1-Ethylcyclohexene

Details

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Internal ID c788cd8f-3664-4b10-8645-fca78b4fe52a
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1-ethylcyclohexene
SMILES (Canonical) CCC1=CCCCC1
SMILES (Isomeric) CCC1=CCCCC1
InChI InChI=1S/C8H14/c1-2-8-6-4-3-5-7-8/h6H,2-5,7H2,1H3
InChI Key IFVMAGPISVKRAR-UHFFFAOYSA-N
Popularity 67 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14
Molecular Weight 110.20 g/mol
Exact Mass 110.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1453-24-3
Cyclohexene, 1-ethyl-
ethylcyclohexene
NSC74155
1-ethyl-cyclohexene
EINECS 215-922-0
1-Ethylcyclohexene-1
1-ethylcyclohex-1-ene
1-Ethyl-1-cyclohexene #
DTXSID60162971
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-Ethylcyclohexene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.9613 96.13%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.5363 53.63%
OATP2B1 inhibitior - 0.8446 84.46%
OATP1B1 inhibitior + 0.9410 94.10%
OATP1B3 inhibitior + 0.9357 93.57%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9229 92.29%
P-glycoprotein inhibitior - 0.9883 98.83%
P-glycoprotein substrate - 0.9718 97.18%
CYP3A4 substrate - 0.7705 77.05%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9542 95.42%
CYP2C9 inhibition - 0.9172 91.72%
CYP2C19 inhibition - 0.8943 89.43%
CYP2D6 inhibition - 0.9178 91.78%
CYP1A2 inhibition - 0.5991 59.91%
CYP2C8 inhibition - 0.9341 93.41%
CYP inhibitory promiscuity + 0.6402 64.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.4621 46.21%
Eye corrosion + 0.9108 91.08%
Eye irritation + 0.9825 98.25%
Skin irritation + 0.7472 74.72%
Skin corrosion - 0.9722 97.22%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6072 60.72%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6428 64.28%
skin sensitisation + 0.9619 96.19%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.6970 69.70%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.8043 80.43%
Acute Oral Toxicity (c) III 0.8171 81.71%
Estrogen receptor binding - 0.9691 96.91%
Androgen receptor binding - 0.8980 89.80%
Thyroid receptor binding - 0.9259 92.59%
Glucocorticoid receptor binding - 0.9041 90.41%
Aromatase binding - 0.8611 86.11%
PPAR gamma - 0.8840 88.40%
Honey bee toxicity - 0.9671 96.71%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9931 99.31%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.51% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.33% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.86% 97.25%
CHEMBL4208 P20618 Proteasome component C5 86.64% 90.00%
CHEMBL230 P35354 Cyclooxygenase-2 84.49% 89.63%
CHEMBL221 P23219 Cyclooxygenase-1 82.28% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.56% 95.56%

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.
Caryocar coriaceum

Cross-Links

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PubChem 73937
LOTUS LTS0256171
wikiData Q83031794