(1S,13R,16S,18S)-18-methoxy-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9-trien-11-one

Details

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Internal ID 81023943-26e0-46af-9dc5-3db140871d37
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (1S,13R,16S,18S)-18-methoxy-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9-trien-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H19NO5/c1-20-9-2-3-17-11-6-13-12(21-8-22-13)5-10(11)16(19)23-15(17)7-18-14(17)4-9/h5-6,9,14-15,18H,2-4,7-8H2,1H3/t9-,14-,15-,17-/m0/s1
InChI Key BNNZKHPAYFIGHL-CHKZYTGQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H19NO5
Molecular Weight 317.34 g/mol
Exact Mass 317.12632271 g/mol
Topological Polar Surface Area (TPSA) 66.00 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.36
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 (1S,13R,16S,18S)-18-methoxy-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9-trien-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 + 0.9864 98.64%
Caco-2 + 0.7009 70.09%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.5102 51.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9147 91.47%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.6901 69.01%
P-glycoprotein inhibitior - 0.8452 84.52%
P-glycoprotein substrate - 0.6768 67.68%
CYP3A4 substrate + 0.6268 62.68%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.7189 71.89%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.8944 89.44%
CYP2C19 inhibition - 0.6032 60.32%
CYP2D6 inhibition - 0.5080 50.80%
CYP1A2 inhibition - 0.6985 69.85%
CYP2C8 inhibition - 0.6964 69.64%
CYP inhibitory promiscuity - 0.5808 58.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6008 60.08%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9322 93.22%
Skin irritation - 0.7475 74.75%
Skin corrosion - 0.9312 93.12%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7349 73.49%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.5055 50.55%
skin sensitisation - 0.7976 79.76%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.6034 60.34%
Acute Oral Toxicity (c) III 0.5432 54.32%
Estrogen receptor binding + 0.7508 75.08%
Androgen receptor binding + 0.5554 55.54%
Thyroid receptor binding + 0.6419 64.19%
Glucocorticoid receptor binding + 0.7429 74.29%
Aromatase binding + 0.5424 54.24%
PPAR gamma + 0.7007 70.07%
Honey bee toxicity - 0.7760 77.60%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity - 0.6005 60.05%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.53% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.81% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.54% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.45% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 94.33% 94.80%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 91.88% 80.96%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.67% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.46% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.99% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.48% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.86% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.60% 99.23%
CHEMBL2581 P07339 Cathepsin D 88.53% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 88.13% 94.75%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.05% 96.21%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.90% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.66% 82.69%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.64% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.01% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.40% 97.14%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.41% 93.40%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.23% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.08% 89.00%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 82.62% 88.84%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.00% 93.04%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 81.43% 96.09%

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.
Ungernia spiralis

Cross-Links

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PubChem 163032174
LOTUS LTS0206141
wikiData Q104938933