Veprisine

Details

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Internal ID 7a2bfa96-15c9-4262-9070-8d5c1e727c5f
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Pyranoquinolines
IUPAC Name 7,8-dimethoxy-2,2,6-trimethylpyrano[3,2-c]quinolin-5-one
SMILES (Canonical) CC1(C=CC2=C(O1)C3=C(C(=C(C=C3)OC)OC)N(C2=O)C)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C3=C(C(=C(C=C3)OC)OC)N(C2=O)C)C
InChI InChI=1S/C17H19NO4/c1-17(2)9-8-11-14(22-17)10-6-7-12(20-4)15(21-5)13(10)18(3)16(11)19/h6-9H,1-5H3
InChI Key DWZSQRJGZJNUEK-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C17H19NO4
Molecular Weight 301.34 g/mol
Exact Mass 301.13140809 g/mol
Topological Polar Surface Area (TPSA) 48.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.74
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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NSC363785
76525-26-3
CHEMBL21801
DTXSID00320710
NSC-363785
NCI60_003332

2D Structure

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2D Structure of Veprisine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9399 93.99%
Caco-2 + 0.9341 93.41%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4175 41.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9298 92.98%
OATP1B3 inhibitior + 0.9569 95.69%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6111 61.11%
P-glycoprotein inhibitior - 0.6418 64.18%
P-glycoprotein substrate - 0.6917 69.17%
CYP3A4 substrate + 0.6206 62.06%
CYP2C9 substrate - 0.7936 79.36%
CYP2D6 substrate - 0.8462 84.62%
CYP3A4 inhibition + 0.5283 52.83%
CYP2C9 inhibition - 0.8089 80.89%
CYP2C19 inhibition - 0.5324 53.24%
CYP2D6 inhibition - 0.9277 92.77%
CYP1A2 inhibition + 0.8089 80.89%
CYP2C8 inhibition - 0.7712 77.12%
CYP inhibitory promiscuity + 0.5929 59.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Danger 0.4925 49.25%
Eye corrosion - 0.9898 98.98%
Eye irritation + 0.6778 67.78%
Skin irritation - 0.8351 83.51%
Skin corrosion - 0.9518 95.18%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7901 79.01%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.6522 65.22%
skin sensitisation - 0.8849 88.49%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6154 61.54%
Acute Oral Toxicity (c) III 0.6724 67.24%
Estrogen receptor binding + 0.8677 86.77%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.6755 67.55%
Glucocorticoid receptor binding + 0.6925 69.25%
Aromatase binding + 0.6754 67.54%
PPAR gamma + 0.5811 58.11%
Honey bee toxicity - 0.7856 78.56%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.7597 75.97%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.05% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.66% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.47% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.14% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.50% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.09% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.51% 85.14%
CHEMBL1255126 O15151 Protein Mdm4 86.50% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.29% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.56% 97.14%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.51% 89.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.36% 93.99%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.03% 96.77%

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.
Euxylophora paraensis
Geijera balansae
Rauia resinosa
Stauranthus perforatus
Vepris louisii
Vepris renieri
Vepris soyauxii
Vepris stolzii

Cross-Links

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PubChem 338941
LOTUS LTS0109073
wikiData Q82078125