(3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol

Details

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Internal ID 0565443c-418c-4015-ae5f-004b8aef9bb1
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives > Naphthylisoquinolines
IUPAC Name (3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol
SMILES (Canonical) CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O
SMILES (Isomeric) C[C@@H]1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O
InChI InChI=1S/C24H27NO3/c1-13-11-20(28-5)23-17(7-6-8-19(23)27-4)21(13)18-10-9-16-12-14(2)25-15(3)22(16)24(18)26/h6-11,14-15,25-26H,12H2,1-5H3/t14-,15?/m1/s1
InChI Key MXIZZLBQRBAZEX-GICMACPYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H27NO3
Molecular Weight 377.50 g/mol
Exact Mass 377.19909372 g/mol
Topological Polar Surface Area (TPSA) 50.70 Ų
XlogP 5.00
Atomic LogP (AlogP) 5.13
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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NSC-656296

2D Structure

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2D Structure of (3R)-7-(4,5-dimethoxy-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 + 0.7261 72.61%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5238 52.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8512 85.12%
OATP1B3 inhibitior + 0.9487 94.87%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9363 93.63%
P-glycoprotein inhibitior + 0.6149 61.49%
P-glycoprotein substrate + 0.7700 77.00%
CYP3A4 substrate + 0.6765 67.65%
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 + 0.6887 68.87%
CYP inhibitory promiscuity + 0.6521 65.21%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5514 55.14%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.8853 88.53%
Skin irritation - 0.8239 82.39%
Skin corrosion - 0.8950 89.50%
Ames mutagenesis + 0.6763 67.63%
Human Ether-a-go-go-Related Gene inhibition + 0.8264 82.64%
Micronuclear + 0.6000 60.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.9098 90.98%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.9155 91.55%
Acute Oral Toxicity (c) III 0.5319 53.19%
Estrogen receptor binding + 0.8038 80.38%
Androgen receptor binding + 0.5830 58.30%
Thyroid receptor binding + 0.7755 77.55%
Glucocorticoid receptor binding + 0.9045 90.45%
Aromatase binding + 0.6344 63.44%
PPAR gamma + 0.7083 70.83%
Honey bee toxicity - 0.8656 86.56%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6000 60.00%
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 99.18% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.21% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.00% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.95% 95.56%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 94.33% 91.79%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.61% 95.89%
CHEMBL2535 P11166 Glucose transporter 92.40% 98.75%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 92.23% 96.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.03% 86.33%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 90.92% 89.62%
CHEMBL1907 P15144 Aminopeptidase N 89.67% 93.31%
CHEMBL1951 P21397 Monoamine oxidase A 88.98% 91.49%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.30% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.89% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.70% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.58% 93.99%
CHEMBL217 P14416 Dopamine D2 receptor 87.24% 95.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.17% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.11% 99.17%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 86.72% 94.03%
CHEMBL213 P08588 Beta-1 adrenergic receptor 86.10% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.80% 99.15%
CHEMBL4208 P20618 Proteasome component C5 85.20% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.62% 96.95%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.49% 90.24%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.09% 91.71%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.90% 96.67%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.52% 97.21%
CHEMBL4361 Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 80.34% 95.52%
CHEMBL1795185 Q58F21 Bromodomain testis-specific protein 80.08% 89.76%

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.
Ancistrocladus barteri
Ancistrocladus korupensis
Ancistrocladus tectorius
Dioncophyllum thollonii
Habropetalum dawei
Triphyophyllum peltatum

Cross-Links

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PubChem 375943
LOTUS LTS0015033
wikiData Q105174204