Lycopersene

Details

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Internal ID ef593d42-b5ab-4f04-b01d-970bdb044d26
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Carotenes
IUPAC Name (6E,10E,14E,18E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,14,18,22,26,30-octaene
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CC/C(=C/CC/C(=C/CC/C=C(/CC/C=C(/CC/C=C(/CCC=C(C)C)\C)\C)\C)/C)/C)/C)C
InChI InChI=1S/C40H66/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/h19-22,27-30H,11-18,23-26,31-32H2,1-10H3/b35-21+,36-22+,37-27+,38-28+,39-29+,40-30+
InChI Key BGVXBZXEFXMRGJ-DPOFWPLISA-N
Popularity 48 references in papers

Physical and Chemical Properties

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Molecular Formula C40H66
Molecular Weight 547.00 g/mol
Exact Mass 546.516452105 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 15.30
Atomic LogP (AlogP) 14.06
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 21

Synonyms

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lycopaoctaene
502-62-5
(6E,10E,14E,18E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,14,18,22,26,30-octaene
Lycopersen
all-trans-lycopaoctaene
15,15'-dihydrophytoene
CHEBI:142538
DTXSID901318251
C22055
7,7',8,8',11,11',12,12',15,15'-Decahydro-psi,psi-carotene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Lycopersene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 - 0.6598 65.98%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Nucleus 0.6684 66.84%
OATP2B1 inhibitior - 0.7156 71.56%
OATP1B1 inhibitior + 0.9462 94.62%
OATP1B3 inhibitior + 0.9380 93.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9789 97.89%
P-glycoprotein inhibitior + 0.7606 76.06%
P-glycoprotein substrate - 0.9803 98.03%
CYP3A4 substrate - 0.6864 68.64%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9716 97.16%
CYP2C9 inhibition - 0.9099 90.99%
CYP2C19 inhibition - 0.9168 91.68%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.7354 73.54%
CYP2C8 inhibition - 0.9863 98.63%
CYP inhibitory promiscuity - 0.6923 69.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Warning 0.4712 47.12%
Eye corrosion + 0.7181 71.81%
Eye irritation - 0.8128 81.28%
Skin irritation + 0.8835 88.35%
Skin corrosion - 0.9656 96.56%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6533 65.33%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation + 0.9505 95.05%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.6624 66.24%
Acute Oral Toxicity (c) III 0.8971 89.71%
Estrogen receptor binding + 0.7240 72.40%
Androgen receptor binding - 0.8474 84.74%
Thyroid receptor binding + 0.5872 58.72%
Glucocorticoid receptor binding - 0.5176 51.76%
Aromatase binding - 0.5571 55.71%
PPAR gamma + 0.5889 58.89%
Honey bee toxicity - 0.8442 84.42%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9916 99.16%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.43% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.16% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.96% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.68% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.29% 91.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Lemna minor
Zea mays

Cross-Links

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PubChem 5365816
LOTUS LTS0007754
wikiData Q74418198