[(2E,14R)-3,19-dimethoxy-17-oxo-16-azabicyclo[13.4.0]nonadeca-1(15),2,18-trien-14-yl] acetate

Details

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Internal ID fe7ce4db-07a3-4972-8abc-8dbf265f4674
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Alkyl aryl ethers
IUPAC Name [(2E,14R)-3,19-dimethoxy-17-oxo-16-azabicyclo[13.4.0]nonadeca-1(15),2,18-trien-14-yl] acetate
SMILES (Canonical) CC(=O)OC1CCCCCCCCCCC(=CC2=C1NC(=O)C=C2OC)OC
SMILES (Isomeric) CC(=O)O[C@@H]1CCCCCCCCCC/C(=C\C2=C1NC(=O)C=C2OC)/OC
InChI InChI=1S/C22H33NO5/c1-16(24)28-19-13-11-9-7-5-4-6-8-10-12-17(26-2)14-18-20(27-3)15-21(25)23-22(18)19/h14-15,19H,4-13H2,1-3H3,(H,23,25)/b17-14+/t19-/m1/s1
InChI Key CKRMHXONECUIGK-DQSGYLJSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H33NO5
Molecular Weight 391.50 g/mol
Exact Mass 391.23587315 g/mol
Topological Polar Surface Area (TPSA) 73.90 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.89
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2E,14R)-3,19-dimethoxy-17-oxo-16-azabicyclo[13.4.0]nonadeca-1(15),2,18-trien-14-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9713 97.13%
Caco-2 + 0.5377 53.77%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8058 80.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9033 90.33%
OATP1B3 inhibitior + 0.9304 93.04%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8072 80.72%
BSEP inhibitior + 0.9011 90.11%
P-glycoprotein inhibitior - 0.4530 45.30%
P-glycoprotein substrate - 0.5609 56.09%
CYP3A4 substrate + 0.5694 56.94%
CYP2C9 substrate - 0.7791 77.91%
CYP2D6 substrate - 0.8510 85.10%
CYP3A4 inhibition - 0.8911 89.11%
CYP2C9 inhibition - 0.8392 83.92%
CYP2C19 inhibition - 0.5498 54.98%
CYP2D6 inhibition - 0.9273 92.73%
CYP1A2 inhibition + 0.5296 52.96%
CYP2C8 inhibition - 0.6343 63.43%
CYP inhibitory promiscuity - 0.7844 78.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9425 94.25%
Carcinogenicity (trinary) Non-required 0.6952 69.52%
Eye corrosion - 0.9872 98.72%
Eye irritation - 0.9092 90.92%
Skin irritation - 0.8069 80.69%
Skin corrosion - 0.9555 95.55%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8797 87.97%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8821 88.21%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8425 84.25%
Acute Oral Toxicity (c) III 0.5903 59.03%
Estrogen receptor binding + 0.6084 60.84%
Androgen receptor binding + 0.6722 67.22%
Thyroid receptor binding + 0.5256 52.56%
Glucocorticoid receptor binding + 0.7261 72.61%
Aromatase binding - 0.6281 62.81%
PPAR gamma + 0.5413 54.13%
Honey bee toxicity - 0.8933 89.33%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8190 81.90%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.09% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.41% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.43% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.15% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.30% 85.14%
CHEMBL2535 P11166 Glucose transporter 92.18% 98.75%
CHEMBL340 P08684 Cytochrome P450 3A4 90.56% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.13% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.41% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.21% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.55% 95.56%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 85.85% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.19% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.06% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.62% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.38% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.77% 97.09%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 82.52% 94.78%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.80% 89.50%
CHEMBL5255 O00206 Toll-like receptor 4 81.50% 92.50%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.86% 94.80%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.68% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.62% 82.69%

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.
Lysimachia patungensis

Cross-Links

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PubChem 163188880
LOTUS LTS0259294
wikiData Q104962701