxin, citrate-free can be dissolved in slightly acidic buffer. Tetrodotoxin, with citrate can be dissolved in water to obtain TTX in pH 4.8 citrate buffer.Properties: C11H17N3O8; MW: 319.28; [4368-28-9]
Medchemexpress LLC HY-N0488 50mg Medchemexpress, Vincristine (sulfate) CAS:2068-78-2 Purity:>98%
Medchemexpress, HY-N0488 50mg Vincristine (sulfate) CAS:2068-78-2 Vincristine sulfate is an antitumor vinca alkaloid which inhibits microtubule formation in mitotic spindle, resulting in an arrest of dividing cells at the metaphase stage. It binds to microtubule with a Ki of 85 nM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Cayman Chemical GABAA RECPTR a2 SubunIt Pol
An antispasmodic agent suppresses contractions induced by potassium or ACh in isolated guinea pig detrusor smooth muscle blocks spontaneous and vagal-stimulated colonic motility in rabbits reduces the number of abdominal contractions induced by 5-HTP or high volume rectal distension in rats at 75 g/animal
Cayman Chemical GABAA RECPTR a4 SubunIt Pol
An antispasmodic agent suppresses contractions induced by potassium or ACh in isolated guinea pig detrusor smooth muscle blocks spontaneous and vagal-stimulated colonic motility in rabbits reduces the number of abdominal contractions induced by 5-HTP or high volume rectal distension in rats at 75 g/animal
Medchemexpress LLC Cucurbitacin Q1 | 99530-82-2 | 5 MG
Cucurbitacin Q1 is a tetracyclic triterpene, isolated from *Cucumis prophetarum*. It is a white to off-white solid with a molecular weight of 560.72 and chemical formula C32H48O8. Cucurbitacin Q1 exhibits potent cytotoxicity against various human cancer cell lines, including HT-29 (IC50: 0.54 μM), MCF7 (GI50: 0.11 μM), NCI-H460 (GI50: 0.065 μM), and SF-268 (GI50: 0.087 μM), indicating its potential in anti-cancer research. Its CAS number is 99530-82-2.
- High purity: 98.39%.
- Available in various package sizes.
- Comprehensive documentation including data sheet, SDS, COA, and more.
- Detailed protocols for dissolution in both in vitro and in vivo studies.
- Recommended storage at 4°C, protected from light.
Enzo Life Sciences 2-Methoxyestradiol (10 mg). CAS: 362-07-2
An endogenous estrogen metabolite with low affinity for the estrogen receptor but which disrupts microtubule function. Potent inhibitor of endothelial cell proliferation and migration. Inhibits bFGF and VEGF-induced corneal neovascularization in mice. Posttranscriptionally downregulates HIF-1α expression. Alternative name: 2-ME. Purity: ≥95% (TLC). Long Term Storage: Ambient.
Sigma Aldrich Fine Chemicals Biosciences Berberine chloride dihydrate phyproof(R) Reference Substance | 5956-60-5 | MFCD00011939 | 100MG
Berberine chloride dihydrate phyproof(R) Reference Substance | Purity: >=95.0% (HPLC) | Mol Wt: 389.83 | 5956-60-5 | MFCD00011939 | 100MG
Cayman Chemical Werner Syndrome RecQ Helicase
An inhibitor of WRN (IC50 = 60 nM); selectively inhibits the growth of SW48 cells over DLD-1-WRN-KO cells (GI50s = 70 and >10,000 nM, respectively); reduces tumor volume in an SW48 mouse xenograft model at 240 mg/kg per day