Stevastelin E3

Details

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Internal ID 8e5d8788-74b7-47cc-95a4-7249a0eeb657
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name 6-(1-hydroxyethyl)-13-(3-hydroxyhexadecan-2-yl)-12-methyl-3-methylidene-9-propan-2-yl-1-oxa-4,7,10-triazacyclotridecane-2,5,8,11-tetrone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H57N3O7/c1-8-9-10-11-12-13-14-15-16-17-18-19-25(37)21(4)28-22(5)29(38)34-26(20(2)3)30(39)35-27(24(7)36)31(40)33-23(6)32(41)42-28/h20-22,24-28,36-37H,6,8-19H2,1-5,7H3,(H,33,40)(H,34,38)(H,35,39)
InChI Key PQPBSHSHOPBRGI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H57N3O7
Molecular Weight 595.80 g/mol
Exact Mass 595.41965117 g/mol
Topological Polar Surface Area (TPSA) 154.00 Ų
XlogP 7.70
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 16

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Stevastelin E3

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7953 79.53%
Caco-2 - 0.8248 82.48%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6514 65.14%
OATP2B1 inhibitior - 0.5672 56.72%
OATP1B1 inhibitior + 0.8693 86.93%
OATP1B3 inhibitior + 0.8719 87.19%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8140 81.40%
BSEP inhibitior - 0.4896 48.96%
P-glycoprotein inhibitior + 0.6631 66.31%
P-glycoprotein substrate + 0.6484 64.84%
CYP3A4 substrate + 0.5969 59.69%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8703 87.03%
CYP3A4 inhibition + 0.7515 75.15%
CYP2C9 inhibition - 0.8376 83.76%
CYP2C19 inhibition - 0.8217 82.17%
CYP2D6 inhibition - 0.9159 91.59%
CYP1A2 inhibition - 0.8404 84.04%
CYP2C8 inhibition - 0.7339 73.39%
CYP inhibitory promiscuity - 0.9257 92.57%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5969 59.69%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.9148 91.48%
Skin irritation - 0.7540 75.40%
Skin corrosion - 0.9276 92.76%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5993 59.93%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.5086 50.86%
skin sensitisation - 0.8442 84.42%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6921 69.21%
Acute Oral Toxicity (c) III 0.6195 61.95%
Estrogen receptor binding + 0.7165 71.65%
Androgen receptor binding + 0.5572 55.72%
Thyroid receptor binding - 0.5744 57.44%
Glucocorticoid receptor binding + 0.6859 68.59%
Aromatase binding + 0.6356 63.56%
PPAR gamma + 0.6481 64.81%
Honey bee toxicity - 0.9058 90.58%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5488 54.88%
Fish aquatic toxicity + 0.9529 95.29%

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 98.12% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 97.35% 97.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.49% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.68% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.15% 97.25%
CHEMBL299 P17252 Protein kinase C alpha 94.21% 98.03%
CHEMBL5103 Q969S8 Histone deacetylase 10 93.39% 90.08%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.93% 97.29%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 91.82% 96.47%
CHEMBL255 P29275 Adenosine A2b receptor 89.81% 98.59%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.46% 94.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.39% 93.56%
CHEMBL221 P23219 Cyclooxygenase-1 89.07% 90.17%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 89.02% 92.88%
CHEMBL3045 P05771 Protein kinase C beta 88.41% 97.63%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.15% 89.00%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.47% 85.94%
CHEMBL4227 P25090 Lipoxin A4 receptor 87.17% 100.00%
CHEMBL230 P35354 Cyclooxygenase-2 87.11% 89.63%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.57% 93.03%
CHEMBL3310 Q96DB2 Histone deacetylase 11 84.38% 88.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.20% 99.23%
CHEMBL1949 P62937 Cyclophilin A 83.43% 98.57%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.37% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.19% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.18% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 82.64% 94.73%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.39% 92.86%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.91% 100.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.23% 91.81%

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 85211058
LOTUS LTS0252045
wikiData Q105213326