2-Hydroxy-5-methylcyclopent-2-en-1-one

Details

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Internal ID 4487eddf-fed7-4fd5-9c05-57171e338feb
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 2-hydroxy-5-methylcyclopent-2-en-1-one
SMILES (Canonical) CC1CC=C(C1=O)O
SMILES (Isomeric) CC1CC=C(C1=O)O
InChI InChI=1S/C6H8O2/c1-4-2-3-5(7)6(4)8/h3-4,7H,2H2,1H3
InChI Key LTMNDGSOQVSRMK-UHFFFAOYSA-N
Popularity 1 reference 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 1.00
Atomic LogP (AlogP) 1.04
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Hydroxy-5-methylcyclopent-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.4911 49.11%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7390 73.90%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.9677 96.77%
OATP1B3 inhibitior + 0.9635 96.35%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9378 93.78%
P-glycoprotein inhibitior - 0.9870 98.70%
P-glycoprotein substrate - 0.9461 94.61%
CYP3A4 substrate - 0.6396 63.96%
CYP2C9 substrate - 0.8030 80.30%
CYP2D6 substrate - 0.8573 85.73%
CYP3A4 inhibition - 0.9583 95.83%
CYP2C9 inhibition - 0.9086 90.86%
CYP2C19 inhibition - 0.8792 87.92%
CYP2D6 inhibition - 0.9170 91.70%
CYP1A2 inhibition - 0.7711 77.11%
CYP2C8 inhibition - 0.9938 99.38%
CYP inhibitory promiscuity - 0.8570 85.70%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.5081 50.81%
Eye corrosion + 0.6545 65.45%
Eye irritation + 0.9843 98.43%
Skin irritation + 0.7181 71.81%
Skin corrosion + 0.6481 64.81%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8143 81.43%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.6533 65.33%
skin sensitisation + 0.7519 75.19%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.4587 45.87%
Acute Oral Toxicity (c) III 0.5962 59.62%
Estrogen receptor binding - 0.9532 95.32%
Androgen receptor binding - 0.8918 89.18%
Thyroid receptor binding - 0.9048 90.48%
Glucocorticoid receptor binding - 0.9191 91.91%
Aromatase binding - 0.9018 90.18%
PPAR gamma - 0.9308 93.08%
Honey bee toxicity - 0.9714 97.14%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.7717 77.17%

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 91.48% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.99% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.49% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.61% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.62% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.44% 90.71%

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.
Glycyrrhiza glabra

Cross-Links

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PubChem 14886368
LOTUS LTS0226274
wikiData Q105157030