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Price | Qty |
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L651857-1mg
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1mg |
Available within 8-12 weeks(?)
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$320.90
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Phenols Polyphenols Others
| Synonyms | DTXSID50331917 | BDBM246496 | 2,5-Dihydroxy-7-methoxy-9,10-dihydrophenanthrene (14) | CHEBI:28678 | FS-7984 | 4,7-Dihydroxy-2-methoxy-9,10-dihydrophenanthrene | SCHEMBL4743850 | 7-methoxy-9,10-dihydrophenanthrene-2,5-diol | Q27103833 | HY-121418 | Lusiant |
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| Specifications & Purity | ≥98% |
| Biochemical and Physiological Mechanisms | Lusianthridin, a pure compound from Dendrobium venustum , have an anti-migratory effect. Lusianthridin enhances c-Myc degradation through the inhibition of Src-STAT3 signaling. |
| Storage Temp | Protected from light,Store at -80°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
Lusianthridin, a pure compound from Dendrobium venustum , have an anti-migratory effect. Lusianthridin enhances c-Myc degradation through the inhibition of Src-STAT3 signaling. In Vitro Lusianthridin (0-100 μM) inhibits cell viability at concentrations greater than 50 μM in both H460 and H292 cells. Lusianthridin significantly reduces the CSC populations in both H460 and H292 cells of the CSC spheres, with a significant decrease in the size of the H460 CSC spheres by approximately 10%, 63%, and 77% at day 3 at concentration 5, 10, and 20 μM Lusianthridin, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: The human non-small cell lung cancer cell lines, NCI-H460, and NCI-H292 cells.\n0-100 μM. Concentration: 0-100 μM. Incubation Time: 24 h. Result: Caused a significant reduction in terms of cell viability at concentrations greater than 50 μM in both H460 and H292 cells. Form:Solid |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Phenanthrenes and derivatives |
| Subclass | Hydrophenanthrenes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Hydrophenanthrenes |
| Alternative Parents | Naphthols and derivatives Anisoles Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Hydrophenanthrene - 1-naphthol - Naphthalene - Anisole - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as hydrophenanthrenes. These are a phenanthrene derivative where at least one ring CC bond is substituted by hydrogenation. |
| External Descriptors | dihydrophenanthrene |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| IUPAC Name | 7-methoxy-9,10-dihydrophenanthrene-2,5-diol |
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| INCHI | InChI=1S/C15H14O3/c1-18-12-7-10-3-2-9-6-11(16)4-5-13(9)15(10)14(17)8-12/h4-8,16-17H,2-3H2,1H3 |
| InChIKey | RDKDIPDDUFMMMT-UHFFFAOYSA-N |
| Smiles | COC1=CC2=C(C3=C(CC2)C=C(C=C3)O)C(=C1)O |
| Isomeric SMILES | COC1=CC2=C(C3=C(CC2)C=C(C=C3)O)C(=C1)O |
| Alternate CAS | 87530-30-1 |
| PubChem CID | 442702 |
| MeSH Entry Terms | 4,7-dihydroxy-2-methoxy-9,10-dihydrophenanthrene;lusianthridin |
| Molecular Weight | 242.27 |
| Molecular Weight | 242.270 g/mol |
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| XLogP3 | 3.100 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 1 |
| Exact Mass | 242.094 Da |
| Monoisotopic Mass | 242.094 Da |
| Topological Polar Surface Area | 49.700 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 293.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |