7-Methoxyflindersine

Details

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Internal ID 73149db0-c6a2-455c-9f95-9a9d3b307bfc
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Pyranoquinolines
IUPAC Name 8-methoxy-2,2-dimethyl-6H-pyrano[3,2-c]quinolin-5-one
SMILES (Canonical) CC1(C=CC2=C(O1)C3=C(C=C(C=C3)OC)NC2=O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C3=C(C=C(C=C3)OC)NC2=O)C
InChI InChI=1S/C15H15NO3/c1-15(2)7-6-11-13(19-15)10-5-4-9(18-3)8-12(10)16-14(11)17/h4-8H,1-3H3,(H,16,17)
InChI Key MSNTXSKOUDIFMS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H15NO3
Molecular Weight 257.28 g/mol
Exact Mass 257.10519334 g/mol
Topological Polar Surface Area (TPSA) 47.60 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.72
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Methoxyflindersine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.7054 70.54%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6658 66.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9165 91.65%
OATP1B3 inhibitior + 0.9688 96.88%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.4896 48.96%
P-glycoprotein inhibitior - 0.7930 79.30%
P-glycoprotein substrate - 0.7524 75.24%
CYP3A4 substrate + 0.5764 57.64%
CYP2C9 substrate - 0.6070 60.70%
CYP2D6 substrate - 0.8552 85.52%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.6651 66.51%
CYP2C19 inhibition + 0.5584 55.84%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition + 0.9107 91.07%
CYP2C8 inhibition - 0.7576 75.76%
CYP inhibitory promiscuity + 0.5679 56.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Danger 0.4491 44.91%
Eye corrosion - 0.9884 98.84%
Eye irritation + 0.8771 87.71%
Skin irritation - 0.8533 85.33%
Skin corrosion - 0.9657 96.57%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4870 48.70%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.6576 65.76%
skin sensitisation - 0.8482 84.82%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.5590 55.90%
Acute Oral Toxicity (c) III 0.5517 55.17%
Estrogen receptor binding + 0.9665 96.65%
Androgen receptor binding + 0.7796 77.96%
Thyroid receptor binding + 0.8021 80.21%
Glucocorticoid receptor binding + 0.9116 91.16%
Aromatase binding + 0.9275 92.75%
PPAR gamma + 0.8225 82.25%
Honey bee toxicity - 0.8345 83.45%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.6841 68.41%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.97% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.75% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.79% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.80% 94.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 91.29% 85.30%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.92% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 89.45% 93.31%
CHEMBL2535 P11166 Glucose transporter 89.37% 98.75%
CHEMBL1951 P21397 Monoamine oxidase A 88.11% 91.49%
CHEMBL255 P29275 Adenosine A2b receptor 86.79% 98.59%
CHEMBL4208 P20618 Proteasome component C5 86.53% 90.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.48% 86.92%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.38% 96.77%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.77% 94.80%
CHEMBL2581 P07339 Cathepsin D 82.23% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.99% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.67% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.52% 92.62%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.40% 95.71%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.34% 100.00%

Cross-Links

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PubChem 101995295
NPASS NPC73369
LOTUS LTS0216325
wikiData Q105171289