3,7,11,15,19-Pentamethylicos-2-en-1-ol

Details

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Internal ID dfee24e1-19d4-456e-9475-0693e8a1779f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesterterpenoids
IUPAC Name 3,7,11,15,19-pentamethylicos-2-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H50O/c1-21(2)11-7-12-22(3)13-8-14-23(4)15-9-16-24(5)17-10-18-25(6)19-20-26/h19,21-24,26H,7-18,20H2,1-6H3
InChI Key IRJHFRKRPYTYCQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H50O
Molecular Weight 366.70 g/mol
Exact Mass 366.386166214 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 10.60
Atomic LogP (AlogP) 8.17
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 3,7,11,15,19-Pentamethylicos-2-en-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 + 0.6404 64.04%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.5576 55.76%
OATP2B1 inhibitior - 0.8526 85.26%
OATP1B1 inhibitior + 0.9484 94.84%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5213 52.13%
P-glycoprotein inhibitior - 0.7667 76.67%
P-glycoprotein substrate - 0.8261 82.61%
CYP3A4 substrate - 0.6011 60.11%
CYP2C9 substrate - 0.6591 65.91%
CYP2D6 substrate - 0.7543 75.43%
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 - 0.9687 96.87%
CYP inhibitory promiscuity - 0.7650 76.50%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6507 65.07%
Eye corrosion + 0.5325 53.25%
Eye irritation + 0.5938 59.38%
Skin irritation + 0.8492 84.92%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3736 37.36%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.9000 90.00%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.9812 98.12%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.7132 71.32%
Acute Oral Toxicity (c) III 0.8552 85.52%
Estrogen receptor binding - 0.7022 70.22%
Androgen receptor binding - 0.8177 81.77%
Thyroid receptor binding + 0.6439 64.39%
Glucocorticoid receptor binding - 0.5198 51.98%
Aromatase binding - 0.5452 54.52%
PPAR gamma + 0.5217 52.17%
Honey bee toxicity - 0.9714 97.14%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7400 74.00%
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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.84% 97.29%
CHEMBL2581 P07339 Cathepsin D 89.18% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.65% 93.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.39% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 86.16% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.29% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.82% 91.11%
CHEMBL2885 P07451 Carbonic anhydrase III 82.76% 87.45%
CHEMBL2039 P27338 Monoamine oxidase B 82.22% 92.51%
CHEMBL3401 O75469 Pregnane X receptor 81.02% 94.73%

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.
Croton hieronymi

Cross-Links

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PubChem 53931403
LOTUS LTS0014537
wikiData Q105118905