(8R,9E,11Z,14Z)-heptadeca-1,9,11,14-tetraen-8-ol

Details

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Internal ID 6af98a79-6cb2-42d4-933d-bade01263f6d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (8R,9E,11Z,14Z)-heptadeca-1,9,11,14-tetraen-8-ol
SMILES (Canonical) CCC=CCC=CC=CC(CCCCCC=C)O
SMILES (Isomeric) CC/C=C\C/C=C\C=C\[C@@H](CCCCCC=C)O
InChI InChI=1S/C17H28O/c1-3-5-7-9-10-12-14-16-17(18)15-13-11-8-6-4-2/h4-5,7,10,12,14,16-18H,2-3,6,8-9,11,13,15H2,1H3/b7-5-,12-10-,16-14+/t17-/m1/s1
InChI Key XRQOZSDRIZPYNO-IPRFWXIGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H28O
Molecular Weight 248.40 g/mol
Exact Mass 248.214015512 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.95
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8R,9E,11Z,14Z)-heptadeca-1,9,11,14-tetraen-8-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 + 0.7555 75.55%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.4101 41.01%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.8261 82.61%
OATP1B3 inhibitior + 0.8922 89.22%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6265 62.65%
P-glycoprotein inhibitior - 0.8441 84.41%
P-glycoprotein substrate - 0.8424 84.24%
CYP3A4 substrate - 0.5244 52.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7357 73.57%
CYP3A4 inhibition - 0.9543 95.43%
CYP2C9 inhibition - 0.8837 88.37%
CYP2C19 inhibition - 0.8993 89.93%
CYP2D6 inhibition - 0.9418 94.18%
CYP1A2 inhibition + 0.5502 55.02%
CYP2C8 inhibition - 0.8080 80.80%
CYP inhibitory promiscuity - 0.7922 79.22%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6530 65.30%
Eye corrosion + 0.7650 76.50%
Eye irritation + 0.5843 58.43%
Skin irritation + 0.7218 72.18%
Skin corrosion - 0.8718 87.18%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6480 64.80%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5574 55.74%
skin sensitisation + 0.9117 91.17%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.8884 88.84%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.7848 78.48%
Acute Oral Toxicity (c) III 0.5386 53.86%
Estrogen receptor binding + 0.7914 79.14%
Androgen receptor binding - 0.8317 83.17%
Thyroid receptor binding + 0.6183 61.83%
Glucocorticoid receptor binding + 0.5922 59.22%
Aromatase binding + 0.5702 57.02%
PPAR gamma + 0.8222 82.22%
Honey bee toxicity - 0.9158 91.58%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.7221 72.21%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.08% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.96% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.40% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 88.98% 90.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.13% 97.29%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.55% 91.11%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 83.15% 90.75%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.38% 100.00%

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.
Cirsium nipponicum

Cross-Links

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PubChem 162971596
LOTUS LTS0238993
wikiData Q105340681