Alcohols and polyols
Inositol, FCC, 97%, Spectrum™ Chemical
CAS: 87-89-8 Molecular Formula: C6H12O6 Molecular Weight (g/mol): 180.16 InChI Key: CDAISMWEOUEBRE-UHFFFAOYSA-N IUPAC Name: cyclohexane-1,2,3,4,5,6-hexol SMILES: OC1C(O)C(O)C(O)C(O)C1O
Inositol, NF, 97-102%, Spectrum™ Chemical
CAS: 87-89-8 Molecular Formula: C6H12O6 Molecular Weight (g/mol): 180.16 InChI Key: CDAISMWEOUEBRE-UHFFFAOYSA-N IUPAC Name: cyclohexane-1,2,3,4,5,6-hexol SMILES: OC1C(O)C(O)C(O)C(O)C1O
(1alpha,3alpha,5alpha)-1,3,5-Cyclohexanetriol 98.0+%, TCI America™
CAS: 50409-12-6 Molecular Formula: C6H12O3 Molecular Weight (g/mol): 132.159 MDL Number: MFCD00043062 InChI Key: FSDSKERRNURGGO-UHFFFAOYSA-N PubChem CID: 230351 IUPAC Name: cyclohexane-1,3,5-triol SMILES: C1C(CC(CC1O)O)O
5-Norbornene-2,2-dimethanol 98.0+%, TCI America™
CAS: 6707-12-6 Molecular Formula: C9H14O2 Molecular Weight (g/mol): 154.21 MDL Number: MFCD00167595 InChI Key: DSHXMENPUICESR-UHFFFAOYNA-N Synonym: Bicyclo[2.2.1]hept-5-ene-2,2-dimethanol, 2,2-Bis(hydroxymethyl)-5-norbornene PubChem CID: 110917 IUPAC Name: [5-(hydroxymethyl)-5-bicyclo[2.2.1]hept-2-enyl]methanol SMILES: C1C2CC(C1C=C2)(CO)CO
Medchemexpress LLC 12-Epinapelline | 110064-71-6 | 5 MG
12-Epinapelline is a diterpene alkaloid isolated from Aconitum baikalense. It exhibits anti-inflammatory activity and stimulates the growth of colonies from fibroblast precursors. The initial source is identified as Aconitum carmichaeli Debx. from the Ranunculaceae family of plants.
- Isolated from Aconitum baikalense
- Exhibits anti-inflammatory activity
- Stimulates the growth of colonies from fibroblast precursors
- Derived from Aconitum carmichaeli Debx.
Medchemexpress LLC 12-epinapelline | 110064-71-6 | 99.9% | 359.50 g/mol | C22H33NO3 | 10 MG
12-epinapelline is a diterpene alkaloid isolated from Aconitum baikalense. It has demonstrated anti-inflammatory activity and promotes the growth of colonies from fibroblast precursors. The compound is a white to off-white solid with high purity and defined storage recommendations.
- Exhibits anti-inflammatory activity
- Stimulates fibroblast colony growth
- Chemical formula C22H33NO3 and molecular weight 359.50 g/mol
- White to off-white solid appearance
- High purity (99.92% as listed by manufacturer)
- Available in small research pack sizes suitable for biological assays
- Store protected from light at 4°C; in solvent, long-term storage at -80°C
Medchemexpress LLC Cardiotoxin Analog (CTX) IV (6-12) | 115722-23-1 | 99.95% | 899.13 | 10 MG
Cardiotoxin Analog (CTX) IV (6-12) is a membrane-active peptide isolated from the venom of the Taiwan cobra. It specifically targets negatively charged phospholipid membranes, such as phosphatidylserine and phosphatidylinositol. This snake venom cardiotoxin binds to cell membranes and embeds into lipid bilayers through hydrophobic interactions and electrostatic attraction, disrupting membrane stability. It can induce membrane lipid disorder and cell lysis, exhibiting hemolysis and cytotoxicity.
- Targets negatively charged phospholipid membranes
- Isolated from Taiwan cobra venom
- Binds to cell membranes and embeds into lipid bilayers
- Disrupts membrane stability
- Induces membrane lipid disorder and cell lysis
- Exhibits hemolysis and cytotoxicity
- Shows specific binding to negatively charged lipid membranes in vitro (10 μM)
- Causes complete hemolysis of erythrocytes in vitro (25 μM)
Sigma Aldrich tert-Butyl 12-hydroxy-4,7,10-trioxadodecanoate
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
eMolecules 21-Chloro-3,6,9,12,15-pentaoxahenicosan-1-ol | 1355956-01-2 | | 1g
Synthonix - Stock | 21-Chloro-3,6,9,12,15-pentaoxahenicosan-1-ol | 1g | 495875377 | C61861 | | 1355956-01-2 | | 356.880 | C16H33ClO6
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Apexbio Technology LLC CHAPS,5g CAS# 75621-03-3
CHAPS is a zwitterionic nondenaturing detergent for solubilizing membrane proteins. CHAPS is often used as a detergent in the solubilization and purification of membrane proteins for several advantageous reasons. CHAPS detergent is non-denaturing to membrane proteins, can solubilize proteins, disaggregate protein-protein interactions and is electrically neutral. CHAPS is also useful in ion exchange chromatography and isoelectric focusing as it is zwitterionic and does not exhibit a net charge between pH 2 to 12. The critical micelle concentration of CHAPS is 6-10mM. Other sizes are also available. Please inqury us for quote.
Apexbio Technology LLC Pexmetinib (ARRY-614) 945614-12-0 100mg
Pexmetinib (ARRY-614 CAS 945614-12-0) is a small molecule inhibitor targeting both p38 mitogen-activated protein kinase (MAPK) and Tie2/Tek receptor tyrosine kinase It demonstrates in vitro IC50 values of 1000 ng/mL for Tie2 and 100 ng/mL for p38 MAPK and inhibits basal cytokine production in primary human bone marrow stromal cells with IC50 values between 50 100 nM In human whole blood assays it suppresses LPS-induced cytokine production (IC50 50 120 nM) and reduces IL-6 release in mouse models (ED50 10 mg/kg) Pexmetinib is studied for its impact on cytokine synthesis bone marrow biomarkers and inflammatory signaling highlighting its potential utility in hematologic and inflammatory research
Apexbio Technology LLC Pexmetinib (ARRY-614) 945614-12-0 25mg
Pexmetinib (ARRY-614 CAS 945614-12-0) is a small molecule inhibitor targeting both p38 mitogen-activated protein kinase (MAPK) and Tie2/Tek receptor tyrosine kinase It demonstrates in vitro IC50 values of 1000 ng/mL for Tie2 and 100 ng/mL for p38 MAPK and inhibits basal cytokine production in primary human bone marrow stromal cells with IC50 values between 50 100 nM In human whole blood assays it suppresses LPS-induced cytokine production (IC50 50 120 nM) and reduces IL-6 release in mouse models (ED50 10 mg/kg) Pexmetinib is studied for its impact on cytokine synthesis bone marrow biomarkers and inflammatory signaling highlighting its potential utility in hematologic and inflammatory research