Deferrihydroxyneocoprogen I

Details

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Internal ID e8d7afad-3807-4e23-af3e-ea246a19c2d6
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > N-acyl-alpha amino acids and derivatives
IUPAC Name [(E)-5-[3-[5-[3-[[(E)-4,5-dihydroxy-3-methylpent-2-enoyl]-hydroxyamino]propyl]-3,6-dioxopiperazin-2-yl]propyl-hydroxyamino]-3-methyl-5-oxopent-3-enyl] 2-acetamido-5-[acetyl(hydroxy)amino]pentanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H50N6O13/c1-19(11-15-50-31(46)25(32-21(3)39)10-7-12-35(47)22(4)40)16-27(42)36(48)13-5-8-23-29(44)34-24(30(45)33-23)9-6-14-37(49)28(43)17-20(2)26(41)18-38/h16-17,23-26,38,41,47-49H,5-15,18H2,1-4H3,(H,32,39)(H,33,45)(H,34,44)/b19-16+,20-17+
InChI Key XQOVEZMAFQKFSK-VQZJLROISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H50N6O13
Molecular Weight 714.80 g/mol
Exact Mass 714.34358567 g/mol
Topological Polar Surface Area (TPSA) 276.00 Ų
XlogP -1.90
Atomic LogP (AlogP) -1.33
H-Bond Acceptor 13
H-Bond Donor 8
Rotatable Bonds 21

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Deferrihydroxyneocoprogen I

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5536 55.36%
Caco-2 - 0.8555 85.55%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7828 78.28%
OATP2B1 inhibitior - 0.5751 57.51%
OATP1B1 inhibitior + 0.8732 87.32%
OATP1B3 inhibitior + 0.9305 93.05%
MATE1 inhibitior - 0.8866 88.66%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8071 80.71%
P-glycoprotein inhibitior + 0.7427 74.27%
P-glycoprotein substrate + 0.7164 71.64%
CYP3A4 substrate + 0.6916 69.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8756 87.56%
CYP3A4 inhibition - 0.7654 76.54%
CYP2C9 inhibition - 0.7707 77.07%
CYP2C19 inhibition - 0.7842 78.42%
CYP2D6 inhibition - 0.8855 88.55%
CYP1A2 inhibition - 0.8439 84.39%
CYP2C8 inhibition - 0.6404 64.04%
CYP inhibitory promiscuity - 0.9773 97.73%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.4812 48.12%
Eye corrosion - 0.9811 98.11%
Eye irritation - 0.9106 91.06%
Skin irritation - 0.7554 75.54%
Skin corrosion - 0.9251 92.51%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4001 40.01%
Micronuclear + 0.7300 73.00%
Hepatotoxicity - 0.5073 50.73%
skin sensitisation - 0.8396 83.96%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.6091 60.91%
Acute Oral Toxicity (c) III 0.6095 60.95%
Estrogen receptor binding + 0.8013 80.13%
Androgen receptor binding + 0.7015 70.15%
Thyroid receptor binding + 0.5211 52.11%
Glucocorticoid receptor binding + 0.6228 62.28%
Aromatase binding + 0.6522 65.22%
PPAR gamma + 0.6715 67.15%
Honey bee toxicity - 0.8196 81.96%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.4646 46.46%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.66% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.63% 94.45%
CHEMBL2581 P07339 Cathepsin D 98.01% 98.95%
CHEMBL5103 Q969S8 Histone deacetylase 10 95.98% 90.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.33% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.24% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.99% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.96% 89.34%
CHEMBL221 P23219 Cyclooxygenase-1 89.61% 90.17%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 88.91% 91.24%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 88.47% 96.90%
CHEMBL3401 O75469 Pregnane X receptor 87.93% 94.73%
CHEMBL255 P29275 Adenosine A2b receptor 87.44% 98.59%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.00% 97.29%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 86.24% 97.64%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 86.19% 96.47%
CHEMBL340 P08684 Cytochrome P450 3A4 85.94% 91.19%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.49% 94.33%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.88% 92.88%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 84.41% 98.75%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.07% 97.28%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 82.52% 95.71%
CHEMBL3310 Q96DB2 Histone deacetylase 11 82.50% 88.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.21% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.02% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.35% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.48% 86.33%

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 139584860
LOTUS LTS0031550
wikiData Q77377042