(6aS)-2,9,10-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol

Details

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Internal ID 56f2fded-b4d6-4f0e-9b7c-cf55307205a8
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name (6aS)-2,9,10-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol
SMILES (Canonical) COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)OC)NCCC3=C1)O
SMILES (Isomeric) COC1=C(C2=C3[C@H](CC4=CC(=C(C=C42)OC)OC)NCCC3=C1)O
InChI InChI=1S/C19H21NO4/c1-22-14-8-11-6-13-17-10(4-5-20-13)7-16(24-3)19(21)18(17)12(11)9-15(14)23-2/h7-9,13,20-21H,4-6H2,1-3H3/t13-/m0/s1
InChI Key MDUPNPFWUYFJQG-ZDUSSCGKSA-N
Popularity 2 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) 60.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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(6aS)-2,9,10-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol
(6aS)-5,6,6a,7-Tetrahydro-2,9,10-trimethoxy-4H-dibenzo[de,g]quinolin-1-ol
(+)-6As-Wilsonirine
CHEMBL2332233

2D Structure

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2D Structure of (6aS)-2,9,10-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9563 95.63%
Caco-2 + 0.8165 81.65%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6022 60.22%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.8767 87.67%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6145 61.45%
P-glycoprotein inhibitior - 0.7256 72.56%
P-glycoprotein substrate - 0.5488 54.88%
CYP3A4 substrate + 0.5602 56.02%
CYP2C9 substrate - 0.6360 63.60%
CYP2D6 substrate + 0.7728 77.28%
CYP3A4 inhibition - 0.8208 82.08%
CYP2C9 inhibition - 0.9102 91.02%
CYP2C19 inhibition - 0.8293 82.93%
CYP2D6 inhibition + 0.5346 53.46%
CYP1A2 inhibition - 0.5676 56.76%
CYP2C8 inhibition + 0.5403 54.03%
CYP inhibitory promiscuity - 0.8829 88.29%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.7340 73.40%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.9436 94.36%
Skin irritation - 0.7035 70.35%
Skin corrosion - 0.9233 92.33%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4484 44.84%
Micronuclear - 0.5100 51.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation - 0.8869 88.69%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8341 83.41%
Acute Oral Toxicity (c) III 0.4846 48.46%
Estrogen receptor binding + 0.7901 79.01%
Androgen receptor binding - 0.5707 57.07%
Thyroid receptor binding + 0.8198 81.98%
Glucocorticoid receptor binding + 0.8094 80.94%
Aromatase binding + 0.5584 55.84%
PPAR gamma + 0.7659 76.59%
Honey bee toxicity - 0.8864 88.64%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5149 51.49%
Fish aquatic toxicity - 0.5562 55.62%

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 96.87% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.31% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 96.23% 92.94%
CHEMBL1951 P21397 Monoamine oxidase A 93.70% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.68% 97.09%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 92.00% 91.79%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.37% 95.89%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.84% 96.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.47% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.40% 98.95%
CHEMBL4208 P20618 Proteasome component C5 89.27% 90.00%
CHEMBL3438 Q05513 Protein kinase C zeta 88.46% 88.48%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.41% 93.99%
CHEMBL213 P08588 Beta-1 adrenergic receptor 86.96% 95.56%
CHEMBL217 P14416 Dopamine D2 receptor 86.50% 95.62%
CHEMBL2535 P11166 Glucose transporter 85.87% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.27% 99.17%
CHEMBL2056 P21728 Dopamine D1 receptor 84.51% 91.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.05% 92.68%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.52% 92.62%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.95% 91.03%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.63% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.26% 100.00%

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.
Artabotrys monteiroae
Corydalis paniculigera
Corydalis pseudoadunca
Corydalis stricta
Miliusa cuneata

Cross-Links

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PubChem 10860413
LOTUS LTS0059407
wikiData Q104391503