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Triptonodiol
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Product Name Triptonodiol
Price:
CAS No.: 117456-87-8
Catalog No.: CFN96476
Molecular Formula: C21H30O4
Molecular Weight: 346.46 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The roots of Tripterygium wilfordii Hook.f.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Triptonodiol is a natural product from Tripterygium wilfordii Hook.f.
Triptonodiol Description
Source: The roots of Tripterygium wilfordii Hook.f.
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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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.8863 mL 14.4317 mL 28.8634 mL 57.7267 mL 72.1584 mL
5 mM 0.5773 mL 2.8863 mL 5.7727 mL 11.5453 mL 14.4317 mL
10 mM 0.2886 mL 1.4432 mL 2.8863 mL 5.7727 mL 7.2158 mL
50 mM 0.0577 mL 0.2886 mL 0.5773 mL 1.1545 mL 1.4432 mL
100 mM 0.0289 mL 0.1443 mL 0.2886 mL 0.5773 mL 0.7216 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:
Helvetica Chimica Acta, 2013 , 96 (2) :313-9.
Two New Abietane Diterpenoids from the Roots of Tripterygium wilfordii HOOK. f.[Reference: WebLink]

METHODS AND RESULTS:
Two new abietane-type diterpenoids, named triptobenzene R (1) and triptobenzene S (2), together with three known abietane-type diterpenoids, triptophenolide (3), Triptonodiol (4), and triptonoterpene methyl ether (5), were isolated from the roots of Tripterygium wilfordii Hook. f. Their structures and relative configurations were established by detailed spectral studies, including 1D- and 2D-NMR (HSQC, HMBC, and NOESY), and HR-ESI-TOF-MS, and by comparison with published data.
CONCLUSIONS:
Their absolute configurations were assigned by the CD technique, applied for the first time to abietane diterpenes from Tripterygium wilfordii. Compound 2 is the first abietane-type norditerpenoid isolated from the genus Tripterygium.
Planta Med. 1988 Aug;54(4):330-2.
Studies on New Components and Stereochemistry of Diterpenoids from Trypterygium wilfordii.[Pubmed: 17265278 ]
An extensive investigation of the petroleum ether extract of TRIPTERYGIUM WILFORDII plants have revealed the presence of four new compounds, triptonoterpene, neotriptonoterpene, Triptonodiol, and neotriptonolide, in addition to the diterpenes isolated and characterized earlier. The structures of these novel natural products have been elucidated.
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