Emodacidamide E

Details

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Internal ID 74f2eed7-c722-4a8f-8392-1efa292bad9f
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name (2S,3S)-3-methyl-2-[(4,5,7-trihydroxy-9,10-dioxoanthracene-2-carbonyl)amino]pentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H19NO8/c1-3-8(2)17(21(29)30)22-20(28)9-4-11-15(13(24)5-9)19(27)16-12(18(11)26)6-10(23)7-14(16)25/h4-8,17,23-25H,3H2,1-2H3,(H,22,28)(H,29,30)/t8-,17-/m0/s1
InChI Key UVFFSOBWYUVHFJ-QPFGOUBPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H19NO8
Molecular Weight 413.40 g/mol
Exact Mass 413.11106656 g/mol
Topological Polar Surface Area (TPSA) 161.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 1.81
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Emodacidamide E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8958 89.58%
Caco-2 - 0.7511 75.11%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6466 64.66%
OATP2B1 inhibitior - 0.5717 57.17%
OATP1B1 inhibitior + 0.8376 83.76%
OATP1B3 inhibitior + 0.9371 93.71%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5971 59.71%
P-glycoprotein inhibitior - 0.7557 75.57%
P-glycoprotein substrate - 0.7151 71.51%
CYP3A4 substrate - 0.5203 52.03%
CYP2C9 substrate - 0.6054 60.54%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.8809 88.09%
CYP2C9 inhibition - 0.7776 77.76%
CYP2C19 inhibition - 0.7940 79.40%
CYP2D6 inhibition - 0.8417 84.17%
CYP1A2 inhibition - 0.6046 60.46%
CYP2C8 inhibition - 0.8056 80.56%
CYP inhibitory promiscuity - 0.8278 82.78%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8491 84.91%
Carcinogenicity (trinary) Non-required 0.6563 65.63%
Eye corrosion - 0.9961 99.61%
Eye irritation - 0.9311 93.11%
Skin irritation - 0.8420 84.20%
Skin corrosion - 0.9559 95.59%
Ames mutagenesis - 0.5898 58.98%
Human Ether-a-go-go-Related Gene inhibition - 0.3631 36.31%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.6711 67.11%
skin sensitisation - 0.9054 90.54%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.6269 62.69%
Acute Oral Toxicity (c) III 0.6468 64.68%
Estrogen receptor binding + 0.6432 64.32%
Androgen receptor binding + 0.6348 63.48%
Thyroid receptor binding - 0.6377 63.77%
Glucocorticoid receptor binding + 0.5698 56.98%
Aromatase binding - 0.5745 57.45%
PPAR gamma + 0.6833 68.33%
Honey bee toxicity - 0.9393 93.93%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9818 98.18%

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 98.98% 98.95%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 98.71% 96.38%
CHEMBL4208 P20618 Proteasome component C5 92.54% 90.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 91.55% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.35% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.28% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.38% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.96% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.28% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.98% 91.11%
CHEMBL4072 P07858 Cathepsin B 87.25% 93.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.16% 89.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.42% 93.56%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 83.97% 80.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.66% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 83.08% 94.73%
CHEMBL2535 P11166 Glucose transporter 80.19% 98.75%

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 132489980
LOTUS LTS0163199
wikiData Q105279795