4,6-Dihydroxy-5-methoxy-7-methyl-1,3-dihydroisobenzofuran

Details

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Internal ID 06bac031-dbf5-4bb1-bb74-3664557f6a88
Taxonomy Organoheterocyclic compounds > Isocoumarans
IUPAC Name 5-methoxy-7-methyl-1,3-dihydro-2-benzofuran-4,6-diol
SMILES (Canonical) CC1=C2COCC2=C(C(=C1O)OC)O
SMILES (Isomeric) CC1=C2COCC2=C(C(=C1O)OC)O
InChI InChI=1S/C10H12O4/c1-5-6-3-14-4-7(6)9(12)10(13-2)8(5)11/h11-12H,3-4H2,1-2H3
InChI Key CCIMZPYSIJENDN-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O4
Molecular Weight 196.20 g/mol
Exact Mass 196.07355886 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.45
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,6-Dihydroxy-5-methoxy-7-methyl-1,3-dihydroisobenzofuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9508 95.08%
Caco-2 + 0.5825 58.25%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5405 54.05%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.9377 93.77%
OATP1B3 inhibitior + 0.9627 96.27%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8510 85.10%
P-glycoprotein inhibitior - 0.9422 94.22%
P-glycoprotein substrate - 0.9542 95.42%
CYP3A4 substrate - 0.5688 56.88%
CYP2C9 substrate - 0.7850 78.50%
CYP2D6 substrate + 0.4213 42.13%
CYP3A4 inhibition - 0.5286 52.86%
CYP2C9 inhibition - 0.6353 63.53%
CYP2C19 inhibition - 0.5629 56.29%
CYP2D6 inhibition - 0.8340 83.40%
CYP1A2 inhibition + 0.5834 58.34%
CYP2C8 inhibition - 0.8550 85.50%
CYP inhibitory promiscuity + 0.5162 51.62%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5642 56.42%
Eye corrosion - 0.9814 98.14%
Eye irritation + 0.9536 95.36%
Skin irritation - 0.7571 75.71%
Skin corrosion - 0.9331 93.31%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6504 65.04%
Micronuclear - 0.6419 64.19%
Hepatotoxicity + 0.5034 50.34%
skin sensitisation - 0.7437 74.37%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.6836 68.36%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7725 77.25%
Acute Oral Toxicity (c) III 0.6004 60.04%
Estrogen receptor binding - 0.7301 73.01%
Androgen receptor binding - 0.5667 56.67%
Thyroid receptor binding - 0.6684 66.84%
Glucocorticoid receptor binding - 0.6393 63.93%
Aromatase binding - 0.8777 87.77%
PPAR gamma - 0.6503 65.03%
Honey bee toxicity - 0.9500 95.00%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.8577 85.77%

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 94.20% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.47% 96.09%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 83.91% 92.68%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.38% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.10% 95.56%
CHEMBL5905 Q04828 Aldo-keto reductase family 1 member C1 81.24% 91.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.04% 97.09%

Cross-Links

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PubChem 123784052
NPASS NPC38343
LOTUS LTS0146333
wikiData Q104953361