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Physalien
Physalien
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Physalien
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CAS No.: 144-67-2
Catalog No.: CFN70273
Molecular Formula: C72H116O4
Molecular Weight: 1045.7 g/mol
Purity: >=98%
Type of Compound: Miscellaneous
Physical Desc.: Powder
Source: The fruits of Zea mays L.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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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
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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: Reference standards.
Physalien Description
Source: The fruits of Zea mays 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.
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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 0.9563 mL 4.7815 mL 9.563 mL 19.1259 mL 23.9074 mL
5 mM 0.1913 mL 0.9563 mL 1.9126 mL 3.8252 mL 4.7815 mL
10 mM 0.0956 mL 0.4781 mL 0.9563 mL 1.9126 mL 2.3907 mL
50 mM 0.0191 mL 0.0956 mL 0.1913 mL 0.3825 mL 0.4781 mL
100 mM 0.0096 mL 0.0478 mL 0.0956 mL 0.1913 mL 0.2391 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:
Journal of the Chemical Society, 1993.
(Z/E)-photoisomerization of C40-carotenoids by iodine.[Reference: WebLink]

METHODS AND RESULTS:
The compositions of stereoisomeric mixtures of β-carotene (1), zeaxanthin (2), Physaliene (3), natural violaxanthin (4), ‘semi-synthetic’ violaxanthin (5), capsorubin (6), capsanthin (7) and lutein-epoxide (8) have been investigated.
CONCLUSIONS:
The effect of end groups with different structures and stereochemistry on the cis-trans equilibrium, the rates of photo-induced cis–trans rearrangement of the zeaxanthin (2) set, and the ‘specific rate’(per unit light energy at a given wavelength) for several 13-cis carotenoids (2, 4, 6, 7, 9) have been determined.
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Licochalcone D

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Schizandrin B

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