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Glycozolinine
Glycozolinine
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Glycozolinine
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CAS No.: 5257-08-9
Catalog No.: CFN98862
Molecular Formula: C13H11NO
Molecular Weight: 197.2 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Micromelum sp.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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Description: Standard reference
Glycozolinine Description
Source: The herbs of Micromelum sp.
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.
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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

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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 5.071 mL 25.355 mL 50.7099 mL 101.4199 mL 126.7748 mL
5 mM 1.0142 mL 5.071 mL 10.142 mL 20.284 mL 25.355 mL
10 mM 0.5071 mL 2.5355 mL 5.071 mL 10.142 mL 12.6775 mL
50 mM 0.1014 mL 0.5071 mL 1.0142 mL 2.0284 mL 2.5355 mL
100 mM 0.0507 mL 0.2535 mL 0.5071 mL 1.0142 mL 1.2677 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.
Glycozolinine References Information
Citation [1]

Phytochemistry Volume 22, Issue 4, 1983, Pages 1064-1065

Glycozolinine, a carbazole derivative from Glycosmis pentaphilla[Reference: WebLink]
A new carbazole derivative, Glycozolinine, was isolated from the seeds of Glycosmis pentaphylla. From physical and chemical evidence its structure is 6-hydroxy-3-methylcarbazole.
Citation [2]

Tetrahedron Volume 71, Issue 21, 27 May 2015, Pages 3485–3490

Total synthesis of glycomaurrol and eustifoline-C by DIBAL-H promoted reductive ring opening of pyrano[2,3-c]carbazoles[Reference: WebLink]
The palladium-catalyzed construction of the carbazole framework provides an efficient access to 3-hydroxy-6-methylcarbazole (Glycozolinine) (5). Regioselective annulation of a pyran ring at Glycozolinine (5) using either a C5- or a C10-building block leads to the pyrano[2,3-c]carbazole alkaloids glycomaurin (5,6-pyranoglycozoline, eustifoline-A) (2) and eustifoline-B (4), respectively.
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Bavachin

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