4-Hydroxy-3-methoxy-4-methylcyclohexa-1,5-diene-1-carboxylic acid

Details

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Internal ID 96f75e41-49c4-4a83-9b2d-4502da3e4608
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 4-hydroxy-3-methoxy-4-methylcyclohexa-1,5-diene-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12O4/c1-9(12)4-3-6(8(10)11)5-7(9)13-2/h3-5,7,12H,1-2H3,(H,10,11)
InChI Key MLHQQVVHYTXTMJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O4
Molecular Weight 184.19 g/mol
Exact Mass 184.07355886 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.33
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-3-methoxy-4-methylcyclohexa-1,5-diene-1-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9649 96.49%
Caco-2 + 0.7208 72.08%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8658 86.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9163 91.63%
OATP1B3 inhibitior + 0.9612 96.12%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9555 95.55%
P-glycoprotein inhibitior - 0.9614 96.14%
P-glycoprotein substrate - 0.9379 93.79%
CYP3A4 substrate - 0.5710 57.10%
CYP2C9 substrate - 0.7875 78.75%
CYP2D6 substrate - 0.9081 90.81%
CYP3A4 inhibition - 0.9557 95.57%
CYP2C9 inhibition - 0.8804 88.04%
CYP2C19 inhibition - 0.8367 83.67%
CYP2D6 inhibition - 0.9280 92.80%
CYP1A2 inhibition - 0.9411 94.11%
CYP2C8 inhibition - 0.9536 95.36%
CYP inhibitory promiscuity - 0.8854 88.54%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6956 69.56%
Carcinogenicity (trinary) Non-required 0.5900 59.00%
Eye corrosion - 0.9260 92.60%
Eye irritation + 0.9246 92.46%
Skin irritation - 0.5466 54.66%
Skin corrosion - 0.9668 96.68%
Ames mutagenesis - 0.6754 67.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8357 83.57%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.6858 68.58%
skin sensitisation + 0.4757 47.57%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6038 60.38%
Acute Oral Toxicity (c) III 0.5595 55.95%
Estrogen receptor binding + 0.5734 57.34%
Androgen receptor binding - 0.8682 86.82%
Thyroid receptor binding - 0.6904 69.04%
Glucocorticoid receptor binding - 0.8007 80.07%
Aromatase binding - 0.9311 93.11%
PPAR gamma - 0.8406 84.06%
Honey bee toxicity - 0.9064 90.64%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity + 0.8624 86.24%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.12% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.43% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.89% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.78% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.94% 86.33%
CHEMBL2581 P07339 Cathepsin D 81.18% 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 163192287
LOTUS LTS0113223
wikiData Q105166661