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Murrayacarpin B
Murrayacarpin B
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Murrayacarpin B
Price:
CAS No.: 120693-44-9
Catalog No.: CFN92670
Molecular Formula: C12H12O5
Molecular Weight: 236.2 g/mol
Purity: >=98%
Type of Compound: Coumarins
Physical Desc.: Cryst.
Source: The herbs of Murraya paniculata
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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Description: Murrayacarpin B is a natural product from Murraya paniculata.
Murrayacarpin B Description
Source: The herbs of Murraya paniculata
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
More...

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 4.2337 mL 21.1685 mL 42.337 mL 84.674 mL 105.8425 mL
5 mM 0.8467 mL 4.2337 mL 8.4674 mL 16.9348 mL 21.1685 mL
10 mM 0.4234 mL 2.1169 mL 4.2337 mL 8.4674 mL 10.5843 mL
50 mM 0.0847 mL 0.4234 mL 0.8467 mL 1.6935 mL 2.1169 mL
100 mM 0.0423 mL 0.2117 mL 0.4234 mL 0.8467 mL 1.0584 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:
Phytochemistry, 2015 , 28 (1) :293-294.
Coumarins of the flowers of Murraya paniculata.[Reference: WebLink]

METHODS AND RESULTS:
Four new coumarins, omphalocarpin, (−)-murracarpin, murrayacarpin A and Murrayacarpin B together with known coumarins, scopolin, scopoletin, 5,7-dimethoxy-8-(3′-methyl-2′-oxobutyl)coumarin, (±)-murracarpin and mupanidin have been isolated from the flowers of Murraya paniculata var. omphalocarpa.
CONCLUSIONS:
Their structures have been characterized from spectral analysis, chemical transformation and/or synthesis.
CFN91660Neoartanin104196-69-2290.31C16H18O5
CFN993448-Geranyloxy-5,7-dimethoxycoumarin1228175-65-2358.4 C21H26O5
CFN92736Arteminin466639-11-2222.2C11H10O5
CFN98768Fraxinol486-28-2222.2 C11H10O5
CFN70362Umckalin43053-62-9222.2C11H10O5
CFN98347Tomentin28449-62-9222.2 C11H10O5
CFN893095,6,7-Trimethoxycoumarin55085-47-7236.22C12H12O5
CFN891825-Hydroxy-6,7,8-trimethoxycoumarin1581248-32-9252.22C12H12O6
CFN989415,6,7,8-Tetramethoxycoumarin56317-15-8266.3 C13H14O6
CFN704388-Acetyl-7-hydroxycoumarin6748-68-1204.2C11H8O4
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