Target intelligence / Profile preview

Lycopene

Molecular classification
Other (Carotenoid), Tetraterpene
01

Overview

Lycopene is a naturally occurring red carotenoid pigment with the molecular formula C₄₀H₅₆ and a molecular weight of approximately 536.9 g/mol. It is a symmetrical tetraterpene composed of eight isoprene units arranged in an acyclic open-chain structure containing 13 double bonds—11 of which are conjugated—giving it strong antioxidant properties and its characteristic deep red color[1][3][4]. Lycopene is highly lipophilic and insoluble in water but soluble in organic solvents such as hexane and chloroform. It occurs predominantly in the all-trans form in nature but can exist as various cis-isomers due to light or heat-induced isomerization[3][5]. Found abundantly in tomatoes and other red fruits like watermelon and pink grapefruit, lycopene acts primarily as an antioxidant by quenching singlet oxygen and neutralizing free radicals more efficiently than many other carotenoids or vitamin E[1][4]. Unlike some related carotenoids such as beta-carotene, lycopene does not have provitamin A activity because it lacks terminal beta-ionone rings[4]. Epidemiological studies suggest that higher dietary intake of lycopene may be associated with reduced risk for certain cancers (notably prostate cancer) and cardiovascular diseases; however, lycopene itself does not act on a specific therapeutic target such as a receptor or enzyme—it functions through general antioxidative mechanisms rather than direct modulation of biological targets typically considered "therapeutic targets" in pharmacology[8]. Note: Lycopene itself is not considered a therapeutic target like receptors or enzymes; rather it is a bioactive compound/nutrient with health-related effects via its chemical properties. Thus "is_target" should be marked false; "is_incorrect" should be true if the intent was to identify druggable protein/nucleic acid targets rather than nutrients or small molecule antioxidants.

Other names
all-trans-lycopeneΨ,Ψ-carotenepsi,psi-carotenetrans-lycopene9-cis-lycopene (for isomer)(all-E)-lycopene[6][9]
02

Mechanism of action

Scavenges reactive oxygen species and singlet oxygen as an antioxidant[1][4]

03

Biological functions

Antioxidant activityFree radical scavenging
04

Disease associations

Cancer (preventive/epidemiological association)Cardiovascular disease (preventive/epidemiological association)
05

Safety considerations

Generally recognized as safe; no major safety concerns at dietary levels[1]

Beyond the preview

Go deeper on Lycopene.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Lycopene.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call