2-(6,10-Dimethylundeca-1,5,9-trien-2-yl)-5,9,14-trimethylpentadeca-4,8,13-trien-1-ol

Details

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Internal ID d9bd77c5-b7b8-4874-8766-bae1f0970ebf
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 2-(6,10-dimethylundeca-1,5,9-trien-2-yl)-5,9,14-trimethylpentadeca-4,8,13-trien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H52O/c1-25(2)14-9-10-16-27(5)18-12-19-29(7)22-23-31(24-32)30(8)21-13-20-28(6)17-11-15-26(3)4/h14-15,18,20,22,31-32H,8-13,16-17,19,21,23-24H2,1-7H3
InChI Key PZHZGNSCKVIFBY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H52O
Molecular Weight 440.70 g/mol
Exact Mass 440.401816278 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 11.00
Atomic LogP (AlogP) 9.82
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 2-(6,10-Dimethylundeca-1,5,9-trien-2-yl)-5,9,14-trimethylpentadeca-4,8,13-trien-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 + 0.9837 98.37%
Caco-2 - 0.5999 59.99%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.5673 56.73%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9205 92.05%
OATP1B3 inhibitior + 0.9461 94.61%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9471 94.71%
P-glycoprotein inhibitior + 0.7186 71.86%
P-glycoprotein substrate - 0.8422 84.22%
CYP3A4 substrate - 0.5104 51.04%
CYP2C9 substrate - 0.6591 65.91%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.8452 84.52%
CYP2C9 inhibition - 0.8534 85.34%
CYP2C19 inhibition - 0.8772 87.72%
CYP2D6 inhibition - 0.9201 92.01%
CYP1A2 inhibition - 0.8698 86.98%
CYP2C8 inhibition - 0.8814 88.14%
CYP inhibitory promiscuity - 0.7882 78.82%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6586 65.86%
Eye corrosion - 0.5861 58.61%
Eye irritation - 0.8463 84.63%
Skin irritation + 0.6756 67.56%
Skin corrosion - 0.9437 94.37%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7268 72.68%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation + 0.8832 88.32%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9830 98.30%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6363 63.63%
Estrogen receptor binding + 0.6729 67.29%
Androgen receptor binding - 0.7123 71.23%
Thyroid receptor binding + 0.5723 57.23%
Glucocorticoid receptor binding - 0.4878 48.78%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6508 65.08%
Honey bee toxicity - 0.8296 82.96%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9831 98.31%

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
CHEMBL2581 P07339 Cathepsin D 90.36% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.53% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.30% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.57% 96.09%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 85.11% 93.10%
CHEMBL2885 P07451 Carbonic anhydrase III 85.09% 87.45%
CHEMBL3401 O75469 Pregnane X receptor 84.68% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.07% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.84% 97.29%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.03% 94.45%

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.
Euphorbia guyoniana

Cross-Links

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PubChem 163092396
LOTUS LTS0163698
wikiData Q105216981