cis-Tetradec-11-enoic acid

Details

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Internal ID dc5bcbed-49da-42f6-8b2f-e4e291cfb704
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (Z)-tetradec-11-enoic acid
SMILES (Canonical) CCC=CCCCCCCCCCC(=O)O
SMILES (Isomeric) CC/C=C\CCCCCCCCCC(=O)O
InChI InChI=1S/C14H26O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14(15)16/h3-4H,2,5-13H2,1H3,(H,15,16)/b4-3-
InChI Key FWWOMPFHMRPXIH-ARJAWSKDSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C14H26O2
Molecular Weight 226.35 g/mol
Exact Mass 226.193280068 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.55
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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(Z)-11-tetradecenoic acid
(Z)-tetradec-11-enoic acid
11Z-tetradecenoic acid
cis-11-tetradecenoic acid
C14:1n-3
79039-46-6
CHEBI:37273
Z-11-Tetradecenoic acid
C18:1 n-3 cis
acide cis-11-tetradecenoique
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of cis-Tetradec-11-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.8393 83.93%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Plasma membrane 0.5044 50.44%
OATP2B1 inhibitior - 0.8503 85.03%
OATP1B1 inhibitior + 0.7531 75.31%
OATP1B3 inhibitior - 0.3406 34.06%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.4776 47.76%
P-glycoprotein inhibitior - 0.9663 96.63%
P-glycoprotein substrate - 0.9680 96.80%
CYP3A4 substrate - 0.6851 68.51%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.9465 94.65%
CYP2C9 inhibition - 0.8798 87.98%
CYP2C19 inhibition - 0.9638 96.38%
CYP2D6 inhibition - 0.9631 96.31%
CYP1A2 inhibition + 0.6915 69.15%
CYP2C8 inhibition - 0.9557 95.57%
CYP inhibitory promiscuity - 0.9426 94.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6935 69.35%
Carcinogenicity (trinary) Non-required 0.6373 63.73%
Eye corrosion + 0.9371 93.71%
Eye irritation + 0.9549 95.49%
Skin irritation + 0.7676 76.76%
Skin corrosion - 0.6260 62.60%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3693 36.93%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation + 0.8470 84.70%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity - 0.6531 65.31%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.8415 84.15%
Acute Oral Toxicity (c) IV 0.6387 63.87%
Estrogen receptor binding - 0.5397 53.97%
Androgen receptor binding - 0.9134 91.34%
Thyroid receptor binding - 0.4947 49.47%
Glucocorticoid receptor binding + 0.6032 60.32%
Aromatase binding - 0.6917 69.17%
PPAR gamma + 0.8634 86.34%
Honey bee toxicity - 0.9905 99.05%
Biodegradation + 0.9500 95.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.8175 81.75%

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 96.90% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.43% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.50% 98.95%
CHEMBL1781 P11387 DNA topoisomerase I 91.24% 97.00%
CHEMBL221 P23219 Cyclooxygenase-1 85.94% 90.17%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 82.05% 92.26%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.25% 96.95%

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.
Cnidium monnieri

Cross-Links

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PubChem 5362743
NPASS NPC20120