1-Tridecene

Details

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Internal ID 38f1cdc4-4054-49c3-8bf3-dffc972c95ee
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Unsaturated aliphatic hydrocarbons
IUPAC Name tridec-1-ene
SMILES (Canonical) CCCCCCCCCCCC=C
SMILES (Isomeric) CCCCCCCCCCCC=C
InChI InChI=1S/C13H26/c1-3-5-7-9-11-13-12-10-8-6-4-2/h3H,1,4-13H2,2H3
InChI Key VQOXUMQBYILCKR-UHFFFAOYSA-N
Popularity 256 references in papers

Physical and Chemical Properties

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Molecular Formula C13H26
Molecular Weight 182.35 g/mol
Exact Mass 182.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 7.30
Atomic LogP (AlogP) 5.09
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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2437-56-1
tridec-1-ene
N-Tridec-1-ene
Tridecylene
Undecylethylene
alpha-Tridecene
1-Tridecene, 97%
Tridecene-1
.alpha.-Tridecene
CCRIS 5719
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Tridecene

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 + 0.9262 92.62%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.4578 45.78%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9249 92.49%
OATP1B3 inhibitior + 0.9239 92.39%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7182 71.82%
P-glycoprotein inhibitior - 0.9693 96.93%
P-glycoprotein substrate - 0.9510 95.10%
CYP3A4 substrate - 0.6997 69.97%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
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 - 0.8997 89.97%
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 + 0.9890 98.90%
Skin irritation + 0.8622 86.22%
Skin corrosion - 0.9742 97.42%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5149 51.49%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5475 54.75%
skin sensitisation + 0.9605 96.05%
Respiratory toxicity - 0.9889 98.89%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6384 63.84%
Acute Oral Toxicity (c) III 0.6572 65.72%
Estrogen receptor binding - 0.9224 92.24%
Androgen receptor binding - 0.8599 85.99%
Thyroid receptor binding - 0.6372 63.72%
Glucocorticoid receptor binding - 0.7296 72.96%
Aromatase binding - 0.8719 87.19%
PPAR gamma - 0.7702 77.02%
Honey bee toxicity - 0.9654 96.54%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.8700 87.00%
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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.47% 92.08%
CHEMBL240 Q12809 HERG 95.26% 89.76%
CHEMBL230 P35354 Cyclooxygenase-2 91.40% 89.63%
CHEMBL2581 P07339 Cathepsin D 90.78% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.99% 92.86%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.54% 85.94%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 89.21% 85.40%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.06% 97.29%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.64% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.37% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 87.83% 87.45%
CHEMBL221 P23219 Cyclooxygenase-1 86.18% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.65% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.98% 89.34%
CHEMBL2996 Q05655 Protein kinase C delta 80.95% 97.79%
CHEMBL1907 P15144 Aminopeptidase N 80.71% 93.31%

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.
Angelica sinensis
Asarum heterotropoides
Asarum sieboldii
Astilbe rubra
Camellia saluenensis
Elaeis guineensis
Hoehnephytum imbricatum
Inula helenium
Leuzea uniflora
Ophrys sphegodes
Panax notoginseng
Pectis elongata
Tussilago farfara

Cross-Links

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PubChem 17095
NPASS NPC287191
LOTUS LTS0122180
wikiData Q27162003