(7E,9E,15E)-heptadeca-7,9,15-trien-11,13-diyn-1-ol

Details

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Internal ID 2c1c45b7-986f-44b4-9de0-ec1257db7aa3
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (7E,9E,15E)-heptadeca-7,9,15-trien-11,13-diyn-1-ol
SMILES (Canonical) CC=CC#CC#CC=CC=CCCCCCCO
SMILES (Isomeric) C/C=C/C#CC#C/C=C/C=C/CCCCCCO
InChI InChI=1S/C17H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h2-3,8-11,18H,12-17H2,1H3/b3-2+,9-8+,11-10+
InChI Key CGLLCCUJRHGHTR-MMOYHAHMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O
Molecular Weight 242.36 g/mol
Exact Mass 242.167065321 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.62
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (7E,9E,15E)-heptadeca-7,9,15-trien-11,13-diyn-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 + 0.9810 98.10%
Caco-2 + 0.6523 65.23%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Lysosomes 0.4640 46.40%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.8214 82.14%
OATP1B3 inhibitior + 0.9360 93.60%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7632 76.32%
P-glycoprotein inhibitior - 0.9135 91.35%
P-glycoprotein substrate - 0.8840 88.40%
CYP3A4 substrate - 0.5443 54.43%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7877 78.77%
CYP3A4 inhibition - 0.8773 87.73%
CYP2C9 inhibition - 0.7995 79.95%
CYP2C19 inhibition - 0.9042 90.42%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.5745 57.45%
CYP2C8 inhibition - 0.8490 84.90%
CYP inhibitory promiscuity - 0.8161 81.61%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6449 64.49%
Eye corrosion + 0.8009 80.09%
Eye irritation - 0.5927 59.27%
Skin irritation + 0.7242 72.42%
Skin corrosion - 0.8548 85.48%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6581 65.81%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5492 54.92%
skin sensitisation + 0.8058 80.58%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.6691 66.91%
Acute Oral Toxicity (c) III 0.6391 63.91%
Estrogen receptor binding + 0.5425 54.25%
Androgen receptor binding - 0.5526 55.26%
Thyroid receptor binding + 0.6658 66.58%
Glucocorticoid receptor binding - 0.5644 56.44%
Aromatase binding + 0.6843 68.43%
PPAR gamma + 0.5794 57.94%
Honey bee toxicity - 0.9340 93.40%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5987 59.87%
Fish aquatic toxicity - 0.5855 58.55%

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 90.49% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 90.22% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.50% 99.17%
CHEMBL2581 P07339 Cathepsin D 82.05% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.50% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 81.22% 92.86%

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.
Pleiotaxis rugosa

Cross-Links

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PubChem 15081405
LOTUS LTS0096738
wikiData Q104957830