5-hydroxy-2-(4-methoxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

Details

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Internal ID 35648bb7-bdc8-4d8a-a1f1-40b2c25a4cb4
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 5-hydroxy-2-(4-methoxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
SMILES (Canonical) CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)OC)O)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)OC)O)O)O)O
InChI InChI=1S/C22H22O9/c1-10-19(25)20(26)21(27)22(29-10)30-13-7-14(23)18-15(24)9-16(31-17(18)8-13)11-3-5-12(28-2)6-4-11/h3-10,19-23,25-27H,1-2H3/t10-,19-,20+,21+,22-/m0/s1
InChI Key SNYZBYGDUMJVSM-VOIWBUMZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H22O9
Molecular Weight 430.40 g/mol
Exact Mass 430.12638228 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.38
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-hydroxy-2-(4-methoxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7703 77.03%
Caco-2 - 0.6675 66.75%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.6640 66.40%
OATP2B1 inhibitior - 0.5496 54.96%
OATP1B1 inhibitior + 0.9442 94.42%
OATP1B3 inhibitior + 0.9078 90.78%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.7816 78.16%
P-glycoprotein inhibitior - 0.5592 55.92%
P-glycoprotein substrate - 0.6642 66.42%
CYP3A4 substrate + 0.5707 57.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8527 85.27%
CYP3A4 inhibition + 0.5181 51.81%
CYP2C9 inhibition - 0.9219 92.19%
CYP2C19 inhibition - 0.8626 86.26%
CYP2D6 inhibition - 0.8753 87.53%
CYP1A2 inhibition - 0.8368 83.68%
CYP2C8 inhibition + 0.6521 65.21%
CYP inhibitory promiscuity - 0.5948 59.48%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5217 52.17%
Eye corrosion - 0.9831 98.31%
Eye irritation - 0.8759 87.59%
Skin irritation - 0.7036 70.36%
Skin corrosion - 0.9531 95.31%
Ames mutagenesis - 0.5264 52.64%
Human Ether-a-go-go-Related Gene inhibition - 0.4762 47.62%
Micronuclear + 0.8800 88.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.9297 92.97%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.8763 87.63%
Acute Oral Toxicity (c) III 0.6135 61.35%
Estrogen receptor binding + 0.7639 76.39%
Androgen receptor binding + 0.7247 72.47%
Thyroid receptor binding + 0.5517 55.17%
Glucocorticoid receptor binding + 0.7253 72.53%
Aromatase binding + 0.6502 65.02%
PPAR gamma + 0.8080 80.80%
Honey bee toxicity - 0.8010 80.10%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8856 88.56%

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 99.39% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.50% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.32% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.00% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.24% 89.00%
CHEMBL2581 P07339 Cathepsin D 95.02% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.92% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.75% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.34% 95.56%
CHEMBL3714130 P46095 G-protein coupled receptor 6 90.90% 97.36%
CHEMBL3401 O75469 Pregnane X receptor 87.70% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.65% 90.71%
CHEMBL3194 P02766 Transthyretin 86.77% 90.71%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 85.61% 81.11%
CHEMBL4208 P20618 Proteasome component C5 84.98% 90.00%
CHEMBL1907 P15144 Aminopeptidase N 84.20% 93.31%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.28% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.00% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.51% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.21% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.34% 99.23%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.15% 86.92%

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.
Carthamus tinctorius
Peganum harmala

Cross-Links

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PubChem 102442676
LOTUS LTS0114999
wikiData Q105256779