8aalpha-Hydroxy-3,3,6,6,8,8-hexamethyl-3,8a-dihydro-1,2-benzodioxin-5,7(6H,8H)-dione

Details

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Internal ID 12bcd2d7-6f88-49ca-b76d-42868397fec7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclic alcohols and derivatives
IUPAC Name (8aR)-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([C@]2(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/t14-/m0/s1
InChI Key UBYZFUSXTLJWFM-AWEZNQCLSA-N
Popularity 1 reference 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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8aalpha-Hydroxy-3,3,6,6,8,8-hexamethyl-3,8a-dihydro-1,2-benzodioxin-5,7(6H,8H)-dione

2D Structure

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2D Structure of 8aalpha-Hydroxy-3,3,6,6,8,8-hexamethyl-3,8a-dihydro-1,2-benzodioxin-5,7(6H,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 + 0.9736 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%

Cross-Links

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PubChem 44281346
NPASS NPC227925
ChEMBL CHEMBL34459
LOTUS LTS0133609
wikiData Q105269755