10E-Pentadecen-6,8-diynoic acid

Details

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Internal ID 707a7d5a-ce64-4462-89b8-b214fbf0bd72
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (E)-pentadec-10-en-6,8-diynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(16)17/h5-6H,2-4,11-14H2,1H3,(H,16,17)/b6-5+
InChI Key VLPCQMHZJMTSIW-AATRIKPKSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O2
Molecular Weight 232.32 g/mol
Exact Mass 232.146329876 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.38
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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10-Pentadecen-6,8-diynoic acid, (E)-
(E)-pentadec-10-en-6,8-diynoic Acid
CHEMBL448670
CHEBI:186712
LMFA01031097
trans-pentadec-10-en-6,8-diynoic acid

2D Structure

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2D Structure of 10E-Pentadecen-6,8-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 + 0.9918 99.18%
Caco-2 + 0.5090 50.90%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Plasma membrane 0.5344 53.44%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.6861 68.61%
OATP1B3 inhibitior - 0.2917 29.17%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8742 87.42%
P-glycoprotein inhibitior - 0.9482 94.82%
P-glycoprotein substrate - 0.8633 86.33%
CYP3A4 substrate - 0.5436 54.36%
CYP2C9 substrate + 0.6009 60.09%
CYP2D6 substrate - 0.8767 87.67%
CYP3A4 inhibition - 0.8709 87.09%
CYP2C9 inhibition - 0.7999 79.99%
CYP2C19 inhibition - 0.8839 88.39%
CYP2D6 inhibition - 0.9364 93.64%
CYP1A2 inhibition + 0.8890 88.90%
CYP2C8 inhibition - 0.7910 79.10%
CYP inhibitory promiscuity - 0.8732 87.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6135 61.35%
Carcinogenicity (trinary) Non-required 0.6619 66.19%
Eye corrosion + 0.9335 93.35%
Eye irritation - 0.7344 73.44%
Skin irritation + 0.8726 87.26%
Skin corrosion + 0.9488 94.88%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5178 51.78%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation + 0.8537 85.37%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.9170 91.70%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.4910 49.10%
Acute Oral Toxicity (c) III 0.4627 46.27%
Estrogen receptor binding - 0.5080 50.80%
Androgen receptor binding - 0.7351 73.51%
Thyroid receptor binding - 0.5198 51.98%
Glucocorticoid receptor binding - 0.5830 58.30%
Aromatase binding - 0.5662 56.62%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9668 96.68%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9342 93.42%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 96.56% 99.17%
CHEMBL2581 P07339 Cathepsin D 94.52% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.37% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.96% 92.08%
CHEMBL1781 P11387 DNA topoisomerase I 89.68% 97.00%
CHEMBL221 P23219 Cyclooxygenase-1 85.68% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.73% 96.00%
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!
To see more specific details click the taxa you are interested in.
Heisteria acuminata

Cross-Links

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PubChem 10443953
LOTUS LTS0158313
wikiData Q76415676