Hexadec-11-en-7,9-diynoic acid

Details

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Internal ID 3b9abe2f-e691-463a-bc60-e96e00730e76
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name hexadec-11-en-7,9-diynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H22O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h5-6H,2-4,11-15H2,1H3,(H,17,18)
InChI Key ZYKRBUYXWXJLBD-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H22O2
Molecular Weight 246.34 g/mol
Exact Mass 246.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.77
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hexadec-11-en-7,9-diynoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.6048 60.48%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Plasma membrane 0.5985 59.85%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.7222 72.22%
OATP1B3 inhibitior - 0.3673 36.73%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7093 70.93%
P-glycoprotein inhibitior - 0.9387 93.87%
P-glycoprotein substrate - 0.8525 85.25%
CYP3A4 substrate - 0.5288 52.88%
CYP2C9 substrate + 0.6009 60.09%
CYP2D6 substrate - 0.8767 87.67%
CYP3A4 inhibition - 0.8712 87.12%
CYP2C9 inhibition - 0.7677 76.77%
CYP2C19 inhibition - 0.8960 89.60%
CYP2D6 inhibition - 0.9443 94.43%
CYP1A2 inhibition + 0.9102 91.02%
CYP2C8 inhibition - 0.7668 76.68%
CYP inhibitory promiscuity - 0.8882 88.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6335 63.35%
Carcinogenicity (trinary) Non-required 0.6967 69.67%
Eye corrosion + 0.9302 93.02%
Eye irritation - 0.6386 63.86%
Skin irritation + 0.7953 79.53%
Skin corrosion + 0.7203 72.03%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4212 42.12%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation + 0.8570 85.70%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.8026 80.26%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.4921 49.21%
Acute Oral Toxicity (c) IV 0.5117 51.17%
Estrogen receptor binding - 0.6178 61.78%
Androgen receptor binding - 0.7117 71.17%
Thyroid receptor binding + 0.5857 58.57%
Glucocorticoid receptor binding - 0.5400 54.00%
Aromatase binding - 0.5722 57.22%
PPAR gamma + 0.7530 75.30%
Honey bee toxicity - 0.9667 96.67%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.9701 97.01%

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 97.10% 99.17%
CHEMBL2581 P07339 Cathepsin D 94.56% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.29% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.10% 92.08%
CHEMBL1781 P11387 DNA topoisomerase I 90.54% 97.00%
CHEMBL221 P23219 Cyclooxygenase-1 87.91% 90.17%
CHEMBL4040 P28482 MAP kinase ERK2 87.08% 83.82%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.73% 96.00%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 81.93% 92.26%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.80% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 85138962
LOTUS LTS0108280
wikiData Q105386228