Gentioflavine

Details

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Internal ID af68398a-32db-4538-ba0a-b817d8117718
Taxonomy Organoheterocyclic compounds > Lactones > Delta valerolactones
IUPAC Name 6-methyl-1-oxo-3,4,6,7-tetrahydropyrano[3,4-c]pyridine-5-carbaldehyde
SMILES (Canonical) CC1C(=C2CCOC(=O)C2=CN1)C=O
SMILES (Isomeric) CC1C(=C2CCOC(=O)C2=CN1)C=O
InChI InChI=1S/C10H11NO3/c1-6-9(5-12)7-2-3-14-10(13)8(7)4-11-6/h4-6,11H,2-3H2,1H3
InChI Key GLNRAZLQBMAROT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H11NO3
Molecular Weight 193.20 g/mol
Exact Mass 193.07389321 g/mol
Topological Polar Surface Area (TPSA) 55.40 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.30
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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Gentioflavin
18058-50-9
6-methyl-1-oxo-3,4,6,7-tetrahydropyrano[3,4-c]pyridine-5-carbaldehyde
C09962
1H-Pyrano[3,4-c]pyridine-5-carboxaldehyde, 3,4,6,7-tetrahydro-6-methyl-1-oxo- (9CI)
AC1L9D18
CTK0H8040
CHEBI:5320
DTXSID60331867
HY-N10810
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Gentioflavine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9871 98.71%
Caco-2 + 0.7276 72.76%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7400 74.00%
OATP2B1 inhibitior - 0.8631 86.31%
OATP1B1 inhibitior + 0.8696 86.96%
OATP1B3 inhibitior + 0.9555 95.55%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8631 86.31%
P-glycoprotein inhibitior - 0.9702 97.02%
P-glycoprotein substrate - 0.8183 81.83%
CYP3A4 substrate - 0.5356 53.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8617 86.17%
CYP3A4 inhibition - 0.9171 91.71%
CYP2C9 inhibition - 0.7106 71.06%
CYP2C19 inhibition - 0.6793 67.93%
CYP2D6 inhibition - 0.8812 88.12%
CYP1A2 inhibition + 0.5408 54.08%
CYP2C8 inhibition - 0.9139 91.39%
CYP inhibitory promiscuity - 0.7786 77.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5030 50.30%
Eye corrosion - 0.9733 97.33%
Eye irritation + 0.7629 76.29%
Skin irritation - 0.7303 73.03%
Skin corrosion - 0.9101 91.01%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6897 68.97%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8005 80.05%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.6363 63.63%
Acute Oral Toxicity (c) III 0.6253 62.53%
Estrogen receptor binding - 0.7408 74.08%
Androgen receptor binding - 0.5988 59.88%
Thyroid receptor binding - 0.7189 71.89%
Glucocorticoid receptor binding - 0.7199 71.99%
Aromatase binding - 0.8575 85.75%
PPAR gamma - 0.8674 86.74%
Honey bee toxicity - 0.9082 90.82%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity - 0.3940 39.40%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.84% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.60% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.18% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 89.47% 93.40%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.15% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.14% 85.14%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.58% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.16% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.42% 97.09%
CHEMBL230 P35354 Cyclooxygenase-2 81.03% 89.63%

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.
Gentiana scabra
Swertia marginata

Cross-Links

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PubChem 442536
NPASS NPC137399
LOTUS LTS0209900
wikiData Q27106717