Gustastatin

Details

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Internal ID 1861bdba-f184-4bb2-8a1d-898cd3fc50fe
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name [3-methoxy-4-methoxycarbonyl-5-(2-oxoheptyl)phenyl] 2-hydroxy-4-methoxy-6-(2-oxoheptyl)benzoate
SMILES (Canonical) CCCCCC(=O)CC1=C(C(=CC(=C1)OC)O)C(=O)OC2=CC(=C(C(=C2)OC)C(=O)OC)CC(=O)CCCCC
SMILES (Isomeric) CCCCCC(=O)CC1=C(C(=CC(=C1)OC)O)C(=O)OC2=CC(=C(C(=C2)OC)C(=O)OC)CC(=O)CCCCC
InChI InChI=1S/C31H40O9/c1-6-8-10-12-22(32)14-20-16-24(37-3)18-26(34)28(20)31(36)40-25-17-21(15-23(33)13-11-9-7-2)29(30(35)39-5)27(19-25)38-4/h16-19,34H,6-15H2,1-5H3
InChI Key FHOVJOXBAHBKGJ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C31H40O9
Molecular Weight 556.60 g/mol
Exact Mass 556.26723285 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 6.40
Atomic LogP (AlogP) 5.80
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 17

Synonyms

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[3-methoxy-4-methoxycarbonyl-5-(2-oxoheptyl)phenyl] 2-hydroxy-4-methoxy-6-(2-oxoheptyl)benzoate
(3-methoxy-4-methoxycarbonyl-5-(2-oxoheptyl)phenyl) 2-hydroxy-4-methoxy-6-(2-oxoheptyl)benzoate
RefChem:144800
720698-33-9
CHEBI:67822
CHEMBL481267
Q27136298

2D Structure

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2D Structure of Gustastatin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9831 98.31%
Caco-2 - 0.6355 63.55%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8932 89.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9074 90.74%
OATP1B3 inhibitior + 0.8537 85.37%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9609 96.09%
P-glycoprotein inhibitior + 0.8930 89.30%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.5579 55.79%
CYP2C9 substrate - 0.5995 59.95%
CYP2D6 substrate - 0.8440 84.40%
CYP3A4 inhibition - 0.5973 59.73%
CYP2C9 inhibition - 0.7092 70.92%
CYP2C19 inhibition + 0.5510 55.10%
CYP2D6 inhibition - 0.8548 85.48%
CYP1A2 inhibition + 0.5381 53.81%
CYP2C8 inhibition + 0.8445 84.45%
CYP inhibitory promiscuity - 0.7680 76.80%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7254 72.54%
Carcinogenicity (trinary) Non-required 0.7172 71.72%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.8400 84.00%
Skin irritation - 0.8471 84.71%
Skin corrosion - 0.9217 92.17%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8502 85.02%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6177 61.77%
skin sensitisation - 0.9458 94.58%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.5200 52.00%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6503 65.03%
Acute Oral Toxicity (c) III 0.4162 41.62%
Estrogen receptor binding + 0.6690 66.90%
Androgen receptor binding + 0.6542 65.42%
Thyroid receptor binding - 0.5062 50.62%
Glucocorticoid receptor binding + 0.7454 74.54%
Aromatase binding - 0.5400 54.00%
PPAR gamma + 0.6305 63.05%
Honey bee toxicity - 0.8647 86.47%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6813 68.13%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.10% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.87% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.09% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 94.90% 95.17%
CHEMBL240 Q12809 HERG 94.84% 89.76%
CHEMBL2581 P07339 Cathepsin D 93.81% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.49% 92.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.46% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 85.97% 94.73%
CHEMBL2535 P11166 Glucose transporter 85.65% 98.75%
CHEMBL230 P35354 Cyclooxygenase-2 85.55% 89.63%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.11% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.58% 92.62%
CHEMBL4208 P20618 Proteasome component C5 81.57% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.19% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.71% 95.50%

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.
Cupania cinerea
Gustavia hexapetala

Cross-Links

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PubChem 11757435
NPASS NPC60413
ChEMBL CHEMBL481267
LOTUS LTS0131009
wikiData Q27136298