8a-Hydroxy-3,3,6,6,8,8-hexamethyl-1,2-benzodioxine-5,7-dione

Details

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Internal ID 1d66203b-3d46-4e1c-88dc-80e4e969187d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclic alcohols and derivatives
IUPAC Name 8a-hydroxy-3,3,6,6,8,8-hexamethyl-1,2-benzodioxine-5,7-dione
SMILES (Canonical) CC1(C=C2C(=O)C(C(=O)C(C2(OO1)O)(C)C)(C)C)C
SMILES (Isomeric) CC1(C=C2C(=O)C(C(=O)C(C2(OO1)O)(C)C)(C)C)C
InChI InChI=1S/C14H20O5/c1-11(2)7-8-9(15)12(3,4)10(16)13(5,6)14(8,17)19-18-11/h7,17H,1-6H3
InChI Key UBYZFUSXTLJWFM-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C14H20O5
Molecular Weight 268.30 g/mol
Exact Mass 268.13107373 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.55
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CHEMBL445267
AKOS040739442
1-Hydroxy-4,4,8,8,10,10-hexamethyl-2,3-dioxabicyclo[4.4.0]deca-5-ene-7,9-dione

2D Structure

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2D Structure of 8a-Hydroxy-3,3,6,6,8,8-hexamethyl-1,2-benzodioxine-5,7-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9736 97.36%
Caco-2 + 0.5874 58.74%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7267 72.67%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.9137 91.37%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8793 87.93%
P-glycoprotein inhibitior - 0.8885 88.85%
P-glycoprotein substrate - 0.9435 94.35%
CYP3A4 substrate - 0.5481 54.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8509 85.09%
CYP3A4 inhibition - 0.7481 74.81%
CYP2C9 inhibition - 0.8412 84.12%
CYP2C19 inhibition - 0.8787 87.87%
CYP2D6 inhibition - 0.9205 92.05%
CYP1A2 inhibition - 0.8812 88.12%
CYP2C8 inhibition - 0.9404 94.04%
CYP inhibitory promiscuity - 0.8919 89.19%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Danger 0.5333 53.33%
Eye corrosion - 0.9697 96.97%
Eye irritation + 0.6799 67.99%
Skin irritation - 0.5878 58.78%
Skin corrosion - 0.9246 92.46%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8214 82.14%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.5783 57.83%
skin sensitisation - 0.7084 70.84%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.6749 67.49%
Acute Oral Toxicity (c) III 0.5635 56.35%
Estrogen receptor binding + 0.6068 60.68%
Androgen receptor binding - 0.4868 48.68%
Thyroid receptor binding - 0.5146 51.46%
Glucocorticoid receptor binding - 0.6883 68.83%
Aromatase binding - 0.5285 52.85%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9539 95.39%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9366 93.66%

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 95.04% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.02% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.78% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.17% 95.56%
CHEMBL2581 P07339 Cathepsin D 84.90% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 84.88% 89.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.01% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.98% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.07% 99.23%

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.
Eucalyptus grandis
Melaleuca squarrosa
Rhodomyrtus tomentosa

Cross-Links

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PubChem 11207902
NPASS NPC204701
LOTUS LTS0048388
wikiData Q105269758