Olivetoric acid

Details

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Internal ID cab20dfe-876a-4d05-bf95-d26cd6e2f5a1
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 4-[2,4-dihydroxy-6-(2-oxoheptyl)benzoyl]oxy-2-hydroxy-6-pentylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H32O8/c1-3-5-7-9-16-13-20(15-22(30)23(16)25(31)32)34-26(33)24-17(12-19(28)14-21(24)29)11-18(27)10-8-6-4-2/h12-15,28-30H,3-11H2,1-2H3,(H,31,32)
InChI Key VZPLPGICHZXOCQ-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C26H32O8
Molecular Weight 472.50 g/mol
Exact Mass 472.20971797 g/mol
Topological Polar Surface Area (TPSA) 141.00 Ų
XlogP 6.80
Atomic LogP (AlogP) 5.15
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 13

Synonyms

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491-47-4
DTXSID101316863
RefChem:928180
DTXCID201746689
CHEMBL3770253
4-[2,4-dihydroxy-6-(2-oxoheptyl)benzoyl]oxy-2-hydroxy-6-pentylbenzoic acid
SCHEMBL30055925
CHEBI:144183
VZPLPGICHZXOCQ-UHFFFAOYSA-N
BDBM50369678
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Olivetoric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9460 94.60%
Caco-2 - 0.7372 73.72%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.9094 90.94%
OATP2B1 inhibitior - 0.5677 56.77%
OATP1B1 inhibitior + 0.9257 92.57%
OATP1B3 inhibitior + 0.8769 87.69%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.7685 76.85%
P-glycoprotein inhibitior + 0.6646 66.46%
P-glycoprotein substrate - 0.7040 70.40%
CYP3A4 substrate + 0.5441 54.41%
CYP2C9 substrate + 0.5904 59.04%
CYP2D6 substrate - 0.8840 88.40%
CYP3A4 inhibition + 0.6613 66.13%
CYP2C9 inhibition - 0.5108 51.08%
CYP2C19 inhibition - 0.5148 51.48%
CYP2D6 inhibition - 0.7612 76.12%
CYP1A2 inhibition - 0.5144 51.44%
CYP2C8 inhibition + 0.7883 78.83%
CYP inhibitory promiscuity - 0.5966 59.66%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8034 80.34%
Carcinogenicity (trinary) Non-required 0.7630 76.30%
Eye corrosion - 0.9923 99.23%
Eye irritation - 0.6338 63.38%
Skin irritation - 0.7777 77.77%
Skin corrosion - 0.8720 87.20%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7162 71.62%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.5949 59.49%
skin sensitisation - 0.8716 87.16%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.6733 67.33%
Acute Oral Toxicity (c) III 0.4398 43.98%
Estrogen receptor binding + 0.7835 78.35%
Androgen receptor binding + 0.6975 69.75%
Thyroid receptor binding - 0.5656 56.56%
Glucocorticoid receptor binding + 0.7219 72.19%
Aromatase binding + 0.6208 62.08%
PPAR gamma + 0.6781 67.81%
Honey bee toxicity - 0.8472 84.72%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6260 62.60%
Fish aquatic toxicity + 1.0000 100.00%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL5658 O14684 Prostaglandin E synthase 400 nM
IC50
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 98.69% 95.17%
CHEMBL2581 P07339 Cathepsin D 97.92% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.75% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 96.44% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.62% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.12% 92.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.42% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 90.67% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.32% 96.09%
CHEMBL3194 P02766 Transthyretin 88.72% 90.71%
CHEMBL1929 P47989 Xanthine dehydrogenase 88.02% 96.12%
CHEMBL4208 P20618 Proteasome component C5 84.62% 90.00%
CHEMBL1907 P15144 Aminopeptidase N 84.24% 93.31%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.09% 96.95%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.96% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.13% 95.56%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 81.12% 96.09%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.92% 94.42%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.39% 97.29%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 591238
LOTUS LTS0000246
wikiData Q105299916