Chilenine

Details

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Internal ID d7e8dc61-1db1-4b69-9020-cab0f435412e
Taxonomy Organoheterocyclic compounds > Benzazepines
IUPAC Name 3-hydroxy-7,8-dimethoxy-17,19-dioxa-11-azapentacyclo[12.7.0.03,11.04,9.016,20]henicosa-1(21),4(9),5,7,14,16(20)-hexaene-2,10-dione
SMILES (Canonical) COC1=C(C2=C(C=C1)C3(C(=O)C4=CC5=C(C=C4CCN3C2=O)OCO5)O)OC
SMILES (Isomeric) COC1=C(C2=C(C=C1)C3(C(=O)C4=CC5=C(C=C4CCN3C2=O)OCO5)O)OC
InChI InChI=1S/C20H17NO7/c1-25-13-4-3-12-16(17(13)26-2)19(23)21-6-5-10-7-14-15(28-9-27-14)8-11(10)18(22)20(12,21)24/h3-4,7-8,24H,5-6,9H2,1-2H3
InChI Key DJCOYPJXFKNBCF-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C20H17NO7
Molecular Weight 383.40 g/mol
Exact Mass 383.10050188 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.47
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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71700-15-7
Xylolin
AKOS040761484
3-hydroxy-7,8-dimethoxy-17,19-dioxa-11-azapentacyclo[12.7.0.03,11.04,9.016,20]henicosa-1(21),4(9),5,7,14,16(20)-hexaene-2,10-dione

2D Structure

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2D Structure of Chilenine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6858 68.58%
Caco-2 + 0.6703 67.03%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5421 54.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9445 94.45%
OATP1B3 inhibitior + 0.9379 93.79%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7544 75.44%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.4569 45.69%
P-glycoprotein substrate - 0.7875 78.75%
CYP3A4 substrate + 0.6265 62.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8222 82.22%
CYP3A4 inhibition + 0.6832 68.32%
CYP2C9 inhibition - 0.6913 69.13%
CYP2C19 inhibition - 0.6449 64.49%
CYP2D6 inhibition - 0.7939 79.39%
CYP1A2 inhibition - 0.8363 83.63%
CYP2C8 inhibition - 0.7418 74.18%
CYP inhibitory promiscuity - 0.5676 56.76%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5801 58.01%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.8334 83.34%
Skin irritation - 0.7893 78.93%
Skin corrosion - 0.9378 93.78%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7994 79.94%
Micronuclear + 0.7474 74.74%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.8796 87.96%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.4872 48.72%
Acute Oral Toxicity (c) III 0.6445 64.45%
Estrogen receptor binding + 0.9048 90.48%
Androgen receptor binding + 0.6963 69.63%
Thyroid receptor binding + 0.5808 58.08%
Glucocorticoid receptor binding + 0.7313 73.13%
Aromatase binding + 0.5364 53.64%
PPAR gamma + 0.7678 76.78%
Honey bee toxicity - 0.8728 87.28%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5951 59.51%
Fish aquatic toxicity + 0.7329 73.29%

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 98.46% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.42% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.98% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.33% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.88% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.29% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.22% 95.56%
CHEMBL4208 P20618 Proteasome component C5 93.75% 90.00%
CHEMBL261 P00915 Carbonic anhydrase I 93.65% 96.76%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 93.60% 93.40%
CHEMBL4040 P28482 MAP kinase ERK2 92.25% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.12% 94.45%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 90.92% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.00% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.54% 85.14%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 89.33% 82.38%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 89.05% 82.67%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.65% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.49% 89.00%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 85.80% 80.78%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.46% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.43% 100.00%
CHEMBL5747 Q92793 CREB-binding protein 80.91% 95.12%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.59% 99.23%
CHEMBL2056 P21728 Dopamine D1 receptor 80.06% 91.00%

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.
Berberis darwinii
Berberis vulgaris
Coptis chinensis
Coptis deltoidea
Coptis japonica
Coptis teeta
Phellodendron amurense
Phellodendron chinense

Cross-Links

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PubChem 11025386
NPASS NPC114721
LOTUS LTS0125162
wikiData Q104396960