(1R,9S,10S,12R)-4,5,12-trimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6-trien-13-one

Details

Top
Internal ID a2d56817-e16f-43e9-9312-efdcf509cc02
Taxonomy Alkaloids and derivatives > Morphinans
IUPAC Name (1R,9S,10S,12R)-4,5,12-trimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6-trien-13-one
SMILES (Canonical) CN1CCC23CC(=O)C(CC2C1CC4=CC(=C(C=C34)OC)OC)OC
SMILES (Isomeric) CN1CC[C@@]23CC(=O)[C@@H](C[C@@H]2[C@@H]1CC4=CC(=C(C=C34)OC)OC)OC
InChI InChI=1S/C20H27NO4/c1-21-6-5-20-11-16(22)17(23-2)10-14(20)15(21)7-12-8-18(24-3)19(25-4)9-13(12)20/h8-9,14-15,17H,5-7,10-11H2,1-4H3/t14-,15+,17-,20+/m1/s1
InChI Key KDFCXHYXRVENIS-MJEZEWASSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H27NO4
Molecular Weight 345.40 g/mol
Exact Mass 345.19400834 g/mol
Topological Polar Surface Area (TPSA) 48.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (1R,9S,10S,12R)-4,5,12-trimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6-trien-13-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9701 97.01%
Caco-2 + 0.9100 91.00%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5604 56.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8165 81.65%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.7023 70.23%
P-glycoprotein inhibitior - 0.7822 78.22%
P-glycoprotein substrate + 0.7159 71.59%
CYP3A4 substrate + 0.7183 71.83%
CYP2C9 substrate - 0.8144 81.44%
CYP2D6 substrate + 0.6473 64.73%
CYP3A4 inhibition - 0.5976 59.76%
CYP2C9 inhibition - 0.9166 91.66%
CYP2C19 inhibition - 0.9189 91.89%
CYP2D6 inhibition + 0.6367 63.67%
CYP1A2 inhibition - 0.8324 83.24%
CYP2C8 inhibition - 0.9217 92.17%
CYP inhibitory promiscuity - 0.9411 94.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6588 65.88%
Eye corrosion - 0.9931 99.31%
Eye irritation - 0.9604 96.04%
Skin irritation - 0.7768 77.68%
Skin corrosion - 0.9420 94.20%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6990 69.90%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.8822 88.22%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.6789 67.89%
Acute Oral Toxicity (c) III 0.6913 69.13%
Estrogen receptor binding + 0.5841 58.41%
Androgen receptor binding + 0.6014 60.14%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7083 70.83%
Aromatase binding - 0.6020 60.20%
PPAR gamma - 0.7243 72.43%
Honey bee toxicity - 0.6698 66.98%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.7900 79.00%
Fish aquatic toxicity + 0.8030 80.30%

Targets

Top

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 98.47% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.77% 95.56%
CHEMBL217 P14416 Dopamine D2 receptor 91.56% 95.62%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.53% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.97% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.33% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.28% 86.33%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 89.19% 93.40%
CHEMBL233 P35372 Mu opioid receptor 88.47% 97.93%
CHEMBL4208 P20618 Proteasome component C5 88.47% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.33% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.64% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.89% 95.89%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 86.74% 91.03%
CHEMBL2413 P32246 C-C chemokine receptor type 1 86.31% 89.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.86% 97.14%
CHEMBL236 P41143 Delta opioid receptor 84.76% 99.35%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.06% 90.71%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.13% 95.89%
CHEMBL1902 P62942 FK506-binding protein 1A 82.98% 97.05%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.96% 93.04%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.95% 99.18%
CHEMBL2581 P07339 Cathepsin D 82.69% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.29% 93.99%
CHEMBL2535 P11166 Glucose transporter 80.33% 98.75%

Plants that contains it

Top
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.
Stephania zippeliana

Cross-Links

Top
PubChem 163019760
LOTUS LTS0248715
wikiData Q105139124