dapdiamide E

Details

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Internal ID 2ece6285-b1fd-47c9-8a0b-de7e894c722d
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Dipeptides
IUPAC Name (2S)-2-[[(2S)-3-amino-2-[(3-carbamoyloxirane-2-carbonyl)amino]propanoyl]amino]-3-methylbutanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H20N4O6/c1-4(2)6(12(20)21)16-10(18)5(3-13)15-11(19)8-7(22-8)9(14)17/h4-8H,3,13H2,1-2H3,(H2,14,17)(H,15,19)(H,16,18)(H,20,21)/t5-,6-,7?,8?/m0/s1
InChI Key BQMJFERCSPVSGR-LHZZQDSXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20N4O6
Molecular Weight 316.31 g/mol
Exact Mass 316.13828437 g/mol
Topological Polar Surface Area (TPSA) 177.00 Ų
XlogP -4.70
Atomic LogP (AlogP) -3.09
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of dapdiamide E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5498 54.98%
Caco-2 - 0.9207 92.07%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.4907 49.07%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.9226 92.26%
OATP1B3 inhibitior + 0.9357 93.57%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9663 96.63%
P-glycoprotein inhibitior - 0.8611 86.11%
P-glycoprotein substrate - 0.6285 62.85%
CYP3A4 substrate - 0.5308 53.08%
CYP2C9 substrate - 0.6070 60.70%
CYP2D6 substrate - 0.8386 83.86%
CYP3A4 inhibition - 0.9107 91.07%
CYP2C9 inhibition - 0.9248 92.48%
CYP2C19 inhibition - 0.8933 89.33%
CYP2D6 inhibition - 0.9423 94.23%
CYP1A2 inhibition - 0.8941 89.41%
CYP2C8 inhibition - 0.9402 94.02%
CYP inhibitory promiscuity - 0.9848 98.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.6794 67.94%
Eye corrosion - 0.9838 98.38%
Eye irritation - 0.9842 98.42%
Skin irritation - 0.7760 77.60%
Skin corrosion - 0.9459 94.59%
Ames mutagenesis - 0.7048 70.48%
Human Ether-a-go-go-Related Gene inhibition - 0.7743 77.43%
Micronuclear + 0.7800 78.00%
Hepatotoxicity - 0.5660 56.60%
skin sensitisation - 0.8769 87.69%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5593 55.93%
Estrogen receptor binding - 0.5902 59.02%
Androgen receptor binding - 0.5843 58.43%
Thyroid receptor binding - 0.6458 64.58%
Glucocorticoid receptor binding - 0.5199 51.99%
Aromatase binding - 0.7087 70.87%
PPAR gamma - 0.4845 48.45%
Honey bee toxicity - 0.9292 92.92%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.9172 91.72%

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
CHEMBL2730 P21980 Protein-glutamine gamma-glutamyltransferase 95.93% 92.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.07% 96.09%
CHEMBL4072 P07858 Cathepsin B 95.00% 93.67%
CHEMBL2581 P07339 Cathepsin D 94.73% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.92% 99.17%
CHEMBL3837 P07711 Cathepsin L 89.61% 96.61%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.50% 93.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 88.73% 96.47%
CHEMBL2514 O95665 Neurotensin receptor 2 88.37% 100.00%
CHEMBL3776 Q14790 Caspase-8 87.92% 97.06%
CHEMBL2413 P32246 C-C chemokine receptor type 1 85.57% 89.50%
CHEMBL221 P23219 Cyclooxygenase-1 85.46% 90.17%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 85.43% 92.29%
CHEMBL340 P08684 Cytochrome P450 3A4 84.52% 91.19%
CHEMBL5028 O14672 ADAM10 84.46% 97.50%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.16% 100.00%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 84.15% 98.33%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.62% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.38% 91.11%
CHEMBL3308 P55212 Caspase-6 82.94% 97.56%
CHEMBL4816 Q9Y243 Serine/threonine-protein kinase AKT3 82.40% 96.28%
CHEMBL2094135 Q96BI3 Gamma-secretase 81.20% 98.05%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.96% 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 45379525
LOTUS LTS0004117
wikiData Q77382028