Heptadeca-8,10-dien-4,6-diyne-1,14-diol

Details

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Internal ID b1e45881-9fc4-4e56-91f4-8bde817da144
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name heptadeca-8,10-dien-4,6-diyne-1,14-diol
SMILES (Canonical) CCCC(CCC=CC=CC#CC#CCCCO)O
SMILES (Isomeric) CCCC(CCC=CC=CC#CC#CCCCO)O
InChI InChI=1S/C17H24O2/c1-2-14-17(19)15-12-10-8-6-4-3-5-7-9-11-13-16-18/h4,6,8,10,17-19H,2,11-16H2,1H3
InChI Key SZYKBBPFQKNSPD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H24O2
Molecular Weight 260.40 g/mol
Exact Mass 260.177630004 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.82
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Heptadeca-8,10-dien-4,6-diyne-1,14-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.6961 69.61%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4801 48.01%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.8415 84.15%
OATP1B3 inhibitior + 0.9152 91.52%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8417 84.17%
P-glycoprotein inhibitior - 0.8968 89.68%
P-glycoprotein substrate - 0.6662 66.62%
CYP3A4 substrate + 0.5223 52.23%
CYP2C9 substrate - 0.8056 80.56%
CYP2D6 substrate - 0.7828 78.28%
CYP3A4 inhibition - 0.6996 69.96%
CYP2C9 inhibition - 0.8740 87.40%
CYP2C19 inhibition - 0.8589 85.89%
CYP2D6 inhibition - 0.8982 89.82%
CYP1A2 inhibition + 0.5757 57.57%
CYP2C8 inhibition - 0.7935 79.35%
CYP inhibitory promiscuity - 0.6868 68.68%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6776 67.76%
Eye corrosion - 0.6844 68.44%
Eye irritation - 0.8060 80.60%
Skin irritation - 0.7308 73.08%
Skin corrosion - 0.9616 96.16%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7516 75.16%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5631 56.31%
skin sensitisation + 0.6653 66.53%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.7478 74.78%
Acute Oral Toxicity (c) III 0.6070 60.70%
Estrogen receptor binding - 0.4850 48.50%
Androgen receptor binding - 0.5345 53.45%
Thyroid receptor binding + 0.6321 63.21%
Glucocorticoid receptor binding + 0.6553 65.53%
Aromatase binding - 0.5474 54.74%
PPAR gamma + 0.6406 64.06%
Honey bee toxicity - 0.8939 89.39%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7655 76.55%
Fish aquatic toxicity - 0.4542 45.42%

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 94.92% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 94.17% 92.86%
CHEMBL2581 P07339 Cathepsin D 92.74% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.27% 97.29%
CHEMBL2885 P07451 Carbonic anhydrase III 89.66% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.18% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.07% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.06% 96.00%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 82.39% 95.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.80% 93.56%
CHEMBL242 Q92731 Estrogen receptor beta 81.46% 98.35%

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.
Oenanthe crocata
Oenanthe fistulosa

Cross-Links

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PubChem 74932187
LOTUS LTS0262858
wikiData Q105264485