(3R)-5-(5-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-6-ol

Details

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Internal ID 03225402-7fa9-474e-91c3-9d28b279af90
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives > Naphthylisoquinolines
IUPAC Name (3R)-5-(5-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H25NO4/c1-12-8-16-15(6-7-20(28-4)24(16)18(26)9-12)23-17-10-13(2)25-14(3)22(17)21(29-5)11-19(23)27/h6-9,11,13,26-27H,10H2,1-5H3/t13-/m1/s1
InChI Key CAGBCZAJHUAFBK-CYBMUJFWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H25NO4
Molecular Weight 391.50 g/mol
Exact Mass 391.17835828 g/mol
Topological Polar Surface Area (TPSA) 71.30 Ų
XlogP 4.50
Atomic LogP (AlogP) 5.00
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R)-5-(5-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-6-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9529 95.29%
Caco-2 + 0.7674 76.74%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7051 70.51%
OATP2B1 inhibitior - 0.8623 86.23%
OATP1B1 inhibitior + 0.9079 90.79%
OATP1B3 inhibitior + 0.9544 95.44%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8361 83.61%
BSEP inhibitior + 0.8441 84.41%
P-glycoprotein inhibitior + 0.5844 58.44%
P-glycoprotein substrate - 0.5428 54.28%
CYP3A4 substrate + 0.6225 62.25%
CYP2C9 substrate - 0.6040 60.40%
CYP2D6 substrate - 0.7309 73.09%
CYP3A4 inhibition + 0.5926 59.26%
CYP2C9 inhibition - 0.5146 51.46%
CYP2C19 inhibition + 0.5719 57.19%
CYP2D6 inhibition + 0.5359 53.59%
CYP1A2 inhibition - 0.5315 53.15%
CYP2C8 inhibition + 0.7273 72.73%
CYP inhibitory promiscuity + 0.6478 64.78%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5585 55.85%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.7097 70.97%
Skin irritation - 0.8192 81.92%
Skin corrosion - 0.9360 93.60%
Ames mutagenesis + 0.5263 52.63%
Human Ether-a-go-go-Related Gene inhibition + 0.8252 82.52%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.5564 55.64%
skin sensitisation - 0.9038 90.38%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7156 71.56%
Acute Oral Toxicity (c) III 0.5229 52.29%
Estrogen receptor binding + 0.7891 78.91%
Androgen receptor binding + 0.5819 58.19%
Thyroid receptor binding + 0.7461 74.61%
Glucocorticoid receptor binding + 0.7238 72.38%
Aromatase binding + 0.7073 70.73%
PPAR gamma + 0.7241 72.41%
Honey bee toxicity - 0.8515 85.15%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.7734 77.34%

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
CHEMBL1951 P21397 Monoamine oxidase A 99.30% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.01% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.11% 96.09%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 94.14% 97.31%
CHEMBL2535 P11166 Glucose transporter 92.97% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.87% 95.56%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 92.04% 91.79%
CHEMBL5747 Q92793 CREB-binding protein 91.88% 95.12%
CHEMBL2243 O00519 Anandamide amidohydrolase 91.59% 97.53%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.28% 94.00%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 90.98% 85.40%
CHEMBL3438 Q05513 Protein kinase C zeta 90.77% 88.48%
CHEMBL1907 P15144 Aminopeptidase N 90.06% 93.31%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.54% 92.94%
CHEMBL2581 P07339 Cathepsin D 88.53% 98.95%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.50% 96.21%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.83% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.33% 95.89%
CHEMBL4208 P20618 Proteasome component C5 87.30% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.96% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.17% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.31% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.69% 99.15%
CHEMBL2056 P21728 Dopamine D1 receptor 83.67% 91.00%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 83.66% 95.78%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.53% 96.67%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.51% 89.62%
CHEMBL213 P08588 Beta-1 adrenergic receptor 82.05% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.60% 94.80%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.05% 93.40%

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 likoko

Cross-Links

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PubChem 163000264
LOTUS LTS0177821
wikiData Q104951238