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Triptoquinone B
Triptoquinone B
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Product Name Triptoquinone B
Price:
CAS No.: 142937-50-6
Catalog No.: CFN99474
Molecular Formula: C20H26O4
Molecular Weight: 330.4 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The vines of Tripterygium wilfordii
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF    Manual
Similar structural: Comparison (Web)  (SDF)
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Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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Product Use Citation
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: Triptoquinone B is a novel interleukin-1 inhibitor, shows extremely potent inhibitory activities against interleukin-lα and β releases for human peripheral mononticlear cells, it shows the significant immunosuppressive activity.
Targets: IL Receptor
In vitro:
Chinese Traditional & Herbal Drugs, 2007, 38(4):493-6.
Diterpenoids possessed immunosuppressive activity from Tripterygium hypoglaucum.[Reference: WebLink]
To study the diterpenoids possessed immunosuppressive activity from Tripterygium hypoglaucum.
METHODS AND RESULTS:
The chemical constituents were isolated from the CHCl3 extracts of T. hypoglaucum by repeated column chromatography, including silica gel, Sephadex LH-20, and preparative HPLC. Their structures were elucidated on the basis of spectroscopic studies. The immunosuppressive activity of these compounds was tested using the lymphocyte transformation test. Compounds I-VI were identified as triptobenzene H (I), triptoquinone A (II), Triptoquinone B (IIII), triptoquinone H (IV), triptonediol (V), triptonoterpene (VI).
CONCLUSIONS:
Compound I-III are isolated from this medicinal plant for the first time and all the compounds show the significant immunosuppressive activity.
Triptoquinone B Description
Source: The vines of Tripterygium wilfordii
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.

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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
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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)

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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.0266 mL 15.1332 mL 30.2663 mL 60.5327 mL 75.6659 mL
5 mM 0.6053 mL 3.0266 mL 6.0533 mL 12.1065 mL 15.1332 mL
10 mM 0.3027 mL 1.5133 mL 3.0266 mL 6.0533 mL 7.5666 mL
50 mM 0.0605 mL 0.3027 mL 0.6053 mL 1.2107 mL 1.5133 mL
100 mM 0.0303 mL 0.1513 mL 0.3027 mL 0.6053 mL 0.7567 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:
Tetrahedron Letters,1997,38(9):4121–4124.
Enantiocontrolled total synthesis of the diterpenoids, triptoquinone B, C and triptocallol[Reference: WebLink]

METHODS AND RESULTS:
An efficient and enantiocontrolled synthesis of Triptoquinone B and C, which possess interleukin-1 inhibitory activity, has been accomplished employing the lipase-catalyzed kinetic resolution and a highly diastereoselective radical cyclization as key synthetic steps. In addition, the first total synthesis of triptocallol has been achieved utilizing the same strategy.
CFN96479Triptinin B189389-05-7314.42C20H26O3
CFN96478Triptobenzene H146900-55-2344.45C21H28O4
CFN91646Triptonoterpene99694-87-8300.4C20H28O2
CFN99197Tripdiolide38647-10-8376.40C20H24O7
CFN99134Triptonide38647-11-9358.39C20H22O6
CFN91653Tripchlorolide132368-08-2396.86C20H25ClO6
CFN90404Triptophenolide74285-86-2312.4C20H24O3
CFN99690Triptoquinonide163513-81-3326.4 C20H22O4
CFN91917Triptobenzene K198129-88-3342.39C20H22O5
CFN91913Neotriptophenolide81827-74-9342.43C21H26O4
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