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6-Hydroxysugiol
6-Hydroxysugiol
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 6-Hydroxysugiol
Price:
CAS No.: 55898-07-2
Catalog No.: CFN92177
Molecular Formula: C20H28O3
Molecular Weight: 316.4 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The herbs of Salvia yunnanensis
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
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Biological Activity
Description: 6-Hydroxysugiol inhibits proliferation and migration of HepG2 cells and exhibits potent anti-angiogenic activity.
Targets: VEGFR
In vitro:
Latin American Journal of Pharmacy, 2012 , 31 (10) :1457-1463.
6-Hydroxysugiol Isolated from Salvia yunnanensis Inhibits Proliferation and Migration of HepG2 Cells as well as Exhibits Potent Anti-Angiogenic Activity[Reference: WebLink]
The aim of our study was to investigate the anti-angiogenic effect and anti-tumor activity of 6-Hydroxysugiol isolated from Salvia yunnanensis.
METHODS AND RESULTS:
The cell proliferation was evaluated by MTT assay. The apoptosis of HepG2 was studied through the fluorescence microscope. Anti-angiogenic activity of 6-Hydroxysugiol was tested by chicken chorioallantoic membrane (CAM) model in vivo. In order to study the mechanism of 6-Hydroxysugiol inhibiting angiogenesis, the expression of VEGF in the HepG2 cell and the cell culture fluid were determined by immunocytochemistry and ELISA assay. The results showed that the cell proliferation was inhibited to 76.2% by 6-Hydroxysugiol, at the concentration 0.32 mmol/L. The ability of cells to migrate was significantly reduced by 6-Hydroxysugiol and the 59.72% cells showed the typically apoptotic chromatin fragmentation that were treated with 6-Hydroxysugiol at 0.64 mmol/L. The ex- pression of VEGF in the HepG2 cell and in the cell culture medium were all decreased to by 6-Hydroxysugiol.
CONCLUSIONS:
6-Hydroxysugiol is able to suppress angiogenesis on CAM models. These results suggest that it is de- served further investigation as a promising anti-tumor angiogenesis compound.
6-Hydroxysugiol Description
Source: The herbs of Salvia yunnanensis
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Cell. 2018 Jan 11;172(1-2):249-261.e12.
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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.1606 mL 15.8028 mL 31.6056 mL 63.2111 mL 79.0139 mL
5 mM 0.6321 mL 3.1606 mL 6.3211 mL 12.6422 mL 15.8028 mL
10 mM 0.3161 mL 1.5803 mL 3.1606 mL 6.3211 mL 7.9014 mL
50 mM 0.0632 mL 0.3161 mL 0.6321 mL 1.2642 mL 1.5803 mL
100 mM 0.0316 mL 0.158 mL 0.3161 mL 0.6321 mL 0.7901 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Synthesis , 2010 (13) :2223-2232.
Connecting C19 Norditerpenoids to C20 Diterpenes: Total Syntheses of 6Hydroxy5,6-dehydrosugiol, 6-Hydroxysugiol, and Taiwaniaquinone H, and Formal Synthesis of Dichroanone[Reference: WebLink]

METHODS AND RESULTS:
Oxidation of the B-ring of abietane derivatives by Sharpless- dihydroxylation gave the natural products 6-hydroxy-5,6-dehydrosugiol and 6-Hydroxysugiol. Moreover, further oxidation gave a hydroxy dione derivative that provides a synthetic entry into the C19 taiwaniaquinoid family of natural products.
CONCLUSIONS:
This route is based on biosynthetic considerations and involves a benzilic acid rearrangement followed by decarboxylation. On the basis of this approach, a total synthesis of (-)-taiwaniaquinone H and a formal synthesis of (-)-dichroanone have been achieved.
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