17-Methoxy-5,7,19,21-tetraoxa-13-azahexacyclo[10.10.1.02,10.04,8.016,23.018,22]tricosa-1(22),2,4(8),9,16(23),17-hexaene

Details

Top
Internal ID 708251b4-a0de-4b5d-bddb-cc931931e947
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 17-methoxy-5,7,19,21-tetraoxa-13-azahexacyclo[10.10.1.02,10.04,8.016,23.018,22]tricosa-1(22),2,4(8),9,16(23),17-hexaene
SMILES (Canonical) COC1=C2C(=C3C4=CC5=C(C=C4CC6C3=C1CCN6)OCO5)OCO2
SMILES (Isomeric) COC1=C2C(=C3C4=CC5=C(C=C4CC6C3=C1CCN6)OCO5)OCO2
InChI InChI=1S/C19H17NO5/c1-21-17-10-2-3-20-12-4-9-5-13-14(23-7-22-13)6-11(9)16(15(10)12)18-19(17)25-8-24-18/h5-6,12,20H,2-4,7-8H2,1H3
InChI Key BLQMKAOCFLGRCD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C19H17NO5
Molecular Weight 339.30 g/mol
Exact Mass 339.11067264 g/mol
Topological Polar Surface Area (TPSA) 58.20 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.56
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 17-Methoxy-5,7,19,21-tetraoxa-13-azahexacyclo[10.10.1.02,10.04,8.016,23.018,22]tricosa-1(22),2,4(8),9,16(23),17-hexaene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9804 98.04%
Caco-2 + 0.8626 86.26%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.4525 45.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9163 91.63%
OATP1B3 inhibitior + 0.9508 95.08%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.7197 71.97%
P-glycoprotein inhibitior - 0.6469 64.69%
P-glycoprotein substrate - 0.7445 74.45%
CYP3A4 substrate + 0.5684 56.84%
CYP2C9 substrate - 0.8281 82.81%
CYP2D6 substrate + 0.6636 66.36%
CYP3A4 inhibition + 0.6528 65.28%
CYP2C9 inhibition - 0.7785 77.85%
CYP2C19 inhibition - 0.5717 57.17%
CYP2D6 inhibition + 0.6710 67.10%
CYP1A2 inhibition + 0.7957 79.57%
CYP2C8 inhibition - 0.6688 66.88%
CYP inhibitory promiscuity + 0.7380 73.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5967 59.67%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.9090 90.90%
Skin irritation - 0.7206 72.06%
Skin corrosion - 0.9366 93.66%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7865 78.65%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8183 81.83%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.5532 55.32%
Acute Oral Toxicity (c) III 0.5237 52.37%
Estrogen receptor binding + 0.7786 77.86%
Androgen receptor binding + 0.5198 51.98%
Thyroid receptor binding + 0.7837 78.37%
Glucocorticoid receptor binding + 0.8322 83.22%
Aromatase binding + 0.5513 55.13%
PPAR gamma + 0.7339 73.39%
Honey bee toxicity - 0.8061 80.61%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.5405 54.05%

Targets

Top

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 98.38% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.82% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.44% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.82% 97.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.91% 93.40%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 91.41% 95.55%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.07% 86.33%
CHEMBL2581 P07339 Cathepsin D 90.72% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.58% 94.45%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 90.01% 82.67%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.99% 93.99%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 89.63% 80.96%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.62% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.17% 95.89%
CHEMBL4208 P20618 Proteasome component C5 85.88% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 85.81% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.35% 95.56%
CHEMBL261 P00915 Carbonic anhydrase I 84.34% 96.76%
CHEMBL3438 Q05513 Protein kinase C zeta 84.30% 88.48%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 83.20% 95.53%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.19% 94.80%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.62% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.32% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.41% 89.00%

Plants that contains it

Top
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.
Annona glabra
Cassytha filiformis

Cross-Links

Top
PubChem 5315733
NPASS NPC76637
LOTUS LTS0160428
wikiData Q104399697