Sinomenine N-oxide

Details

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Internal ID 995d0c08-fe78-4a5f-8fe5-7292860e050e
Taxonomy Alkaloids and derivatives > Morphinans
IUPAC Name (1R,9S,10S)-3-hydroxy-4,12-dimethoxy-17-methyl-17-oxido-17-azoniatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5,11-tetraen-13-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H23NO5/c1-20(23)7-6-19-10-14(21)16(25-3)9-12(19)13(20)8-11-4-5-15(24-2)18(22)17(11)19/h4-5,9,12-13,22H,6-8,10H2,1-3H3/t12-,13+,19-,20?/m1/s1
InChI Key IQCNMIIBBLJCAC-SLAUIZBQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H23NO5
Molecular Weight 345.40 g/mol
Exact Mass 345.15762283 g/mol
Topological Polar Surface Area (TPSA) 73.80 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.03
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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1000026-77-6
(+)-SINOMENINE N-OXIDE
HY-151241
CS-0610728
E87207

2D Structure

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2D Structure of Sinomenine N-oxide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5760 57.60%
Caco-2 + 0.7317 73.17%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4648 46.48%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.9174 91.74%
OATP1B3 inhibitior + 0.9378 93.78%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.5366 53.66%
P-glycoprotein inhibitior - 0.7567 75.67%
P-glycoprotein substrate - 0.6005 60.05%
CYP3A4 substrate + 0.6520 65.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8271 82.71%
CYP3A4 inhibition - 0.6958 69.58%
CYP2C9 inhibition - 0.8320 83.20%
CYP2C19 inhibition - 0.7999 79.99%
CYP2D6 inhibition - 0.6939 69.39%
CYP1A2 inhibition - 0.7918 79.18%
CYP2C8 inhibition - 0.6134 61.34%
CYP inhibitory promiscuity - 0.9461 94.61%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8115 81.15%
Carcinogenicity (trinary) Non-required 0.5733 57.33%
Eye corrosion - 0.9837 98.37%
Eye irritation - 0.9376 93.76%
Skin irritation - 0.7577 75.77%
Skin corrosion - 0.9261 92.61%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5332 53.32%
Micronuclear - 0.6000 60.00%
Hepatotoxicity - 0.6226 62.26%
skin sensitisation - 0.8384 83.84%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.7286 72.86%
Acute Oral Toxicity (c) III 0.6722 67.22%
Estrogen receptor binding + 0.6193 61.93%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.6002 60.02%
Glucocorticoid receptor binding + 0.7756 77.56%
Aromatase binding + 0.5322 53.22%
PPAR gamma + 0.5419 54.19%
Honey bee toxicity - 0.8271 82.71%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9362 93.62%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.07% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.50% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.30% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 93.77% 95.89%
CHEMBL1951 P21397 Monoamine oxidase A 93.47% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.89% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.99% 93.99%
CHEMBL2535 P11166 Glucose transporter 90.59% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.43% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.72% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.55% 99.23%
CHEMBL2581 P07339 Cathepsin D 83.35% 98.95%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 83.12% 98.00%
CHEMBL1902 P62942 FK506-binding protein 1A 82.53% 97.05%
CHEMBL1937 Q92769 Histone deacetylase 2 82.47% 94.75%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.09% 93.03%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.67% 90.71%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.49% 92.94%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Sinomenium acutum

Cross-Links

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PubChem 11175374
LOTUS LTS0010644
wikiData Q105117697