1-Ethyl-1-cyclopentene

Details

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Internal ID 01d264ed-7ef2-4fb4-91f2-eb5a199f42a4
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1-ethylcyclopentene
SMILES (Canonical) CCC1=CCCC1
SMILES (Isomeric) CCC1=CCCC1
InChI InChI=1S/C7H12/c1-2-7-5-3-4-6-7/h5H,2-4,6H2,1H3
InChI Key QYYQTLLGVAPKPN-UHFFFAOYSA-N
Popularity 30 references in papers

Physical and Chemical Properties

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Molecular Formula C7H12
Molecular Weight 96.17 g/mol
Exact Mass 96.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.51
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1-Ethylcyclopentene
2146-38-5
Cyclopentene, 1-ethyl-
1-ethylcyclopent-1-ene
Ethylcyclopentene
N5HEF75LON
NSC-73920
NSC73920
1-Ethyl1-cyclopentene
1-Ethylcyclopentene-1
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-Ethyl-1-cyclopentene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.9623 96.23%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.5986 59.86%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.9568 95.68%
OATP1B3 inhibitior + 0.9482 94.82%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9262 92.62%
P-glycoprotein inhibitior - 0.9875 98.75%
P-glycoprotein substrate - 0.9765 97.65%
CYP3A4 substrate - 0.7733 77.33%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9721 97.21%
CYP2C9 inhibition - 0.8924 89.24%
CYP2C19 inhibition - 0.8608 86.08%
CYP2D6 inhibition - 0.9201 92.01%
CYP1A2 inhibition - 0.5875 58.75%
CYP2C8 inhibition - 0.9635 96.35%
CYP inhibitory promiscuity + 0.5923 59.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.4414 44.14%
Eye corrosion + 0.8671 86.71%
Eye irritation + 0.9878 98.78%
Skin irritation + 0.7775 77.75%
Skin corrosion - 0.9728 97.28%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6294 62.94%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6678 66.78%
skin sensitisation + 0.9381 93.81%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7192 71.92%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.6986 69.86%
Acute Oral Toxicity (c) III 0.8350 83.50%
Estrogen receptor binding - 0.9677 96.77%
Androgen receptor binding - 0.9161 91.61%
Thyroid receptor binding - 0.9382 93.82%
Glucocorticoid receptor binding - 0.9148 91.48%
Aromatase binding - 0.8739 87.39%
PPAR gamma - 0.9056 90.56%
Honey bee toxicity - 0.9804 98.04%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9884 98.84%

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 90.67% 96.09%
CHEMBL4208 P20618 Proteasome component C5 87.50% 90.00%
CHEMBL2581 P07339 Cathepsin D 86.64% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 86.26% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.55% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 81.74% 90.17%

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 137448
LOTUS LTS0255891
wikiData Q83046056