6-Hydroxy-9-methoxy-4,4,8-trimethyl-benzo[h]isochromene-1,3-dione

Details

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Internal ID d1017c22-cd75-43d1-a97b-977661e6fc77
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name 6-hydroxy-9-methoxy-4,4,8-trimethylbenzo[h]isochromene-1,3-dione
SMILES (Canonical) CC1=CC2=C(C=C3C(=C2C=C1OC)C(=O)OC(=O)C3(C)C)O
SMILES (Isomeric) CC1=CC2=C(C=C3C(=C2C=C1OC)C(=O)OC(=O)C3(C)C)O
InChI InChI=1S/C17H16O5/c1-8-5-9-10(6-13(8)21-4)14-11(7-12(9)18)17(2,3)16(20)22-15(14)19/h5-7,18H,1-4H3
InChI Key HTIPWCMGJSDMSU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H16O5
Molecular Weight 300.30 g/mol
Exact Mass 300.09977361 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.84
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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6-hydroxy-9-methoxy-4,4,8-trimethyl-benzo[h]isochromene-1,3-dione

2D Structure

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2D Structure of 6-Hydroxy-9-methoxy-4,4,8-trimethyl-benzo[h]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 + 0.9674 96.74%
Caco-2 + 0.6521 65.21%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7228 72.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8566 85.66%
OATP1B3 inhibitior + 0.9732 97.32%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7937 79.37%
P-glycoprotein inhibitior - 0.7241 72.41%
P-glycoprotein substrate - 0.9112 91.12%
CYP3A4 substrate + 0.6099 60.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7951 79.51%
CYP3A4 inhibition - 0.7908 79.08%
CYP2C9 inhibition - 0.7988 79.88%
CYP2C19 inhibition - 0.9249 92.49%
CYP2D6 inhibition - 0.9343 93.43%
CYP1A2 inhibition + 0.5132 51.32%
CYP2C8 inhibition - 0.6169 61.69%
CYP inhibitory promiscuity - 0.8671 86.71%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.5650 56.50%
Eye corrosion - 0.9830 98.30%
Eye irritation + 0.6153 61.53%
Skin irritation - 0.8022 80.22%
Skin corrosion - 0.9728 97.28%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6401 64.01%
Micronuclear + 0.6500 65.00%
Hepatotoxicity - 0.5198 51.98%
skin sensitisation - 0.9452 94.52%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.5704 57.04%
Acute Oral Toxicity (c) III 0.4585 45.85%
Estrogen receptor binding + 0.8742 87.42%
Androgen receptor binding + 0.5401 54.01%
Thyroid receptor binding - 0.6177 61.77%
Glucocorticoid receptor binding - 0.5855 58.55%
Aromatase binding + 0.7575 75.75%
PPAR gamma + 0.6310 63.10%
Honey bee toxicity - 0.9281 92.81%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9719 97.19%

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 99.14% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.22% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.72% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.43% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.04% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.84% 99.23%
CHEMBL2535 P11166 Glucose transporter 87.52% 98.75%
CHEMBL1937 Q92769 Histone deacetylase 2 87.27% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.05% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.79% 93.99%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 84.41% 95.70%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.02% 85.14%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.98% 82.38%
CHEMBL2581 P07339 Cathepsin D 83.67% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.64% 92.94%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.57% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 80.69% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Strophioblachia fimbricalyx

Cross-Links

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PubChem 71746809
LOTUS LTS0241042
wikiData Q105033451