2-Ethyl-1-decene

Details

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Internal ID 688d4ee8-a3ce-466b-bb2e-6794c5c35664
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 3-methylideneundecane
SMILES (Canonical) CCCCCCCCC(=C)CC
SMILES (Isomeric) CCCCCCCCC(=C)CC
InChI InChI=1S/C12H24/c1-4-6-7-8-9-10-11-12(3)5-2/h3-11H2,1-2H3
InChI Key KOGYHNNTUZDGRV-UHFFFAOYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C12H24
Molecular Weight 168.32 g/mol
Exact Mass 168.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.20
Atomic LogP (AlogP) 4.70
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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RefChem:901039
615-254-3
2-Ethyl-1-decene
71138-64-2
2-Ethyl-1-decene #
SCHEMBL718036
SCHEMBL1173858
SCHEMBL3284709
SCHEMBL8220265
DTXSID20338716
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Ethyl-1-decene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9892 98.92%
Caco-2 + 0.9632 96.32%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.4502 45.02%
OATP2B1 inhibitior - 0.8466 84.66%
OATP1B1 inhibitior + 0.9294 92.94%
OATP1B3 inhibitior + 0.9377 93.77%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8244 82.44%
P-glycoprotein inhibitior - 0.9550 95.50%
P-glycoprotein substrate - 0.9015 90.15%
CYP3A4 substrate - 0.6857 68.57%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9595 95.95%
CYP2C9 inhibition - 0.9179 91.79%
CYP2C19 inhibition - 0.9117 91.17%
CYP2D6 inhibition - 0.9301 93.01%
CYP1A2 inhibition - 0.5761 57.61%
CYP2C8 inhibition - 0.9111 91.11%
CYP inhibitory promiscuity - 0.5959 59.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.4727 47.27%
Eye corrosion + 0.8457 84.57%
Eye irritation + 0.9931 99.31%
Skin irritation + 0.7420 74.20%
Skin corrosion - 0.9875 98.75%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6257 62.57%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6268 62.68%
skin sensitisation + 0.9460 94.60%
Respiratory toxicity - 1.0000 100.00%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity - 0.5674 56.74%
Acute Oral Toxicity (c) III 0.8543 85.43%
Estrogen receptor binding - 0.9268 92.68%
Androgen receptor binding - 0.8042 80.42%
Thyroid receptor binding - 0.7877 78.77%
Glucocorticoid receptor binding - 0.8140 81.40%
Aromatase binding - 0.8656 86.56%
PPAR gamma - 0.7920 79.20%
Honey bee toxicity - 0.9878 98.78%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity + 0.7980 79.80%
Fish aquatic toxicity + 0.9971 99.71%

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 94.17% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.11% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 91.84% 85.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.20% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.01% 97.29%
CHEMBL2581 P07339 Cathepsin D 89.96% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 88.13% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 87.57% 92.86%
CHEMBL2885 P07451 Carbonic anhydrase III 86.45% 87.45%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.26% 91.81%
CHEMBL4040 P28482 MAP kinase ERK2 84.66% 83.82%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 84.14% 85.40%
CHEMBL2996 Q05655 Protein kinase C delta 83.73% 97.79%

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.
Houttuynia cordata
Lycium barbarum
Lycium chinense

Cross-Links

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PubChem 550798
NPASS NPC273390
LOTUS LTS0085393
wikiData Q82107303