(Z)-Isoconiferin

Details

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Internal ID 6073a65b-2d15-4ac3-b409-1aa0f920738a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl glycosides > Fatty acyl glycosides of mono- and disaccharides
IUPAC Name (2R,3R,4S,5S,6R)-2-[(Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) COC1=C(C=CC(=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)/C=C\CO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O
InChI InChI=1S/C16H22O8/c1-22-11-7-9(4-5-10(11)18)3-2-6-23-16-15(21)14(20)13(19)12(8-17)24-16/h2-5,7,12-21H,6,8H2,1H3/b3-2-/t12-,13-,14+,15-,16-/m1/s1
InChI Key JOIDTHZGWZZGMU-JNDSXIQISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H22O8
Molecular Weight 342.34 g/mol
Exact Mass 342.13146766 g/mol
Topological Polar Surface Area (TPSA) 129.00 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.77
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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66791-74-0
(2Z)-3-(4-Hydroxy-3-methoxyphenyl)-2-propen-1-yl beta-D-glucopyranoside

2D Structure

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2D Structure of (Z)-Isoconiferin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7680 76.80%
Caco-2 - 0.7428 74.28%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5647 56.47%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8625 86.25%
OATP1B3 inhibitior + 0.9775 97.75%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7748 77.48%
P-glycoprotein inhibitior - 0.9109 91.09%
P-glycoprotein substrate - 0.9187 91.87%
CYP3A4 substrate + 0.5098 50.98%
CYP2C9 substrate - 0.6100 61.00%
CYP2D6 substrate - 0.8073 80.73%
CYP3A4 inhibition - 0.8726 87.26%
CYP2C9 inhibition - 0.8603 86.03%
CYP2C19 inhibition - 0.8011 80.11%
CYP2D6 inhibition - 0.8955 89.55%
CYP1A2 inhibition - 0.8672 86.72%
CYP2C8 inhibition + 0.5295 52.95%
CYP inhibitory promiscuity - 0.5395 53.95%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6529 65.29%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9285 92.85%
Skin irritation - 0.8308 83.08%
Skin corrosion - 0.9511 95.11%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5527 55.27%
Micronuclear - 0.5541 55.41%
Hepatotoxicity - 0.9040 90.40%
skin sensitisation - 0.8190 81.90%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.8105 81.05%
Acute Oral Toxicity (c) III 0.7481 74.81%
Estrogen receptor binding - 0.6302 63.02%
Androgen receptor binding - 0.5544 55.44%
Thyroid receptor binding + 0.5748 57.48%
Glucocorticoid receptor binding - 0.5754 57.54%
Aromatase binding - 0.6022 60.22%
PPAR gamma - 0.5458 54.58%
Honey bee toxicity - 0.8626 86.26%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity - 0.4401 44.01%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.40% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 96.23% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.64% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.59% 86.33%
CHEMBL3194 P02766 Transthyretin 91.22% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.19% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 90.10% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.80% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.33% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 88.06% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 86.72% 91.49%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.87% 86.92%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.23% 99.15%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.43% 95.89%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.43% 91.71%

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.
Fagus grandifolia
Fagus sylvatica
Juniperus communis

Cross-Links

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PubChem 14330981
LOTUS LTS0255846
wikiData Q105132350