1,6-Dihydro-1-methyl-6-oxo-3-pyridinecarbonitrile

Details

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Internal ID 04698f8c-0687-4182-9cd6-69c69671ed53
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > 3-pyridinecarbonitriles
IUPAC Name 1-methyl-6-oxopyridine-3-carbonitrile
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H6N2O/c1-9-5-6(4-8)2-3-7(9)10/h2-3,5H,1H3
InChI Key XICDFLICODYZJE-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C7H6N2O
Molecular Weight 134.14 g/mol
Exact Mass 134.048012819 g/mol
Topological Polar Surface Area (TPSA) 44.10 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.26
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1,6-Dihydro-1-methyl-6-oxo-3-pyridinecarbonitrile
3-Pyridinecarbonitrile, 1,6-dihydro-1-methyl-6-oxo-
DTXSID20227611
RefChem:1053507
DTXCID70150102
1-Methyl-6-oxo-1,6-dihydropyridine-3-carbonitrile
1-methyl-6-oxopyridine-3-carbonitrile
MFCD11975500
1-Methyl-6-oxo-1,6-dihydro-pyridine-3-carbonitrile
Nudiflorine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,6-Dihydro-1-methyl-6-oxo-3-pyridinecarbonitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9652 96.52%
Caco-2 + 0.9474 94.74%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.9429 94.29%
Subcellular localzation Mitochondria 0.7398 73.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9660 96.60%
OATP1B3 inhibitior + 0.9564 95.64%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8261 82.61%
P-glycoprotein inhibitior - 0.9842 98.42%
P-glycoprotein substrate - 0.9586 95.86%
CYP3A4 substrate - 0.6442 64.42%
CYP2C9 substrate - 0.7919 79.19%
CYP2D6 substrate - 0.8566 85.66%
CYP3A4 inhibition - 0.8602 86.02%
CYP2C9 inhibition - 0.9359 93.59%
CYP2C19 inhibition - 0.9817 98.17%
CYP2D6 inhibition - 0.9751 97.51%
CYP1A2 inhibition - 0.7961 79.61%
CYP2C8 inhibition - 0.9922 99.22%
CYP inhibitory promiscuity - 0.8981 89.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6531 65.31%
Eye corrosion - 0.9431 94.31%
Eye irritation + 0.9861 98.61%
Skin irritation - 0.6378 63.78%
Skin corrosion - 0.9374 93.74%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7108 71.08%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.8501 85.01%
skin sensitisation - 0.8319 83.19%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6451 64.51%
Nephrotoxicity + 0.5872 58.72%
Acute Oral Toxicity (c) III 0.6481 64.81%
Estrogen receptor binding - 0.9396 93.96%
Androgen receptor binding - 0.7316 73.16%
Thyroid receptor binding - 0.8450 84.50%
Glucocorticoid receptor binding - 0.7476 74.76%
Aromatase binding - 0.8709 87.09%
PPAR gamma - 0.8133 81.33%
Honey bee toxicity - 0.9059 90.59%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity - 0.8617 86.17%

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 94.45% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 91.19% 93.65%
CHEMBL1871 P10275 Androgen Receptor 90.50% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.20% 96.09%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.20% 96.12%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.66% 95.56%
CHEMBL2487 P05067 Beta amyloid A4 protein 82.05% 96.74%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.63% 86.33%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 81.45% 96.42%

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.
Mallotus nudiflorus

Cross-Links

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PubChem 69851
LOTUS LTS0097756
wikiData Q83107420