(4R,5E,11E)-trideca-5,11-dien-7,9-diyn-4-ol

Details

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Internal ID 80631dbf-f79b-4bd8-bff5-6101d9561fda
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (4R,5E,11E)-trideca-5,11-dien-7,9-diyn-4-ol
SMILES (Canonical) CCCC(C=CC#CC#CC=CC)O
SMILES (Isomeric) CCC[C@H](/C=C/C#CC#C/C=C/C)O
InChI InChI=1S/C13H16O/c1-3-5-6-7-8-9-10-12-13(14)11-4-2/h3,5,10,12-14H,4,11H2,1-2H3/b5-3+,12-10+/t13-/m1/s1
InChI Key GEENZQOWBUUIOA-DJCVSYIJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O
Molecular Weight 188.26 g/mol
Exact Mass 188.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.29
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R,5E,11E)-trideca-5,11-dien-7,9-diyn-4-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 - 0.7439 74.39%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.3687 36.87%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.8581 85.81%
OATP1B3 inhibitior + 0.9359 93.59%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8808 88.08%
P-glycoprotein inhibitior - 0.9623 96.23%
P-glycoprotein substrate - 0.8805 88.05%
CYP3A4 substrate - 0.6330 63.30%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.7649 76.49%
CYP3A4 inhibition - 0.8806 88.06%
CYP2C9 inhibition - 0.8736 87.36%
CYP2C19 inhibition - 0.8153 81.53%
CYP2D6 inhibition - 0.9175 91.75%
CYP1A2 inhibition + 0.5792 57.92%
CYP2C8 inhibition - 0.9465 94.65%
CYP inhibitory promiscuity - 0.7541 75.41%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.6379 63.79%
Eye corrosion - 0.6387 63.87%
Eye irritation - 0.7755 77.55%
Skin irritation + 0.6201 62.01%
Skin corrosion - 0.7829 78.29%
Ames mutagenesis - 0.7737 77.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5453 54.53%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5572 55.72%
skin sensitisation + 0.8931 89.31%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.4878 48.78%
Acute Oral Toxicity (c) II 0.5436 54.36%
Estrogen receptor binding - 0.6384 63.84%
Androgen receptor binding - 0.9011 90.11%
Thyroid receptor binding + 0.5416 54.16%
Glucocorticoid receptor binding + 0.5446 54.46%
Aromatase binding - 0.6122 61.22%
PPAR gamma - 0.7482 74.82%
Honey bee toxicity - 0.9067 90.67%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.6595 65.95%

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
CHEMBL4040 P28482 MAP kinase ERK2 94.15% 83.82%
CHEMBL2581 P07339 Cathepsin D 91.68% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.24% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 88.33% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.26% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.20% 92.86%

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.
Aethusa cynapium

Cross-Links

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PubChem 101424593
LOTUS LTS0140115
wikiData Q105007113