4,4a,8-trihydroxy-2,9-bis(1-hydroxyhexa-2,4-dienylidene)-4,5a,7,9b-tetramethyl-9aH-dibenzofuran-1,3,6-trione

Details

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Internal ID 75fff6f1-13ef-4f60-9624-3e864b29b3c2
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 4,4a,8-trihydroxy-2,9-bis(1-hydroxyhexa-2,4-dienylidene)-4,5a,7,9b-tetramethyl-9aH-dibenzofuran-1,3,6-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H32O9/c1-7-9-11-13-16(29)18-20(31)15(3)22(32)26(5)21(18)25(4)23(33)19(17(30)14-12-10-8-2)24(34)27(6,35)28(25,36)37-26/h7-14,21,29-31,35-36H,1-6H3
InChI Key NWYGQCMFWAOARK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H32O9
Molecular Weight 512.50 g/mol
Exact Mass 512.20463259 g/mol
Topological Polar Surface Area (TPSA) 162.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.29
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,4a,8-trihydroxy-2,9-bis(1-hydroxyhexa-2,4-dienylidene)-4,5a,7,9b-tetramethyl-9aH-dibenzofuran-1,3,6-trione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9391 93.91%
Caco-2 - 0.7363 73.63%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6235 62.35%
OATP2B1 inhibitior + 0.5792 57.92%
OATP1B1 inhibitior + 0.8423 84.23%
OATP1B3 inhibitior + 0.9448 94.48%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8335 83.35%
P-glycoprotein inhibitior + 0.6339 63.39%
P-glycoprotein substrate - 0.7420 74.20%
CYP3A4 substrate + 0.6253 62.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8877 88.77%
CYP3A4 inhibition - 0.8791 87.91%
CYP2C9 inhibition - 0.8872 88.72%
CYP2C19 inhibition - 0.9387 93.87%
CYP2D6 inhibition - 0.9582 95.82%
CYP1A2 inhibition - 0.8395 83.95%
CYP2C8 inhibition - 0.5845 58.45%
CYP inhibitory promiscuity - 0.7235 72.35%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Danger 0.4995 49.95%
Eye corrosion - 0.9816 98.16%
Eye irritation - 0.8494 84.94%
Skin irritation - 0.5189 51.89%
Skin corrosion - 0.9061 90.61%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4886 48.86%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.5928 59.28%
skin sensitisation - 0.7323 73.23%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.6825 68.25%
Acute Oral Toxicity (c) III 0.4055 40.55%
Estrogen receptor binding + 0.7360 73.60%
Androgen receptor binding + 0.7563 75.63%
Thyroid receptor binding + 0.6063 60.63%
Glucocorticoid receptor binding + 0.6246 62.46%
Aromatase binding + 0.6075 60.75%
PPAR gamma + 0.6704 67.04%
Honey bee toxicity - 0.7815 78.15%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9572 95.72%

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 96.91% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.15% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 93.95% 83.82%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.70% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.05% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.27% 99.23%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.23% 91.71%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 84.23% 85.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.53% 86.33%
CHEMBL2581 P07339 Cathepsin D 82.93% 98.95%

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 71434527
LOTUS LTS0005821
wikiData Q104180102