Ethyl Tumonoate A

Details

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Internal ID 999b9fb9-e3ce-45f2-837d-ea737e4acc0d
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > N-acyl-alpha amino acids
IUPAC Name ethyl (2S)-1-[(E,2R,3S)-3-hydroxy-2,4-dimethyldodec-4-enoyl]pyrrolidine-2-carboxylate
SMILES (Canonical) CCCCCCCC=C(C)C(C(C)C(=O)N1CCCC1C(=O)OCC)O
SMILES (Isomeric) CCCCCCC/C=C(\C)/[C@H]([C@@H](C)C(=O)N1CCC[C@H]1C(=O)OCC)O
InChI InChI=1S/C21H37NO4/c1-5-7-8-9-10-11-13-16(3)19(23)17(4)20(24)22-15-12-14-18(22)21(25)26-6-2/h13,17-19,23H,5-12,14-15H2,1-4H3/b16-13+/t17-,18+,19-/m1/s1
InChI Key ATSNGULFDLCUIL-BFJJTLHJSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H37NO4
Molecular Weight 367.50 g/mol
Exact Mass 367.27225866 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 5.00
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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DTXSID501046585
RefChem:139068
DTXCID501528410
ethyl (2S)-1-((E,2R,3S)-3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylate
CHEBI:69215
CHEMBL1822612
Q27137554

2D Structure

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2D Structure of Ethyl Tumonoate A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8528 85.28%
Caco-2 + 0.6957 69.57%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6685 66.85%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.9039 90.39%
OATP1B3 inhibitior + 0.9345 93.45%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.5358 53.58%
P-glycoprotein inhibitior - 0.5884 58.84%
P-glycoprotein substrate - 0.6563 65.63%
CYP3A4 substrate + 0.6230 62.30%
CYP2C9 substrate - 0.6221 62.21%
CYP2D6 substrate - 0.8522 85.22%
CYP3A4 inhibition - 0.8170 81.70%
CYP2C9 inhibition - 0.7943 79.43%
CYP2C19 inhibition - 0.7063 70.63%
CYP2D6 inhibition - 0.8598 85.98%
CYP1A2 inhibition - 0.7434 74.34%
CYP2C8 inhibition - 0.7943 79.43%
CYP inhibitory promiscuity - 0.5332 53.32%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5137 51.37%
Eye corrosion - 0.9816 98.16%
Eye irritation - 0.9130 91.30%
Skin irritation - 0.7674 76.74%
Skin corrosion - 0.9241 92.41%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4344 43.44%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.5542 55.42%
skin sensitisation - 0.8653 86.53%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6985 69.85%
Acute Oral Toxicity (c) III 0.6835 68.35%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.5328 53.28%
Thyroid receptor binding - 0.5936 59.36%
Glucocorticoid receptor binding + 0.6113 61.13%
Aromatase binding - 0.6614 66.14%
PPAR gamma - 0.6597 65.97%
Honey bee toxicity - 0.9233 92.33%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5649 56.49%
Fish aquatic toxicity + 0.9465 94.65%

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 97.98% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.68% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.41% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 94.25% 92.86%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 93.69% 96.47%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 93.49% 100.00%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 92.81% 97.47%
CHEMBL321 P14780 Matrix metalloproteinase 9 92.40% 92.12%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 92.11% 98.33%
CHEMBL230 P35354 Cyclooxygenase-2 91.19% 89.63%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.95% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.87% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.46% 99.17%
CHEMBL205 P00918 Carbonic anhydrase II 89.52% 98.44%
CHEMBL340 P08684 Cytochrome P450 3A4 89.48% 91.19%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.23% 97.29%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.07% 91.81%
CHEMBL5203 P33316 dUTP pyrophosphatase 88.86% 99.18%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.62% 97.09%
CHEMBL4588 P22894 Matrix metalloproteinase 8 88.30% 94.66%
CHEMBL4227 P25090 Lipoxin A4 receptor 87.74% 100.00%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 86.73% 98.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.68% 90.71%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.41% 97.21%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.65% 94.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.17% 96.95%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.05% 93.03%
CHEMBL2514 O95665 Neurotensin receptor 2 84.87% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 84.66% 92.50%
CHEMBL5103 Q969S8 Histone deacetylase 10 84.32% 90.08%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.06% 95.89%
CHEMBL261 P00915 Carbonic anhydrase I 83.25% 96.76%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.12% 95.50%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 83.10% 90.24%
CHEMBL1944495 P28065 Proteasome subunit beta type-9 82.67% 97.50%
CHEMBL3238 P23786 Carnitine palmitoyltransferase 2 82.65% 94.05%
CHEMBL221 P23219 Cyclooxygenase-1 82.49% 90.17%
CHEMBL299 P17252 Protein kinase C alpha 82.45% 98.03%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.41% 95.89%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 82.28% 95.34%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 82.23% 82.38%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 81.74% 97.64%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.28% 97.50%

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.
Panax japonicus

Cross-Links

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PubChem 53493313
NPASS NPC188785
ChEMBL CHEMBL1822612
LOTUS LTS0007741
wikiData Q27137554