3-(1-Butenyl)-4-vinylcyclopentene

Details

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Internal ID d203d4e6-2fd3-4d1c-bf79-e160e4f14918
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Cyclic olefins > Cycloalkenes
IUPAC Name 3-but-1-enyl-4-ethenylcyclopentene
SMILES (Canonical) CCC=CC1C=CCC1C=C
SMILES (Isomeric) CCC=CC1C=CCC1C=C
InChI InChI=1S/C11H16/c1-3-5-7-11-9-6-8-10(11)4-2/h4-7,9-11H,2-3,8H2,1H3
InChI Key BEUUCPGMRTUNSM-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H16
Molecular Weight 148.24 g/mol
Exact Mass 148.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.33
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(1-Butenyl)-4-vinylcyclopentene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.8121 81.21%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.5318 53.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9011 90.11%
OATP1B3 inhibitior + 0.9532 95.32%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8317 83.17%
P-glycoprotein inhibitior - 0.9770 97.70%
P-glycoprotein substrate - 0.8890 88.90%
CYP3A4 substrate - 0.5843 58.43%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.7561 75.61%
CYP3A4 inhibition - 0.9403 94.03%
CYP2C9 inhibition - 0.8455 84.55%
CYP2C19 inhibition - 0.7723 77.23%
CYP2D6 inhibition - 0.9421 94.21%
CYP1A2 inhibition - 0.6786 67.86%
CYP2C8 inhibition - 0.9240 92.40%
CYP inhibitory promiscuity - 0.5546 55.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Warning 0.4820 48.20%
Eye corrosion + 0.9697 96.97%
Eye irritation + 0.9420 94.20%
Skin irritation + 0.8076 80.76%
Skin corrosion - 0.7501 75.01%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5263 52.63%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5051 50.51%
skin sensitisation + 0.9343 93.43%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.4770 47.70%
Acute Oral Toxicity (c) III 0.6600 66.00%
Estrogen receptor binding - 0.8802 88.02%
Androgen receptor binding - 0.9079 90.79%
Thyroid receptor binding - 0.8116 81.16%
Glucocorticoid receptor binding - 0.7384 73.84%
Aromatase binding - 0.7857 78.57%
PPAR gamma - 0.8166 81.66%
Honey bee toxicity - 0.7612 76.12%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9566 95.66%

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 92.52% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 82.55% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.21% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.68% 97.25%
CHEMBL2581 P07339 Cathepsin D 80.55% 98.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 556410
LOTUS LTS0060169
wikiData Q104933599