3,4,5-Trihydroxy-4-methoxycyclohexa-1,5-diene-1-carboxylic acid

Details

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Internal ID 5adba9f0-9844-4cb1-b2be-67bd901c40d3
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Hemiacetals
IUPAC Name 3,4,5-trihydroxy-4-methoxycyclohexa-1,5-diene-1-carboxylic acid
SMILES (Canonical) COC1(C(C=C(C=C1O)C(=O)O)O)O
SMILES (Isomeric) COC1(C(C=C(C=C1O)C(=O)O)O)O
InChI InChI=1S/C8H10O6/c1-14-8(13)5(9)2-4(7(11)12)3-6(8)10/h2-3,5,9-10,13H,1H3,(H,11,12)
InChI Key HKJDFWCBAWZFCB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O6
Molecular Weight 202.16 g/mol
Exact Mass 202.04773803 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP -1.70
Atomic LogP (AlogP) -0.85
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,4,5-Trihydroxy-4-methoxycyclohexa-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 + 0.7942 79.42%
Caco-2 - 0.8419 84.19%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7936 79.36%
OATP2B1 inhibitior - 0.8652 86.52%
OATP1B1 inhibitior + 0.9111 91.11%
OATP1B3 inhibitior + 0.9704 97.04%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9838 98.38%
BSEP inhibitior - 0.9822 98.22%
P-glycoprotein inhibitior - 0.9793 97.93%
P-glycoprotein substrate - 0.9404 94.04%
CYP3A4 substrate - 0.5955 59.55%
CYP2C9 substrate - 0.7887 78.87%
CYP2D6 substrate - 0.8904 89.04%
CYP3A4 inhibition - 0.9622 96.22%
CYP2C9 inhibition - 0.7931 79.31%
CYP2C19 inhibition - 0.8505 85.05%
CYP2D6 inhibition - 0.9547 95.47%
CYP1A2 inhibition - 0.8831 88.31%
CYP2C8 inhibition - 0.9230 92.30%
CYP inhibitory promiscuity - 0.8925 89.25%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.7766 77.66%
Carcinogenicity (trinary) Non-required 0.6335 63.35%
Eye corrosion - 0.9473 94.73%
Eye irritation - 0.7110 71.10%
Skin irritation - 0.5482 54.82%
Skin corrosion - 0.9326 93.26%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8420 84.20%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.6477 64.77%
skin sensitisation - 0.6491 64.91%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5662 56.62%
Acute Oral Toxicity (c) IV 0.5485 54.85%
Estrogen receptor binding - 0.6513 65.13%
Androgen receptor binding - 0.6884 68.84%
Thyroid receptor binding - 0.7778 77.78%
Glucocorticoid receptor binding - 0.6088 60.88%
Aromatase binding - 0.6404 64.04%
PPAR gamma - 0.7703 77.03%
Honey bee toxicity - 0.8102 81.02%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.8131 81.31%

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
CHEMBL2581 P07339 Cathepsin D 92.67% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.32% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 90.58% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.46% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.68% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.28% 95.56%

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.
Epilobium hirsutum
Rhus glabra

Cross-Links

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PubChem 162513630
LOTUS LTS0216172
wikiData Q105029691