12,12,16-Trimethyl-10,19,21-triazahexacyclo[13.5.2.01,13.03,11.04,9.015,19]docosa-3(11),4,6,8-tetraen-22-one

Details

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Internal ID bfd8fb6a-749e-4fb2-8e19-6367a7a104ca
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Pyrroloquinolines
IUPAC Name 12,12,16-trimethyl-10,19,21-triazahexacyclo[13.5.2.01,13.03,11.04,9.015,19]docosa-3(11),4,6,8-tetraen-22-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H27N3O/c1-13-8-9-25-12-21-10-15-14-6-4-5-7-16(14)23-18(15)20(2,3)17(21)11-22(13,25)19(26)24-21/h4-7,13,17,23H,8-12H2,1-3H3,(H,24,26)
InChI Key FBXHMCWNISYEEV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H27N3O
Molecular Weight 349.50 g/mol
Exact Mass 349.215412493 g/mol
Topological Polar Surface Area (TPSA) 48.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 12,12,16-Trimethyl-10,19,21-triazahexacyclo[13.5.2.01,13.03,11.04,9.015,19]docosa-3(11),4,6,8-tetraen-22-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 + 0.5844 58.44%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.5987 59.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8993 89.93%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.6479 64.79%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.6881 68.81%
P-glycoprotein inhibitior - 0.6383 63.83%
P-glycoprotein substrate + 0.5454 54.54%
CYP3A4 substrate + 0.6604 66.04%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate + 0.3571 35.71%
CYP3A4 inhibition - 0.6444 64.44%
CYP2C9 inhibition - 0.7705 77.05%
CYP2C19 inhibition - 0.6932 69.32%
CYP2D6 inhibition + 0.5469 54.69%
CYP1A2 inhibition - 0.7302 73.02%
CYP2C8 inhibition - 0.6846 68.46%
CYP inhibitory promiscuity - 0.6747 67.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6972 69.72%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9943 99.43%
Skin irritation - 0.7736 77.36%
Skin corrosion - 0.9106 91.06%
Ames mutagenesis - 0.5837 58.37%
Human Ether-a-go-go-Related Gene inhibition + 0.9012 90.12%
Micronuclear + 0.5200 52.00%
Hepatotoxicity - 0.5102 51.02%
skin sensitisation - 0.8669 86.69%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.5302 53.02%
Acute Oral Toxicity (c) III 0.5955 59.55%
Estrogen receptor binding + 0.7933 79.33%
Androgen receptor binding + 0.6803 68.03%
Thyroid receptor binding + 0.6398 63.98%
Glucocorticoid receptor binding - 0.5603 56.03%
Aromatase binding + 0.7421 74.21%
PPAR gamma + 0.5312 53.12%
Honey bee toxicity - 0.8448 84.48%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.8609 86.09%

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
CHEMBL2581 P07339 Cathepsin D 96.86% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.25% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.05% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.18% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.06% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.17% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.65% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.10% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.53% 89.00%
CHEMBL3310 Q96DB2 Histone deacetylase 11 88.54% 88.56%
CHEMBL1937 Q92769 Histone deacetylase 2 88.16% 94.75%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 87.13% 90.71%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.42% 93.40%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.41% 97.25%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.08% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 85.55% 90.17%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 83.91% 94.78%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 83.00% 97.64%
CHEMBL4523377 Q86WV6 Stimulator of interferon genes protein 82.60% 95.48%
CHEMBL2535 P11166 Glucose transporter 82.33% 98.75%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.18% 90.08%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 80.90% 94.23%
CHEMBL255 P29275 Adenosine A2b receptor 80.88% 98.59%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.73% 93.99%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.16% 82.69%

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 73112083
LOTUS LTS0234871
wikiData Q104992999