rel-(2R,3R)-2,3-Dihydro-2-(4-hydroxyphenyl)-3-methyl-5-benzofurancarboxaldehyde

Details

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Internal ID 029c17ae-3902-477c-a624-09abbbd10bab
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name (2R,3R)-2-(4-hydroxyphenyl)-3-methyl-2,3-dihydro-1-benzofuran-5-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H14O3/c1-10-14-8-11(9-17)2-7-15(14)19-16(10)12-3-5-13(18)6-4-12/h2-10,16,18H,1H3/t10-,16-/m1/s1
InChI Key WAURLMRAHQJPGC-QLJPJBMISA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O3
Molecular Weight 254.28 g/mol
Exact Mass 254.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.44
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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rel-(2R,3R)-2,3-Dihydro-2-(4-hydroxyphenyl)-3-methyl-5-benzofurancarboxaldehyde
172617-91-3

2D Structure

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2D Structure of rel-(2R,3R)-2,3-Dihydro-2-(4-hydroxyphenyl)-3-methyl-5-benzofurancarboxaldehyde

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 + 0.6050 60.50%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8219 82.19%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior - 0.3531 35.31%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7691 76.91%
P-glycoprotein inhibitior - 0.8813 88.13%
P-glycoprotein substrate - 0.9161 91.61%
CYP3A4 substrate - 0.5172 51.72%
CYP2C9 substrate - 0.7790 77.90%
CYP2D6 substrate - 0.7019 70.19%
CYP3A4 inhibition - 0.7740 77.40%
CYP2C9 inhibition + 0.9273 92.73%
CYP2C19 inhibition + 0.8192 81.92%
CYP2D6 inhibition - 0.9326 93.26%
CYP1A2 inhibition + 0.9608 96.08%
CYP2C8 inhibition + 0.4624 46.24%
CYP inhibitory promiscuity + 0.7536 75.36%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Warning 0.4662 46.62%
Eye corrosion - 0.9895 98.95%
Eye irritation + 0.5980 59.80%
Skin irritation + 0.5517 55.17%
Skin corrosion - 0.9804 98.04%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4248 42.48%
Micronuclear + 0.7559 75.59%
Hepatotoxicity - 0.6128 61.28%
skin sensitisation - 0.8172 81.72%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.4677 46.77%
Acute Oral Toxicity (c) III 0.7101 71.01%
Estrogen receptor binding + 0.7291 72.91%
Androgen receptor binding + 0.5289 52.89%
Thyroid receptor binding - 0.5506 55.06%
Glucocorticoid receptor binding - 0.5512 55.12%
Aromatase binding + 0.6801 68.01%
PPAR gamma + 0.5357 53.57%
Honey bee toxicity - 0.9005 90.05%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9752 97.52%

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
CHEMBL1951 P21397 Monoamine oxidase A 97.37% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.62% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.40% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.40% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.08% 89.00%
CHEMBL2581 P07339 Cathepsin D 88.76% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.35% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.16% 96.09%
CHEMBL3194 P02766 Transthyretin 85.39% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.65% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.47% 85.14%

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.
Piper aequale
Piper regnellii

Cross-Links

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PubChem 101712154
LOTUS LTS0139871
wikiData Q105300486