7',8',11',12'-Tetrahydro-gamma-carotene

Details

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Internal ID 8fc81655-69e4-4ae2-a6eb-6968d464b261
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Carotenes
IUPAC Name 2-[(1E,3E,5E,7E,9E,11E,15E,19E)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,15,19,23-nonaenyl]-1,3,3-trimethylcyclohexene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C40H60/c1-32(2)18-13-21-35(5)24-15-26-36(6)25-14-22-33(3)19-11-12-20-34(4)23-16-27-37(7)29-30-39-38(8)28-17-31-40(39,9)10/h11-12,16,18-20,23-25,27,29-30H,13-15,17,21-22,26,28,31H2,1-10H3/b12-11+,23-16+,30-29+,33-19+,34-20+,35-24+,36-25+,37-27+
InChI Key CJPVGWWWFOEZJV-FOBJUVIXSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C40H60
Molecular Weight 540.90 g/mol
Exact Mass 540.469501914 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 14.40
Atomic LogP (AlogP) 13.22
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7',8',11',12'-Tetrahydro-gamma-carotene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 - 0.7415 74.15%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.5479 54.79%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior - 0.5727 57.27%
OATP1B3 inhibitior - 0.2942 29.42%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 1.0000 100.00%
P-glycoprotein inhibitior + 0.8502 85.02%
P-glycoprotein substrate - 0.8181 81.81%
CYP3A4 substrate + 0.6568 65.68%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.8896 88.96%
CYP2C9 inhibition - 0.8919 89.19%
CYP2C19 inhibition - 0.8956 89.56%
CYP2D6 inhibition - 0.9502 95.02%
CYP1A2 inhibition - 0.8451 84.51%
CYP2C8 inhibition - 0.6561 65.61%
CYP inhibitory promiscuity - 0.5752 57.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Warning 0.4901 49.01%
Eye corrosion - 0.8210 82.10%
Eye irritation - 0.9122 91.22%
Skin irritation + 0.5691 56.91%
Skin corrosion - 0.9860 98.60%
Ames mutagenesis - 0.5512 55.12%
Human Ether-a-go-go-Related Gene inhibition + 0.8843 88.43%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5206 52.06%
skin sensitisation + 0.9289 92.89%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.7563 75.63%
Acute Oral Toxicity (c) III 0.7043 70.43%
Estrogen receptor binding + 0.8264 82.64%
Androgen receptor binding + 0.6861 68.61%
Thyroid receptor binding + 0.7196 71.96%
Glucocorticoid receptor binding + 0.6012 60.12%
Aromatase binding - 0.6196 61.96%
PPAR gamma + 0.7150 71.50%
Honey bee toxicity - 0.8599 85.99%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.46% 91.11%
CHEMBL2061 P19793 Retinoid X receptor alpha 93.33% 91.67%
CHEMBL1870 P28702 Retinoid X receptor beta 93.27% 95.00%
CHEMBL2004 P48443 Retinoid X receptor gamma 92.56% 100.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.50% 95.50%
CHEMBL1937 Q92769 Histone deacetylase 2 90.00% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.48% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.08% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 88.99% 90.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.07% 91.71%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.93% 92.08%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.59% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.72% 94.45%
CHEMBL2581 P07339 Cathepsin D 84.92% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 82.13% 89.63%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.07% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 81.51% 94.73%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.54% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163184446
LOTUS LTS0274331
wikiData Q104961522