4-(2-Heptyl-6-hydroxy-4-methoxybenzoyl)oxy-2-hydroxy-6-methylbenzoic acid

Details

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Internal ID ccb5f296-745d-4bb6-b876-de23899659c1
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 4-(2-heptyl-6-hydroxy-4-methoxybenzoyl)oxy-2-hydroxy-6-methylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H28O7/c1-4-5-6-7-8-9-15-11-16(29-3)12-19(25)21(15)23(28)30-17-10-14(2)20(22(26)27)18(24)13-17/h10-13,24-25H,4-9H2,1-3H3,(H,26,27)
InChI Key OYEWMEUDOVKFPP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H28O7
Molecular Weight 416.50 g/mol
Exact Mass 416.18350323 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 7.10
Atomic LogP (AlogP) 4.85
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(2-Heptyl-6-hydroxy-4-methoxybenzoyl)oxy-2-hydroxy-6-methylbenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9408 94.08%
Caco-2 + 0.5434 54.34%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8955 89.55%
OATP2B1 inhibitior - 0.7165 71.65%
OATP1B1 inhibitior + 0.9264 92.64%
OATP1B3 inhibitior - 0.2175 21.75%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6650 66.50%
P-glycoprotein inhibitior + 0.6002 60.02%
P-glycoprotein substrate - 0.7286 72.86%
CYP3A4 substrate + 0.5287 52.87%
CYP2C9 substrate - 0.6131 61.31%
CYP2D6 substrate - 0.8804 88.04%
CYP3A4 inhibition + 0.5467 54.67%
CYP2C9 inhibition - 0.5175 51.75%
CYP2C19 inhibition - 0.5129 51.29%
CYP2D6 inhibition - 0.7910 79.10%
CYP1A2 inhibition - 0.5083 50.83%
CYP2C8 inhibition + 0.7270 72.70%
CYP inhibitory promiscuity - 0.5934 59.34%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7934 79.34%
Carcinogenicity (trinary) Non-required 0.7612 76.12%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.7629 76.29%
Skin irritation - 0.8194 81.94%
Skin corrosion - 0.8963 89.63%
Ames mutagenesis - 0.7515 75.15%
Human Ether-a-go-go-Related Gene inhibition + 0.7290 72.90%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5785 57.85%
skin sensitisation - 0.8938 89.38%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.5364 53.64%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.5066 50.66%
Acute Oral Toxicity (c) II 0.4430 44.30%
Estrogen receptor binding + 0.7812 78.12%
Androgen receptor binding + 0.7330 73.30%
Thyroid receptor binding + 0.5469 54.69%
Glucocorticoid receptor binding + 0.7889 78.89%
Aromatase binding + 0.6633 66.33%
PPAR gamma + 0.7877 78.77%
Honey bee toxicity - 0.9093 90.93%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6143 61.43%
Fish aquatic toxicity + 1.0000 100.00%

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 95.34% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.02% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.84% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.87% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.05% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.02% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.57% 96.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.63% 95.17%
CHEMBL3401 O75469 Pregnane X receptor 88.60% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.77% 95.56%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.86% 97.29%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.12% 91.71%
CHEMBL3194 P02766 Transthyretin 83.86% 90.71%
CHEMBL1907 P15144 Aminopeptidase N 82.17% 93.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.87% 96.00%
CHEMBL2535 P11166 Glucose transporter 81.76% 98.75%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.75% 100.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.52% 97.21%
CHEMBL4208 P20618 Proteasome component C5 81.14% 90.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 80.97% 92.68%
CHEMBL230 P35354 Cyclooxygenase-2 80.92% 89.63%

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.
There are no matching plants.

Cross-Links

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PubChem 163187266
LOTUS LTS0236946
wikiData Q104253076