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Lycopene

$65

  • Brand : BIOFRON

  • Catalogue Number : BD-D1220

  • Specification : 98%(HPLC)

  • CAS number : 502-65-8

  • Formula : C40H56

  • Molecular Weight : 536.87

  • PUBCHEM ID : 446925

  • Volume : 20mg

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Catalogue Number

BD-D1220

Analysis Method

HPLC,NMR,MS

Specification

98%(HPLC)

Storage

-20?

Molecular Weight

536.87

Appearance

Red crystalline powder

Botanical Source

Lycopersicon esculentum Mill.

Structure Type

Other Terpenoids

Category

Standards;Natural Pytochemical;API

SMILES

CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C

Synonyms

lycopen/LYCOSOURCE/y,y-Carotene/Lycopene,Redivivo/?,?-Carotene/LYCOVIT/LycopinE 160d/Lycopene all-trans-/Lycopene/(all-E)-2,6,10,14,19,23,27,31-Octamethyl-2,6,8,10,12,14,16,18,20,22,24,26,30-dotriacontatridecaene/(all-trans)-Lycopene/y-Carotene/(6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-Octamethyl-2,6,8,10,12,14,16,18,20,22,24,26,30dotriacontatridecaene/(6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-Octamethyl-2,6,8,10,12,14,16,18,20,22,24,26,30-dotriacontatridecaene/all-trans-Lyc/(6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-Octamethyl-2,6,8,10,12,14,16,18,20,22,24,26,30-dotriacontatridecaen/4,4-CAROTENE

IUPAC Name

(6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaene

Applications

Lycopene is naturally occurring carotenoids found in tomato, tomato products, and in other red fruits and vegetables; exhibits antioxidant effects.

Density

0.9±0.1 g/cm3

Solubility

Dichloromethane

Flash Point

350.7±19.4 °C

Boiling Point

660.9±30.0 °C at 760 mmHg

Melting Point

172-173°C

InChl

InChI=1S/C40H56/c1-33(2)19-13-23-37(7)27-17-31-39(9)29-15-25-35(5)21-11-12-22-36(6)26-16-30-40(10)32-18-28-38(8)24-14-20-34(3)4/h11-12,15-22,25-32H,13-14,23-24H2,1-10H3/b12-11+,25-15+,26-16+,31-17+,32-18+,35-21+,36-22+,37-27+,38-28+,39-29+,40-30+

InChl Key

OAIJSZIZWZSQBC-GYZMGTAESA-N

WGK Germany

RID/ADR

HS Code Reference

2922500000

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:502-65-8) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

No Technical Documents Available For This Product.

PMID

31933364

Abstract

Carotenoids are essential phytonutrients synthesized by all photosynthetic organisms. Acyclic lycopene is the first branching point for carotenoid biosynthesis. Lycopene ?- and ?-cyclases (LCYB and LCYE, respectively) catalyze the cyclization of its open ends and direct the metabolic flux into different downstream branches. Carotenoids of the ?,?-branch (e.g., ?-carotene) are found in all photosynthetic organisms, but those of the ?,?-branch (e.g., lutein) are generally absent in cyanobacteria, heterokonts, and some red algae. Although both LCYBs and LCYEs have been characterized from land plants, there are only a few reports on LCYs from cyanobacteria and algae. Here, we cloned four LCY genes from Porphyra umbilicalis and Pyropia yezoensis (susabi-nori) of Bangiales, the most primitive red algal order that synthesizes lutein. Our functional characterization in both Escherichia coli and Arabidopsis thaliana demonstrated that each species has a pair of LCYB and LCYE. Similar to LCYs from higher plants, red algal LCYBs cyclize both ends of lycopene, and their LCYEs only cyclize a single end. The characterization of LCYEs from red algae resolved the first bifurcation step toward ?-carotene and lutein biosynthesis. Our phylogenetic analysis suggests that LCYEs of the green lineage and the red algae originated separately during evolution.

KEYWORDS

Porphyra umbilicalis; Pyropia yezoensis; carotenoid; evolution; lutein; lycopene; lycopene cyclase; red algae

Title

Functional Characterization of Lycopene Cyclases Illustrates the Metabolic Pathway toward Lutein in Red Algal Seaweeds.

Author

Deng YY1,2, Cheng L1, Wang Q1, Ge ZH1, Zheng H1, Cao TJ1, Lu QQ2, Yang LE1,2, Lu S1.

Publish date

2020 Feb 5

PMID

31891495

Abstract

Lycopene, one of the most dominant carotenoids in a person’s diet, is a well-known natural compound that has protective effects against chronic diseases. Industrial and domestic processing and storage conditions significantly influence retention and isomerization of lycopene; thus, in recent years, great attention has been given for their preservative effects of lycopene. This review highlights recent strategies that have been developed to preserve lycopene in processed products, especially in tomato pulp, puree, paste, and juice. The key factors influencing lycopene degradation and isomerization, such as ingredients and intensity of thermal treatments, are also discussed. Special attention was paid to the crystalline structures of lycopene which facilitate its resistance to degradation and isomerization. Emerging non-thermal processing methods, such as ultrasound and high-pressure processing (HPP), are critically evaluated for their preservation of thermo-labile compounds. Novel trends to improve lycopene stability by micro- and nanoencapsulation and addition of antioxidants are also included to examine their efficacy to protect against light, heat, oxygen, and other oxidative processes. Finally, recommended processing and storage conditions are discussed to provide strategies to retain the highest possible amount of bioactive lycopene until consumption.

KEYWORDS

bioactive compounds; carotenoids; encapsulation; processing methods; tomato

Title

Chemical Stability of Lycopene in Processed Products: A Review of the Effects of Processing Methods and Modern Preservation Strategies.

Author

Saini RK1,2,3, A Bekhit AE4, Roohinejad S5, Rengasamy KRR1, Keum YS3.

Publish date

2020 Jan 22

PMID

31855051

Abstract

OBJECTIVE:
The aim of the present study is to investigate the cardioprotective effect of lycopene, known for its antioxidant and anti-inflammatory effect, in a rat sepsis model induced by lypopolysaccharide (LPS).

METHODS:
The oxidative stress parameters, antioxidant parameters and cytokine levels with or without lycopene treatment in LPS?induced septic rats as well as in controls were measured in serum and tissue. Histologic examinations of the cardiac tissues were also performed. The Kruskal-Wallis and the Bonferroni-adjusted Mann-Whitney U Test was used for analysis. A p value < 0.05 was considered significant. RESULTS: The data of this study showed that lycopene pretreatment reduced the oxidative stres parametersand , proinflammatory cytokines as well as increased the antoxidant enzyme activities in both serum and cardiac tissues in LPS?induced septic rats.. Moreover, hyperaemia and haemorrhage in the epicardium, myocardium and endocardium were lower in the lycopene pretreated group as compared to the LPS alone group. CONCLUSION: These results suggest that lycopene could be beneficial for the prevention of cardiac injury caused by sepsis through reducing the cytokine levels and oxidative stress parameters (Tab. 4, Fig. 1, Ref.?35).

KEYWORDS

antioxidant anti-inflammatory.; lycopene; sepsis

Title

Lycopene has a protective effect on septic shock?induced cardiac injury in rats.

Author

Duzen IV, Oguz E, Yilmaz R, Taskin A, Vuruskan E, Cekici Y, Bilgel ZG, Goksuluk H, Candemir B, Sucu M.

Publish date

2019