1,3-Benzodioxole-5-carboxylic acid, 6-(2-(dimethylamino)ethyl)-

Details

Top
Internal ID 511b32e6-c592-4167-970b-855201c39f5e
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 6-[2-(dimethylamino)ethyl]-1,3-benzodioxole-5-carboxylic acid
SMILES (Canonical) CN(C)CCC1=CC2=C(C=C1C(=O)O)OCO2
SMILES (Isomeric) CN(C)CCC1=CC2=C(C=C1C(=O)O)OCO2
InChI InChI=1S/C12H15NO4/c1-13(2)4-3-8-5-10-11(17-7-16-10)6-9(8)12(14)15/h5-6H,3-4,7H2,1-2H3,(H,14,15)
InChI Key BOZYJTCKDCTZDN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H15NO4
Molecular Weight 237.25 g/mol
Exact Mass 237.10010796 g/mol
Topological Polar Surface Area (TPSA) 59.00 Ų
XlogP -0.70
Atomic LogP (AlogP) 1.22
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
76948-81-7
DTXSID00227735

2D Structure

Top
2D Structure of 1,3-Benzodioxole-5-carboxylic acid, 6-(2-(dimethylamino)ethyl)-

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8767 87.67%
Caco-2 + 0.7733 77.33%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.5374 53.74%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9363 93.63%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.8809 88.09%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8745 87.45%
P-glycoprotein inhibitior - 0.9424 94.24%
P-glycoprotein substrate - 0.9380 93.80%
CYP3A4 substrate - 0.6126 61.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7230 72.30%
CYP3A4 inhibition - 0.7756 77.56%
CYP2C9 inhibition - 0.7883 78.83%
CYP2C19 inhibition - 0.7974 79.74%
CYP2D6 inhibition + 0.5000 50.00%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9838 98.38%
CYP inhibitory promiscuity - 0.8143 81.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6097 60.97%
Eye corrosion - 0.9812 98.12%
Eye irritation + 0.7911 79.11%
Skin irritation - 0.7229 72.29%
Skin corrosion - 0.8753 87.53%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7539 75.39%
Micronuclear - 0.6826 68.26%
Hepatotoxicity + 0.6431 64.31%
skin sensitisation - 0.7706 77.06%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6709 67.09%
Acute Oral Toxicity (c) III 0.6204 62.04%
Estrogen receptor binding - 0.6456 64.56%
Androgen receptor binding - 0.8103 81.03%
Thyroid receptor binding - 0.6627 66.27%
Glucocorticoid receptor binding - 0.5162 51.62%
Aromatase binding + 0.5966 59.66%
PPAR gamma + 0.5726 57.26%
Honey bee toxicity - 0.9524 95.24%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.9600 96.00%
Fish aquatic toxicity + 0.7562 75.62%

Targets

Top

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.02% 96.77%
CHEMBL2581 P07339 Cathepsin D 94.77% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.46% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.08% 91.11%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.76% 93.00%
CHEMBL3401 O75469 Pregnane X receptor 86.71% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.60% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.26% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.19% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.48% 89.00%

Plants that contains it

Top
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.
Fumaria indica

Cross-Links

Top
PubChem 156979
LOTUS LTS0194819
wikiData Q83107557