3-Methoxysampangine

Details

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Internal ID b4ea5f71-8fea-4778-8756-2949531f58aa
Taxonomy Alkaloids and derivatives > 1-azaoxoaporphines
IUPAC Name 14-methoxy-10,16-diazatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2,4,6,9,11,13(17),14-octaen-8-one
SMILES (Canonical) COC1=CN=C2C3=CC=CC=C3C(=O)C4=NC=CC1=C24
SMILES (Isomeric) COC1=CN=C2C3=CC=CC=C3C(=O)C4=NC=CC1=C24
InChI InChI=1S/C16H10N2O2/c1-20-12-8-18-14-9-4-2-3-5-10(9)16(19)15-13(14)11(12)6-7-17-15/h2-8H,1H3
InChI Key FBVVMYZYZXYLIA-UHFFFAOYSA-N
Popularity 3 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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128129-42-0
CHEMBL335181
SCHEMBL7804334
DTXSID70155819
FBVVMYZYZXYLIA-UHFFFAOYSA-N
7H-Naphtho(1,2,3-ij)(2,7)naphthyridin-7-one, 3-methoxy-
14-methoxy-10,16-diazatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2,4,6,9,11,13(17),14-octaen-8-one

2D Structure

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2D Structure of 3-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 + 0.7904 79.04%
Blood Brain Barrier + 0.8129 81.29%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8541 85.41%
OATP2B1 inhibitior - 0.8553 85.53%
OATP1B1 inhibitior + 0.9549 95.49%
OATP1B3 inhibitior + 0.9793 97.93%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6854 68.54%
P-glycoprotein inhibitior - 0.7547 75.47%
P-glycoprotein substrate - 0.8136 81.36%
CYP3A4 substrate + 0.5851 58.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4887 48.87%
CYP3A4 inhibition - 0.5051 50.51%
CYP2C9 inhibition - 0.6403 64.03%
CYP2C19 inhibition + 0.7201 72.01%
CYP2D6 inhibition - 0.9088 90.88%
CYP1A2 inhibition + 0.9530 95.30%
CYP2C8 inhibition + 0.5317 53.17%
CYP inhibitory promiscuity + 0.6549 65.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.6639 66.39%
Eye corrosion - 0.9911 99.11%
Eye irritation + 0.7089 70.89%
Skin irritation - 0.7983 79.83%
Skin corrosion - 0.9772 97.72%
Ames mutagenesis + 0.7236 72.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5988 59.88%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.6114 61.14%
skin sensitisation - 0.9165 91.65%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.5371 53.71%
Acute Oral Toxicity (c) III 0.8274 82.74%
Estrogen receptor binding + 0.9230 92.30%
Androgen receptor binding + 0.7157 71.57%
Thyroid receptor binding + 0.7969 79.69%
Glucocorticoid receptor binding + 0.9450 94.50%
Aromatase binding + 0.9485 94.85%
PPAR gamma + 0.6586 65.86%
Honey bee toxicity - 0.6786 67.86%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity - 0.8005 80.05%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.80% 94.00%
CHEMBL240 Q12809 HERG 93.75% 89.76%
CHEMBL2581 P07339 Cathepsin D 93.64% 98.95%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 93.33% 96.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.66% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.55% 96.09%
CHEMBL2535 P11166 Glucose transporter 91.94% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.70% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.33% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.01% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.87% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.60% 99.23%
CHEMBL255 P29275 Adenosine A2b receptor 87.35% 98.59%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 86.94% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 86.75% 93.31%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 84.10% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 83.71% 94.75%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.71% 94.03%
CHEMBL2094121 P14867 GABA-A receptor; alpha-1/beta-3/gamma-2 82.17% 95.50%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 81.42% 96.47%

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.
Cleistopholis patens
Duguetia hadrantha

Cross-Links

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PubChem 122683
LOTUS LTS0209756
wikiData Q83023797