8-Oxocanadine

Details

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Internal ID d5542979-87e2-4b06-b6b5-06ee8f72ed8a
Taxonomy Alkaloids and derivatives > Protoberberine alkaloids and derivatives
IUPAC Name 16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-14-one
SMILES (Canonical) COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2=O)OCO5)C=C1)OC
SMILES (Isomeric) COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2=O)OCO5)C=C1)OC
InChI InChI=1S/C20H19NO5/c1-23-15-4-3-12-7-14-13-9-17-16(25-10-26-17)8-11(13)5-6-21(14)20(22)18(12)19(15)24-2/h3-4,8-9,14H,5-7,10H2,1-2H3
InChI Key DESORMZUMYIKSG-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H19NO5
Molecular Weight 353.40 g/mol
Exact Mass 353.12632271 g/mol
Topological Polar Surface Area (TPSA) 57.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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CHEMBL518062
O-Methyl-8-oxotetrahydrothalifendine

2D Structure

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2D Structure of 8-Oxocanadine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9576 95.76%
Caco-2 + 0.8509 85.09%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6152 61.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9308 93.08%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.8506 85.06%
P-glycoprotein inhibitior + 0.5741 57.41%
P-glycoprotein substrate - 0.8230 82.30%
CYP3A4 substrate + 0.6100 61.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8044 80.44%
CYP3A4 inhibition + 0.7508 75.08%
CYP2C9 inhibition - 0.7376 73.76%
CYP2C19 inhibition + 0.7530 75.30%
CYP2D6 inhibition + 0.5000 50.00%
CYP1A2 inhibition + 0.7074 70.74%
CYP2C8 inhibition - 0.7776 77.76%
CYP inhibitory promiscuity + 0.7686 76.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5890 58.90%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.9503 95.03%
Skin irritation - 0.8134 81.34%
Skin corrosion - 0.9527 95.27%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3813 38.13%
Micronuclear + 0.6500 65.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.8643 86.43%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.5483 54.83%
Acute Oral Toxicity (c) III 0.7026 70.26%
Estrogen receptor binding + 0.8628 86.28%
Androgen receptor binding + 0.5529 55.29%
Thyroid receptor binding + 0.5445 54.45%
Glucocorticoid receptor binding + 0.8683 86.83%
Aromatase binding - 0.7372 73.72%
PPAR gamma + 0.5445 54.45%
Honey bee toxicity - 0.8546 85.46%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.8346 83.46%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.47% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.17% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.78% 96.77%
CHEMBL4040 P28482 MAP kinase ERK2 96.27% 83.82%
CHEMBL2581 P07339 Cathepsin D 96.01% 98.95%
CHEMBL261 P00915 Carbonic anhydrase I 95.47% 96.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.58% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.95% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.91% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 93.63% 93.40%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.19% 85.14%
CHEMBL1902 P62942 FK506-binding protein 1A 90.57% 97.05%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 90.50% 96.86%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.27% 93.99%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 89.50% 82.67%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 88.75% 82.38%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.01% 92.62%
CHEMBL2056 P21728 Dopamine D1 receptor 86.85% 91.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.73% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.44% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.22% 89.00%
CHEMBL217 P14416 Dopamine D2 receptor 85.84% 95.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.84% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.50% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.28% 89.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.12% 100.00%
CHEMBL4208 P20618 Proteasome component C5 81.90% 90.00%
CHEMBL2535 P11166 Glucose transporter 81.80% 98.75%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.27% 95.78%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 81.09% 90.95%
CHEMBL1951 P21397 Monoamine oxidase A 80.29% 91.49%

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.
Coscinium fenestratum
Hydrastis canadensis
Pericampylus glaucus

Cross-Links

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PubChem 470418
LOTUS LTS0242598
wikiData Q104399897