Cyclotene

Details

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Internal ID 50b7ade8-28d9-47ee-9648-f7b2aa78b321
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 2-hydroxy-3-methylcyclopent-2-en-1-one
SMILES (Canonical) CC1=C(C(=O)CC1)O
SMILES (Isomeric) CC1=C(C(=O)CC1)O
InChI InChI=1S/C6H8O2/c1-4-2-3-5(7)6(4)8/h8H,2-3H2,1H3
InChI Key CFAKWWQIUFSQFU-UHFFFAOYSA-N
Popularity 257 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8O2
Molecular Weight 112.13 g/mol
Exact Mass 112.052429494 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 0.30
Atomic LogP (AlogP) 1.18
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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Cyclotene
2-Hydroxy-3-methylcyclopent-2-enone
Methyl cyclopentenolone
Corylone
Corylon
Maple lactone
2-HYDROXY-3-METHYL-2-CYCLOPENTEN-1-ONE
Cycloten
2-hydroxy-3-methylcyclopent-2-en-1-one
2-Hydroxy-3-methyl-2-cyclopentenone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyclotene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 + 0.6627 66.27%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6993 69.93%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9501 95.01%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9289 92.89%
P-glycoprotein inhibitior - 0.9826 98.26%
P-glycoprotein substrate - 0.9879 98.79%
CYP3A4 substrate - 0.6957 69.57%
CYP2C9 substrate - 0.8076 80.76%
CYP2D6 substrate - 0.8529 85.29%
CYP3A4 inhibition - 0.9633 96.33%
CYP2C9 inhibition - 0.9276 92.76%
CYP2C19 inhibition - 0.8772 87.72%
CYP2D6 inhibition - 0.8973 89.73%
CYP1A2 inhibition - 0.6661 66.61%
CYP2C8 inhibition - 0.9954 99.54%
CYP inhibitory promiscuity - 0.8783 87.83%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8728 87.28%
Carcinogenicity (trinary) Non-required 0.5268 52.68%
Eye corrosion - 0.8193 81.93%
Eye irritation + 0.9862 98.62%
Skin irritation + 0.7612 76.12%
Skin corrosion - 0.7171 71.71%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8084 80.84%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.7283 72.83%
skin sensitisation + 0.6364 63.64%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.6405 64.05%
Acute Oral Toxicity (c) III 0.6549 65.49%
Estrogen receptor binding - 0.9516 95.16%
Androgen receptor binding - 0.8251 82.51%
Thyroid receptor binding - 0.8574 85.74%
Glucocorticoid receptor binding - 0.8433 84.33%
Aromatase binding - 0.9096 90.96%
PPAR gamma - 0.8019 80.19%
Honey bee toxicity - 0.9682 96.82%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.7148 71.48%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.32% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.87% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.01% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.34% 93.40%
CHEMBL4040 P28482 MAP kinase ERK2 83.89% 83.82%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.44% 99.23%

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.
Capsicum annuum
Foeniculum vulgare
Panax ginseng

Cross-Links

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PubChem 6660
NPASS NPC247093
LOTUS LTS0237850
wikiData Q25101336