2,12-Tridecadiene-4,6,8,10-tetrayne-1-ol

Details

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Internal ID 9d98c9e7-0c80-436c-9f75-800c74c05947
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (2E)-trideca-2,12-dien-4,6,8,10-tetrayn-1-ol
SMILES (Canonical) C=CC#CC#CC#CC#CC=CCO
SMILES (Isomeric) C=CC#CC#CC#CC#C/C=C/CO
InChI InChI=1S/C13H8O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h2,11-12,14H,1,13H2/b12-11+
InChI Key VWCBEKGFBBBSSO-VAWYXSNFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8O
Molecular Weight 180.20 g/mol
Exact Mass 180.057514874 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 0.73
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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trideca-2,12-dien-4,6,8,10-tetrayn-1-ol
(E)-2,12-Tridecadiene-4,6,8,10-tetryn-1-ol

2D Structure

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2D Structure of 2,12-Tridecadiene-4,6,8,10-tetrayne-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9798 97.98%
Caco-2 - 0.5964 59.64%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4844 48.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8725 87.25%
OATP1B3 inhibitior + 0.9541 95.41%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9245 92.45%
P-glycoprotein inhibitior - 0.9527 95.27%
P-glycoprotein substrate - 0.9710 97.10%
CYP3A4 substrate - 0.6487 64.87%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7902 79.02%
CYP3A4 inhibition - 0.9029 90.29%
CYP2C9 inhibition - 0.8832 88.32%
CYP2C19 inhibition - 0.8248 82.48%
CYP2D6 inhibition - 0.9648 96.48%
CYP1A2 inhibition - 0.6075 60.75%
CYP2C8 inhibition - 0.9382 93.82%
CYP inhibitory promiscuity - 0.8210 82.10%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.6083 60.83%
Carcinogenicity (trinary) Non-required 0.6345 63.45%
Eye corrosion + 0.9752 97.52%
Eye irritation - 0.6676 66.76%
Skin irritation + 0.8484 84.84%
Skin corrosion + 0.9581 95.81%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7870 78.70%
Micronuclear - 0.8341 83.41%
Hepatotoxicity + 0.5482 54.82%
skin sensitisation + 0.5562 55.62%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5736 57.36%
Acute Oral Toxicity (c) II 0.5191 51.91%
Estrogen receptor binding - 0.8882 88.82%
Androgen receptor binding - 0.7127 71.27%
Thyroid receptor binding - 0.5701 57.01%
Glucocorticoid receptor binding - 0.6247 62.47%
Aromatase binding + 0.5550 55.50%
PPAR gamma - 0.5467 54.67%
Honey bee toxicity - 0.8113 81.13%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.5000 50.00%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.84% 89.34%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.52% 86.92%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.35% 96.09%

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.
Allium ampeloprasum
Bidens andicola
Coreopsis nuecensis
Coreopsis verticillata
Dahlia coccinea
Dahlia merckii
Dahlia tubulata

Cross-Links

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PubChem 14729085
NPASS NPC181945
LOTUS LTS0063108
wikiData Q105297993