2,6-Di((methoxythio)carbonyl)pyridine

Details

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Internal ID a24009ff-9838-414b-ac05-ceab2933f224
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Pyridinecarboxylic acids and derivatives
IUPAC Name 2-S,6-S-dimethoxy pyridine-2,6-dicarbothioate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H9NO4S2/c1-13-15-8(11)6-4-3-5-7(10-6)9(12)16-14-2/h3-5H,1-2H3
InChI Key CVXQTZDTQXJFEV-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C9H9NO4S2
Molecular Weight 259.30 g/mol
Exact Mass 258.99730012 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.95
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,6-Di((methoxythio)carbonyl)pyridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9515 95.15%
Caco-2 - 0.6687 66.87%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7264 72.64%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9783 97.83%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8641 86.41%
P-glycoprotein inhibitior - 0.9382 93.82%
P-glycoprotein substrate - 0.9690 96.90%
CYP3A4 substrate - 0.6141 61.41%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8593 85.93%
CYP3A4 inhibition - 0.9383 93.83%
CYP2C9 inhibition - 0.7535 75.35%
CYP2C19 inhibition - 0.7175 71.75%
CYP2D6 inhibition - 0.9171 91.71%
CYP1A2 inhibition - 0.6288 62.88%
CYP2C8 inhibition - 0.7957 79.57%
CYP inhibitory promiscuity - 0.9161 91.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5807 58.07%
Carcinogenicity (trinary) Non-required 0.6747 67.47%
Eye corrosion - 0.9160 91.60%
Eye irritation + 0.9607 96.07%
Skin irritation - 0.6579 65.79%
Skin corrosion - 0.9152 91.52%
Ames mutagenesis - 0.6078 60.78%
Human Ether-a-go-go-Related Gene inhibition - 0.7707 77.07%
Micronuclear + 0.6100 61.00%
Hepatotoxicity - 0.5341 53.41%
skin sensitisation - 0.8022 80.22%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.7050 70.50%
Acute Oral Toxicity (c) III 0.5097 50.97%
Estrogen receptor binding - 0.6504 65.04%
Androgen receptor binding - 0.8078 80.78%
Thyroid receptor binding - 0.6950 69.50%
Glucocorticoid receptor binding - 0.7465 74.65%
Aromatase binding - 0.5707 57.07%
PPAR gamma - 0.7808 78.08%
Honey bee toxicity - 0.9799 97.99%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5345 53.45%
Fish aquatic toxicity - 0.5528 55.28%

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 93.35% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.04% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.94% 94.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.77% 81.11%
CHEMBL2581 P07339 Cathepsin D 84.31% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.16% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.44% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 82.00% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 13715969
LOTUS LTS0169725
wikiData Q75067395