(4R)-8-hydroxy-4,5,6,7-tetramethyl-4H-isochromene-1,3-dione

Details

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Internal ID d0670803-3266-4ec7-9483-c201225f01cb
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (4R)-8-hydroxy-4,5,6,7-tetramethyl-4H-isochromene-1,3-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14O4/c1-5-6(2)9-8(4)12(15)17-13(16)10(9)11(14)7(5)3/h8,14H,1-4H3/t8-/m1/s1
InChI Key PXPDDNZJJKVTBG-MRVPVSSYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O4
Molecular Weight 234.25 g/mol
Exact Mass 234.08920892 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.12
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R)-8-hydroxy-4,5,6,7-tetramethyl-4H-isochromene-1,3-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9707 97.07%
Caco-2 - 0.6185 61.85%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6794 67.94%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.7963 79.63%
OATP1B3 inhibitior + 0.9681 96.81%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9258 92.58%
P-glycoprotein inhibitior - 0.9037 90.37%
P-glycoprotein substrate - 0.9392 93.92%
CYP3A4 substrate - 0.5689 56.89%
CYP2C9 substrate + 0.7917 79.17%
CYP2D6 substrate - 0.8704 87.04%
CYP3A4 inhibition - 0.9221 92.21%
CYP2C9 inhibition - 0.8724 87.24%
CYP2C19 inhibition - 0.9878 98.78%
CYP2D6 inhibition - 0.9763 97.63%
CYP1A2 inhibition + 0.6482 64.82%
CYP2C8 inhibition - 0.9178 91.78%
CYP inhibitory promiscuity - 0.9199 91.99%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.6305 63.05%
Eye corrosion - 0.9706 97.06%
Eye irritation + 0.7083 70.83%
Skin irritation - 0.5322 53.22%
Skin corrosion - 0.9600 96.00%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8080 80.80%
Micronuclear + 0.8259 82.59%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8982 89.82%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.5541 55.41%
Acute Oral Toxicity (c) II 0.6446 64.46%
Estrogen receptor binding + 0.5622 56.22%
Androgen receptor binding + 0.5412 54.12%
Thyroid receptor binding - 0.6993 69.93%
Glucocorticoid receptor binding - 0.7437 74.37%
Aromatase binding - 0.7032 70.32%
PPAR gamma - 0.8169 81.69%
Honey bee toxicity - 0.9552 95.52%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9480 94.80%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.81% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.40% 99.23%
CHEMBL2581 P07339 Cathepsin D 90.31% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.40% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.54% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.04% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 80.97% 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 97042235
LOTUS LTS0200349
wikiData Q105216310