Determine the necessary mass, volume, or concentration for preparing a solution.
This is a demo store. No orders will be fulfilled.
| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
|
F649588-5mg
|
5mg |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$370.90
|
|
|
F649588-10mg
|
10mg |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$600.90
|
|
| Synonyms | 1,9-Heptadecadiene-4,6-diyne-3,8-diol | SCHEMBL40936 | (E)-Heptadeca-1,9-dien-4,6-diyne-3,8-diol | Falcarindiol | heptadeca-1,9-dien-4,6-diyne-3,8-diol | (9E)-heptadeca-1,9-dien-4,6-diyne-3,8-diol | 1,9-Heptadecadiene-4,6-diyne-3,8-diol, (3S,8S,9Z)- | AKO |
|---|---|
| Specifications & Purity | ≥99% |
| Biochemical and Physiological Mechanisms | Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy . Falcarindiol has anti-inflammatory, antifungal , anticancer |
| Storage Temp | Store at 2-8°C,Protected from light,Desiccated |
| Shipped In |
Wet ice This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy . Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties In Vitro Falcarindiol (3, 6, 12, 24 µM; for 24 hours) significantly decreases cell viability of MDA-MB-231 and MDA-MB-468 cells. Cell viability of MCF-10A cells is unchanged until the dose of Falcarindiol reaches to 24 uM. Falcarindiol preferentially induces cell death in breast cancer cells. Falcarindiol (6 uM; for 2 hours) induces autophagy and causes significant level of LC3-I converted to LC3-II in MDA-MB-231, MDA-MB-468 and SKBR3 cells. Falcarindiol (6 uM; for 2, 4, 8, 24 hours) increases the level of GRP78 in MDA-MB-231 cells in dose- and time-dependent manner. Falcarindiol (1-20 µM) has no effect on hMSCs and HT-29 cell viability. Falcarindiol with only concentrations above 50 µM exhibits a toxic effect on the cells. Falcarindiol (5 µM; 10 min, 1 h and 24 h) causes a significant upregulation on PPARγ2 expression at 24 h. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo Falcarindiol (7 µg/g; diet) increases ABCA1 expression in neoplastic tissue in five weeks old male rats. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Oil IC50& Target:PPARγ |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty alcohols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Long-chain fatty alcohols |
| Alternative Parents | Secondary alcohols Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Long chain fatty alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. |
| External Descriptors | Fatty alcohols |
|
|
|
| IUPAC Name | (9E)-heptadeca-1,9-dien-4,6-diyne-3,8-diol |
|---|---|
| INCHI | InChI=1S/C17H24O2/c1-3-5-6-7-8-9-10-14-17(19)15-12-11-13-16(18)4-2/h4,10,14,16-19H,2-3,5-9H2,1H3/b14-10+ |
| InChIKey | QWCNQXNAFCBLLV-GXDHUFHOSA-N |
| Smiles | CCCCCCCC=CC(C#CC#CC(C=C)O)O |
| Isomeric SMILES | CCCCCCC/C=C/C(C#CC#CC(C=C)O)O |
| Molecular Weight | 260.399 |
| Reaxy-Rn | 9786761 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9786761&ln= |
| Solubility | DMSO : ≥ 33.33 mg/mL (128.01 mM) |
|---|---|
| Molecular Weight | 260.399 g/mol |
| XLogP3 | 4.400 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 9 |
| Exact Mass | 260.178 Da |
| Monoisotopic Mass | 260.178 Da |
| Topological Polar Surface Area | 40.500 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 394.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |