Acutifolin

Details

Top
Internal ID ffe67a6f-e573-4e5b-8842-900b91d8a32e
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 3-(2-hydroxy-3-methylbut-3-enyl)-4,8-dimethoxy-1-methylquinolin-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H21NO4/c1-10(2)13(19)9-12-16(22-5)11-7-6-8-14(21-4)15(11)18(3)17(12)20/h6-8,13,19H,1,9H2,2-5H3
InChI Key BIJMYZRFCGRNCV-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H21NO4
Molecular Weight 303.35 g/mol
Exact Mass 303.14705815 g/mol
Topological Polar Surface Area (TPSA) 59.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.04
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

Top
SCHEMBL29519736
CHEBI:229044
3-(2-hydroxy-3-methylbut-3-enyl)-4,8-dimethoxy-1-methylquinolin-2-one

2D Structure

Top
2D Structure of Acutifolin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9657 96.57%
Caco-2 + 0.8261 82.61%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.3966 39.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9166 91.66%
OATP1B3 inhibitior + 0.9399 93.99%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6215 62.15%
P-glycoprotein inhibitior - 0.8355 83.55%
P-glycoprotein substrate - 0.6808 68.08%
CYP3A4 substrate + 0.6244 62.44%
CYP2C9 substrate - 0.6124 61.24%
CYP2D6 substrate - 0.8017 80.17%
CYP3A4 inhibition + 0.6052 60.52%
CYP2C9 inhibition - 0.7993 79.93%
CYP2C19 inhibition - 0.5468 54.68%
CYP2D6 inhibition - 0.8694 86.94%
CYP1A2 inhibition + 0.6144 61.44%
CYP2C8 inhibition - 0.7597 75.97%
CYP inhibitory promiscuity + 0.5869 58.69%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5410 54.10%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.8416 84.16%
Skin irritation - 0.8159 81.59%
Skin corrosion - 0.9477 94.77%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4002 40.02%
Micronuclear + 0.6759 67.59%
Hepatotoxicity - 0.5591 55.91%
skin sensitisation - 0.8789 87.89%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.7881 78.81%
Acute Oral Toxicity (c) III 0.6113 61.13%
Estrogen receptor binding + 0.7071 70.71%
Androgen receptor binding - 0.6680 66.80%
Thyroid receptor binding + 0.6345 63.45%
Glucocorticoid receptor binding - 0.4944 49.44%
Aromatase binding - 0.5785 57.85%
PPAR gamma + 0.5752 57.52%
Honey bee toxicity - 0.8519 85.19%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.8015 80.15%

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
CHEMBL2581 P07339 Cathepsin D 98.76% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.74% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.74% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.48% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.55% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.24% 94.00%
CHEMBL1255126 O15151 Protein Mdm4 88.70% 90.20%
CHEMBL2535 P11166 Glucose transporter 87.65% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.48% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.81% 89.00%

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.
Glycosmis pentaphylla
Zanthoxylum rhoifolium

Cross-Links

Top
PubChem 5316376
NPASS NPC299323
LOTUS LTS0168769
wikiData Q103816771