2,3,8-Trimethyl-4H-1-benzopyran-4,7(8H)-dione

Details

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Internal ID ea7bc26b-9d2e-4bfb-b7fc-f8600b2f9dc3
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 8-ethyl-2,3,8-trimethylchromene-4,7-dione
SMILES (Canonical) CCC1(C(=O)C=CC2=C1OC(=C(C2=O)C)C)C
SMILES (Isomeric) CCC1(C(=O)C=CC2=C1OC(=C(C2=O)C)C)C
InChI InChI=1S/C14H16O3/c1-5-14(4)11(15)7-6-10-12(16)8(2)9(3)17-13(10)14/h6-7H,5H2,1-4H3
InChI Key QMMMQWRPZIJGPT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O3
Molecular Weight 232.27 g/mol
Exact Mass 232.109944368 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.52
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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2,3,8-Trimethyl-4H-1-benzopyran-4,7(8H)-dione
8-ethyl-2,3,8-trimethylchromene-4,7-dione

2D Structure

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2D Structure of 2,3,8-Trimethyl-4H-1-benzopyran-4,7(8H)-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.8906 89.06%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.6519 65.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8698 86.98%
OATP1B3 inhibitior + 0.9833 98.33%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6123 61.23%
P-glycoprotein inhibitior - 0.9318 93.18%
P-glycoprotein substrate - 0.8666 86.66%
CYP3A4 substrate - 0.5484 54.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8670 86.70%
CYP3A4 inhibition - 0.6688 66.88%
CYP2C9 inhibition - 0.5151 51.51%
CYP2C19 inhibition - 0.5402 54.02%
CYP2D6 inhibition - 0.9203 92.03%
CYP1A2 inhibition + 0.8304 83.04%
CYP2C8 inhibition - 0.9011 90.11%
CYP inhibitory promiscuity + 0.7000 70.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.5534 55.34%
Eye corrosion - 0.9681 96.81%
Eye irritation + 0.6776 67.76%
Skin irritation - 0.6865 68.65%
Skin corrosion - 0.9055 90.55%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6426 64.26%
Micronuclear - 0.5441 54.41%
Hepatotoxicity + 0.6710 67.10%
skin sensitisation - 0.5479 54.79%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.6698 66.98%
Acute Oral Toxicity (c) II 0.4288 42.88%
Estrogen receptor binding - 0.5745 57.45%
Androgen receptor binding + 0.5634 56.34%
Thyroid receptor binding - 0.6399 63.99%
Glucocorticoid receptor binding - 0.6827 68.27%
Aromatase binding + 0.5707 57.07%
PPAR gamma - 0.5698 56.98%
Honey bee toxicity - 0.9453 94.53%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9807 98.07%

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 93.48% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 91.49% 89.63%
CHEMBL3401 O75469 Pregnane X receptor 88.52% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.12% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.06% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.74% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.05% 94.00%

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 14443155
LOTUS LTS0039812
wikiData Q77502994