3,4-Dimethoxy-N,N-dimethylbenzamide

Details

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Internal ID 58fe5143-3011-40ec-a715-fbb43fe9f0a9
Taxonomy Benzenoids > Benzene and substituted derivatives > Methoxybenzenes > Dimethoxybenzenes
IUPAC Name 3,4-dimethoxy-N,N-dimethylbenzamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H15NO3/c1-12(2)11(13)8-5-6-9(14-3)10(7-8)15-4/h5-7H,1-4H3
InChI Key WSSLDBVWUSSAGE-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C11H15NO3
Molecular Weight 209.24 g/mol
Exact Mass 209.10519334 g/mol
Topological Polar Surface Area (TPSA) 38.80 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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6967-45-9
DTXSID60290369
RefChem:91171
DTXCID80241515
NSC 68327
NSC68327
CHEMBL442652
SCHEMBL6409033
NSC-68327
AKOS008933487
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,4-Dimethoxy-N,N-dimethylbenzamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9808 98.08%
Caco-2 + 0.9160 91.60%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.8177 81.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9574 95.74%
OATP1B3 inhibitior + 0.9590 95.90%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9252 92.52%
P-glycoprotein inhibitior - 0.9522 95.22%
P-glycoprotein substrate - 0.8586 85.86%
CYP3A4 substrate - 0.5808 58.08%
CYP2C9 substrate - 0.7939 79.39%
CYP2D6 substrate - 0.7770 77.70%
CYP3A4 inhibition - 0.8744 87.44%
CYP2C9 inhibition - 0.9523 95.23%
CYP2C19 inhibition - 0.7877 78.77%
CYP2D6 inhibition - 0.9593 95.93%
CYP1A2 inhibition + 0.7257 72.57%
CYP2C8 inhibition - 0.6975 69.75%
CYP inhibitory promiscuity - 0.7606 76.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7843 78.43%
Carcinogenicity (trinary) Non-required 0.6149 61.49%
Eye corrosion - 0.9214 92.14%
Eye irritation + 0.9587 95.87%
Skin irritation - 0.7905 79.05%
Skin corrosion - 0.9665 96.65%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4576 45.76%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.5870 58.70%
skin sensitisation - 0.9210 92.10%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6274 62.74%
Acute Oral Toxicity (c) III 0.5979 59.79%
Estrogen receptor binding - 0.7019 70.19%
Androgen receptor binding - 0.8095 80.95%
Thyroid receptor binding - 0.6551 65.51%
Glucocorticoid receptor binding - 0.7224 72.24%
Aromatase binding - 0.5774 57.74%
PPAR gamma - 0.7795 77.95%
Honey bee toxicity - 0.9664 96.64%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6266 62.66%
Fish aquatic toxicity + 0.6785 67.85%

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
CHEMBL1255126 O15151 Protein Mdm4 95.25% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.14% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.36% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.84% 86.33%
CHEMBL2535 P11166 Glucose transporter 89.88% 98.75%
CHEMBL4208 P20618 Proteasome component C5 88.40% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.13% 95.56%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 81.22% 95.48%
CHEMBL340 P08684 Cytochrome P450 3A4 80.39% 91.19%

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.
Aristolochia kaempferi

Cross-Links

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PubChem 249720
LOTUS LTS0121527
wikiData Q82028011