20-Hydroxy-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 e2369894-df3f-496c-aa2d-de76a9bf0ff8
Taxonomy Organoheterocyclic compounds > Pyrimidodiazepines
IUPAC Name 20-hydroxy-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/C20H17N3O4/c1-27-11-9-13-17(16(24)10-11)21-18-15-7-4-8-22(15)19(25)12-5-2-3-6-14(12)23(18)20(13)26/h2-3,5-6,9-10,15,24H,4,7-8H2,1H3
InChI Key JIIDXCQQSWFYCR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H17N3O4
Molecular Weight 363.40 g/mol
Exact Mass 363.12190603 g/mol
Topological Polar Surface Area (TPSA) 82.40 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.39
H-Bond Acceptor 6
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 20-Hydroxy-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 + 0.9821 98.21%
Caco-2 + 0.5837 58.37%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7886 78.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8917 89.17%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.6400 64.00%
OCT2 inhibitior - 0.6390 63.90%
BSEP inhibitior + 0.6087 60.87%
P-glycoprotein inhibitior + 0.5713 57.13%
P-glycoprotein substrate + 0.5384 53.84%
CYP3A4 substrate + 0.6600 66.00%
CYP2C9 substrate + 0.5992 59.92%
CYP2D6 substrate - 0.8391 83.91%
CYP3A4 inhibition - 0.8329 83.29%
CYP2C9 inhibition - 0.8279 82.79%
CYP2C19 inhibition - 0.8081 80.81%
CYP2D6 inhibition - 0.9192 91.92%
CYP1A2 inhibition - 0.5853 58.53%
CYP2C8 inhibition - 0.5657 56.57%
CYP inhibitory promiscuity - 0.7413 74.13%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6499 64.99%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9768 97.68%
Skin irritation - 0.8293 82.93%
Skin corrosion - 0.9549 95.49%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7272 72.72%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.6070 60.70%
skin sensitisation - 0.9163 91.63%
Respiratory toxicity + 0.9111 91.11%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.6432 64.32%
Acute Oral Toxicity (c) III 0.7149 71.49%
Estrogen receptor binding + 0.5947 59.47%
Androgen receptor binding + 0.7245 72.45%
Thyroid receptor binding + 0.6292 62.92%
Glucocorticoid receptor binding + 0.8177 81.77%
Aromatase binding - 0.5486 54.86%
PPAR gamma + 0.5843 58.43%
Honey bee toxicity - 0.9169 91.69%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.5490 54.90%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.55% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 99.38% 91.49%
CHEMBL2581 P07339 Cathepsin D 98.09% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.05% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.92% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 95.91% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.90% 99.15%
CHEMBL2535 P11166 Glucose transporter 92.75% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.11% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.93% 86.33%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.34% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.82% 91.11%
CHEMBL204 P00734 Thrombin 90.60% 96.01%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 90.51% 92.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.27% 95.89%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 87.17% 98.46%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.63% 97.09%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.99% 93.65%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.94% 99.18%
CHEMBL3438 Q05513 Protein kinase C zeta 83.82% 88.48%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.37% 96.67%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.77% 80.78%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.69% 93.03%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.19% 99.17%

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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There are no matching plants.

Cross-Links

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PubChem 21588225
LOTUS LTS0106490
wikiData Q104169570