4-methoxy-3H-1,2-benzodioxole

Details

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Internal ID ceaf684e-97f0-4209-9d34-fa82f5a3b559
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 4-methoxy-3H-1,2-benzodioxole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H8O3/c1-9-7-3-2-4-8-6(7)5-10-11-8/h2-4H,5H2,1H3
InChI Key SMUNJBNGTHEKIO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O3
Molecular Weight 152.15 g/mol
Exact Mass 152.047344113 g/mol
Topological Polar Surface Area (TPSA) 27.70 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.52
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-methoxy-3H-1,2-benzodioxole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8535 85.35%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6245 62.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9786 97.86%
OATP1B3 inhibitior + 0.9777 97.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8845 88.45%
P-glycoprotein inhibitior - 0.9903 99.03%
P-glycoprotein substrate - 0.8908 89.08%
CYP3A4 substrate - 0.5914 59.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4613 46.13%
CYP3A4 inhibition - 0.9333 93.33%
CYP2C9 inhibition - 0.6281 62.81%
CYP2C19 inhibition + 0.5184 51.84%
CYP2D6 inhibition - 0.8494 84.94%
CYP1A2 inhibition + 0.8760 87.60%
CYP2C8 inhibition - 0.7127 71.27%
CYP inhibitory promiscuity + 0.5898 58.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8308 83.08%
Carcinogenicity (trinary) Warning 0.4435 44.35%
Eye corrosion - 0.8848 88.48%
Eye irritation + 0.9672 96.72%
Skin irritation - 0.7377 73.77%
Skin corrosion - 0.9550 95.50%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6227 62.27%
Micronuclear - 0.5719 57.19%
Hepatotoxicity + 0.6784 67.84%
skin sensitisation - 0.5739 57.39%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.6831 68.31%
Acute Oral Toxicity (c) III 0.7074 70.74%
Estrogen receptor binding - 0.9194 91.94%
Androgen receptor binding - 0.7862 78.62%
Thyroid receptor binding - 0.8842 88.42%
Glucocorticoid receptor binding - 0.9241 92.41%
Aromatase binding - 0.8550 85.50%
PPAR gamma - 0.8352 83.52%
Honey bee toxicity - 0.9081 90.81%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.5838 58.38%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.14% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.45% 96.09%
CHEMBL2535 P11166 Glucose transporter 88.45% 98.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.35% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.20% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.38% 86.33%
CHEMBL2581 P07339 Cathepsin D 83.53% 98.95%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.94% 94.03%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.18% 96.00%
CHEMBL240 Q12809 HERG 81.47% 89.76%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.42% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.27% 94.00%

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.
Cornus officinalis
Syzygium aromaticum

Cross-Links

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PubChem 5319407
NPASS NPC232914