(6aS)-10-hydroxy-1,2-dimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-11-olate

Details

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Internal ID 50cd1ca4-2f3d-49a9-8c4f-eb15588b075e
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name (6aS)-10-hydroxy-1,2-dimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-11-olate
SMILES (Canonical) C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)[O-])OC)OC)C
SMILES (Isomeric) C[N+]1(CCC2=CC(=C(C3=C2[C@@H]1CC4=C3C(=C(C=C4)O)[O-])OC)OC)C
InChI InChI=1S/C20H23NO4/c1-21(2)8-7-12-10-15(24-3)20(25-4)18-16(12)13(21)9-11-5-6-14(22)19(23)17(11)18/h5-6,10,13H,7-9H2,1-4H3,(H-,22,23)/t13-/m0/s1
InChI Key BNLBUVFPTCUHTE-ZDUSSCGKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H23NO4
Molecular Weight 341.40 g/mol
Exact Mass 341.16270821 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.38
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6aS)-10-hydroxy-1,2-dimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-11-olate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9152 91.52%
Caco-2 + 0.8052 80.52%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5305 53.05%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9258 92.58%
OATP1B3 inhibitior + 0.9502 95.02%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior - 0.6177 61.77%
P-glycoprotein inhibitior - 0.7583 75.83%
P-glycoprotein substrate - 0.7983 79.83%
CYP3A4 substrate + 0.5964 59.64%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate + 0.3827 38.27%
CYP3A4 inhibition - 0.8720 87.20%
CYP2C9 inhibition - 0.9180 91.80%
CYP2C19 inhibition - 0.8932 89.32%
CYP2D6 inhibition + 0.5611 56.11%
CYP1A2 inhibition - 0.7331 73.31%
CYP2C8 inhibition + 0.6422 64.22%
CYP inhibitory promiscuity - 0.9712 97.12%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7116 71.16%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.8341 83.41%
Skin irritation - 0.7690 76.90%
Skin corrosion - 0.9268 92.68%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8122 81.22%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.6469 64.69%
skin sensitisation - 0.8791 87.91%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.9276 92.76%
Acute Oral Toxicity (c) III 0.7522 75.22%
Estrogen receptor binding + 0.7399 73.99%
Androgen receptor binding + 0.7369 73.69%
Thyroid receptor binding + 0.7023 70.23%
Glucocorticoid receptor binding + 0.8395 83.95%
Aromatase binding + 0.6105 61.05%
PPAR gamma + 0.7641 76.41%
Honey bee toxicity - 0.8754 87.54%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9181 91.81%

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
CHEMBL3192 Q9BY41 Histone deacetylase 8 99.14% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.34% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.25% 96.09%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 95.36% 91.79%
CHEMBL241 Q14432 Phosphodiesterase 3A 95.34% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.78% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.71% 99.15%
CHEMBL2535 P11166 Glucose transporter 89.06% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.56% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.11% 89.62%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 86.50% 92.68%
CHEMBL261 P00915 Carbonic anhydrase I 86.38% 96.76%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.18% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.88% 94.45%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.51% 93.40%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.77% 86.33%
CHEMBL3438 Q05513 Protein kinase C zeta 84.70% 88.48%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.46% 95.89%
CHEMBL4208 P20618 Proteasome component C5 84.24% 90.00%
CHEMBL217 P14416 Dopamine D2 receptor 83.14% 95.62%
CHEMBL2056 P21728 Dopamine D1 receptor 82.92% 91.00%
CHEMBL1951 P21397 Monoamine oxidase A 82.38% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.07% 97.09%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 80.61% 97.31%
CHEMBL2581 P07339 Cathepsin D 80.36% 98.95%

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.
Thalictrum orientale

Cross-Links

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PubChem 163194783
LOTUS LTS0177179
wikiData Q104938868