3,4,4,5-Tetramethoxycyclohexa-2,5-dien-1-one

Details

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Internal ID 6a987d1f-9cd0-4a78-b16d-3f5f5861d1fa
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals > Ketals
IUPAC Name 3,4,4,5-tetramethoxycyclohexa-2,5-dien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O5/c1-12-8-5-7(11)6-9(13-2)10(8,14-3)15-4/h5-6H,1-4H3
InChI Key DEQOWNUIAOHMGK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O5
Molecular Weight 214.21 g/mol
Exact Mass 214.08412354 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.62
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,4,4,5-Tetramethoxycyclohexa-2,5-dien-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9718 97.18%
Caco-2 + 0.8769 87.69%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8125 81.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9344 93.44%
OATP1B3 inhibitior + 0.9739 97.39%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9152 91.52%
P-glycoprotein inhibitior - 0.9278 92.78%
P-glycoprotein substrate - 0.9753 97.53%
CYP3A4 substrate - 0.6283 62.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8580 85.80%
CYP3A4 inhibition - 0.8668 86.68%
CYP2C9 inhibition - 0.9860 98.60%
CYP2C19 inhibition - 0.8418 84.18%
CYP2D6 inhibition - 0.9658 96.58%
CYP1A2 inhibition - 0.9061 90.61%
CYP2C8 inhibition - 0.9794 97.94%
CYP inhibitory promiscuity - 0.8240 82.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6814 68.14%
Carcinogenicity (trinary) Non-required 0.5764 57.64%
Eye corrosion - 0.7339 73.39%
Eye irritation + 0.8894 88.94%
Skin irritation - 0.6777 67.77%
Skin corrosion - 0.9923 99.23%
Ames mutagenesis - 0.5270 52.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6617 66.17%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.6886 68.86%
skin sensitisation - 0.7125 71.25%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.8311 83.11%
Acute Oral Toxicity (c) IV 0.4493 44.93%
Estrogen receptor binding + 0.5824 58.24%
Androgen receptor binding - 0.5435 54.35%
Thyroid receptor binding - 0.6927 69.27%
Glucocorticoid receptor binding - 0.7589 75.89%
Aromatase binding - 0.7760 77.60%
PPAR gamma - 0.7674 76.74%
Honey bee toxicity - 0.8736 87.36%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.8861 88.61%

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 89.74% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.38% 91.11%
CHEMBL2581 P07339 Cathepsin D 86.55% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.35% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.49% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.01% 94.45%

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.
Pisonia umbellifera

Cross-Links

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PubChem 13815814
LOTUS LTS0210243
wikiData Q104977430