Gentianadine

Details

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Internal ID d74e74c0-2e3d-4258-8722-bd667905b023
Taxonomy Organoheterocyclic compounds > Pyranopyridines
IUPAC Name 3,4-dihydropyrano[3,4-c]pyridin-1-one
SMILES (Canonical) C1COC(=O)C2=C1C=CN=C2
SMILES (Isomeric) C1COC(=O)C2=C1C=CN=C2
InChI InChI=1S/C8H7NO2/c10-8-7-5-9-3-1-6(7)2-4-11-8/h1,3,5H,2,4H2
InChI Key SIIDHCZFMSEKDS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H7NO2
Molecular Weight 149.15 g/mol
Exact Mass 149.047678466 g/mol
Topological Polar Surface Area (TPSA) 39.20 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.79
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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6790-32-5
3,4-dihydropyrano[3,4-c]pyridin-1-one
1H,3H,4H-Pyrano[3,4-c]pyridin-1-one
3,4-Dihydro-1H-pyrano[3,4-c]pyridin-1-one
C09957
AC1L9D0Z
SureCN798279
SCHEMBL798279
CHEBI:5314
DTXSID40331865
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Gentianadine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.8401 84.01%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7753 77.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9680 96.80%
OATP1B3 inhibitior + 0.9615 96.15%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8960 89.60%
P-glycoprotein inhibitior - 0.9899 98.99%
P-glycoprotein substrate - 0.9689 96.89%
CYP3A4 substrate - 0.6536 65.36%
CYP2C9 substrate - 0.7907 79.07%
CYP2D6 substrate - 0.8501 85.01%
CYP3A4 inhibition - 0.8850 88.50%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.6130 61.30%
CYP2D6 inhibition - 0.8735 87.35%
CYP1A2 inhibition + 0.8341 83.41%
CYP2C8 inhibition - 0.8081 80.81%
CYP inhibitory promiscuity - 0.8921 89.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6209 62.09%
Eye corrosion - 0.9470 94.70%
Eye irritation + 0.9831 98.31%
Skin irritation - 0.6065 60.65%
Skin corrosion - 0.9467 94.67%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6982 69.82%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.5921 59.21%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.4671 46.71%
Acute Oral Toxicity (c) III 0.6896 68.96%
Estrogen receptor binding - 0.9279 92.79%
Androgen receptor binding - 0.7006 70.06%
Thyroid receptor binding - 0.7962 79.62%
Glucocorticoid receptor binding - 0.8758 87.58%
Aromatase binding - 0.7698 76.98%
PPAR gamma - 0.7653 76.53%
Honey bee toxicity - 0.9258 92.58%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity - 0.8732 87.32%

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
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 91.77% 95.72%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 90.07% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.06% 86.33%
CHEMBL4040 P28482 MAP kinase ERK2 88.21% 83.82%
CHEMBL2581 P07339 Cathepsin D 87.96% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 87.10% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.12% 95.56%

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.
Cephalaria nachiczevanica
Gentiana olivieri

Cross-Links

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PubChem 442532
NPASS NPC101506
LOTUS LTS0227413
wikiData Q27106713