(8R,9Z,15Z)-heptadeca-1,9,15-trien-11,13-diyn-8-ol

Details

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Internal ID eec6d880-1456-44d6-8e0a-06ac02cc2e28
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (8R,9Z,15Z)-heptadeca-1,9,15-trien-11,13-diyn-8-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O/c1-3-5-7-9-10-12-14-16-17(18)15-13-11-8-6-4-2/h3-5,14,16-18H,2,6,8,11,13,15H2,1H3/b5-3-,16-14-/t17-/m1/s1
InChI Key DDWUABWPXPSLAB-JPZFZPFNSA-N
Popularity 2 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 (8R,9Z,15Z)-heptadeca-1,9,15-trien-11,13-diyn-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 - 0.5630 56.30%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.5052 50.52%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.8905 89.05%
OATP1B3 inhibitior + 0.9336 93.36%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7778 77.78%
P-glycoprotein inhibitior - 0.9161 91.61%
P-glycoprotein substrate - 0.8304 83.04%
CYP3A4 substrate - 0.5052 50.52%
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 - 0.8544 85.44%
CYP inhibitory promiscuity - 0.7780 77.80%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.6419 64.19%
Eye corrosion + 0.7583 75.83%
Eye irritation - 0.8466 84.66%
Skin irritation + 0.6997 69.97%
Skin corrosion - 0.6876 68.76%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3944 39.44%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6216 62.16%
skin sensitisation + 0.8609 86.09%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.9411 94.11%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.5593 55.93%
Acute Oral Toxicity (c) II 0.4997 49.97%
Estrogen receptor binding + 0.5847 58.47%
Androgen receptor binding - 0.8496 84.96%
Thyroid receptor binding + 0.5134 51.34%
Glucocorticoid receptor binding + 0.6407 64.07%
Aromatase binding + 0.5207 52.07%
PPAR gamma + 0.5905 59.05%
Honey bee toxicity - 0.8191 81.91%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5124 51.24%
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 93.10% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.96% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.17% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 87.19% 90.17%
CHEMBL4040 P28482 MAP kinase ERK2 85.75% 83.82%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.20% 97.29%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.15% 91.11%
CHEMBL1829 O15379 Histone deacetylase 3 84.61% 95.00%
CHEMBL2885 P07451 Carbonic anhydrase III 82.02% 87.45%
CHEMBL206 P03372 Estrogen receptor alpha 81.93% 97.64%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.36% 96.00%

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.
Cousinia pterocaulos

Cross-Links

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PubChem 162969188
LOTUS LTS0177524
wikiData Q104976989