11-Methoxysampangine

Details

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Internal ID 4d74df40-a6cd-49d3-99a8-f0c01e22e2d2
Taxonomy Alkaloids and derivatives > 1-azaoxoaporphines
IUPAC Name 3-methoxy-10,16-diazatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2(7),3,5,9,11,13(17),14-octaen-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H10N2O2/c1-20-11-4-2-3-10-13(11)14-12-9(5-7-17-14)6-8-18-15(12)16(10)19/h2-8H,1H3
InChI Key ZLDFQCLGYOKBIH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H10N2O2
Molecular Weight 262.26 g/mol
Exact Mass 262.074227566 g/mol
Topological Polar Surface Area (TPSA) 52.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.85
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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CHEBI:67603
CHEMBL1801765
Q27136073

2D Structure

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2D Structure of 11-Methoxysampangine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5194 51.94%
Blood Brain Barrier + 0.8379 83.79%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.8914 89.14%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.9634 96.34%
OATP1B3 inhibitior + 0.9773 97.73%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6526 65.26%
P-glycoprotein inhibitior - 0.7906 79.06%
P-glycoprotein substrate - 0.8235 82.35%
CYP3A4 substrate + 0.5408 54.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4887 48.87%
CYP3A4 inhibition - 0.5988 59.88%
CYP2C9 inhibition - 0.6699 66.99%
CYP2C19 inhibition + 0.7176 71.76%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition + 0.9537 95.37%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.6055 60.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6272 62.72%
Eye corrosion - 0.9922 99.22%
Eye irritation + 0.5598 55.98%
Skin irritation - 0.8347 83.47%
Skin corrosion - 0.9794 97.94%
Ames mutagenesis + 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6653 66.53%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.7407 74.07%
skin sensitisation - 0.9148 91.48%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.8530 85.30%
Acute Oral Toxicity (c) III 0.8371 83.71%
Estrogen receptor binding + 0.8852 88.52%
Androgen receptor binding + 0.7724 77.24%
Thyroid receptor binding + 0.7507 75.07%
Glucocorticoid receptor binding + 0.8761 87.61%
Aromatase binding + 0.9070 90.70%
PPAR gamma + 0.5599 55.99%
Honey bee toxicity - 0.8777 87.77%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity - 0.8062 80.62%

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
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 95.75% 94.03%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 95.25% 96.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.91% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.95% 86.33%
CHEMBL2581 P07339 Cathepsin D 93.34% 98.95%
CHEMBL2535 P11166 Glucose transporter 92.36% 98.75%
CHEMBL301 P24941 Cyclin-dependent kinase 2 92.10% 91.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.58% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 91.11% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.93% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.45% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.24% 96.09%
CHEMBL3116 P50750 Cyclin-dependent kinase 9 89.24% 96.31%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 88.73% 96.00%
CHEMBL5014 O43353 Serine/threonine-protein kinase RIPK2 88.30% 86.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.76% 95.56%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 86.48% 96.09%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 86.46% 96.47%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.91% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.41% 94.75%
CHEMBL1907 P15144 Aminopeptidase N 83.92% 93.31%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.88% 100.00%
CHEMBL5747 Q92793 CREB-binding protein 81.63% 95.12%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 81.60% 92.38%

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.
Ambavia gerrardii

Cross-Links

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PubChem 53262837
LOTUS LTS0214703
wikiData Q27136073