ChemFaces is a professional high-purity natural products manufacturer.
Product Intended Use
1. Reference standards
2. Pharmacological research
3. Inhibitors
Citing Use of our Products
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* Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.
According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
| Size /Price /Stock |
10 mM * 1 mL in DMSO / Inquiry |
Other Packaging |
*Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap |
More articles cited ChemFaces products.
Int J Biol Macromol.2021, 199:189-200.J Ethnopharmacol.2017, 209:305-316Arch Toxicol.2017, 91(10):3225-3245Eur J Pharm Sci.2016, 94:33-45Exp Parasitol.2015, 153:160-4J Ethnopharmacol.2020, 260:112988.Food Chem Toxicol.2020, 135:110863Appl. Sci.2020, 10(20), 7323.
Biomed Pharmacother.2021, 139:111585. Processes2021, 9(11),2065.Molecules.2020, 25(17):3783.International Food Research Journ...2018...Evid Based Complement Alternat Me...2017...Biomol Ther (Seoul).2019, 10.4062Aquaculture2017, 481:94-102Food Chem.2019, 274:345-350
Biochem Biophys Res Commun....2021...Food Res Int.2020, 133:109130.African J. Agricultural Research ...2017...Institute of Food Science & Techn...2021...Plos One.2020, 10.1371Molecules 2022, 27(3),1047.South African J of Botany...2020...
More...
Our products had been exported to the following research institutions and universities, And still growing.
Agricultural Research Organizat... (Israel)Institute of Tropical Disease U... (Indonesia)Universidad de La Salle (Mexico)University of Helsinki (Finland)
University of Oslo (Norway)Chinese University of Hong Kong (China)Max-Planck-Insitut (Germany)Copenhagen University (Denmark)
Mahidol University (Thailand)University of Limpopo (South Africa)Tohoku University (Japan)
More...
Paniculidine C
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
bioRxiv2021, 462065.Journal of Ginseng Research2019, 10.1016Medicinal Chemistry Research 2021, 30:1117-1124.Processes2021, 9(1), 153;Sci Rep.2021, 11(1):11936.Food Chem.2017, 228:301-314Korean Herb. Med. Inf. 2016, 4(1):35-42Int J Biol Macromol.2020, 161:1230-1239.Plant Sci.2020, 301:110656.Molecules.2018, 23(11):E2837
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 |
Alkaloids Compound Library |
| Description: |
Standard reference |
Paniculidine C Description
| Source: |
The herbs of Murraya exotica L. |
| 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. |
ChemFaces New Products and Compounds
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 |
4.9188 mL |
24.5942 mL |
49.1884 mL |
98.3768 mL |
122.971 mL |
| 5 mM |
0.9838 mL |
4.9188 mL |
9.8377 mL |
19.6754 mL |
24.5942 mL |
| 10 mM |
0.4919 mL |
2.4594 mL |
4.9188 mL |
9.8377 mL |
12.2971 mL |
| 50 mM |
0.0984 mL |
0.4919 mL |
0.9838 mL |
1.9675 mL |
2.4594 mL |
| 100 mM |
0.0492 mL |
0.2459 mL |
0.4919 mL |
0.9838 mL |
1.2297 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.
| Structure Identification: |
| J Org Chem. 2004 Jun 25;69(13):4429-32. | | Efficient total syntheses of phytoalexin and (+/-)-paniculidine B and C based on the novel methodology for the preparation of 1-methoxyindoles.[Pubmed: 15202897 ] | A general route to 2-unsubstituted-1-methoxyindoles, based on our methodology for the synthesis of 1-methoxyindoles, is reported.
METHODS AND RESULTS:
This synthesis renders accessibility to a variety of natural products possessing the said skeleton. A direct synthesis of phytoalexin (1), (+/-)-paniculidine B (2), and (+/-)-Paniculidine C (3) is disclosed based on the methodology.
CONCLUSIONS:
The synthesis of paniculidine B (2) has been achieved from aldehyde 10 in only two steps in 88% yield and in five steps from a methoxyindole compound 8 obtained using our earlier methodology. |
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