5,6,7-Trimethoxy-2-methyl-3,4-dihydroisoquinolin-1-one

Details

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Internal ID 1c0976de-c3a6-4e1b-9ee2-473438cb60d2
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives > Isoquinolones and derivatives
IUPAC Name 5,6,7-trimethoxy-2-methyl-3,4-dihydroisoquinolin-1-one
SMILES (Canonical) CN1CCC2=C(C(=C(C=C2C1=O)OC)OC)OC
SMILES (Isomeric) CN1CCC2=C(C(=C(C=C2C1=O)OC)OC)OC
InChI InChI=1S/C13H17NO4/c1-14-6-5-8-9(13(14)15)7-10(16-2)12(18-4)11(8)17-3/h7H,5-6H2,1-4H3
InChI Key KBMHMJUDNKXZBG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H17NO4
Molecular Weight 251.28 g/mol
Exact Mass 251.11575802 g/mol
Topological Polar Surface Area (TPSA) 48.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.34
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,6,7-Trimethoxy-2-methyl-3,4-dihydroisoquinolin-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9542 95.42%
Caco-2 + 0.9336 93.36%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4523 45.23%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.9587 95.87%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9281 92.81%
P-glycoprotein inhibitior - 0.9489 94.89%
P-glycoprotein substrate - 0.8911 89.11%
CYP3A4 substrate - 0.5231 52.31%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7436 74.36%
CYP3A4 inhibition - 0.8374 83.74%
CYP2C9 inhibition - 0.9006 90.06%
CYP2C19 inhibition - 0.8885 88.85%
CYP2D6 inhibition - 0.9375 93.75%
CYP1A2 inhibition + 0.7849 78.49%
CYP2C8 inhibition - 0.9528 95.28%
CYP inhibitory promiscuity - 0.9210 92.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6644 66.44%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.5659 56.59%
Skin irritation - 0.7843 78.43%
Skin corrosion - 0.9388 93.88%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5915 59.15%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8994 89.94%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6591 65.91%
Acute Oral Toxicity (c) III 0.7374 73.74%
Estrogen receptor binding - 0.5752 57.52%
Androgen receptor binding - 0.7224 72.24%
Thyroid receptor binding + 0.5780 57.80%
Glucocorticoid receptor binding - 0.5208 52.08%
Aromatase binding - 0.6904 69.04%
PPAR gamma - 0.8069 80.69%
Honey bee toxicity - 0.8997 89.97%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity - 0.4703 47.03%

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 96.65% 96.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 96.02% 93.40%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.48% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.87% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.63% 95.56%
CHEMBL4208 P20618 Proteasome component C5 90.96% 90.00%
CHEMBL5747 Q92793 CREB-binding protein 86.66% 95.12%
CHEMBL2535 P11166 Glucose transporter 86.03% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.65% 94.00%
CHEMBL2056 P21728 Dopamine D1 receptor 85.56% 91.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.63% 96.77%
CHEMBL4302 P08183 P-glycoprotein 1 81.16% 92.98%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.30% 82.38%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.05% 91.11%

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 fendleri

Cross-Links

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PubChem 162931699
LOTUS LTS0275623
wikiData Q105138343