Evocarpine

Details

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Internal ID e96bc8c0-2112-486b-be3b-00178a6d7667
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 1-methyl-2-[(Z)-tridec-8-enyl]quinolin-4-one
SMILES (Canonical) CCCCC=CCCCCCCCC1=CC(=O)C2=CC=CC=C2N1C
SMILES (Isomeric) CCCC/C=C\CCCCCCCC1=CC(=O)C2=CC=CC=C2N1C
InChI InChI=1S/C23H33NO/c1-3-4-5-6-7-8-9-10-11-12-13-16-20-19-23(25)21-17-14-15-18-22(21)24(20)2/h6-7,14-15,17-19H,3-5,8-13,16H2,1-2H3/b7-6-
InChI Key HWFYWIVOYBPLQU-SREVYHEPSA-N
Popularity 20 references in papers

Physical and Chemical Properties

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Molecular Formula C23H33NO
Molecular Weight 339.50 g/mol
Exact Mass 339.256214676 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 7.30
Atomic LogP (AlogP) 6.17
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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15266-38-3
(Z)-1-Methyl-2-(tridec-8-en-1-yl)quinolin-4(1H)-one
1-methyl-2-[(Z)-tridec-8-enyl]quinolin-4-one
CHEMBL5173740
SCHEMBL15944383
CHEBI:80821
HY-N2060
AKOS016010722
MS-25177
CS-0018549
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Evocarpine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 + 0.6837 68.37%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.5115 51.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8667 86.67%
OATP1B3 inhibitior + 0.9510 95.10%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.7250 72.50%
BSEP inhibitior + 0.8398 83.98%
P-glycoprotein inhibitior + 0.7086 70.86%
P-glycoprotein substrate - 0.6048 60.48%
CYP3A4 substrate + 0.5883 58.83%
CYP2C9 substrate - 0.5824 58.24%
CYP2D6 substrate - 0.8409 84.09%
CYP3A4 inhibition - 0.8156 81.56%
CYP2C9 inhibition - 0.7545 75.45%
CYP2C19 inhibition - 0.5331 53.31%
CYP2D6 inhibition + 0.5383 53.83%
CYP1A2 inhibition + 0.8422 84.22%
CYP2C8 inhibition - 0.7254 72.54%
CYP inhibitory promiscuity + 0.8018 80.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6384 63.84%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9278 92.78%
Skin irritation - 0.7572 75.72%
Skin corrosion - 0.8686 86.86%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9026 90.26%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.5014 50.14%
skin sensitisation - 0.8198 81.98%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.6503 65.03%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.5933 59.33%
Acute Oral Toxicity (c) III 0.6532 65.32%
Estrogen receptor binding + 0.8217 82.17%
Androgen receptor binding + 0.7187 71.87%
Thyroid receptor binding + 0.7073 70.73%
Glucocorticoid receptor binding - 0.4788 47.88%
Aromatase binding - 0.5466 54.66%
PPAR gamma + 0.7965 79.65%
Honey bee toxicity - 0.9700 97.00%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7700 77.00%
Fish aquatic toxicity + 0.9676 96.76%

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
CHEMBL2581 P07339 Cathepsin D 99.28% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.45% 95.56%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 97.10% 92.08%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.84% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.85% 86.33%
CHEMBL240 Q12809 HERG 91.45% 89.76%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.91% 85.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.77% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 89.34% 89.63%
CHEMBL1781 P11387 DNA topoisomerase I 89.09% 97.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.74% 91.11%
CHEMBL255 P29275 Adenosine A2b receptor 88.21% 98.59%
CHEMBL3401 O75469 Pregnane X receptor 88.01% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.54% 89.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 84.42% 96.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.11% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 83.69% 93.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.25% 96.00%

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.
Hesperocyparis abramsiana
Tetradium ruticarpum
Vincetoxicum indicum var. indicum

Cross-Links

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PubChem 5317303
NPASS NPC289145
LOTUS LTS0193684
wikiData Q27149864