4-Ethyl-3,4,5-trihydroxycyclohexa-1,5-diene-1-carboxylic acid

Details

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Internal ID 6115c2e5-f846-48d9-a05e-8943ff0ab3ac
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 4-ethyl-3,4,5-trihydroxycyclohexa-1,5-diene-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12O5/c1-2-9(14)6(10)3-5(8(12)13)4-7(9)11/h3-4,6,10-11,14H,2H2,1H3,(H,12,13)
InChI Key CVBUORIIECEHBO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O5
Molecular Weight 200.19 g/mol
Exact Mass 200.06847348 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.05
H-Bond Acceptor 4
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 4-Ethyl-3,4,5-trihydroxycyclohexa-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 + 0.9255 92.55%
Caco-2 - 0.8129 81.29%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7751 77.51%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.8712 87.12%
OATP1B3 inhibitior + 0.9609 96.09%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9088 90.88%
BSEP inhibitior - 0.9799 97.99%
P-glycoprotein inhibitior - 0.9884 98.84%
P-glycoprotein substrate - 0.8882 88.82%
CYP3A4 substrate - 0.6473 64.73%
CYP2C9 substrate - 0.5878 58.78%
CYP2D6 substrate - 0.8966 89.66%
CYP3A4 inhibition - 0.9544 95.44%
CYP2C9 inhibition - 0.8865 88.65%
CYP2C19 inhibition - 0.9037 90.37%
CYP2D6 inhibition - 0.9439 94.39%
CYP1A2 inhibition - 0.9567 95.67%
CYP2C8 inhibition - 0.9499 94.99%
CYP inhibitory promiscuity - 0.9540 95.40%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6404 64.04%
Eye corrosion - 0.9810 98.10%
Eye irritation - 0.7268 72.68%
Skin irritation - 0.5311 53.11%
Skin corrosion - 0.8570 85.70%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8322 83.22%
Micronuclear + 0.5018 50.18%
Hepatotoxicity + 0.6043 60.43%
skin sensitisation + 0.5676 56.76%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5383 53.83%
Acute Oral Toxicity (c) III 0.5744 57.44%
Estrogen receptor binding - 0.7377 73.77%
Androgen receptor binding - 0.7195 71.95%
Thyroid receptor binding - 0.7037 70.37%
Glucocorticoid receptor binding - 0.5158 51.58%
Aromatase binding - 0.7918 79.18%
PPAR gamma - 0.7184 71.84%
Honey bee toxicity - 0.9298 92.98%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity + 0.7825 78.25%

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
CHEMBL221 P23219 Cyclooxygenase-1 96.19% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.89% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.89% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.52% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.18% 91.11%

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.
Mimosa hamata

Cross-Links

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PubChem 163192760
LOTUS LTS0062352
wikiData Q104970654