Diethyl 2,6-dimethylpyridine-3,5-dicarboxylate

Details

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Internal ID 86958841-3429-412e-87e5-288461c34c69
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Pyridinecarboxylic acids and derivatives > Pyridinecarboxylic acids
IUPAC Name diethyl 2,6-dimethylpyridine-3,5-dicarboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H17NO4/c1-5-17-12(15)10-7-11(13(16)18-6-2)9(4)14-8(10)3/h7H,5-6H2,1-4H3
InChI Key DIIWSYPKAJVXBV-UHFFFAOYSA-N
Popularity 64 references in papers

Physical and Chemical Properties

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Molecular Formula C13H17NO4
Molecular Weight 251.28 g/mol
Exact Mass 251.11575802 g/mol
Topological Polar Surface Area (TPSA) 65.50 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.05
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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DTXSID70289002
RefChem:587082
DTXCID20240148
625-393-1
1149-24-2
Diethyl 2,6-dimethyl-3,5-pyridinedicarboxylate
MFCD00023506
3,5-diethyl 2,6-dimethylpyridine-3,5-dicarboxylate
2,6-Dimethyl-pyridine-3,5-dicarboxylic acid diethyl ester
3,5-Pyridinedicarboxylic acid, 2,6-dimethyl-, 3,5-diethyl ester
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Diethyl 2,6-dimethylpyridine-3,5-dicarboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9802 98.02%
Caco-2 + 0.8531 85.31%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.8798 87.98%
OATP2B1 inhibitior - 0.8617 86.17%
OATP1B1 inhibitior + 0.9591 95.91%
OATP1B3 inhibitior + 0.9563 95.63%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7226 72.26%
P-glycoprotein inhibitior - 0.8046 80.46%
P-glycoprotein substrate - 0.9793 97.93%
CYP3A4 substrate - 0.6437 64.37%
CYP2C9 substrate - 0.8338 83.38%
CYP2D6 substrate - 0.9099 90.99%
CYP3A4 inhibition - 0.6969 69.69%
CYP2C9 inhibition - 0.6144 61.44%
CYP2C19 inhibition - 0.6593 65.93%
CYP2D6 inhibition - 0.9284 92.84%
CYP1A2 inhibition + 0.6739 67.39%
CYP2C8 inhibition - 0.7886 78.86%
CYP inhibitory promiscuity - 0.5634 56.34%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6507 65.07%
Carcinogenicity (trinary) Non-required 0.6133 61.33%
Eye corrosion - 0.9755 97.55%
Eye irritation + 0.9803 98.03%
Skin irritation - 0.6998 69.98%
Skin corrosion - 0.9559 95.59%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6302 63.02%
Micronuclear - 0.6026 60.26%
Hepatotoxicity + 0.5677 56.77%
skin sensitisation - 0.8513 85.13%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.6192 61.92%
Acute Oral Toxicity (c) III 0.6425 64.25%
Estrogen receptor binding + 0.6230 62.30%
Androgen receptor binding - 0.8350 83.50%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.4669 46.69%
Aromatase binding + 0.6841 68.41%
PPAR gamma - 0.6319 63.19%
Honey bee toxicity - 0.9775 97.75%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7005 70.05%
Fish aquatic toxicity + 0.7411 74.11%

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 93.40% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 88.85% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.96% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.87% 93.65%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.57% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.66% 99.17%
CHEMBL2581 P07339 Cathepsin D 85.61% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.97% 96.95%

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.
Viburnum tinus

Cross-Links

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PubChem 245983
LOTUS LTS0229801
wikiData Q82026148