(2E,8E,10E)-heptadeca-2,8,10,16-tetraen-4,6-diyn-1-ol

Details

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Internal ID 9a279b2f-d42e-4dc1-8ed1-a7bc128a0f1d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (2E,8E,10E)-heptadeca-2,8,10,16-tetraen-4,6-diyn-1-ol
SMILES (Canonical) C=CCCCCC=CC=CC#CC#CC=CCO
SMILES (Isomeric) C=CCCCC/C=C/C=C/C#CC#C/C=C/CO
InChI InChI=1S/C17H20O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h2,7-10,15-16,18H,1,3-6,17H2/b8-7+,10-9+,16-15+
InChI Key VNZGFKQARLEAQK-YJWTVKCOSA-N
Popularity 0 references 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 4.60
Atomic LogP (AlogP) 3.40
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 (2E,8E,10E)-heptadeca-2,8,10,16-tetraen-4,6-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 + 0.9729 97.29%
Caco-2 + 0.5543 55.43%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4024 40.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8786 87.86%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7766 77.66%
P-glycoprotein inhibitior - 0.9115 91.15%
P-glycoprotein substrate - 0.8951 89.51%
CYP3A4 substrate - 0.5327 53.27%
CYP2C9 substrate - 0.8075 80.75%
CYP2D6 substrate - 0.7593 75.93%
CYP3A4 inhibition - 0.8828 88.28%
CYP2C9 inhibition - 0.8312 83.12%
CYP2C19 inhibition - 0.8411 84.11%
CYP2D6 inhibition - 0.9539 95.39%
CYP1A2 inhibition - 0.6468 64.68%
CYP2C8 inhibition - 0.8023 80.23%
CYP inhibitory promiscuity - 0.7382 73.82%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5000 50.00%
Carcinogenicity (trinary) Non-required 0.5565 55.65%
Eye corrosion + 0.9747 97.47%
Eye irritation - 0.5961 59.61%
Skin irritation + 0.7886 78.86%
Skin corrosion + 0.6432 64.32%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4711 47.11%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.6932 69.32%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6642 66.42%
Acute Oral Toxicity (c) II 0.4798 47.98%
Estrogen receptor binding + 0.6677 66.77%
Androgen receptor binding - 0.5356 53.56%
Thyroid receptor binding + 0.5580 55.80%
Glucocorticoid receptor binding + 0.5804 58.04%
Aromatase binding + 0.7160 71.60%
PPAR gamma + 0.7621 76.21%
Honey bee toxicity - 0.7783 77.83%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6855 68.55%
Fish aquatic toxicity - 0.4049 40.49%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 87.48% 99.17%
CHEMBL242 Q92731 Estrogen receptor beta 86.15% 98.35%
CHEMBL1977 P11473 Vitamin D receptor 83.14% 99.43%
CHEMBL279 P35968 Vascular endothelial growth factor receptor 2 82.74% 95.52%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.91% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.06% 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.
Cirsium chinense
Coreopsis gigantea
Coreopsis longula
Jacobaea erucifolia
Jacobaea vulgaris
Tetragonotheca repanda

Cross-Links

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PubChem 14191354
NPASS NPC199745
LOTUS LTS0243109
wikiData Q105290037