17,18-Dimethoxy-5,8-dioxa-14-azapentacyclo[12.8.0.02,11.04,9.016,21]docosa-1(22),2,4(9),10,16(21),17,19-heptaen-15-one

Details

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Internal ID ad1f8e73-6ef6-40a3-a76e-5045f392093c
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives > Isoquinolones and derivatives
IUPAC Name 17,18-dimethoxy-5,8-dioxa-14-azapentacyclo[12.8.0.02,11.04,9.016,21]docosa-1(22),2,4(9),10,16(21),17,19-heptaen-15-one
SMILES (Canonical) COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2=O)OCCO5)OC
SMILES (Isomeric) COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2=O)OCCO5)OC
InChI InChI=1S/C21H19NO5/c1-24-16-4-3-13-9-15-14-11-18-17(26-7-8-27-18)10-12(14)5-6-22(15)21(23)19(13)20(16)25-2/h3-4,9-11H,5-8H2,1-2H3
InChI Key OLIRVMPRFWLUGS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H19NO5
Molecular Weight 365.40 g/mol
Exact Mass 365.12632271 g/mol
Topological Polar Surface Area (TPSA) 57.20 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 17,18-Dimethoxy-5,8-dioxa-14-azapentacyclo[12.8.0.02,11.04,9.016,21]docosa-1(22),2,4(9),10,16(21),17,19-heptaen-15-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9607 96.07%
Caco-2 + 0.8651 86.51%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5675 56.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9374 93.74%
OATP1B3 inhibitior + 0.9521 95.21%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior + 0.7432 74.32%
P-glycoprotein inhibitior + 0.7822 78.22%
P-glycoprotein substrate - 0.7279 72.79%
CYP3A4 substrate + 0.5856 58.56%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.7877 78.77%
CYP3A4 inhibition - 0.6380 63.80%
CYP2C9 inhibition - 0.5620 56.20%
CYP2C19 inhibition - 0.5955 59.55%
CYP2D6 inhibition - 0.9319 93.19%
CYP1A2 inhibition + 0.7473 74.73%
CYP2C8 inhibition - 0.7213 72.13%
CYP inhibitory promiscuity + 0.5772 57.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5661 56.61%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.8985 89.85%
Skin irritation - 0.8258 82.58%
Skin corrosion - 0.9617 96.17%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7162 71.62%
Micronuclear + 0.6800 68.00%
Hepatotoxicity - 0.6302 63.02%
skin sensitisation - 0.8896 88.96%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6496 64.96%
Acute Oral Toxicity (c) III 0.7198 71.98%
Estrogen receptor binding + 0.9529 95.29%
Androgen receptor binding + 0.6850 68.50%
Thyroid receptor binding + 0.6894 68.94%
Glucocorticoid receptor binding + 0.9080 90.80%
Aromatase binding - 0.6797 67.97%
PPAR gamma + 0.7421 74.21%
Honey bee toxicity - 0.8537 85.37%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity - 0.8777 87.77%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.25% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.16% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.15% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.91% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.67% 98.95%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 92.40% 80.78%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.81% 93.40%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.38% 85.14%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.96% 96.77%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 87.91% 95.78%
CHEMBL4208 P20618 Proteasome component C5 87.28% 90.00%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 87.14% 92.38%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.03% 93.99%
CHEMBL5747 Q92793 CREB-binding protein 86.56% 95.12%
CHEMBL3714079 Q9NQS5 G-protein coupled receptor 84 85.32% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.69% 89.00%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 82.51% 95.53%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 81.26% 96.39%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.21% 90.71%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 80.86% 82.67%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.64% 92.62%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.32% 82.38%

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.
Coscinium fenestratum

Cross-Links

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PubChem 162895741
LOTUS LTS0097464
wikiData Q105193994