3,5,7-trimethyl-3,4-dihydro-1H-isochromene-6,8-diol

Details

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Internal ID 28c4516c-319e-4eda-bfc4-02602312d20d
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3S)-3,5,7-trimethyl-3,4-dihydro-1H-isochromene-6,8-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O3/c1-6-4-9-7(2)11(13)8(3)12(14)10(9)5-15-6/h6,13-14H,4-5H2,1-3H3/t6-/m0/s1
InChI Key ZXRZTYYXLVSFMP-LURJTMIESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O3
Molecular Weight 208.25 g/mol
Exact Mass 208.109944368 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,5,7-trimethyl-3,4-dihydro-1H-isochromene-6,8-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9704 97.04%
Caco-2 + 0.6847 68.47%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6745 67.45%
OATP2B1 inhibitior - 0.8508 85.08%
OATP1B1 inhibitior + 0.8950 89.50%
OATP1B3 inhibitior + 0.9320 93.20%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9140 91.40%
P-glycoprotein inhibitior - 0.9376 93.76%
P-glycoprotein substrate - 0.8987 89.87%
CYP3A4 substrate - 0.5808 58.08%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate + 0.4113 41.13%
CYP3A4 inhibition - 0.7068 70.68%
CYP2C9 inhibition - 0.7494 74.94%
CYP2C19 inhibition - 0.5737 57.37%
CYP2D6 inhibition - 0.8727 87.27%
CYP1A2 inhibition + 0.8436 84.36%
CYP2C8 inhibition - 0.8471 84.71%
CYP inhibitory promiscuity - 0.6675 66.75%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6389 63.89%
Eye corrosion - 0.9841 98.41%
Eye irritation + 0.9007 90.07%
Skin irritation - 0.7517 75.17%
Skin corrosion - 0.9249 92.49%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.7441 74.41%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.7986 79.86%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7578 75.78%
Acute Oral Toxicity (c) III 0.6570 65.70%
Estrogen receptor binding - 0.4758 47.58%
Androgen receptor binding - 0.5262 52.62%
Thyroid receptor binding - 0.4903 49.03%
Glucocorticoid receptor binding - 0.6459 64.59%
Aromatase binding - 0.8607 86.07%
PPAR gamma - 0.5758 57.58%
Honey bee toxicity - 0.9516 95.16%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9470 94.70%

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 91.98% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.23% 97.25%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 81.99% 85.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.34% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 80.40% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.11% 95.56%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 80.10% 91.79%

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 162944707
LOTUS LTS0103521
wikiData Q105385746