1-(Isothiocyanatomethyl)-2-heptyl-3-methyl-4(1H)-quinolone

Details

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Internal ID d283d886-805d-4bda-bdf2-bdca29c18def
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 2-heptyl-1-(isothiocyanatomethyl)-3-methylquinolin-4-one
SMILES (Canonical) CCCCCCCC1=C(C(=O)C2=CC=CC=C2N1CN=C=S)C
SMILES (Isomeric) CCCCCCCC1=C(C(=O)C2=CC=CC=C2N1CN=C=S)C
InChI InChI=1S/C19H24N2OS/c1-3-4-5-6-7-11-17-15(2)19(22)16-10-8-9-12-18(16)21(17)13-20-14-23/h8-10,12H,3-7,11,13H2,1-2H3
InChI Key XYOBWFUHYBVXKR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24N2OS
Molecular Weight 328.50 g/mol
Exact Mass 328.16093457 g/mol
Topological Polar Surface Area (TPSA) 64.80 Ų
XlogP 6.90
Atomic LogP (AlogP) 4.88
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(Isothiocyanatomethyl)-2-heptyl-3-methyl-4(1H)-quinolone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9775 97.75%
Caco-2 + 0.6006 60.06%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6394 63.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8935 89.35%
OATP1B3 inhibitior + 0.9398 93.98%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior + 0.7250 72.50%
BSEP inhibitior + 0.6760 67.60%
P-glycoprotein inhibitior + 0.6018 60.18%
P-glycoprotein substrate - 0.5774 57.74%
CYP3A4 substrate + 0.6120 61.20%
CYP2C9 substrate - 0.5764 57.64%
CYP2D6 substrate - 0.8473 84.73%
CYP3A4 inhibition - 0.6476 64.76%
CYP2C9 inhibition - 0.7120 71.20%
CYP2C19 inhibition - 0.5093 50.93%
CYP2D6 inhibition - 0.7030 70.30%
CYP1A2 inhibition + 0.7793 77.93%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.7961 79.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6694 66.94%
Eye corrosion - 0.9837 98.37%
Eye irritation - 0.9525 95.25%
Skin irritation - 0.7552 75.52%
Skin corrosion - 0.8928 89.28%
Ames mutagenesis - 0.5354 53.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7931 79.31%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.5859 58.59%
skin sensitisation - 0.8224 82.24%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.7792 77.92%
Acute Oral Toxicity (c) III 0.6155 61.55%
Estrogen receptor binding + 0.6472 64.72%
Androgen receptor binding - 0.6212 62.12%
Thyroid receptor binding + 0.6952 69.52%
Glucocorticoid receptor binding - 0.5385 53.85%
Aromatase binding - 0.5057 50.57%
PPAR gamma + 0.7406 74.06%
Honey bee toxicity - 0.9379 93.79%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.7872 78.72%
Fish aquatic toxicity + 0.9641 96.41%

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 98.49% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 98.36% 85.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.90% 95.56%
CHEMBL230 P35354 Cyclooxygenase-2 95.61% 89.63%
CHEMBL240 Q12809 HERG 95.41% 89.76%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.45% 92.08%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 90.47% 80.78%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.14% 86.33%
CHEMBL255 P29275 Adenosine A2b receptor 88.31% 98.59%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.27% 93.99%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.11% 93.65%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 87.73% 85.40%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.61% 99.23%
CHEMBL5805 Q9NR97 Toll-like receptor 8 87.42% 96.25%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.13% 97.25%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.53% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.18% 89.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.96% 91.81%
CHEMBL1978 P11511 Cytochrome P450 19A1 84.31% 91.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.95% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 82.56% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 82.17% 93.31%
CHEMBL2885 P07451 Carbonic anhydrase III 81.91% 87.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.25% 91.11%
CHEMBL3769292 Q9H773 dCTP pyrophosphatase 1 80.50% 94.40%

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.
Zanthoxylum schinifolium

Cross-Links

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PubChem 72206151
NPASS NPC191266