Puberuline E

Details

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Internal ID 647099c1-35bd-4124-a07b-dcf985fa5c40
Taxonomy Benzenoids > Benzene and substituted derivatives > Anilides > Aromatic anilides > Benzanilides
IUPAC Name methyl 4-[(2,5-dihydroxybenzoyl)amino]-3-hydroxybenzoate
SMILES (Canonical) COC(=O)C1=CC(=C(C=C1)NC(=O)C2=C(C=CC(=C2)O)O)O
SMILES (Isomeric) COC(=O)C1=CC(=C(C=C1)NC(=O)C2=C(C=CC(=C2)O)O)O
InChI InChI=1S/C15H13NO6/c1-22-15(21)8-2-4-11(13(19)6-8)16-14(20)10-7-9(17)3-5-12(10)18/h2-7,17-19H,1H3,(H,16,20)
InChI Key QKJXTDDURNMKEZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H13NO6
Molecular Weight 303.27 g/mol
Exact Mass 303.07428713 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.84
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Puberuline E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6261 62.61%
Caco-2 - 0.5406 54.06%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7732 77.32%
OATP2B1 inhibitior - 0.5744 57.44%
OATP1B1 inhibitior + 0.8628 86.28%
OATP1B3 inhibitior + 0.9459 94.59%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8177 81.77%
P-glycoprotein inhibitior - 0.9324 93.24%
P-glycoprotein substrate - 0.7503 75.03%
CYP3A4 substrate - 0.5394 53.94%
CYP2C9 substrate - 0.6334 63.34%
CYP2D6 substrate - 0.8663 86.63%
CYP3A4 inhibition - 0.9100 91.00%
CYP2C9 inhibition - 0.8336 83.36%
CYP2C19 inhibition - 0.9066 90.66%
CYP2D6 inhibition - 0.9410 94.10%
CYP1A2 inhibition - 0.6331 63.31%
CYP2C8 inhibition + 0.6618 66.18%
CYP inhibitory promiscuity - 0.8553 85.53%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7325 73.25%
Carcinogenicity (trinary) Non-required 0.7316 73.16%
Eye corrosion - 0.9956 99.56%
Eye irritation - 0.6185 61.85%
Skin irritation - 0.8932 89.32%
Skin corrosion - 0.9736 97.36%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7775 77.75%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.5072 50.72%
skin sensitisation - 0.9443 94.43%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.7070 70.70%
Acute Oral Toxicity (c) III 0.8061 80.61%
Estrogen receptor binding + 0.8426 84.26%
Androgen receptor binding + 0.8042 80.42%
Thyroid receptor binding + 0.6414 64.14%
Glucocorticoid receptor binding + 0.8593 85.93%
Aromatase binding + 0.6530 65.30%
PPAR gamma + 0.6053 60.53%
Honey bee toxicity - 0.9376 93.76%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9444 94.44%

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
CHEMBL1293294 P51151 Ras-related protein Rab-9A 96.13% 87.67%
CHEMBL1951 P21397 Monoamine oxidase A 94.91% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.26% 91.11%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 93.65% 81.11%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 92.16% 91.07%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 90.65% 94.42%
CHEMBL2535 P11166 Glucose transporter 90.21% 98.75%
CHEMBL4208 P20618 Proteasome component C5 90.20% 90.00%
CHEMBL3194 P02766 Transthyretin 87.35% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.33% 99.17%
CHEMBL4901 P54753 Ephrin type-B receptor 3 86.42% 87.50%
CHEMBL3401 O75469 Pregnane X receptor 85.85% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 85.78% 91.19%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.07% 97.36%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.33% 96.09%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 82.63% 94.67%
CHEMBL2581 P07339 Cathepsin D 81.86% 98.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.28% 94.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.46% 90.71%

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.
Aconitum barbatum

Cross-Links

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PubChem 101472880
LOTUS LTS0126086
wikiData Q105223174