(3R,4E,6Z,9Z)-heptadeca-4,6,9,16-tetraen-3-ol

Details

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Internal ID 064b08cd-fbb4-44ab-9313-175a911cfcc2
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (3R,4E,6Z,9Z)-heptadeca-4,6,9,16-tetraen-3-ol
SMILES (Canonical) CCC(C=CC=CCC=CCCCCCC=C)O
SMILES (Isomeric) CC[C@H](/C=C/C=C\C/C=C\CCCCCC=C)O
InChI InChI=1S/C17H28O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17(18)4-2/h3,10-11,13-18H,1,4-9,12H2,2H3/b11-10-,14-13-,16-15+/t17-/m1/s1
InChI Key AQUQHVOAVQKVSI-XBCMHJSQSA-N
Popularity 1 reference 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 5.60
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 (3R,4E,6Z,9Z)-heptadeca-4,6,9,16-tetraen-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 + 0.8484 84.84%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Plasma membrane 0.4384 43.84%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.7126 71.26%
OATP1B3 inhibitior + 0.9315 93.15%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5650 56.50%
P-glycoprotein inhibitior - 0.8728 87.28%
P-glycoprotein substrate - 0.8740 87.40%
CYP3A4 substrate - 0.5495 54.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7357 73.57%
CYP3A4 inhibition - 0.9462 94.62%
CYP2C9 inhibition - 0.8940 89.40%
CYP2C19 inhibition - 0.8729 87.29%
CYP2D6 inhibition - 0.9557 95.57%
CYP1A2 inhibition - 0.5346 53.46%
CYP2C8 inhibition - 0.7786 77.86%
CYP inhibitory promiscuity - 0.8192 81.92%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.6971 69.71%
Eye corrosion + 0.8893 88.93%
Eye irritation + 0.6939 69.39%
Skin irritation + 0.6955 69.55%
Skin corrosion - 0.9213 92.13%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4086 40.86%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5749 57.49%
skin sensitisation + 0.8723 87.23%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.7360 73.60%
Acute Oral Toxicity (c) III 0.5908 59.08%
Estrogen receptor binding + 0.5752 57.52%
Androgen receptor binding - 0.6907 69.07%
Thyroid receptor binding + 0.6420 64.20%
Glucocorticoid receptor binding + 0.6337 63.37%
Aromatase binding + 0.5479 54.79%
PPAR gamma + 0.8205 82.05%
Honey bee toxicity - 0.9057 90.57%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity - 0.4262 42.62%

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 94.19% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.69% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.56% 99.17%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 88.12% 90.75%
CHEMBL242 Q92731 Estrogen receptor beta 85.60% 98.35%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.02% 97.29%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.63% 97.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.84% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 81.28% 90.17%

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 162915541
LOTUS LTS0226928
wikiData Q104917095