Duguespixine

Details

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Internal ID 9f736a70-95b4-4e93-8f6f-d0e2f32fca51
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 15-hydroxy-16-methoxy-8-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2,4,6,8,13,15-heptaene-10-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H17NO3/c1-11-13-5-3-4-6-14(13)17-16-12(9-15(22)19(17)23-2)7-8-20(10-21)18(11)16/h3-6,9-10,22H,7-8H2,1-2H3
InChI Key CBOXKGYGGIZZOU-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H17NO3
Molecular Weight 307.30 g/mol
Exact Mass 307.12084340 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.53
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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96910-76-8
DTXSID00242625
6H-Dibenzo(de,g)quinoline-6-carboxaldehyde, 4,5-dihydro-2-hydroxy-1-methoxy-7-methyl-

2D Structure

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2D Structure of Duguespixine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8361 83.61%
Caco-2 + 0.8096 80.96%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7744 77.44%
OATP2B1 inhibitior - 0.7090 70.90%
OATP1B1 inhibitior + 0.9111 91.11%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior + 0.5186 51.86%
BSEP inhibitior + 0.6472 64.72%
P-glycoprotein inhibitior - 0.8478 84.78%
P-glycoprotein substrate - 0.8299 82.99%
CYP3A4 substrate + 0.6112 61.12%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.6603 66.03%
CYP3A4 inhibition - 0.6580 65.80%
CYP2C9 inhibition - 0.7180 71.80%
CYP2C19 inhibition - 0.6141 61.41%
CYP2D6 inhibition - 0.7402 74.02%
CYP1A2 inhibition + 0.8115 81.15%
CYP2C8 inhibition - 0.5919 59.19%
CYP inhibitory promiscuity - 0.5343 53.43%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6228 62.28%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9732 97.32%
Skin irritation - 0.7560 75.60%
Skin corrosion - 0.9472 94.72%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3880 38.80%
Micronuclear + 0.5800 58.00%
Hepatotoxicity - 0.5696 56.96%
skin sensitisation - 0.9155 91.55%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.9355 93.55%
Acute Oral Toxicity (c) III 0.7472 74.72%
Estrogen receptor binding + 0.7012 70.12%
Androgen receptor binding + 0.5809 58.09%
Thyroid receptor binding - 0.5657 56.57%
Glucocorticoid receptor binding + 0.8179 81.79%
Aromatase binding + 0.6073 60.73%
PPAR gamma + 0.7770 77.70%
Honey bee toxicity - 0.9053 90.53%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.4421 44.21%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.75% 91.11%
CHEMBL240 Q12809 HERG 98.60% 89.76%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.84% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 94.96% 91.49%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.34% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.90% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.66% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.86% 86.33%
CHEMBL4208 P20618 Proteasome component C5 90.66% 90.00%
CHEMBL2056 P21728 Dopamine D1 receptor 89.78% 91.00%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 88.52% 95.70%
CHEMBL2535 P11166 Glucose transporter 88.46% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.87% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.32% 89.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.14% 93.65%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.84% 99.23%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 86.47% 80.78%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.58% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.03% 95.89%

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.
Duguetia spixiana

Cross-Links

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PubChem 176589
LOTUS LTS0006536
wikiData Q83126435