6,8,14,15-Tetramethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one

Details

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Internal ID 769db332-a9ac-4975-8336-fa6f0338bfe3
Taxonomy Alkaloids and derivatives > Aristolactams
IUPAC Name 6,8,14,15-tetramethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one
SMILES (Canonical) COC1=CC=CC2=C1C(=C3C4=C2C(=C(C=C4C(=O)N3)OC)OC)OC
SMILES (Isomeric) COC1=CC=CC2=C1C(=C3C4=C2C(=C(C=C4C(=O)N3)OC)OC)OC
InChI InChI=1S/C19H17NO5/c1-22-11-7-5-6-9-13(11)18(25-4)16-14-10(19(21)20-16)8-12(23-2)17(24-3)15(9)14/h5-8H,1-4H3,(H,20,21)
InChI Key UGTKGINYNDOEMB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H17NO5
Molecular Weight 339.30 g/mol
Exact Mass 339.11067264 g/mol
Topological Polar Surface Area (TPSA) 66.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.59
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6,8,14,15-Tetramethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2(7),3,5,8,12,14-heptaen-11-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.8811 88.11%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.5464 54.64%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9398 93.98%
OATP1B3 inhibitior + 0.9593 95.93%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7978 79.78%
P-glycoprotein inhibitior - 0.5125 51.25%
P-glycoprotein substrate - 0.7195 71.95%
CYP3A4 substrate + 0.6244 62.44%
CYP2C9 substrate - 0.8100 81.00%
CYP2D6 substrate - 0.8274 82.74%
CYP3A4 inhibition + 0.6145 61.45%
CYP2C9 inhibition - 0.8390 83.90%
CYP2C19 inhibition - 0.8749 87.49%
CYP2D6 inhibition - 0.9624 96.24%
CYP1A2 inhibition + 0.9157 91.57%
CYP2C8 inhibition - 0.6052 60.52%
CYP inhibitory promiscuity + 0.8018 80.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5321 53.21%
Eye corrosion - 0.9922 99.22%
Eye irritation + 0.5280 52.80%
Skin irritation - 0.8712 87.12%
Skin corrosion - 0.9756 97.56%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3752 37.52%
Micronuclear + 0.7859 78.59%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.9463 94.63%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.6595 65.95%
Acute Oral Toxicity (c) III 0.4374 43.74%
Estrogen receptor binding + 0.8417 84.17%
Androgen receptor binding + 0.5837 58.37%
Thyroid receptor binding + 0.7649 76.49%
Glucocorticoid receptor binding + 0.8292 82.92%
Aromatase binding + 0.7224 72.24%
PPAR gamma + 0.6861 68.61%
Honey bee toxicity - 0.8318 83.18%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.7966 79.66%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.26% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.06% 91.11%
CHEMBL2535 P11166 Glucose transporter 95.99% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.58% 94.00%
CHEMBL4302 P08183 P-glycoprotein 1 92.75% 92.98%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.17% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 91.55% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.88% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.53% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.76% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.73% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 86.98% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.87% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.38% 96.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.23% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.11% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.04% 95.50%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.80% 94.03%
CHEMBL1255126 O15151 Protein Mdm4 81.62% 90.20%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 81.01% 92.38%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.93% 99.23%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.53% 96.67%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.36% 100.00%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 80.20% 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.
Aristolochia orbicularis

Cross-Links

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PubChem 163116513
LOTUS LTS0127814
wikiData Q103815906