Hydroxy-3,4-dehydro-apo-8'-lycopene

Details

Top
Internal ID 09081658-10e4-4333-82fb-a16055389e78
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (4E,6E,8E,10E,12E,14E,16E,18E,20E)-2,6,10,14,19,23-hexamethyltetracosa-4,6,8,10,12,14,16,18,20,22-decaen-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H42O/c1-25(2)15-11-18-26(3)16-9-10-17-27(4)19-12-20-28(5)21-13-22-29(6)23-14-24-30(7,8)31/h9-23,31H,24H2,1-8H3/b10-9+,18-11+,19-12+,21-13+,23-14+,26-16+,27-17+,28-20+,29-22+
InChI Key FOIFOTKOVLXQJE-GOWUZQRBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H42O
Molecular Weight 418.70 g/mol
Exact Mass 418.323565959 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 10.40
Atomic LogP (AlogP) 8.68
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Hydroxy-3,4-dehydro-apo-8'-lycopene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9866 98.66%
Caco-2 - 0.5955 59.55%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4077 40.77%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.8495 84.95%
OATP1B3 inhibitior + 0.9589 95.89%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9952 99.52%
P-glycoprotein inhibitior + 0.6539 65.39%
P-glycoprotein substrate - 0.8876 88.76%
CYP3A4 substrate - 0.5318 53.18%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.7761 77.61%
CYP3A4 inhibition - 0.8419 84.19%
CYP2C9 inhibition - 0.8292 82.92%
CYP2C19 inhibition - 0.7159 71.59%
CYP2D6 inhibition - 0.9406 94.06%
CYP1A2 inhibition - 0.8425 84.25%
CYP2C8 inhibition - 0.9241 92.41%
CYP inhibitory promiscuity - 0.7805 78.05%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.5783 57.83%
Carcinogenicity (trinary) Non-required 0.5408 54.08%
Eye corrosion - 0.7026 70.26%
Eye irritation - 0.6967 69.67%
Skin irritation + 0.8215 82.15%
Skin corrosion - 0.8471 84.71%
Ames mutagenesis - 0.6891 68.91%
Human Ether-a-go-go-Related Gene inhibition + 0.9353 93.53%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5196 51.96%
skin sensitisation + 0.9107 91.07%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6454 64.54%
Acute Oral Toxicity (c) III 0.9209 92.09%
Estrogen receptor binding + 0.7613 76.13%
Androgen receptor binding - 0.7494 74.94%
Thyroid receptor binding + 0.7516 75.16%
Glucocorticoid receptor binding + 0.6982 69.82%
Aromatase binding + 0.5746 57.46%
PPAR gamma + 0.7392 73.92%
Honey bee toxicity - 0.8915 89.15%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.5939 59.39%

Targets

Top

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
CHEMBL4040 P28482 MAP kinase ERK2 91.33% 83.82%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 88.65% 89.34%
CHEMBL2061 P19793 Retinoid X receptor alpha 84.54% 91.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.30% 96.09%
CHEMBL1977 P11473 Vitamin D receptor 83.26% 99.43%
CHEMBL2004 P48443 Retinoid X receptor gamma 82.79% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.66% 97.25%
CHEMBL1870 P28702 Retinoid X receptor beta 82.48% 95.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.38% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 82.05% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.60% 91.11%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 46846122
LOTUS LTS0245061
wikiData Q105004920