4H-Dibenzo(de,g)quinoline-1,2-diol, 5,6,6a,7-tetrahydro-9,10-dimethoxy-6-methyl-, (6aS)-

Details

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Internal ID 86afff4e-3f87-4d52-be57-d0ec3e6cf818
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name (6aS)-9,10-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,2-diol
SMILES (Canonical) CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)O)O
SMILES (Isomeric) CN1CCC2=CC(=C(C3=C2[C@@H]1CC4=CC(=C(C=C43)OC)OC)O)O
InChI InChI=1S/C19H21NO4/c1-20-5-4-10-7-14(21)19(22)18-12-9-16(24-3)15(23-2)8-11(12)6-13(20)17(10)18/h7-9,13,21-22H,4-6H2,1-3H3/t13-/m0/s1
InChI Key SBGGUHPMRYOCBS-ZDUSSCGKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H21NO4
Molecular Weight 327.40 g/mol
Exact Mass 327.14705815 g/mol
Topological Polar Surface Area (TPSA) 62.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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4H-Dibenzo(de,g)quinoline-1,2-diol, 5,6,6a,7-tetrahydro-9,10-dimethoxy-6-methyl-, (6aS)-
Lastourvilline
DTXSID60990716
9,10-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,2-diol

2D Structure

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2D Structure of 4H-Dibenzo(de,g)quinoline-1,2-diol, 5,6,6a,7-tetrahydro-9,10-dimethoxy-6-methyl-, (6aS)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6920 69.20%
Caco-2 + 0.8011 80.11%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5711 57.11%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9037 90.37%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.6387 63.87%
P-glycoprotein inhibitior - 0.8549 85.49%
P-glycoprotein substrate - 0.6354 63.54%
CYP3A4 substrate + 0.6003 60.03%
CYP2C9 substrate + 0.7865 78.65%
CYP2D6 substrate + 0.7790 77.90%
CYP3A4 inhibition - 0.9039 90.39%
CYP2C9 inhibition - 0.9002 90.02%
CYP2C19 inhibition - 0.8839 88.39%
CYP2D6 inhibition + 0.6774 67.74%
CYP1A2 inhibition + 0.8734 87.34%
CYP2C8 inhibition - 0.7743 77.43%
CYP inhibitory promiscuity - 0.9615 96.15%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7023 70.23%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9369 93.69%
Skin irritation - 0.7509 75.09%
Skin corrosion - 0.9299 92.99%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3702 37.02%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.7824 78.24%
skin sensitisation - 0.8848 88.48%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8937 89.37%
Acute Oral Toxicity (c) III 0.7003 70.03%
Estrogen receptor binding - 0.4950 49.50%
Androgen receptor binding - 0.5909 59.09%
Thyroid receptor binding + 0.6462 64.62%
Glucocorticoid receptor binding + 0.7941 79.41%
Aromatase binding - 0.5498 54.98%
PPAR gamma + 0.7282 72.82%
Honey bee toxicity - 0.9139 91.39%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9071 90.71%

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 99.01% 96.09%
CHEMBL217 P14416 Dopamine D2 receptor 96.93% 95.62%
CHEMBL2056 P21728 Dopamine D1 receptor 95.85% 91.00%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 95.57% 91.79%
CHEMBL241 Q14432 Phosphodiesterase 3A 95.09% 92.94%
CHEMBL1951 P21397 Monoamine oxidase A 94.46% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.21% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 92.74% 93.40%
CHEMBL2581 P07339 Cathepsin D 92.23% 98.95%
CHEMBL3438 Q05513 Protein kinase C zeta 90.99% 88.48%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.95% 95.56%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 90.53% 91.03%
CHEMBL4208 P20618 Proteasome component C5 90.12% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.49% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.84% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.52% 86.33%
CHEMBL5747 Q92793 CREB-binding protein 86.34% 95.12%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.05% 85.14%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 83.27% 96.86%
CHEMBL2535 P11166 Glucose transporter 82.66% 98.75%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 82.47% 95.70%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.24% 89.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.67% 90.71%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.33% 82.38%
CHEMBL3820 P35557 Hexokinase type IV 81.13% 91.96%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.15% 89.00%

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.
Annona squamosa
Artabotrys lastoursvillensis
Fumaria indica
Glaucium leiocarpum
Luxemburgia octandra

Cross-Links

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PubChem 155514
NPASS NPC58785
LOTUS LTS0000658
wikiData Q105343666