Geovanine

Details

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Internal ID 5c3916cf-f69e-4f56-95d6-249de797049a
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines
IUPAC Name 5,9,10-trimethoxy-4-methyl-1H-benzo[g]quinolin-2-one
SMILES (Canonical) CC1=CC(=O)NC2=C(C3=C(C=CC=C3OC)C(=C12)OC)OC
SMILES (Isomeric) CC1=CC(=O)NC2=C(C3=C(C=CC=C3OC)C(=C12)OC)OC
InChI InChI=1S/C17H17NO4/c1-9-8-12(19)18-15-13(9)16(21-3)10-6-5-7-11(20-2)14(10)17(15)22-4/h5-8H,1-4H3,(H,18,19)
InChI Key LWNCVZAIYGAIFG-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H17NO4
Molecular Weight 299.32 g/mol
Exact Mass 299.11575802 g/mol
Topological Polar Surface Area (TPSA) 56.80 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.02
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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5,9,10-trimethoxy-4-methyl-1H-benzo[g]quinolin-2-one

2D Structure

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2D Structure of Geovanine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 + 0.7083 70.83%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.5946 59.46%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9602 96.02%
OATP1B3 inhibitior + 0.9671 96.71%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7757 77.57%
P-glycoprotein inhibitior - 0.7336 73.36%
P-glycoprotein substrate - 0.8250 82.50%
CYP3A4 substrate + 0.5742 57.42%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.8723 87.23%
CYP3A4 inhibition + 0.5625 56.25%
CYP2C9 inhibition - 0.8816 88.16%
CYP2C19 inhibition - 0.7526 75.26%
CYP2D6 inhibition - 0.9526 95.26%
CYP1A2 inhibition + 0.8496 84.96%
CYP2C8 inhibition + 0.4823 48.23%
CYP inhibitory promiscuity - 0.5353 53.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9223 92.23%
Carcinogenicity (trinary) Non-required 0.6145 61.45%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.5610 56.10%
Skin irritation - 0.8782 87.82%
Skin corrosion - 0.9832 98.32%
Ames mutagenesis + 0.6930 69.30%
Human Ether-a-go-go-Related Gene inhibition - 0.4070 40.70%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.9583 95.83%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.7331 73.31%
Acute Oral Toxicity (c) III 0.6170 61.70%
Estrogen receptor binding + 0.7842 78.42%
Androgen receptor binding + 0.6448 64.48%
Thyroid receptor binding + 0.7078 70.78%
Glucocorticoid receptor binding + 0.8514 85.14%
Aromatase binding + 0.8037 80.37%
PPAR gamma + 0.5202 52.02%
Honey bee toxicity - 0.9166 91.66%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity - 0.7302 73.02%

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 97.38% 95.56%
CHEMBL4302 P08183 P-glycoprotein 1 96.86% 92.98%
CHEMBL2535 P11166 Glucose transporter 96.02% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.27% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.08% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.56% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 90.49% 93.31%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.18% 94.80%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.65% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 89.33% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.97% 99.23%
CHEMBL2581 P07339 Cathepsin D 88.79% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.73% 85.14%
CHEMBL213 P08588 Beta-1 adrenergic receptor 87.78% 95.56%
CHEMBL1255126 O15151 Protein Mdm4 85.19% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.54% 96.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.45% 94.03%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 83.29% 92.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.64% 96.09%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 82.01% 85.00%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.41% 100.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.47% 95.50%
CHEMBL1871 P10275 Androgen Receptor 80.38% 96.43%
CHEMBL3401 O75469 Pregnane X receptor 80.32% 94.73%

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.
Annona ambotay
Annona dioica

Cross-Links

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PubChem 25215758
LOTUS LTS0272757
wikiData Q104399359