7,7-Dibenzyl-3,4,5-trimethyl-3,4-dihydroisochromene-6,8-dione

Details

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Internal ID d9d66181-ea75-4d5c-bbff-5402bcaf9433
Taxonomy Organoheterocyclic compounds > Benzopyrans
IUPAC Name 7,7-dibenzyl-3,4,5-trimethyl-3,4-dihydroisochromene-6,8-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H26O3/c1-17-19(3)29-16-22-23(17)18(2)24(27)26(25(22)28,14-20-10-6-4-7-11-20)15-21-12-8-5-9-13-21/h4-13,16-17,19H,14-15H2,1-3H3
InChI Key SURSMSCPWPKKAE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H26O3
Molecular Weight 386.50 g/mol
Exact Mass 386.18819469 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.87
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7,7-Dibenzyl-3,4,5-trimethyl-3,4-dihydroisochromene-6,8-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.7688 76.88%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6773 67.73%
OATP2B1 inhibitior - 0.7179 71.79%
OATP1B1 inhibitior + 0.7501 75.01%
OATP1B3 inhibitior + 0.9715 97.15%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9684 96.84%
P-glycoprotein inhibitior + 0.8152 81.52%
P-glycoprotein substrate - 0.7822 78.22%
CYP3A4 substrate + 0.5402 54.02%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.8385 83.85%
CYP3A4 inhibition - 0.5594 55.94%
CYP2C9 inhibition - 0.5371 53.71%
CYP2C19 inhibition - 0.5504 55.04%
CYP2D6 inhibition - 0.9224 92.24%
CYP1A2 inhibition + 0.7092 70.92%
CYP2C8 inhibition - 0.6548 65.48%
CYP inhibitory promiscuity + 0.7709 77.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9013 90.13%
Carcinogenicity (trinary) Non-required 0.4597 45.97%
Eye corrosion - 0.9828 98.28%
Eye irritation - 0.9535 95.35%
Skin irritation - 0.6412 64.12%
Skin corrosion - 0.9518 95.18%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6585 65.85%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.6357 63.57%
skin sensitisation - 0.5845 58.45%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.5941 59.41%
Acute Oral Toxicity (c) III 0.5665 56.65%
Estrogen receptor binding + 0.6616 66.16%
Androgen receptor binding + 0.7208 72.08%
Thyroid receptor binding + 0.5499 54.99%
Glucocorticoid receptor binding - 0.4660 46.60%
Aromatase binding - 0.4931 49.31%
PPAR gamma + 0.6282 62.82%
Honey bee toxicity - 0.9043 90.43%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9795 97.95%

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
CHEMBL2581 P07339 Cathepsin D 94.33% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 94.08% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.40% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.92% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.73% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 82.31% 91.49%

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 75602306
LOTUS LTS0190626
wikiData Q104197676