Lipids and Lipid Derivatives
Medchemexpress LLC 7-Epi-docetaxel | 153381-68-1 | 98.8% | 807.88 | 5 MG
7-Epi-10-oxo-docetaxel is an impurity of docetaxel. This product is for research use only and has not been fully validated for medical applications.
- An impurity of docetaxel
- Purity of 98.76%
- Solid appearance, white to light yellow
- Soluble in DMSO at 100 mg/mL (123.78 mM)
- Targets microtubule/tubulin
- Involved in cell cycle/DNA damage and cytoskeleton pathways
- Store as powder at -20°C for 3 years or 4°C for 2 years
- Store in solvent at -80°C for 2 years or -20°C for 1 year
Sigma Aldrich Fine Chemicals Biosciences Paclitaxel from semisynthetic, >=97% | 33069-62-4 | MFCD00869953 | 1MG
Paclitaxel from semisynthetic, >=97% | Purity: >=97% | Mol Wt: 853.91 | 33069-62-4 | MFCD00869953 | 1MG
Medchemexpress LLC 7-epi-docetaxel | 153381-68-1 | MFCD15071206 | 98.8% | 807.88 g·mol⁻¹ | C43H53NO14 | 10 MG
7-Epi-docetaxel is an epimeric impurity of docetaxel used as a research compound and microtubule/tubulin inhibitor. Supplied as a solid powder in a 10 mg quantity, it is intended for laboratory research use only and not for human or clinical applications.
- Impurity/epimer of docetaxel used to study tubulin dynamics and cytotoxicity.
- Solid powder formulation suitable for analytical and cell-based research.
- CAS number 153381-68-1 for unambiguous identification.
- Chemical formula C43H53NO14; molecular weight 807.88 g·mol⁻¹.
- High purity (98.8% reported by supplier) for analytical consistency.
- Store powder at -20°C for long term; store solutions at -80°C for long term per handling instructions.
Selleck Chemical LLC 10-deacetyl-paclitaxel S3933-5mg
10-deacetyl-paclitaxel (10-DAT Deacetyl Paclitaxel) is a semi-synthetic precursor of Paclitaxel
Apexbio Technology LLC Paclitaxel (Taxol) 33069-62-4 100mg
Paclitaxel (Taxol) is a diterpenoid alkaloid initially isolated from the bark of Taxus brevifolia It exhibits antitumor activity primarily by disrupting microtubule dynamics Mechanistically paclitaxel binds tubulin and promotes microtubule polymerization thus stabilizing microtubules and inhibiting their depolymerization This mechanism impairs normal mitotic spindle formation arrests cells in G2-M phase of the cell cycle and induces apoptotic cell death Paclitaxel is extensively employed in biomedical research for investigating antineoplastic mechanisms and testing therapeutic interventions targeting various cancers such as ovarian breast head and neck and lung carcinoma
Medchemexpress LLC Resiniferatoxin | 57444-62-9 | 99.8% | 628.71 g/mol | C37H40O9 | 10 MG
Resiniferatoxin is a highly potent, naturally derived agonist of the transient receptor potential vanilloid 1 (TRPV1) ion channel. It is used in laboratory research to ablate or modulate TRPV1-expressing sensory neurons and to study pain signaling, neurobiology, and cardiac sympathetic afferent reflexes. Supplied as a high-purity solid with storage and solvent guidance, it is intended for research use only (not for human use).
- Potent TRPV1 agonist for targeted neuronal ablation and modulation.
- High chemical purity (99.77%) suitable for sensitive assays.
- Molecular weight 628.71 g/mol and formula C37H40O9.
- Stable solid; store protected from light at -20°C; in solution, store at -80°C for long-term stability.
- Soluble in DMSO; in vitro and in vivo vehicle preparation guidance available.
- Supplied in small milligram-scale quantities appropriate for research applications.
Abcam LDN-57444, UCH-L1 inhibitor, 5MG
MW 397.6 Da, Purity >98%. Reversible, competitive ubiquitin C-terminal hydrolase-L1 (UCH-L1) inhibitor (Ki = 0.4 μM. Increases ubiquitinated protein levels and decreases proteasome activity. Also induces apoptosis.
The product is subject to the following: Abcam Restricted Use Statement