Kaempferol-3-O-glucosyl(1-2)rhamnoside

Details

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Internal ID ac9cf0ff-260e-4582-85fc-649cef571595
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name 3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
SMILES (Canonical) CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)O)O
InChI InChI=1S/C27H30O15/c1-9-17(32)21(36)25(42-26-22(37)20(35)18(33)15(8-28)40-26)27(38-9)41-24-19(34)16-13(31)6-12(30)7-14(16)39-23(24)10-2-4-11(29)5-3-10/h2-7,9,15,17-18,20-22,25-33,35-37H,8H2,1H3/t9-,15+,17-,18+,20-,21+,22+,25+,26-,27-/m0/s1
InChI Key BCNBWICEIXAVQF-DLVIKRKZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H30O15
Molecular Weight 594.50 g/mol
Exact Mass 594.15847025 g/mol
Topological Polar Surface Area (TPSA) 245.00 Ų
XlogP -0.40
Atomic LogP (AlogP) -1.39
H-Bond Acceptor 15
H-Bond Donor 9
Rotatable Bonds 6

Synonyms

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142451-65-8
Kemp-glu-rham
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
Kempferol-3-O-glucosyl(1-2)rhamnoside
3-((6-Deoxy-2-O-beta-D-glucopyranosyl-alpha-L-mannopyranosyl)oxy)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
DTXSID90162045
AKOS040763654
Kaempferol-3-O-b-D-glucosyl(1-2)rhamnoside
E80743
KAEMPFEROL-3-O-??-D-GLUCOSYL(1-2)RHAMNOSIDE
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Kaempferol-3-O-glucosyl(1-2)rhamnoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4777 47.77%
Caco-2 - 0.9112 91.12%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.6881 68.81%
OATP2B1 inhibitior - 0.5560 55.60%
OATP1B1 inhibitior + 0.8824 88.24%
OATP1B3 inhibitior + 0.9552 95.52%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7793 77.93%
P-glycoprotein inhibitior - 0.6137 61.37%
P-glycoprotein substrate - 0.5125 51.25%
CYP3A4 substrate + 0.6555 65.55%
CYP2C9 substrate - 0.6986 69.86%
CYP2D6 substrate - 0.8617 86.17%
CYP3A4 inhibition - 0.9358 93.58%
CYP2C9 inhibition - 0.9271 92.71%
CYP2C19 inhibition - 0.9330 93.30%
CYP2D6 inhibition - 0.9643 96.43%
CYP1A2 inhibition - 0.8830 88.30%
CYP2C8 inhibition + 0.8074 80.74%
CYP inhibitory promiscuity - 0.7188 71.88%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7023 70.23%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.9086 90.86%
Skin irritation - 0.8192 81.92%
Skin corrosion - 0.9626 96.26%
Ames mutagenesis + 0.5063 50.63%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.6433 64.33%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.9312 93.12%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.8771 87.71%
Acute Oral Toxicity (c) III 0.5734 57.34%
Estrogen receptor binding + 0.7981 79.81%
Androgen receptor binding + 0.6785 67.85%
Thyroid receptor binding + 0.5692 56.92%
Glucocorticoid receptor binding + 0.6270 62.70%
Aromatase binding + 0.6203 62.03%
PPAR gamma + 0.7539 75.39%
Honey bee toxicity - 0.7305 73.05%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5450 54.50%
Fish aquatic toxicity + 0.8289 82.89%

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 99.37% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.77% 89.00%
CHEMBL2581 P07339 Cathepsin D 97.72% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 97.37% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.93% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.39% 86.33%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 93.49% 95.64%
CHEMBL3401 O75469 Pregnane X receptor 92.99% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.33% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.99% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.19% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.44% 86.92%
CHEMBL3194 P02766 Transthyretin 84.82% 90.71%
CHEMBL3714130 P46095 G-protein coupled receptor 6 84.61% 97.36%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.59% 99.15%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 82.87% 95.78%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.80% 93.10%
CHEMBL242 Q92731 Estrogen receptor beta 82.05% 98.35%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.72% 95.89%

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.
Beta vulgaris
Crocus speciosus
Ginkgo biloba

Cross-Links

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PubChem 5489470
NPASS NPC110906
LOTUS LTS0168087
wikiData Q105206563