Podocarpiamide

Details

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Internal ID ade73d8f-80fa-4fbc-97e2-ce97a85fa1d2
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acid esters
IUPAC Name 2-acetyloxyethyl-[2-[carboxy-(2-methoxy-2-oxoethyl)amino]phenyl]carbamic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H18N2O8/c1-10(18)25-8-7-16(14(20)21)11-5-3-4-6-12(11)17(15(22)23)9-13(19)24-2/h3-6H,7-9H2,1-2H3,(H,20,21)(H,22,23)
InChI Key APUVOPBXMBRNOU-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18N2O8
Molecular Weight 354.31 g/mol
Exact Mass 354.10631554 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.39
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Podocarpiamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6282 62.82%
Caco-2 + 0.5499 54.99%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8407 84.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9093 90.93%
OATP1B3 inhibitior + 0.9361 93.61%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6564 65.64%
P-glycoprotein inhibitior - 0.8005 80.05%
P-glycoprotein substrate - 0.8057 80.57%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8185 81.85%
CYP2D6 substrate - 0.8499 84.99%
CYP3A4 inhibition - 0.9449 94.49%
CYP2C9 inhibition - 0.8422 84.22%
CYP2C19 inhibition - 0.7115 71.15%
CYP2D6 inhibition - 0.8865 88.65%
CYP1A2 inhibition - 0.7780 77.80%
CYP2C8 inhibition - 0.6570 65.70%
CYP inhibitory promiscuity - 0.7900 79.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8123 81.23%
Carcinogenicity (trinary) Non-required 0.6642 66.42%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.9120 91.20%
Skin irritation - 0.7958 79.58%
Skin corrosion - 0.9510 95.10%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7256 72.56%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.6264 62.64%
skin sensitisation - 0.8896 88.96%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5319 53.19%
Acute Oral Toxicity (c) III 0.6332 63.32%
Estrogen receptor binding - 0.5449 54.49%
Androgen receptor binding + 0.6666 66.66%
Thyroid receptor binding - 0.5740 57.40%
Glucocorticoid receptor binding + 0.7052 70.52%
Aromatase binding - 0.6024 60.24%
PPAR gamma + 0.6634 66.34%
Honey bee toxicity - 0.9570 95.70%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9415 94.15%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.81% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.03% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.40% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.58% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 91.21% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 89.22% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.28% 99.17%
CHEMBL5028 O14672 ADAM10 82.33% 97.50%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 82.10% 89.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.24% 96.00%

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 139585113
LOTUS LTS0271156
wikiData Q77384003