4-hydroxy-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]-2-methoxy-5-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzaldehyde

Details

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Internal ID abfdc823-5c5e-42e6-ad05-b8c3a4891522
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides
IUPAC Name 4-hydroxy-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]-2-methoxy-5-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzaldehyde
SMILES (Canonical) CC1=C(C(=C(C(=C1OC2C(C(C(C(O2)CO)O)O)O)C=O)OC)C(=O)C=CC3=CC=C(C=C3)O)O
SMILES (Isomeric) CC1=C(C(=C(C(=C1O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)C=O)OC)C(=O)/C=C/C3=CC=C(C=C3)O)O
InChI InChI=1S/C24H26O11/c1-11-18(29)17(15(28)8-5-12-3-6-13(27)7-4-12)23(33-2)14(9-25)22(11)35-24-21(32)20(31)19(30)16(10-26)34-24/h3-9,16,19-21,24,26-27,29-32H,10H2,1-2H3/b8-5+/t16-,19-,20+,21-,24+/m1/s1
InChI Key KMSVNFAUWMQQKB-JZFIBNFQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H26O11
Molecular Weight 490.50 g/mol
Exact Mass 490.14751164 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.30
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-hydroxy-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]-2-methoxy-5-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6994 69.94%
Caco-2 - 0.8964 89.64%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.5774 57.74%
OATP2B1 inhibitior - 0.6973 69.73%
OATP1B1 inhibitior + 0.7991 79.91%
OATP1B3 inhibitior + 0.9607 96.07%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7943 79.43%
P-glycoprotein inhibitior - 0.5869 58.69%
P-glycoprotein substrate - 0.7043 70.43%
CYP3A4 substrate + 0.6230 62.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8629 86.29%
CYP3A4 inhibition - 0.6985 69.85%
CYP2C9 inhibition - 0.8371 83.71%
CYP2C19 inhibition - 0.8599 85.99%
CYP2D6 inhibition - 0.8992 89.92%
CYP1A2 inhibition - 0.8692 86.92%
CYP2C8 inhibition + 0.7362 73.62%
CYP inhibitory promiscuity - 0.7706 77.06%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7762 77.62%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9358 93.58%
Skin irritation - 0.8568 85.68%
Skin corrosion - 0.9534 95.34%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6661 66.61%
Micronuclear + 0.5833 58.33%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.8736 87.36%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.8069 80.69%
Acute Oral Toxicity (c) III 0.7266 72.66%
Estrogen receptor binding + 0.7524 75.24%
Androgen receptor binding + 0.5955 59.55%
Thyroid receptor binding + 0.5470 54.70%
Glucocorticoid receptor binding + 0.6680 66.80%
Aromatase binding + 0.5291 52.91%
PPAR gamma + 0.6725 67.25%
Honey bee toxicity - 0.8428 84.28%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6955 69.55%
Fish aquatic toxicity + 0.9003 90.03%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.60% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 96.30% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.61% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.27% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 91.29% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.02% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.41% 99.17%
CHEMBL3194 P02766 Transthyretin 88.06% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.01% 86.33%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 86.92% 89.67%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.06% 97.09%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.45% 91.71%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.82% 95.89%
CHEMBL2581 P07339 Cathepsin D 83.64% 98.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.65% 94.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.66% 95.50%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.58% 89.62%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 80.46% 85.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.17% 93.56%

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.
Syzygium nervosum

Cross-Links

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PubChem 25155517
LOTUS LTS0130075
wikiData Q105143191