Semecarpifoline

Details

Top
Internal ID 899750e4-c01f-433e-934e-0ea58b6a4a3d
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 4,7-dimethoxy-3-(methoxymethyl)-1H-quinolin-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H15NO4/c1-16-7-10-12(18-3)9-5-4-8(17-2)6-11(9)14-13(10)15/h4-6H,7H2,1-3H3,(H,14,15)
InChI Key WBHOECNXRGZKAH-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H15NO4
Molecular Weight 249.26 g/mol
Exact Mass 249.10010796 g/mol
Topological Polar Surface Area (TPSA) 56.80 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.69
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
4,7-dimethoxy-3-(methoxymethyl)-1H-quinolin-2-one
RefChem:182338
366789-86-8
CHEMBL505570
SCHEMBL30514626

2D Structure

Top
2D Structure of Semecarpifoline

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.7220 72.20%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6588 65.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8886 88.86%
OATP1B3 inhibitior + 0.9467 94.67%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5518 55.18%
P-glycoprotein inhibitior - 0.9410 94.10%
P-glycoprotein substrate - 0.8804 88.04%
CYP3A4 substrate - 0.5111 51.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8380 83.80%
CYP3A4 inhibition - 0.6688 66.88%
CYP2C9 inhibition - 0.6680 66.80%
CYP2C19 inhibition + 0.5092 50.92%
CYP2D6 inhibition - 0.9146 91.46%
CYP1A2 inhibition + 0.8613 86.13%
CYP2C8 inhibition - 0.7608 76.08%
CYP inhibitory promiscuity + 0.5726 57.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6453 64.53%
Eye corrosion - 0.9908 99.08%
Eye irritation + 0.8008 80.08%
Skin irritation - 0.8660 86.60%
Skin corrosion - 0.9681 96.81%
Ames mutagenesis + 0.5663 56.63%
Human Ether-a-go-go-Related Gene inhibition - 0.4932 49.32%
Micronuclear + 0.6659 66.59%
Hepatotoxicity + 0.5746 57.46%
skin sensitisation - 0.8979 89.79%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.6825 68.25%
Acute Oral Toxicity (c) III 0.6171 61.71%
Estrogen receptor binding + 0.7211 72.11%
Androgen receptor binding + 0.6955 69.55%
Thyroid receptor binding - 0.5603 56.03%
Glucocorticoid receptor binding + 0.6641 66.41%
Aromatase binding + 0.8221 82.21%
PPAR gamma + 0.5485 54.85%
Honey bee toxicity - 0.9184 91.84%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.6684 66.84%

Targets

Top

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 96.17% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.12% 91.11%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 94.06% 86.92%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.68% 95.56%
CHEMBL2535 P11166 Glucose transporter 91.62% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.00% 94.00%
CHEMBL1907 P15144 Aminopeptidase N 89.85% 93.31%
CHEMBL4208 P20618 Proteasome component C5 86.45% 90.00%
CHEMBL255 P29275 Adenosine A2b receptor 86.38% 98.59%
CHEMBL2581 P07339 Cathepsin D 86.35% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.23% 96.09%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 85.57% 93.24%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.95% 99.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.59% 91.71%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 82.48% 92.67%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.41% 93.99%

Plants that contains it

Top
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.
Melicope semecarpifolia

Cross-Links

Top
PubChem 10857848
NPASS NPC62069
LOTUS LTS0062415
wikiData Q105300758