Benzoic acid, pentahydroxy-

Details

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Internal ID 2daf6e54-f41c-4a73-8a69-ce6d1d5ecae5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylated hydroquinones > Ubiquinols
IUPAC Name 2,3,4,5,6-pentahydroxybenzoic acid
SMILES (Canonical) C1(=C(C(=C(C(=C1O)O)O)O)O)C(=O)O
SMILES (Isomeric) C1(=C(C(=C(C(=C1O)O)O)O)O)C(=O)O
InChI InChI=1S/C7H6O7/c8-2-1(7(13)14)3(9)5(11)6(12)4(2)10/h8-12H,(H,13,14)
InChI Key ZHDKFKAWPYRHSQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C7H6O7
Molecular Weight 202.12 g/mol
Exact Mass 202.01135253 g/mol
Topological Polar Surface Area (TPSA) 138.00 Ų
XlogP 0.80
Atomic LogP (AlogP) -0.09
H-Bond Acceptor 6
H-Bond Donor 6
Rotatable Bonds 1

Synonyms

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145279-23-8
pentahydroxybenzoic acid
SCHEMBL3332818
DTXSID10471040

2D Structure

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2D Structure of Benzoic acid, pentahydroxy-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8929 89.29%
Caco-2 - 0.9248 92.48%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7287 72.87%
OATP2B1 inhibitior - 0.8634 86.34%
OATP1B1 inhibitior + 0.9252 92.52%
OATP1B3 inhibitior + 0.9648 96.48%
MATE1 inhibitior + 0.6200 62.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9796 97.96%
P-glycoprotein inhibitior - 0.9653 96.53%
P-glycoprotein substrate - 0.9923 99.23%
CYP3A4 substrate - 0.8199 81.99%
CYP2C9 substrate - 0.6931 69.31%
CYP2D6 substrate - 0.8961 89.61%
CYP3A4 inhibition - 0.8427 84.27%
CYP2C9 inhibition - 0.9363 93.63%
CYP2C19 inhibition - 0.9782 97.82%
CYP2D6 inhibition - 0.9693 96.93%
CYP1A2 inhibition - 0.9274 92.74%
CYP2C8 inhibition - 0.9747 97.47%
CYP inhibitory promiscuity - 0.9318 93.18%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7923 79.23%
Carcinogenicity (trinary) Non-required 0.7405 74.05%
Eye corrosion - 0.8617 86.17%
Eye irritation + 0.9485 94.85%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.8500 85.00%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7649 76.49%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.8781 87.81%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.7038 70.38%
Acute Oral Toxicity (c) III 0.6904 69.04%
Estrogen receptor binding - 0.7354 73.54%
Androgen receptor binding - 0.7672 76.72%
Thyroid receptor binding - 0.7610 76.10%
Glucocorticoid receptor binding + 0.5515 55.15%
Aromatase binding - 0.7792 77.92%
PPAR gamma - 0.5554 55.54%
Honey bee toxicity - 0.9807 98.07%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.9250 92.50%

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 83.49% 91.11%
CHEMBL3194 P02766 Transthyretin 82.98% 90.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.97% 94.42%

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.
Phyllanthus urinaria

Cross-Links

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PubChem 11715380
LOTUS LTS0155544
wikiData Q82299437