14-Hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one

Details

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Internal ID e6fd9a33-7afe-4db4-a918-9f01cead6ea1
Taxonomy Alkaloids and derivatives > Indolonaphthyridine alkaloids
IUPAC Name 14-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12N2O3/c1-20-11-4-2-8-9-6-7-16-10-3-5-12(18)17(13(9)10)14(8)15(11)19/h2,4,6-7,19H,3,5H2,1H3
InChI Key OCUZCJTWWISTKU-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12N2O3
Molecular Weight 268.27 g/mol
Exact Mass 268.08479225 g/mol
Topological Polar Surface Area (TPSA) 64.40 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.49
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 14-Hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.6992 69.92%
Blood Brain Barrier + 0.7817 78.17%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8753 87.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9610 96.10%
OATP1B3 inhibitior + 0.9503 95.03%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.6140 61.40%
BSEP inhibitior - 0.6580 65.80%
P-glycoprotein inhibitior - 0.9087 90.87%
P-glycoprotein substrate - 0.6874 68.74%
CYP3A4 substrate + 0.5543 55.43%
CYP2C9 substrate - 0.8210 82.10%
CYP2D6 substrate - 0.7932 79.32%
CYP3A4 inhibition - 0.7114 71.14%
CYP2C9 inhibition - 0.8157 81.57%
CYP2C19 inhibition - 0.5863 58.63%
CYP2D6 inhibition - 0.8062 80.62%
CYP1A2 inhibition + 0.8421 84.21%
CYP2C8 inhibition - 0.5720 57.20%
CYP inhibitory promiscuity + 0.6086 60.86%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5536 55.36%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.8839 88.39%
Skin irritation - 0.8300 83.00%
Skin corrosion - 0.9594 95.94%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6791 67.91%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.6461 64.61%
skin sensitisation - 0.9156 91.56%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6832 68.32%
Acute Oral Toxicity (c) III 0.6614 66.14%
Estrogen receptor binding + 0.7548 75.48%
Androgen receptor binding - 0.5814 58.14%
Thyroid receptor binding + 0.5818 58.18%
Glucocorticoid receptor binding + 0.9354 93.54%
Aromatase binding + 0.5317 53.17%
PPAR gamma + 0.7843 78.43%
Honey bee toxicity - 0.9538 95.38%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5649 56.49%
Fish aquatic toxicity - 0.8949 89.49%

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
CHEMBL1951 P21397 Monoamine oxidase A 98.33% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.82% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.35% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.22% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.08% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.24% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.26% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.78% 89.00%
CHEMBL2581 P07339 Cathepsin D 87.69% 98.95%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 87.63% 96.47%
CHEMBL2535 P11166 Glucose transporter 87.50% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.36% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.55% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.93% 99.23%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.54% 96.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.27% 96.67%

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.
Eurycoma longifolia

Cross-Links

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PubChem 162902789
LOTUS LTS0025654
wikiData Q105189611