beta-D-Glucosylisoeugenol

Details

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Internal ID 89beef80-7adf-4305-8728-726d72bfdaa4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[2-methoxy-4-[(E)-prop-1-enyl]phenoxy]oxane-3,4,5-triol
SMILES (Canonical) CC=CC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC
SMILES (Isomeric) C/C=C/C1=CC(=C(C=C1)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)OC
InChI InChI=1S/C16H22O7/c1-3-4-9-5-6-10(11(7-9)21-2)22-16-15(20)14(19)13(18)12(8-17)23-16/h3-7,12-20H,8H2,1-2H3/b4-3+/t12-,13-,14+,15-,16-/m1/s1
InChI Key KEOQVSSHVYLFJO-BSULOXNCSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H22O7
Molecular Weight 326.34 g/mol
Exact Mass 326.13655304 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.09
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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NCGC00385761-01
2-Methoxy-4-(1-propenyl)phenyl beta-D-glucopyranoside
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[2-methoxy-4-[(E)-prop-1-enyl]phenoxy]oxane-3,4,5-triol
120442-72-0

2D Structure

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2D Structure of beta-D-Glucosylisoeugenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7105 71.05%
Caco-2 - 0.7476 74.76%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5666 56.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8834 88.34%
OATP1B3 inhibitior + 0.9741 97.41%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6615 66.15%
P-glycoprotein inhibitior - 0.9152 91.52%
P-glycoprotein substrate - 0.8662 86.62%
CYP3A4 substrate - 0.5126 51.26%
CYP2C9 substrate - 0.6225 62.25%
CYP2D6 substrate - 0.8163 81.63%
CYP3A4 inhibition - 0.7496 74.96%
CYP2C9 inhibition - 0.8671 86.71%
CYP2C19 inhibition - 0.7900 79.00%
CYP2D6 inhibition - 0.8681 86.81%
CYP1A2 inhibition - 0.8426 84.26%
CYP2C8 inhibition + 0.5278 52.78%
CYP inhibitory promiscuity - 0.5530 55.30%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7264 72.64%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9670 96.70%
Skin irritation - 0.8345 83.45%
Skin corrosion - 0.9522 95.22%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4510 45.10%
Micronuclear - 0.5241 52.41%
Hepatotoxicity - 0.7947 79.47%
skin sensitisation - 0.8148 81.48%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.8529 85.29%
Acute Oral Toxicity (c) III 0.7596 75.96%
Estrogen receptor binding - 0.7060 70.60%
Androgen receptor binding - 0.6657 66.57%
Thyroid receptor binding - 0.5464 54.64%
Glucocorticoid receptor binding - 0.4909 49.09%
Aromatase binding - 0.6047 60.47%
PPAR gamma + 0.5262 52.62%
Honey bee toxicity - 0.8384 83.84%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.6603 66.03%

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 96.81% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 96.77% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.38% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.40% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.29% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 87.84% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.77% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 86.99% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.31% 95.56%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.86% 89.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.25% 95.89%
CHEMBL3194 P02766 Transthyretin 81.85% 90.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.56% 86.92%
CHEMBL4208 P20618 Proteasome component C5 80.56% 90.00%

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.
Alluaudia ascendens
Brassica nigra
Cardiocrinum cordatum
Centaurea collina
Echinocereus berlandieri
Euonymus nanus
Isodon weisiensis
Millingtonia hortensis
Physostigma venenosum

Cross-Links

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PubChem 14189874
NPASS NPC261707
LOTUS LTS0011612
wikiData Q105140111