Cyclopentene, 1-ethyl-2-methyl-

Details

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Internal ID e4b84aae-43ef-4ba3-8c1e-46bb5893922d
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1-ethyl-2-methylcyclopentene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H14/c1-3-8-6-4-5-7(8)2/h3-6H2,1-2H3
InChI Key MMYZGQDXYZNAQW-UHFFFAOYSA-N
Popularity 6 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 2.20
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Methyl ethyl cyclopentene
Cyclopentene, 1-ethyl-2-methyl-
2-Methyl-1-ethylcyclopentene
EINECS 243-303-5
DTXSID6066529
RefChem:129880
DTXCID3036157
243-303-5
MMYZGQDXYZNAQW-UHFFFAOYSA-N
19780-56-4
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyclopentene, 1-ethyl-2-methyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.9609 96.09%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Lysosomes 0.5545 55.45%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.9278 92.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9308 93.08%
P-glycoprotein inhibitior - 0.9825 98.25%
P-glycoprotein substrate - 0.9570 95.70%
CYP3A4 substrate - 0.7133 71.33%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9604 96.04%
CYP2C9 inhibition - 0.9010 90.10%
CYP2C19 inhibition - 0.8749 87.49%
CYP2D6 inhibition - 0.9171 91.71%
CYP1A2 inhibition - 0.5855 58.55%
CYP2C8 inhibition - 0.9541 95.41%
CYP inhibitory promiscuity + 0.5739 57.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.4669 46.69%
Eye corrosion + 0.5460 54.60%
Eye irritation + 0.9911 99.11%
Skin irritation + 0.6663 66.63%
Skin corrosion - 0.9792 97.92%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6937 69.37%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.9375 93.75%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.6859 68.59%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.6434 64.34%
Acute Oral Toxicity (c) III 0.8109 81.09%
Estrogen receptor binding - 0.9696 96.96%
Androgen receptor binding - 0.7122 71.22%
Thyroid receptor binding - 0.9031 90.31%
Glucocorticoid receptor binding - 0.9369 93.69%
Aromatase binding - 0.8927 89.27%
PPAR gamma - 0.9148 91.48%
Honey bee toxicity - 0.9830 98.30%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL230 P35354 Cyclooxygenase-2 91.61% 89.63%
CHEMBL2581 P07339 Cathepsin D 89.03% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.89% 96.09%

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.
Ficus carica

Cross-Links

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PubChem 88243
NPASS NPC97735