Isobutyl gallate

Details

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Internal ID 716ea3a7-a3ac-47ec-aa63-fdb9d70a670a
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives > Gallic acid and derivatives > Galloyl esters
IUPAC Name 2-methylpropyl 3,4,5-trihydroxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H14O5/c1-6(2)5-16-11(15)7-3-8(12)10(14)9(13)4-7/h3-4,6,12-14H,5H2,1-2H3
InChI Key UCLHVCFKZSLALE-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O5
Molecular Weight 226.23 g/mol
Exact Mass 226.08412354 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 1.62
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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3856-05-1
Isobutyl 3,4,5-trihydroxybenzoate
Gallic acid iso-butyl ester
2-methylpropyl 3,4,5-trihydroxybenzoate
SR016RR89P
NSC-147482
Benzoic acid, 3,4,5-trihydroxy-, 2-methylpropyl ester
Gallic Acid Isobutyl Ester
UNII-SR016RR89P
SCHEMBL39620
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isobutyl gallate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9143 91.43%
Caco-2 - 0.5936 59.36%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8850 88.50%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.7750 77.50%
OATP1B3 inhibitior + 0.9351 93.51%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9404 94.04%
P-glycoprotein inhibitior - 0.9091 90.91%
P-glycoprotein substrate - 0.9465 94.65%
CYP3A4 substrate - 0.6505 65.05%
CYP2C9 substrate - 0.5914 59.14%
CYP2D6 substrate - 0.8403 84.03%
CYP3A4 inhibition - 0.8809 88.09%
CYP2C9 inhibition - 0.6834 68.34%
CYP2C19 inhibition - 0.8764 87.64%
CYP2D6 inhibition - 0.8819 88.19%
CYP1A2 inhibition + 0.5124 51.24%
CYP2C8 inhibition - 0.9044 90.44%
CYP inhibitory promiscuity - 0.8713 87.13%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7463 74.63%
Carcinogenicity (trinary) Non-required 0.7457 74.57%
Eye corrosion - 0.9681 96.81%
Eye irritation + 0.9228 92.28%
Skin irritation - 0.7098 70.98%
Skin corrosion - 0.9233 92.33%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7410 74.10%
Micronuclear - 0.5871 58.71%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation + 0.6844 68.44%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.8697 86.97%
Acute Oral Toxicity (c) III 0.7657 76.57%
Estrogen receptor binding + 0.8376 83.76%
Androgen receptor binding + 0.7901 79.01%
Thyroid receptor binding - 0.6223 62.23%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.6455 64.55%
PPAR gamma - 0.6240 62.40%
Honey bee toxicity - 0.9748 97.48%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.6350 63.50%
Fish aquatic toxicity + 0.9803 98.03%

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 96.12% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.36% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.28% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.21% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.54% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.40% 86.33%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.39% 100.00%
CHEMBL4208 P20618 Proteasome component C5 84.70% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 84.54% 94.73%
CHEMBL3194 P02766 Transthyretin 82.53% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.03% 96.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.00% 99.15%

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.
Alchornea glandulosa

Cross-Links

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PubChem 77464
LOTUS LTS0225665
wikiData Q83064475