(6R,7E,9E)-heptadeca-1,7,9-trien-11,13,15-triyn-6-ol

Details

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Internal ID 3503eab9-a3ba-4449-b293-1778609ea8b2
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (6R,7E,9E)-heptadeca-1,7,9-trien-11,13,15-triyn-6-ol
SMILES (Canonical) CC#CC#CC#CC=CC=CC(CCCC=C)O
SMILES (Isomeric) CC#CC#CC#C/C=C/C=C/[C@@H](CCCC=C)O
InChI InChI=1S/C17H18O/c1-3-5-7-8-9-10-11-12-14-16-17(18)15-13-6-4-2/h4,11-12,14,16-18H,2,6,13,15H2,1H3/b12-11+,16-14+/t17-/m1/s1
InChI Key BOTZHDRJVZFZFH-CAUYNSQMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O
Molecular Weight 238.32 g/mol
Exact Mass 238.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.10
Atomic LogP (AlogP) 2.85
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6R,7E,9E)-heptadeca-1,7,9-trien-11,13,15-triyn-6-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9732 97.32%
Caco-2 + 0.5563 55.63%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.4767 47.67%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.8923 89.23%
OATP1B3 inhibitior + 0.9450 94.50%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9045 90.45%
P-glycoprotein inhibitior - 0.9175 91.75%
P-glycoprotein substrate - 0.8166 81.66%
CYP3A4 substrate + 0.5263 52.63%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.7649 76.49%
CYP3A4 inhibition - 0.8538 85.38%
CYP2C9 inhibition - 0.8401 84.01%
CYP2C19 inhibition - 0.8076 80.76%
CYP2D6 inhibition - 0.9392 93.92%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.8778 87.78%
CYP inhibitory promiscuity - 0.7613 76.13%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6155 61.55%
Eye corrosion + 0.7679 76.79%
Eye irritation - 0.8862 88.62%
Skin irritation + 0.7879 78.79%
Skin corrosion + 0.8391 83.91%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4018 40.18%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5199 51.99%
skin sensitisation + 0.7857 78.57%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.5747 57.47%
Acute Oral Toxicity (c) II 0.7231 72.31%
Estrogen receptor binding - 0.5139 51.39%
Androgen receptor binding - 0.7682 76.82%
Thyroid receptor binding + 0.5152 51.52%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.5488 54.88%
PPAR gamma + 0.6712 67.12%
Honey bee toxicity - 0.7971 79.71%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.7514 75.14%

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 91.96% 96.09%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 91.17% 97.34%
CHEMBL2581 P07339 Cathepsin D 89.98% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.87% 99.17%
CHEMBL206 P03372 Estrogen receptor alpha 84.71% 97.64%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.46% 97.29%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.39% 91.11%

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.
Artemisia vulgaris subsp. vulgaris

Cross-Links

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PubChem 162949359
LOTUS LTS0098850
wikiData Q104940586