(1R,3S)-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol

Details

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Internal ID ecced98c-5205-43ae-b7de-2eb11c2ea512
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives > Naphthylisoquinolines
IUPAC Name (1R,3S)-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol
SMILES (Canonical) CC1CC2=C(C=CC(=C2C(N1)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)O
SMILES (Isomeric) C[C@H]1CC2=C(C=CC(=C2[C@H](N1)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)O
InChI InChI=1S/C23H25NO3/c1-12-10-20(27-4)23-16(6-5-7-18(23)25)21(12)15-8-9-19(26)22-14(3)24-13(2)11-17(15)22/h5-10,13-14,24-26H,11H2,1-4H3/t13-,14+/m0/s1
InChI Key NALOMJPIDNQZKW-UONOGXRCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H25NO3
Molecular Weight 363.40 g/mol
Exact Mass 363.18344366 g/mol
Topological Polar Surface Area (TPSA) 61.70 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.83
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,3S)-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9835 98.35%
Caco-2 + 0.7089 70.89%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5238 52.38%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.8917 89.17%
OATP1B3 inhibitior + 0.9487 94.87%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8493 84.93%
P-glycoprotein inhibitior - 0.6547 65.47%
P-glycoprotein substrate + 0.6457 64.57%
CYP3A4 substrate + 0.6520 65.20%
CYP2C9 substrate - 0.7713 77.13%
CYP2D6 substrate + 0.7329 73.29%
CYP3A4 inhibition - 0.7298 72.98%
CYP2C9 inhibition - 0.5377 53.77%
CYP2C19 inhibition + 0.5880 58.80%
CYP2D6 inhibition + 0.5377 53.77%
CYP1A2 inhibition - 0.6963 69.63%
CYP2C8 inhibition + 0.7271 72.71%
CYP inhibitory promiscuity + 0.6521 65.21%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5514 55.14%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.9311 93.11%
Skin irritation - 0.8239 82.39%
Skin corrosion - 0.8950 89.50%
Ames mutagenesis + 0.6963 69.63%
Human Ether-a-go-go-Related Gene inhibition + 0.8228 82.28%
Micronuclear + 0.6000 60.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.9098 90.98%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7357 73.57%
Acute Oral Toxicity (c) III 0.5319 53.19%
Estrogen receptor binding + 0.6456 64.56%
Androgen receptor binding + 0.5333 53.33%
Thyroid receptor binding + 0.7186 71.86%
Glucocorticoid receptor binding + 0.7681 76.81%
Aromatase binding + 0.5869 58.69%
PPAR gamma + 0.7550 75.50%
Honey bee toxicity - 0.8110 81.10%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.4199 41.99%

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 99.03% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.56% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 96.51% 91.49%
CHEMBL2581 P07339 Cathepsin D 96.07% 98.95%
CHEMBL2535 P11166 Glucose transporter 94.71% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.49% 99.15%
CHEMBL241 Q14432 Phosphodiesterase 3A 92.75% 92.94%
CHEMBL1907 P15144 Aminopeptidase N 92.69% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.48% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.41% 89.00%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 91.26% 91.79%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.25% 95.89%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 89.30% 97.31%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.51% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.17% 97.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.79% 93.99%
CHEMBL2056 P21728 Dopamine D1 receptor 86.66% 91.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.53% 86.33%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.39% 89.62%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 86.28% 96.21%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 85.37% 100.00%
CHEMBL4208 P20618 Proteasome component C5 85.24% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.94% 94.45%
CHEMBL213 P08588 Beta-1 adrenergic receptor 84.01% 95.56%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 82.75% 95.70%
CHEMBL1937 Q92769 Histone deacetylase 2 82.43% 94.75%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.24% 90.24%
CHEMBL5028 O14672 ADAM10 81.41% 97.50%
CHEMBL3438 Q05513 Protein kinase C zeta 80.94% 88.48%
CHEMBL240 Q12809 HERG 80.92% 89.76%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.54% 99.23%

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.
Triphyophyllum peltatum

Cross-Links

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PubChem 162863866
LOTUS LTS0194249
wikiData Q105176397