(4S)-4-hydroxy-2,5-dimethoxy-4-prop-2-enylcyclohexa-2,5-dien-1-one

Details

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Internal ID bdff5fdc-7cea-4b92-b9d5-7c9e35eae3d7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name (4S)-4-hydroxy-2,5-dimethoxy-4-prop-2-enylcyclohexa-2,5-dien-1-one
SMILES (Canonical) COC1=CC(=O)C(=CC1(CC=C)O)OC
SMILES (Isomeric) COC1=CC(=O)C(=C[C@]1(CC=C)O)OC
InChI InChI=1S/C11H14O4/c1-4-5-11(13)7-9(14-2)8(12)6-10(11)15-3/h4,6-7,13H,1,5H2,2-3H3/t11-/m0/s1
InChI Key DBWCSXUWHNNVMA-NSHDSACASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O4
Molecular Weight 210.23 g/mol
Exact Mass 210.08920892 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.94
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4S)-4-hydroxy-2,5-dimethoxy-4-prop-2-enylcyclohexa-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 + 0.9776 97.76%
Caco-2 + 0.7503 75.03%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7723 77.23%
OATP2B1 inhibitior - 0.8618 86.18%
OATP1B1 inhibitior + 0.9338 93.38%
OATP1B3 inhibitior + 0.9626 96.26%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8950 89.50%
P-glycoprotein inhibitior - 0.9381 93.81%
P-glycoprotein substrate - 0.9230 92.30%
CYP3A4 substrate - 0.5136 51.36%
CYP2C9 substrate - 0.8129 81.29%
CYP2D6 substrate - 0.8325 83.25%
CYP3A4 inhibition - 0.7291 72.91%
CYP2C9 inhibition - 0.9573 95.73%
CYP2C19 inhibition - 0.7823 78.23%
CYP2D6 inhibition - 0.9372 93.72%
CYP1A2 inhibition - 0.9349 93.49%
CYP2C8 inhibition - 0.9070 90.70%
CYP inhibitory promiscuity - 0.9255 92.55%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7571 75.71%
Carcinogenicity (trinary) Non-required 0.6798 67.98%
Eye corrosion - 0.9325 93.25%
Eye irritation + 0.8385 83.85%
Skin irritation - 0.5701 57.01%
Skin corrosion - 0.9488 94.88%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6362 63.62%
Micronuclear - 0.6441 64.41%
Hepatotoxicity - 0.5040 50.40%
skin sensitisation + 0.6253 62.53%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.7687 76.87%
Acute Oral Toxicity (c) III 0.6056 60.56%
Estrogen receptor binding - 0.5152 51.52%
Androgen receptor binding - 0.6560 65.60%
Thyroid receptor binding - 0.7226 72.26%
Glucocorticoid receptor binding - 0.7340 73.40%
Aromatase binding - 0.7289 72.89%
PPAR gamma - 0.6529 65.29%
Honey bee toxicity - 0.8077 80.77%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.6452 64.52%

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 97.46% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.21% 96.09%
CHEMBL4208 P20618 Proteasome component C5 92.00% 90.00%
CHEMBL2581 P07339 Cathepsin D 90.30% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.97% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.86% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.80% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.78% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.53% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.76% 96.00%

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.
Piper kadsura

Cross-Links

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PubChem 52913670
LOTUS LTS0132626
wikiData Q104974892