(2E,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26Z)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaen-1-ol

Details

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Internal ID 2037b1e5-b068-430e-be15-b40e3842c3f1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name (2E,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26Z)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaen-1-ol
SMILES (Canonical) CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)CO)C)C)C)C
SMILES (Isomeric) CC(=CCC/C(=C\C=C\C(=C\C=C\C(=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C=C(/C)\CC/C=C(\C)/CO)\C)\C)/C)C
InChI InChI=1S/C40H56O/c1-33(2)18-12-21-36(5)24-15-27-37(6)25-13-22-34(3)19-10-11-20-35(4)23-14-26-38(7)28-16-29-39(8)30-17-31-40(9)32-41/h10-11,13-16,18-20,22-29,31,41H,12,17,21,30,32H2,1-9H3/b11-10+,22-13+,23-14+,27-15+,28-16+,34-19+,35-20+,36-24-,37-25+,38-26+,39-29+,40-31+
InChI Key IFTRFNLCKUZSNG-OXKLVVMQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C40H56O
Molecular Weight 552.90 g/mol
Exact Mass 552.433116406 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 14.30
Atomic LogP (AlogP) 11.91
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26Z)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaen-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 - 0.7264 72.64%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.5576 55.76%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.8777 87.77%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9953 99.53%
P-glycoprotein inhibitior + 0.8054 80.54%
P-glycoprotein substrate - 0.8813 88.13%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7664 76.64%
CYP3A4 inhibition - 0.9088 90.88%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition - 0.9270 92.70%
CYP inhibitory promiscuity - 0.7650 76.50%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6507 65.07%
Eye corrosion + 0.5325 53.25%
Eye irritation - 0.8890 88.90%
Skin irritation + 0.8492 84.92%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9229 92.29%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7176 71.76%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9812 98.12%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.7558 75.58%
Acute Oral Toxicity (c) III 0.8552 85.52%
Estrogen receptor binding + 0.8650 86.50%
Androgen receptor binding + 0.6703 67.03%
Thyroid receptor binding + 0.8022 80.22%
Glucocorticoid receptor binding - 0.7292 72.92%
Aromatase binding - 0.7925 79.25%
PPAR gamma + 0.7134 71.34%
Honey bee toxicity - 0.8822 88.22%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9500 95.00%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.82% 92.08%
CHEMBL2581 P07339 Cathepsin D 86.97% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.18% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.18% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.48% 99.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.40% 91.71%

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.
Dioscorea communis
Lycoris radiata
Solanum dulcamara
Solanum lycopersicum

Cross-Links

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PubChem 10196509
NPASS NPC299459