Trideca-1,3-diene

Details

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Internal ID c1c419e9-e777-4195-b6dc-c1baa52d418d
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkadienes
IUPAC Name trideca-1,3-diene
SMILES (Canonical) CCCCCCCCCC=CC=C
SMILES (Isomeric) CCCCCCCCCC=CC=C
InChI InChI=1S/C13H24/c1-3-5-7-9-11-13-12-10-8-6-4-2/h3,5,7H,1,4,6,8-13H2,2H3
InChI Key IRVGWDJFZXOKDK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H24
Molecular Weight 180.33 g/mol
Exact Mass 180.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 4.87
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Trideca-1,3-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.9709 97.09%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.4578 45.78%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.8674 86.74%
OATP1B3 inhibitior + 0.9239 92.39%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8161 81.61%
P-glycoprotein inhibitior - 0.9764 97.64%
P-glycoprotein substrate - 0.9353 93.53%
CYP3A4 substrate - 0.6427 64.27%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7603 76.03%
CYP3A4 inhibition - 0.9832 98.32%
CYP2C9 inhibition - 0.9157 91.57%
CYP2C19 inhibition - 0.9190 91.90%
CYP2D6 inhibition - 0.9426 94.26%
CYP1A2 inhibition + 0.5418 54.18%
CYP2C8 inhibition - 0.8966 89.66%
CYP inhibitory promiscuity - 0.6838 68.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.5494 54.94%
Eye corrosion + 0.9841 98.41%
Eye irritation + 0.9916 99.16%
Skin irritation + 0.8622 86.22%
Skin corrosion - 0.9742 97.42%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4577 45.77%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.9605 96.05%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6142 61.42%
Acute Oral Toxicity (c) III 0.6572 65.72%
Estrogen receptor binding - 0.8880 88.80%
Androgen receptor binding - 0.6986 69.86%
Thyroid receptor binding - 0.4887 48.87%
Glucocorticoid receptor binding - 0.5838 58.38%
Aromatase binding - 0.8179 81.79%
PPAR gamma + 0.5956 59.56%
Honey bee toxicity - 0.9015 90.15%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.9253 92.53%
Fish aquatic toxicity + 0.9955 99.55%

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
CHEMBL230 P35354 Cyclooxygenase-2 96.39% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.93% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.39% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.48% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.34% 99.17%
CHEMBL2581 P07339 Cathepsin D 89.79% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.41% 91.81%
CHEMBL2885 P07451 Carbonic anhydrase III 89.03% 87.45%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.75% 85.94%
CHEMBL1907 P15144 Aminopeptidase N 84.50% 93.31%
CHEMBL221 P23219 Cyclooxygenase-1 82.88% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.23% 96.95%
CHEMBL1781 P11387 DNA topoisomerase I 81.28% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.14% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 81.04% 97.79%
CHEMBL240 Q12809 HERG 80.98% 89.76%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.87% 100.00%

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.
Ophrys sphegodes

Cross-Links

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PubChem 181592
LOTUS LTS0060850
wikiData Q105119234