18-Methoxy-6,14,22-triazapentacyclo[12.8.0.02,6.08,13.016,21]docosa-1(22),8,10,12,16(21),17,19-heptaene-7,15-dione

Details

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Internal ID 2af1eaa0-c659-4353-bdf7-d0fd4288efe5
Taxonomy Organoheterocyclic compounds > Pyrimidodiazepines
IUPAC Name 18-methoxy-6,14,22-triazapentacyclo[12.8.0.02,6.08,13.016,21]docosa-1(22),8,10,12,16(21),17,19-heptaene-7,15-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H17N3O3/c1-26-12-8-9-15-14(11-12)20(25)23-16-6-3-2-5-13(16)19(24)22-10-4-7-17(22)18(23)21-15/h2-3,5-6,8-9,11,17H,4,7,10H2,1H3
InChI Key MLEAYJRUKNTODR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H17N3O3
Molecular Weight 347.40 g/mol
Exact Mass 347.12699141 g/mol
Topological Polar Surface Area (TPSA) 62.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 18-Methoxy-6,14,22-triazapentacyclo[12.8.0.02,6.08,13.016,21]docosa-1(22),8,10,12,16(21),17,19-heptaene-7,15-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.7903 79.03%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8378 83.78%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.8694 86.94%
OATP1B3 inhibitior + 0.9465 94.65%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.5072 50.72%
BSEP inhibitior + 0.7811 78.11%
P-glycoprotein inhibitior + 0.7533 75.33%
P-glycoprotein substrate + 0.5166 51.66%
CYP3A4 substrate + 0.6579 65.79%
CYP2C9 substrate - 0.5816 58.16%
CYP2D6 substrate - 0.8397 83.97%
CYP3A4 inhibition - 0.7115 71.15%
CYP2C9 inhibition - 0.6366 63.66%
CYP2C19 inhibition - 0.5863 58.63%
CYP2D6 inhibition - 0.8928 89.28%
CYP1A2 inhibition + 0.7089 70.89%
CYP2C8 inhibition - 0.5916 59.16%
CYP inhibitory promiscuity + 0.5593 55.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6134 61.34%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9905 99.05%
Skin irritation - 0.8384 83.84%
Skin corrosion - 0.9581 95.81%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6470 64.70%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.6086 60.86%
skin sensitisation - 0.9188 91.88%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.5666 56.66%
Acute Oral Toxicity (c) III 0.6236 62.36%
Estrogen receptor binding + 0.7221 72.21%
Androgen receptor binding + 0.7066 70.66%
Thyroid receptor binding + 0.6760 67.60%
Glucocorticoid receptor binding + 0.8432 84.32%
Aromatase binding + 0.6022 60.22%
PPAR gamma - 0.5712 57.12%
Honey bee toxicity - 0.9230 92.30%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity - 0.4269 42.69%

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 99.16% 91.49%
CHEMBL2581 P07339 Cathepsin D 98.44% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.86% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.61% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.69% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.77% 96.09%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 94.55% 92.67%
CHEMBL1907 P15144 Aminopeptidase N 93.65% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.88% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.25% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.10% 99.15%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 90.36% 98.46%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.24% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.82% 95.89%
CHEMBL2535 P11166 Glucose transporter 89.57% 98.75%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 87.25% 91.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.03% 97.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.57% 93.40%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.06% 99.18%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.90% 96.67%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.07% 82.69%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 82.87% 80.78%
CHEMBL204 P00734 Thrombin 81.74% 96.01%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.01% 97.36%
CHEMBL3438 Q05513 Protein kinase C zeta 81.00% 88.48%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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Cross-Links

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PubChem 11336956
LOTUS LTS0151872
wikiData Q104171791