4-[5-[[(1S)-7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-methoxyphenoxy]benzaldehyde

Details

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Internal ID 7ba18e9a-e8fe-4ec4-9fa5-576f569b40e1
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives > Benzylisoquinolines
IUPAC Name 4-[5-[[(1S)-7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-methoxyphenoxy]benzaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H27NO5/c1-27-11-10-19-14-25(31-3)23(29)15-21(19)22(27)12-18-6-9-24(30-2)26(13-18)32-20-7-4-17(16-28)5-8-20/h4-9,13-16,22,29H,10-12H2,1-3H3/t22-/m0/s1
InChI Key LQOWQFUDCYSTIS-QFIPXVFZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H27NO5
Molecular Weight 433.50 g/mol
Exact Mass 433.18892296 g/mol
Topological Polar Surface Area (TPSA) 68.20 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.79
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-[5-[[(1S)-7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-methoxyphenoxy]benzaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9323 93.23%
Caco-2 + 0.5948 59.48%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7362 73.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9057 90.57%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.9864 98.64%
P-glycoprotein inhibitior + 0.9728 97.28%
P-glycoprotein substrate - 0.5116 51.16%
CYP3A4 substrate + 0.6761 67.61%
CYP2C9 substrate + 0.5853 58.53%
CYP2D6 substrate + 0.6158 61.58%
CYP3A4 inhibition - 0.8383 83.83%
CYP2C9 inhibition - 0.9167 91.67%
CYP2C19 inhibition - 0.9331 93.31%
CYP2D6 inhibition + 0.7758 77.58%
CYP1A2 inhibition + 0.5821 58.21%
CYP2C8 inhibition + 0.6285 62.85%
CYP inhibitory promiscuity - 0.9246 92.46%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7203 72.03%
Eye corrosion - 0.9947 99.47%
Eye irritation - 0.9705 97.05%
Skin irritation - 0.7834 78.34%
Skin corrosion - 0.9468 94.68%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8874 88.74%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.9040 90.40%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.8418 84.18%
Acute Oral Toxicity (c) III 0.8377 83.77%
Estrogen receptor binding + 0.7260 72.60%
Androgen receptor binding - 0.5755 57.55%
Thyroid receptor binding + 0.6697 66.97%
Glucocorticoid receptor binding + 0.9086 90.86%
Aromatase binding - 0.5269 52.69%
PPAR gamma + 0.6874 68.74%
Honey bee toxicity - 0.8289 82.89%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9059 90.59%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.41% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.44% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.46% 98.95%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 94.45% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 94.31% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.30% 94.45%
CHEMBL4208 P20618 Proteasome component C5 94.14% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.12% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 94.10% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.03% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.77% 99.17%
CHEMBL2535 P11166 Glucose transporter 90.06% 98.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.84% 91.11%
CHEMBL2056 P21728 Dopamine D1 receptor 87.09% 91.00%
CHEMBL6175 Q9H3R0 Lysine-specific demethylase 4C 86.93% 96.69%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.36% 91.07%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.04% 93.40%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 85.01% 90.95%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 84.38% 91.03%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.83% 94.00%
CHEMBL3474 P14555 Phospholipase A2 group IIA 83.68% 94.05%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.20% 92.62%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.57% 80.78%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.51% 92.94%

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.
Phaeanthus splendens

Cross-Links

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PubChem 23625002
LOTUS LTS0188435
wikiData Q105155647