CID 13853621

Details

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Internal ID f2216962-16e5-43bc-a770-d29983549d6f
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 2,10,11-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,4-diol
SMILES (Canonical) CN1CC(C2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC)O
SMILES (Isomeric) CN1CC(C2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC)O
InChI InChI=1S/C20H23NO5/c1-21-9-13(22)11-8-15(25-3)19(23)18-16-10(7-12(21)17(11)18)5-6-14(24-2)20(16)26-4/h5-6,8,12-13,22-23H,7,9H2,1-4H3
InChI Key DPVUITDUDZIAQO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H23NO5
Molecular Weight 357.40 g/mol
Exact Mass 357.15762283 g/mol
Topological Polar Surface Area (TPSA) 71.40 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 13853621

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9320 93.20%
Caco-2 + 0.8536 85.36%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.3893 38.93%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.8964 89.64%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.6892 68.92%
P-glycoprotein inhibitior - 0.8019 80.19%
P-glycoprotein substrate - 0.6031 60.31%
CYP3A4 substrate + 0.6450 64.50%
CYP2C9 substrate - 0.6075 60.75%
CYP2D6 substrate + 0.8055 80.55%
CYP3A4 inhibition - 0.8803 88.03%
CYP2C9 inhibition - 0.9087 90.87%
CYP2C19 inhibition - 0.7224 72.24%
CYP2D6 inhibition + 0.7846 78.46%
CYP1A2 inhibition + 0.6126 61.26%
CYP2C8 inhibition - 0.5681 56.81%
CYP inhibitory promiscuity - 0.9531 95.31%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6430 64.30%
Eye corrosion - 0.9926 99.26%
Eye irritation - 0.9350 93.50%
Skin irritation - 0.7792 77.92%
Skin corrosion - 0.9400 94.00%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4086 40.86%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8836 88.36%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.9371 93.71%
Acute Oral Toxicity (c) III 0.6800 68.00%
Estrogen receptor binding + 0.7016 70.16%
Androgen receptor binding + 0.6350 63.50%
Thyroid receptor binding + 0.6146 61.46%
Glucocorticoid receptor binding + 0.8098 80.98%
Aromatase binding + 0.5597 55.97%
PPAR gamma + 0.6105 61.05%
Honey bee toxicity - 0.9189 91.89%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity - 0.3729 37.29%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.99% 96.09%
CHEMBL217 P14416 Dopamine D2 receptor 98.61% 95.62%
CHEMBL1951 P21397 Monoamine oxidase A 94.24% 91.49%
CHEMBL2056 P21728 Dopamine D1 receptor 93.03% 91.00%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 91.82% 91.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.78% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.70% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.69% 93.99%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.71% 95.89%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.47% 89.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.25% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.35% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.91% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.42% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.22% 94.45%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.44% 90.71%
CHEMBL3438 Q05513 Protein kinase C zeta 84.39% 88.48%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.54% 94.00%
CHEMBL4208 P20618 Proteasome component C5 81.54% 90.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.48% 82.38%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.36% 92.62%
CHEMBL2535 P11166 Glucose transporter 81.17% 98.75%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.09% 91.03%

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.
Glaucium fimbrilligerum

Cross-Links

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PubChem 13853621
LOTUS LTS0041874
wikiData Q104986734