Isorhamnetin 7-O-alpha-L-rhamnoside

Details

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Internal ID 27c193ae-77c8-41bd-96dd-c4b94dae4493
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 3,5-dihydroxy-2-(4-hydroxy-3-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(=C(C3=O)O)C4=CC(=C(C=C4)O)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(=C(C3=O)O)C4=CC(=C(C=C4)O)OC)O)O)O)O
InChI InChI=1S/C22H22O11/c1-8-16(25)18(27)20(29)22(31-8)32-10-6-12(24)15-14(7-10)33-21(19(28)17(15)26)9-3-4-11(23)13(5-9)30-2/h3-8,16,18,20,22-25,27-29H,1-2H3/t8-,16-,18+,20+,22-/m0/s1
InChI Key XLQFMBLUUSGXQY-FDTPGTFWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H22O11
Molecular Weight 462.40 g/mol
Exact Mass 462.11621151 g/mol
Topological Polar Surface Area (TPSA) 175.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.79
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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17331-72-5
Isorhamnetin 7-O-|A-L-rhamnoside
3,5-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one
Isorhamnetin 7-O-??-L-rhamnoside
HY-N5068
AKOS040760480
FS-7238
CS-0032266
E88775
3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

2D Structure

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2D Structure of Isorhamnetin 7-O-alpha-L-rhamnoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7980 79.80%
Caco-2 - 0.8593 85.93%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6676 66.76%
OATP2B1 inhibitior + 0.5908 59.08%
OATP1B1 inhibitior + 0.9346 93.46%
OATP1B3 inhibitior + 0.9220 92.20%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7297 72.97%
P-glycoprotein inhibitior - 0.5478 54.78%
P-glycoprotein substrate - 0.5384 53.84%
CYP3A4 substrate + 0.6308 63.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8527 85.27%
CYP3A4 inhibition - 0.6056 60.56%
CYP2C9 inhibition - 0.9236 92.36%
CYP2C19 inhibition - 0.8201 82.01%
CYP2D6 inhibition - 0.8906 89.06%
CYP1A2 inhibition - 0.7268 72.68%
CYP2C8 inhibition + 0.8857 88.57%
CYP inhibitory promiscuity - 0.5508 55.08%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6071 60.71%
Eye corrosion - 0.9840 98.40%
Eye irritation - 0.8968 89.68%
Skin irritation - 0.6906 69.06%
Skin corrosion - 0.9434 94.34%
Ames mutagenesis - 0.5629 56.29%
Human Ether-a-go-go-Related Gene inhibition - 0.4346 43.46%
Micronuclear + 0.9200 92.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.9206 92.06%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.9168 91.68%
Acute Oral Toxicity (c) III 0.4825 48.25%
Estrogen receptor binding + 0.7701 77.01%
Androgen receptor binding + 0.5368 53.68%
Thyroid receptor binding + 0.5427 54.27%
Glucocorticoid receptor binding + 0.6650 66.50%
Aromatase binding + 0.5905 59.05%
PPAR gamma + 0.7476 74.76%
Honey bee toxicity - 0.7832 78.32%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5351 53.51%
Fish aquatic toxicity + 0.9150 91.50%

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 99.26% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.65% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.46% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.45% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.86% 86.33%
CHEMBL2581 P07339 Cathepsin D 94.17% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.88% 99.15%
CHEMBL3714130 P46095 G-protein coupled receptor 6 93.13% 97.36%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.40% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.57% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.23% 90.71%
CHEMBL3194 P02766 Transthyretin 88.95% 90.71%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 88.33% 95.78%
CHEMBL3401 O75469 Pregnane X receptor 87.97% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.09% 99.17%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 86.63% 95.64%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.46% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.15% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.00% 85.14%
CHEMBL3438 Q05513 Protein kinase C zeta 83.92% 88.48%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.86% 99.23%
CHEMBL4208 P20618 Proteasome component C5 81.48% 90.00%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 80.45% 95.53%

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.
Barbarea vulgaris

Cross-Links

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PubChem 102007835
LOTUS LTS0188602
wikiData Q105330207