CID 20588088

Details

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Internal ID b31b3b95-6ba3-4ecd-be30-1842883f7df2
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 5-hydroxy-3-methyl-7-oxabicyclo[4.1.0]hept-3-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H8O3/c1-3-2-4(8)6-7(10-6)5(3)9/h2,4,6-8H,1H3
InChI Key WCZPXJJNPSYRIV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8O3
Molecular Weight 140.14 g/mol
Exact Mass 140.047344113 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP -0.40
Atomic LogP (AlogP) -0.36
H-Bond Acceptor 3
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 CID 20588088

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 - 0.6369 63.69%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6332 63.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9131 91.31%
OATP1B3 inhibitior + 0.9760 97.60%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9710 97.10%
P-glycoprotein inhibitior - 0.9623 96.23%
P-glycoprotein substrate - 0.9847 98.47%
CYP3A4 substrate - 0.6018 60.18%
CYP2C9 substrate - 0.7795 77.95%
CYP2D6 substrate - 0.8638 86.38%
CYP3A4 inhibition - 0.9526 95.26%
CYP2C9 inhibition - 0.9359 93.59%
CYP2C19 inhibition - 0.5347 53.47%
CYP2D6 inhibition - 0.9496 94.96%
CYP1A2 inhibition - 0.7944 79.44%
CYP2C8 inhibition - 0.9873 98.73%
CYP inhibitory promiscuity - 0.8103 81.03%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5365 53.65%
Eye corrosion - 0.8066 80.66%
Eye irritation + 0.7185 71.85%
Skin irritation + 0.6973 69.73%
Skin corrosion - 0.8392 83.92%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8231 82.31%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.6283 62.83%
skin sensitisation + 0.5216 52.16%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.7014 70.14%
Acute Oral Toxicity (c) III 0.3957 39.57%
Estrogen receptor binding - 0.9108 91.08%
Androgen receptor binding - 0.6981 69.81%
Thyroid receptor binding - 0.7963 79.63%
Glucocorticoid receptor binding - 0.9175 91.75%
Aromatase binding - 0.8941 89.41%
PPAR gamma - 0.7945 79.45%
Honey bee toxicity - 0.9516 95.16%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.6469 64.69%

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 91.69% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 91.64% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.35% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.18% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.90% 89.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.46% 93.65%
CHEMBL2581 P07339 Cathepsin D 80.38% 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 20588088
LOTUS LTS0029519
wikiData Q105302198