13018-46-7

Usage

Natural pigment

13-CIS-LYCOPENE is a naturally occurring pigment found in various fruits and vegetables.

Carotenoid compound

It is a type of carotenoid, which are organic pigments found in plants and some microorganisms.

Found in

Tomatoes, watermelons, and papayas are some of the sources of 13-CIS-LYCOPENE.

Geometric isomer

It is a geometric isomer of trans-lycopene, which means it has a different molecular structure.

Antioxidant properties

13-CIS-LYCOPENE has the ability to neutralize free radicals, which are unstable molecules that can cause damage to cells and tissues.

Anti-inflammatory properties

It has been found to have potential anti-inflammatory properties, which may help reduce inflammation in the body.

Reduces oxidative stress

By neutralizing free radicals, 13-CIS-LYCOPENE may help reduce oxidative stress, which is a major factor in the development of chronic diseases.

Anti-cancer effects

Some research suggests that 13-CIS-LYCOPENE may have potential anti-cancer effects, although more studies are needed to confirm these findings.

InChI:InChI=1/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+

Upstream product

• 64727-64-6 (9Z)-lycophene 
• 5056-17-7 (2E,4E,6E)-2,7-dimethyl-2,4,6-octatrienedial 
• 145571-84-2 Triphenyl<(2E,4E,6Z)-3,7,11-trimethyldodeca-2,4,6,10-tetraenyl>phosphonium Bromide 
• 103793-14-2 [(2E,6E)-8-(Diethoxy-phosphoryl)-2,7-dimethyl-octa-2,6-dien-4-ynyl]-phosphonic acid diethyl ester 
• 20082-23-9 (4E,6E/Z)-3,7,11-Trimethyldodeca-4,6,10-trien-1-yn-3-ol 
• 1071-89-2 (4E,6E/Z)-3,7,11-Trimethyldodeca-1,4,6,10-tetraen-3-ol 
• 58689-15-9 pseudoionone 
• 101468-86-4 7-cis-lycopene 
• 4418-71-7 lycopene 
• 7553-56-2 iodine 
• 71-43-2 benzene 

Downstream Products

• 4418-71-7 lycopene 
• 502-65-8 lycopene 
• 64727-64-6 (9Z)-lycophene 
• 101468-86-4 7-cis-lycopene 

Relevant academic research and scientific papers

Stable and bioavailable compositions of isomers of carotenoids for skin and hair

Compositions that provide health benefits and methods regarding same are presented. In an embodiment, the present invention provides a primary composition comprising at least one carotenoid-containing material, enriched in Z isomers of the carotenoid compound. For example, the carotenoid-containing material contains by weight a greater percentage of an isomer selected from the group consisting of 5-Z, 9-Z and combinations thereof than of 13-Z isomer.

Stable and bioavailable compositions of isomers of carotenoids for skin and hair

The present invention relates to a method of manufacturing a stable composition enriched in cis-lycopene (z-isomers) by prolonged heating in solvents of tomatoes, parts of tomatoes, derivative thereof or tomato extracts in solvents.

Synthesis, Isolation, and NMR-Spectroscopic Characterization of Fourteen (Z)-Isomers of Lycopene and of Some Acetylenic Didehydro- and Tetradehydrolycopenes

Eight (Z)-isomers of lycopene were prepared by stereocontrolled syntheses and fully characterized by 1H-NMR, 13C-NMR, mass, and UV/VIS-spectroscopy: (5Z)-, (7Z)-, (15Z)-, (5Z,5'Z)-, (7Z,7'Z)-, (7Z,9Z)-, (9Z,9'Z)-, and (7Z,9Z,7'Z,9'Z)-lycopene.Six additional (Z)-isomers, namely (9Z)-, (13Z)-, (5Z,9'Z)-, (9Z,13'Z)-, (5Z,9Z,5'Z)-, and (5Z,13Z,5'Z)-lycopene, were isolated in small quantities from isomer mixtures by semiprep.HPLC and were identified by 1H-NMR spectroscopy.

Synthesen von Carotinen mit ψ-Endgruppen und (Z)-Konfiguration an terminalen konjugierten Doppelbindungen

Five carotenes bearing (5Z)-ψ-end groups were synthesized and carefully characterized: (5Z)-lycopene (6), (5Z,5'Z)-lycopene (7), (5'Z)-neurosporene (8), (5'Z)-β,ψ-carotene (12), and (5'Z)-εψ-carotene (14).