(6R,7aR)-6-hydroxy-5,6,7,7a-tetrahydro-4H-1-benzofuran-2-one

Details

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Internal ID c3ffc3dc-8d2e-4bba-a9a6-2bef304232f4
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name (6R,7aR)-6-hydroxy-5,6,7,7a-tetrahydro-4H-1-benzofuran-2-one
SMILES (Canonical) C1CC2=CC(=O)OC2CC1O
SMILES (Isomeric) C1CC2=CC(=O)O[C@@H]2C[C@@H]1O
InChI InChI=1S/C8H10O3/c9-6-2-1-5-3-8(10)11-7(5)4-6/h3,6-7,9H,1-2,4H2/t6-,7-/m1/s1
InChI Key HVKUASSSTFDQDK-RNFRBKRXSA-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) 0.38
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 (6R,7aR)-6-hydroxy-5,6,7,7a-tetrahydro-4H-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 + 0.5000 50.00%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.5855 58.55%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.9374 93.74%
OATP1B3 inhibitior + 0.9646 96.46%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9658 96.58%
P-glycoprotein inhibitior - 0.9854 98.54%
P-glycoprotein substrate - 0.9244 92.44%
CYP3A4 substrate - 0.5950 59.50%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.8613 86.13%
CYP3A4 inhibition - 0.8888 88.88%
CYP2C9 inhibition - 0.9470 94.70%
CYP2C19 inhibition - 0.8450 84.50%
CYP2D6 inhibition - 0.9362 93.62%
CYP1A2 inhibition - 0.7613 76.13%
CYP2C8 inhibition - 0.9693 96.93%
CYP inhibitory promiscuity - 0.9424 94.24%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5665 56.65%
Eye corrosion + 0.4636 46.36%
Eye irritation + 0.9095 90.95%
Skin irritation - 0.6220 62.20%
Skin corrosion - 0.9586 95.86%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7023 70.23%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.7959 79.59%
skin sensitisation - 0.6889 68.89%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.4524 45.24%
Acute Oral Toxicity (c) III 0.5365 53.65%
Estrogen receptor binding - 0.8411 84.11%
Androgen receptor binding - 0.7103 71.03%
Thyroid receptor binding - 0.8167 81.67%
Glucocorticoid receptor binding - 0.5197 51.97%
Aromatase binding - 0.9177 91.77%
PPAR gamma - 0.7826 78.26%
Honey bee toxicity - 0.9181 91.81%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.7662 76.62%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 89.15% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.79% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.11% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.24% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.27% 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.
Sinomenium acutum

Cross-Links

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PubChem 102386464
LOTUS LTS0167556
wikiData Q105034314