Gaudimycin E

Details

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Internal ID 078d23ae-e780-4d32-aec2-92d052e254e6
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Aminosaccharides > Aminoglycosides
IUPAC Name (3S)-3-[(2S,5S,6R)-5-amino-6-methyloxan-2-yl]oxy-4-[6-[(2S,5S,6S)-5-[(2S,4R,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]-1,5-dihydroxy-9,10-dioxoanthracen-2-yl]-3-methylbutanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H47NO13/c1-16-23(38)9-12-28(48-16)51-37(4,15-27(40)41)14-19-5-6-21-30(33(19)43)35(45)22-8-7-20(34(44)31(22)36(21)46)26-11-10-25(17(2)47-26)50-29-13-24(39)32(42)18(3)49-29/h5-8,16-18,23-26,28-29,32,39,42-44H,9-15,38H2,1-4H3,(H,40,41)/t16-,17+,18-,23+,24-,25+,26+,28+,29+,32-,37+/m1/s1
InChI Key WMKVBRKZBMTQSW-UKINCDMNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C37H47NO13
Molecular Weight 713.80 g/mol
Exact Mass 713.30474055 g/mol
Topological Polar Surface Area (TPSA) 225.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 3.00
H-Bond Acceptor 13
H-Bond Donor 6
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Gaudimycin E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7134 71.34%
Caco-2 - 0.8677 86.77%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Nucleus 0.5975 59.75%
OATP2B1 inhibitior - 0.7151 71.51%
OATP1B1 inhibitior + 0.8603 86.03%
OATP1B3 inhibitior + 0.8960 89.60%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8037 80.37%
BSEP inhibitior + 0.9798 97.98%
P-glycoprotein inhibitior + 0.7070 70.70%
P-glycoprotein substrate + 0.7353 73.53%
CYP3A4 substrate + 0.7045 70.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8590 85.90%
CYP3A4 inhibition - 0.9117 91.17%
CYP2C9 inhibition - 0.9095 90.95%
CYP2C19 inhibition - 0.8921 89.21%
CYP2D6 inhibition - 0.9308 93.08%
CYP1A2 inhibition - 0.6445 64.45%
CYP2C8 inhibition + 0.6149 61.49%
CYP inhibitory promiscuity - 0.8917 89.17%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5843 58.43%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9181 91.81%
Skin irritation - 0.7748 77.48%
Skin corrosion - 0.9219 92.19%
Ames mutagenesis + 0.5246 52.46%
Human Ether-a-go-go-Related Gene inhibition + 0.7046 70.46%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.5830 58.30%
skin sensitisation - 0.8814 88.14%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.9069 90.69%
Acute Oral Toxicity (c) II 0.3382 33.82%
Estrogen receptor binding + 0.8657 86.57%
Androgen receptor binding + 0.7177 71.77%
Thyroid receptor binding + 0.5389 53.89%
Glucocorticoid receptor binding + 0.7693 76.93%
Aromatase binding + 0.7618 76.18%
PPAR gamma + 0.7459 74.59%
Honey bee toxicity - 0.7700 77.00%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9442 94.42%

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 99.50% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.88% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 98.69% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.23% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.73% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 95.72% 95.93%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.10% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.84% 85.14%
CHEMBL284 P27487 Dipeptidyl peptidase IV 92.54% 95.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.36% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.03% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.47% 97.25%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 87.02% 97.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.50% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.22% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.11% 96.00%
CHEMBL4040 P28482 MAP kinase ERK2 82.87% 83.82%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.85% 92.88%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.69% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 81.48% 94.73%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 80.95% 90.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.80% 99.17%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.51% 96.38%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.47% 99.15%

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 139588790
LOTUS LTS0190088
wikiData Q105308641