8-(3-Amino-4,5-dihydroxyoxan-2-yl)oxy-7-hydroxy-7,19-dimethyl-1-azacycloicosa-3,5,9,11,13,15,17-heptaen-2-one

Details

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Internal ID a641f20e-5250-495e-a110-5920332e9710
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name 8-(3-amino-4,5-dihydroxyoxan-2-yl)oxy-7-hydroxy-7,19-dimethyl-1-azacycloicosa-3,5,9,11,13,15,17-heptaen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H36N2O6/c1-19-13-9-7-5-3-4-6-8-10-14-21(34-25-23(27)24(31)20(29)18-33-25)26(2,32)16-12-11-15-22(30)28-17-19/h3-16,19-21,23-25,29,31-32H,17-18,27H2,1-2H3,(H,28,30)
InChI Key QAYDTFSWPPJOQZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H36N2O6
Molecular Weight 472.60 g/mol
Exact Mass 472.25733687 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.19
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-(3-Amino-4,5-dihydroxyoxan-2-yl)oxy-7-hydroxy-7,19-dimethyl-1-azacycloicosa-3,5,9,11,13,15,17-heptaen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9109 91.09%
Caco-2 - 0.8081 80.81%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.5095 50.95%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.8950 89.50%
OATP1B3 inhibitior + 0.9483 94.83%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6700 67.00%
P-glycoprotein inhibitior - 0.5147 51.47%
P-glycoprotein substrate + 0.5633 56.33%
CYP3A4 substrate + 0.6538 65.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8756 87.56%
CYP3A4 inhibition - 0.9919 99.19%
CYP2C9 inhibition - 0.9340 93.40%
CYP2C19 inhibition - 0.9154 91.54%
CYP2D6 inhibition - 0.9243 92.43%
CYP1A2 inhibition - 0.9293 92.93%
CYP2C8 inhibition - 0.5781 57.81%
CYP inhibitory promiscuity - 0.9755 97.55%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6404 64.04%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9770 97.70%
Skin irritation - 0.7866 78.66%
Skin corrosion - 0.9354 93.54%
Ames mutagenesis - 0.5454 54.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6619 66.19%
Micronuclear + 0.7400 74.00%
Hepatotoxicity - 0.5730 57.30%
skin sensitisation - 0.8351 83.51%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.8218 82.18%
Acute Oral Toxicity (c) III 0.6330 63.30%
Estrogen receptor binding + 0.6697 66.97%
Androgen receptor binding - 0.5312 53.12%
Thyroid receptor binding + 0.5854 58.54%
Glucocorticoid receptor binding + 0.6813 68.13%
Aromatase binding + 0.5833 58.33%
PPAR gamma + 0.6445 64.45%
Honey bee toxicity - 0.7107 71.07%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5250 52.50%
Fish aquatic toxicity - 0.9343 93.43%

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 99.18% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.93% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.78% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.17% 97.25%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.36% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.62% 97.09%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 91.86% 92.88%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.23% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.01% 100.00%
CHEMBL2581 P07339 Cathepsin D 87.26% 98.95%
CHEMBL4208 P20618 Proteasome component C5 86.45% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.85% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.07% 94.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.87% 91.07%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.86% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 84.57% 95.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.56% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.71% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.96% 90.71%
CHEMBL1951 P21397 Monoamine oxidase A 80.91% 91.49%

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 75984733
LOTUS LTS0096657
wikiData Q104195643