(8R,9E)-heptadeca-1,9-dien-11,13,15-triyn-8-ol

Details

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Internal ID 48cc9dfb-2915-45d8-9bc3-a1dbd176a17a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (8R,9E)-heptadeca-1,9-dien-11,13,15-triyn-8-ol
SMILES (Canonical) CC#CC#CC#CC=CC(CCCCCC=C)O
SMILES (Isomeric) CC#CC#CC#C/C=C/[C@@H](CCCCCC=C)O
InChI InChI=1S/C17H20O/c1-3-5-7-9-10-12-14-16-17(18)15-13-11-8-6-4-2/h4,14,16-18H,2,6,8,11,13,15H2,1H3/b16-14+/t17-/m1/s1
InChI Key HNLFNCBZIGWOKP-FYPAKXHLSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H20O
Molecular Weight 240.34 g/mol
Exact Mass 240.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.07
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 (8R,9E)-heptadeca-1,9-dien-11,13,15-triyn-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 + 0.9792 97.92%
Caco-2 - 0.5680 56.80%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.5052 50.52%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.9096 90.96%
OATP1B3 inhibitior + 0.9336 93.36%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8840 88.40%
P-glycoprotein inhibitior - 0.9323 93.23%
P-glycoprotein substrate - 0.8419 84.19%
CYP3A4 substrate + 0.5131 51.31%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.7649 76.49%
CYP3A4 inhibition - 0.9014 90.14%
CYP2C9 inhibition - 0.7859 78.59%
CYP2C19 inhibition - 0.8340 83.40%
CYP2D6 inhibition - 0.9447 94.47%
CYP1A2 inhibition + 0.5564 55.64%
CYP2C8 inhibition - 0.8776 87.76%
CYP inhibitory promiscuity - 0.7780 77.80%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.6419 64.19%
Eye corrosion + 0.7583 75.83%
Eye irritation - 0.9022 90.22%
Skin irritation + 0.6997 69.97%
Skin corrosion - 0.6876 68.76%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4820 48.20%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5517 55.17%
skin sensitisation + 0.8609 86.09%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.9411 94.11%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.4659 46.59%
Acute Oral Toxicity (c) II 0.4997 49.97%
Estrogen receptor binding - 0.5824 58.24%
Androgen receptor binding - 0.8270 82.70%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.5337 53.37%
PPAR gamma - 0.5564 55.64%
Honey bee toxicity - 0.8283 82.83%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5024 50.24%
Fish aquatic toxicity + 0.6592 65.92%

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 93.72% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.39% 99.17%
CHEMBL2581 P07339 Cathepsin D 92.11% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 89.52% 90.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.58% 97.29%
CHEMBL1829 O15379 Histone deacetylase 3 85.67% 95.00%
CHEMBL206 P03372 Estrogen receptor alpha 84.39% 97.64%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.34% 92.86%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.23% 91.11%
CHEMBL2885 P07451 Carbonic anhydrase III 80.79% 87.45%

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 162964830
LOTUS LTS0210717
wikiData Q105030930