(3R)-5-hydroxy-4-(hydroxymethyl)-3,7-dimethoxy-6-methyl-3H-2-benzofuran-1-one

Details

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Internal ID 52469c39-0ea9-4615-beba-c4f5e3424bb8
Taxonomy Organoheterocyclic compounds > Benzofurans > Benzofuranones
IUPAC Name (3R)-5-hydroxy-4-(hydroxymethyl)-3,7-dimethoxy-6-methyl-3H-2-benzofuran-1-one
SMILES (Canonical) CC1=C(C(=C2C(OC(=O)C2=C1OC)OC)CO)O
SMILES (Isomeric) CC1=C(C(=C2[C@@H](OC(=O)C2=C1OC)OC)CO)O
InChI InChI=1S/C12H14O6/c1-5-9(14)6(4-13)7-8(10(5)16-2)11(15)18-12(7)17-3/h12-14H,4H2,1-3H3/t12-/m1/s1
InChI Key YKGOAMVCGTXYOR-GFCCVEGCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O6
Molecular Weight 254.24 g/mol
Exact Mass 254.07903816 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.02
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R)-5-hydroxy-4-(hydroxymethyl)-3,7-dimethoxy-6-methyl-3H-2-benzofuran-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 + 0.9584 95.84%
Caco-2 - 0.5957 59.57%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6778 67.78%
OATP2B1 inhibitior - 0.8526 85.26%
OATP1B1 inhibitior + 0.7849 78.49%
OATP1B3 inhibitior + 0.8995 89.95%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9398 93.98%
P-glycoprotein inhibitior - 0.8374 83.74%
P-glycoprotein substrate - 0.8926 89.26%
CYP3A4 substrate + 0.5408 54.08%
CYP2C9 substrate - 0.5966 59.66%
CYP2D6 substrate - 0.8443 84.43%
CYP3A4 inhibition - 0.7616 76.16%
CYP2C9 inhibition - 0.6467 64.67%
CYP2C19 inhibition - 0.6859 68.59%
CYP2D6 inhibition - 0.9483 94.83%
CYP1A2 inhibition + 0.6602 66.02%
CYP2C8 inhibition - 0.7828 78.28%
CYP inhibitory promiscuity + 0.5802 58.02%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6660 66.60%
Eye corrosion - 0.9777 97.77%
Eye irritation + 0.6874 68.74%
Skin irritation - 0.8037 80.37%
Skin corrosion - 0.9646 96.46%
Ames mutagenesis + 0.6446 64.46%
Human Ether-a-go-go-Related Gene inhibition - 0.5898 58.98%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.7711 77.11%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7657 76.57%
Acute Oral Toxicity (c) III 0.5674 56.74%
Estrogen receptor binding + 0.7533 75.33%
Androgen receptor binding - 0.5901 59.01%
Thyroid receptor binding + 0.5746 57.46%
Glucocorticoid receptor binding + 0.6961 69.61%
Aromatase binding - 0.6855 68.55%
PPAR gamma + 0.5247 52.47%
Honey bee toxicity - 0.9124 91.24%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8102 81.02%

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 93.01% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.54% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.85% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.51% 86.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.70% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 81.15% 94.73%

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 162952564
LOTUS LTS0088874
wikiData Q105349671