6-hydroxy-3a,6,7,7a-tetrahydro-3H-1-benzofuran-2-one

Details

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Internal ID ef2b2c14-d4e6-4f31-b7cc-a14332fbd038
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 6-hydroxy-3a,6,7,7a-tetrahydro-3H-1-benzofuran-2-one
SMILES (Canonical) C1C(C=CC2C1OC(=O)C2)O
SMILES (Isomeric) C1C(C=CC2C1OC(=O)C2)O
InChI InChI=1S/C8H10O3/c9-6-2-1-5-3-8(10)11-7(5)4-6/h1-2,5-7,9H,3-4H2
InChI Key MIHZOYYSSYKXBP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O3
Molecular Weight 154.16 g/mol
Exact Mass 154.062994177 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.24
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 6-hydroxy-3a,6,7,7a-tetrahydro-3H-1-benzofuran-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.4905 49.05%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Plasma membrane 0.4845 48.45%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9201 92.01%
OATP1B3 inhibitior + 0.9641 96.41%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9702 97.02%
P-glycoprotein inhibitior - 0.9854 98.54%
P-glycoprotein substrate - 0.9691 96.91%
CYP3A4 substrate - 0.6087 60.87%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8147 81.47%
CYP3A4 inhibition - 0.9315 93.15%
CYP2C9 inhibition - 0.9771 97.71%
CYP2C19 inhibition - 0.8754 87.54%
CYP2D6 inhibition - 0.9652 96.52%
CYP1A2 inhibition - 0.8762 87.62%
CYP2C8 inhibition - 0.9669 96.69%
CYP inhibitory promiscuity - 0.9662 96.62%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9519 95.19%
Carcinogenicity (trinary) Non-required 0.5725 57.25%
Eye corrosion + 0.5466 54.66%
Eye irritation + 0.7775 77.75%
Skin irritation + 0.5784 57.84%
Skin corrosion - 0.9335 93.35%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7748 77.48%
Micronuclear - 0.6500 65.00%
Hepatotoxicity + 0.6666 66.66%
skin sensitisation - 0.6989 69.89%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.6910 69.10%
Acute Oral Toxicity (c) III 0.7010 70.10%
Estrogen receptor binding - 0.8755 87.55%
Androgen receptor binding - 0.8411 84.11%
Thyroid receptor binding - 0.8697 86.97%
Glucocorticoid receptor binding - 0.5978 59.78%
Aromatase binding - 0.9007 90.07%
PPAR gamma - 0.8906 89.06%
Honey bee toxicity - 0.8505 85.05%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.7342 73.42%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.97% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.04% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.70% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.88% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.19% 89.00%

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 130146751
LOTUS LTS0008771
wikiData Q105164797