Nenestatin A

Details

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Internal ID da23ff89-c216-4cd3-a4ca-5780a969da03
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Aminosaccharides > Aminoglycosides
IUPAC Name 2-[(2S,4S,5R,6S)-4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H31NO8/c1-6-28(37-20-12-17(29(3)4)26(35-5)13(2)36-20)10-9-14-15(27(28)34)11-16-21(14)25(33)23-19(31)8-7-18(30)22(23)24(16)32/h7-11,13,17,20,26,30-31,34H,6,12H2,1-5H3/t13-,17-,20-,26-,28?/m0/s1
InChI Key UXGXZONKJVEYNM-SANFDALLSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C28H31NO8
Molecular Weight 509.50 g/mol
Exact Mass 509.20496695 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.34
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Nenestatin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9795 97.95%
Caco-2 - 0.7761 77.61%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.5820 58.20%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.8693 86.93%
OATP1B3 inhibitior + 0.9215 92.15%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8483 84.83%
P-glycoprotein inhibitior + 0.6201 62.01%
P-glycoprotein substrate + 0.6300 63.00%
CYP3A4 substrate + 0.6584 65.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8187 81.87%
CYP3A4 inhibition - 0.8235 82.35%
CYP2C9 inhibition - 0.7444 74.44%
CYP2C19 inhibition - 0.7281 72.81%
CYP2D6 inhibition - 0.8411 84.11%
CYP1A2 inhibition - 0.6427 64.27%
CYP2C8 inhibition - 0.7006 70.06%
CYP inhibitory promiscuity - 0.6001 60.01%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5102 51.02%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.8976 89.76%
Skin irritation - 0.7695 76.95%
Skin corrosion - 0.9297 92.97%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4020 40.20%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.6513 65.13%
skin sensitisation - 0.8481 84.81%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.9084 90.84%
Acute Oral Toxicity (c) III 0.4872 48.72%
Estrogen receptor binding + 0.8543 85.43%
Androgen receptor binding + 0.7104 71.04%
Thyroid receptor binding + 0.6809 68.09%
Glucocorticoid receptor binding + 0.8586 85.86%
Aromatase binding + 0.7455 74.55%
PPAR gamma + 0.7752 77.52%
Honey bee toxicity - 0.8023 80.23%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9722 97.22%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.95% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.14% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.08% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.80% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.29% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.25% 89.00%
CHEMBL4208 P20618 Proteasome component C5 88.14% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.12% 99.23%
CHEMBL2996 Q05655 Protein kinase C delta 88.12% 97.79%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.62% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.94% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 85.39% 94.73%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 85.26% 85.11%
CHEMBL226 P30542 Adenosine A1 receptor 85.20% 95.93%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.93% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.19% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.10% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.91% 90.71%

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 139590198
LOTUS LTS0169451
wikiData Q105280783