2-Cyclopenten-1-one, 2-methyl-5-methylene-3-(1-methylethyl)-

Details

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Internal ID 9b08b11d-2fbd-439c-bae5-74fadcf61ca9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 2-methyl-5-methylidene-3-propan-2-ylcyclopent-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O/c1-6(2)9-5-7(3)10(11)8(9)4/h6H,3,5H2,1-2,4H3
InChI Key HPFXJIUHJKTTLB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.49
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Cyclopenten-1-one, 2-methyl-5-methylene-3-(1-methylethyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.7320 73.20%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.4044 40.44%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9468 94.68%
OATP1B3 inhibitior + 0.9016 90.16%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9306 93.06%
P-glycoprotein inhibitior - 0.9509 95.09%
P-glycoprotein substrate - 0.9778 97.78%
CYP3A4 substrate - 0.6622 66.22%
CYP2C9 substrate - 0.7707 77.07%
CYP2D6 substrate - 0.8414 84.14%
CYP3A4 inhibition - 0.9447 94.47%
CYP2C9 inhibition - 0.8807 88.07%
CYP2C19 inhibition - 0.7309 73.09%
CYP2D6 inhibition - 0.9236 92.36%
CYP1A2 inhibition - 0.6952 69.52%
CYP2C8 inhibition - 0.9939 99.39%
CYP inhibitory promiscuity - 0.7105 71.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7517 75.17%
Carcinogenicity (trinary) Non-required 0.5488 54.88%
Eye corrosion - 0.5991 59.91%
Eye irritation + 0.9308 93.08%
Skin irritation + 0.7486 74.86%
Skin corrosion - 0.8281 82.81%
Ames mutagenesis - 0.8664 86.64%
Human Ether-a-go-go-Related Gene inhibition - 0.7271 72.71%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.8399 83.99%
skin sensitisation + 0.8982 89.82%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.7922 79.22%
Acute Oral Toxicity (c) III 0.5337 53.37%
Estrogen receptor binding - 0.9054 90.54%
Androgen receptor binding - 0.7464 74.64%
Thyroid receptor binding - 0.7754 77.54%
Glucocorticoid receptor binding - 0.9054 90.54%
Aromatase binding - 0.8413 84.13%
PPAR gamma - 0.8401 84.01%
Honey bee toxicity - 0.8005 80.05%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9573 95.73%

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
CHEMBL2581 P07339 Cathepsin D 93.35% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.96% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.66% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.28% 93.56%
CHEMBL4040 P28482 MAP kinase ERK2 83.31% 83.82%
CHEMBL3401 O75469 Pregnane X receptor 80.36% 94.73%

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 45095801
LOTUS LTS0083662
wikiData Q105031690