Imbricaric acid

Details

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Internal ID 18466c29-caad-425c-ae07-0330f7d4fdc2
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 2-hydroxy-4-(2-hydroxy-4-methoxy-6-pentylbenzoyl)oxy-6-propylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H28O7/c1-4-6-7-9-15-10-16(29-3)12-19(25)21(15)23(28)30-17-11-14(8-5-2)20(22(26)27)18(24)13-17/h10-13,24-25H,4-9H2,1-3H3,(H,26,27)
InChI Key QXDIHIOKSGGXLD-UHFFFAOYSA-N
Popularity 3 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 7.00
Atomic LogP (AlogP) 4.71
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 10

Synonyms

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2-hydroxy-4-(2-hydroxy-4-methoxy-6-pentylbenzoyl)oxy-6-propylbenzoic acid
RefChem:147930
SCHEMBL30985285
CHEBI:144259

2D Structure

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2D Structure of Imbricaric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9328 93.28%
Caco-2 + 0.5151 51.51%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8836 88.36%
OATP2B1 inhibitior - 0.7179 71.79%
OATP1B1 inhibitior + 0.9097 90.97%
OATP1B3 inhibitior - 0.2437 24.37%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6482 64.82%
P-glycoprotein inhibitior + 0.6538 65.38%
P-glycoprotein substrate - 0.7107 71.07%
CYP3A4 substrate - 0.5119 51.19%
CYP2C9 substrate - 0.6131 61.31%
CYP2D6 substrate - 0.8804 88.04%
CYP3A4 inhibition - 0.5327 53.27%
CYP2C9 inhibition + 0.5857 58.57%
CYP2C19 inhibition - 0.5298 52.98%
CYP2D6 inhibition - 0.7489 74.89%
CYP1A2 inhibition - 0.5267 52.67%
CYP2C8 inhibition + 0.6907 69.07%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7634 76.34%
Carcinogenicity (trinary) Non-required 0.7394 73.94%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.7328 73.28%
Skin irritation - 0.8154 81.54%
Skin corrosion - 0.8950 89.50%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7049 70.49%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6074 60.74%
skin sensitisation - 0.8880 88.80%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.5364 53.64%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.6442 64.42%
Acute Oral Toxicity (c) II 0.4282 42.82%
Estrogen receptor binding + 0.8490 84.90%
Androgen receptor binding + 0.7428 74.28%
Thyroid receptor binding - 0.4872 48.72%
Glucocorticoid receptor binding + 0.7700 77.00%
Aromatase binding + 0.6916 69.16%
PPAR gamma + 0.8328 83.28%
Honey bee toxicity - 0.9128 91.28%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5040 50.40%
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 96.39% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.81% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.44% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.34% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.19% 92.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.04% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.55% 96.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.21% 95.17%
CHEMBL3401 O75469 Pregnane X receptor 87.13% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.43% 95.56%
CHEMBL3194 P02766 Transthyretin 83.51% 90.71%
CHEMBL2535 P11166 Glucose transporter 82.45% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 82.35% 93.31%
CHEMBL4208 P20618 Proteasome component C5 81.49% 90.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.43% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.38% 96.00%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 81.26% 96.09%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.14% 91.71%

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 15559746
LOTUS LTS0259118
wikiData Q77567742