(3R)-3-methyl-3,4-dihydro-1,2-benzodioxine-5-carbaldehyde

Details

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Internal ID fabd13a9-7aee-413c-adab-b5e53e92d33e
Taxonomy Organoheterocyclic compounds > Benzodioxanes > Benzo-1,2-dioxanes
IUPAC Name (3R)-3-methyl-3,4-dihydro-1,2-benzodioxine-5-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H10O3/c1-7-5-9-8(6-11)3-2-4-10(9)13-12-7/h2-4,6-7H,5H2,1H3/t7-/m1/s1
InChI Key HAVVTRFZWPOIAG-SSDOTTSWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O3
Molecular Weight 178.18 g/mol
Exact Mass 178.062994177 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.75
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 (3R)-3-methyl-3,4-dihydro-1,2-benzodioxine-5-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.8280 82.80%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6419 64.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9088 90.88%
OATP1B3 inhibitior + 0.9820 98.20%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9382 93.82%
P-glycoprotein inhibitior - 0.9629 96.29%
P-glycoprotein substrate - 0.8771 87.71%
CYP3A4 substrate - 0.5814 58.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7601 76.01%
CYP3A4 inhibition - 0.7345 73.45%
CYP2C9 inhibition - 0.5820 58.20%
CYP2C19 inhibition - 0.5148 51.48%
CYP2D6 inhibition - 0.8950 89.50%
CYP1A2 inhibition + 0.9047 90.47%
CYP2C8 inhibition - 0.8729 87.29%
CYP inhibitory promiscuity - 0.5929 59.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7913 79.13%
Carcinogenicity (trinary) Non-required 0.5666 56.66%
Eye corrosion - 0.8297 82.97%
Eye irritation + 0.9335 93.35%
Skin irritation + 0.4922 49.22%
Skin corrosion - 0.9423 94.23%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5828 58.28%
Micronuclear - 0.5259 52.59%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.5231 52.31%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.5361 53.61%
Acute Oral Toxicity (c) III 0.7587 75.87%
Estrogen receptor binding - 0.7477 74.77%
Androgen receptor binding - 0.8235 82.35%
Thyroid receptor binding - 0.7562 75.62%
Glucocorticoid receptor binding - 0.9279 92.79%
Aromatase binding - 0.8712 87.12%
PPAR gamma - 0.7977 79.77%
Honey bee toxicity - 0.8923 89.23%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.7889 78.89%

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 96.52% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.53% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.38% 94.80%
CHEMBL1951 P21397 Monoamine oxidase A 91.36% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 87.76% 94.73%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 87.30% 98.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.18% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.82% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.91% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.49% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.01% 96.09%

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.
Bombax anceps

Cross-Links

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PubChem 162957279
LOTUS LTS0180551
wikiData Q105025096