[(2S,3R,4R)-4-(1,3-benzodioxol-5-yl)-4-(3,4-dimethoxyphenyl)-2,3-dimethylbutyl] acetate

Details

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Internal ID 664cbf97-1629-4a90-9886-6ede4ce46e47
Taxonomy Benzenoids > Benzene and substituted derivatives > Methoxybenzenes > Dimethoxybenzenes
IUPAC Name [(2S,3R,4R)-4-(1,3-benzodioxol-5-yl)-4-(3,4-dimethoxyphenyl)-2,3-dimethylbutyl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H28O6/c1-14(12-27-16(3)24)15(2)23(17-6-8-19(25-4)21(10-17)26-5)18-7-9-20-22(11-18)29-13-28-20/h6-11,14-15,23H,12-13H2,1-5H3/t14-,15+,23-/m1/s1
InChI Key IYHIDVFUEBFZJV-HUYGQZFBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H28O6
Molecular Weight 400.50 g/mol
Exact Mass 400.18858861 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.40
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2S,3R,4R)-4-(1,3-benzodioxol-5-yl)-4-(3,4-dimethoxyphenyl)-2,3-dimethylbutyl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9903 99.03%
Caco-2 + 0.8017 80.17%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6169 61.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9108 91.08%
OATP1B3 inhibitior + 0.9521 95.21%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9458 94.58%
P-glycoprotein inhibitior + 0.8963 89.63%
P-glycoprotein substrate - 0.7005 70.05%
CYP3A4 substrate - 0.5128 51.28%
CYP2C9 substrate - 0.7919 79.19%
CYP2D6 substrate - 0.8306 83.06%
CYP3A4 inhibition + 0.7982 79.82%
CYP2C9 inhibition + 0.8628 86.28%
CYP2C19 inhibition + 0.8850 88.50%
CYP2D6 inhibition + 0.5581 55.81%
CYP1A2 inhibition - 0.5622 56.22%
CYP2C8 inhibition - 0.8771 87.71%
CYP inhibitory promiscuity + 0.8472 84.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4252 42.52%
Eye corrosion - 0.9845 98.45%
Eye irritation - 0.9357 93.57%
Skin irritation - 0.8106 81.06%
Skin corrosion - 0.9646 96.46%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8643 86.43%
Micronuclear - 0.5226 52.26%
Hepatotoxicity + 0.5340 53.40%
skin sensitisation - 0.6377 63.77%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6213 62.13%
Acute Oral Toxicity (c) III 0.6913 69.13%
Estrogen receptor binding + 0.7937 79.37%
Androgen receptor binding + 0.7692 76.92%
Thyroid receptor binding + 0.7149 71.49%
Glucocorticoid receptor binding + 0.7873 78.73%
Aromatase binding + 0.5249 52.49%
PPAR gamma + 0.5880 58.80%
Honey bee toxicity - 0.8832 88.32%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7055 70.55%
Fish aquatic toxicity + 0.9891 98.91%

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 97.33% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.06% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.95% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.17% 96.77%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.20% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.80% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.76% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.21% 98.95%
CHEMBL2413 P32246 C-C chemokine receptor type 1 90.86% 89.50%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.75% 94.80%
CHEMBL4208 P20618 Proteasome component C5 89.18% 90.00%
CHEMBL2535 P11166 Glucose transporter 89.16% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.32% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.65% 89.62%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.86% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.65% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 83.54% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.90% 89.00%

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.
Virola elongata

Cross-Links

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PubChem 162907944
LOTUS LTS0216506
wikiData Q105122747