kaempferol-3-O-(2,3-di-O-acetyl-alpha-L-rhamnopyranoside)

Details

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Internal ID f6de84b4-6d04-41ba-be9a-c49a5945fd39
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name [(2S,3R,4R,5S,6S)-3-acetyloxy-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-5-hydroxy-6-methyloxan-4-yl] acetate
SMILES (Canonical) CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C)OC(=O)C)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)OC(=O)C)OC(=O)C)O
InChI InChI=1S/C25H24O12/c1-10-19(31)22(34-11(2)26)24(35-12(3)27)25(33-10)37-23-20(32)18-16(30)8-15(29)9-17(18)36-21(23)13-4-6-14(28)7-5-13/h4-10,19,22,24-25,28-31H,1-3H3/t10-,19-,22+,24+,25-/m0/s1
InChI Key BHCRVKVXJRBQJR-YPDHAKIYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H24O12
Molecular Weight 516.40 g/mol
Exact Mass 516.12677620 g/mol
Topological Polar Surface Area (TPSA) 178.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 1.92
H-Bond Acceptor 12
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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kaempferol-3-O-(2,3-di-O-acetyl-alpha-L-rhamnopyranoside)
SCHEMBL572336
BDBM50242096
[(2S,3R,4R,5S,6S)-3-acetyloxy-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-5-hydroxy-6-methyloxan-4-yl] acetate

2D Structure

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2D Structure of kaempferol-3-O-(2,3-di-O-acetyl-alpha-L-rhamnopyranoside)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8335 83.35%
Caco-2 - 0.8021 80.21%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7061 70.61%
OATP2B1 inhibitior - 0.5640 56.40%
OATP1B1 inhibitior + 0.8540 85.40%
OATP1B3 inhibitior - 0.3604 36.04%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7930 79.30%
P-glycoprotein inhibitior + 0.7694 76.94%
P-glycoprotein substrate - 0.5275 52.75%
CYP3A4 substrate + 0.6498 64.98%
CYP2C9 substrate + 0.5516 55.16%
CYP2D6 substrate - 0.8795 87.95%
CYP3A4 inhibition - 0.8575 85.75%
CYP2C9 inhibition - 0.8462 84.62%
CYP2C19 inhibition - 0.9348 93.48%
CYP2D6 inhibition - 0.9559 95.59%
CYP1A2 inhibition - 0.8264 82.64%
CYP2C8 inhibition + 0.8341 83.41%
CYP inhibitory promiscuity - 0.6478 64.78%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5276 52.76%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.8487 84.87%
Skin irritation - 0.7512 75.12%
Skin corrosion - 0.9552 95.52%
Ames mutagenesis + 0.5363 53.63%
Human Ether-a-go-go-Related Gene inhibition - 0.5522 55.22%
Micronuclear + 0.8800 88.00%
Hepatotoxicity - 0.5322 53.22%
skin sensitisation - 0.9336 93.36%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7604 76.04%
Acute Oral Toxicity (c) III 0.5465 54.65%
Estrogen receptor binding + 0.7896 78.96%
Androgen receptor binding + 0.8011 80.11%
Thyroid receptor binding + 0.5623 56.23%
Glucocorticoid receptor binding + 0.7609 76.09%
Aromatase binding - 0.6772 67.72%
PPAR gamma + 0.7249 72.49%
Honey bee toxicity - 0.7954 79.54%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5350 53.50%
Fish aquatic toxicity + 0.9663 96.63%

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 99.10% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 98.42% 89.00%
CHEMBL2581 P07339 Cathepsin D 97.89% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 97.46% 91.49%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 96.65% 95.64%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.17% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.54% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 90.78% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.35% 96.09%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 87.75% 95.78%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.60% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.47% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.43% 94.45%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.73% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.34% 95.56%
CHEMBL3194 P02766 Transthyretin 86.28% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.67% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.35% 94.80%
CHEMBL4208 P20618 Proteasome component C5 81.87% 90.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.63% 94.42%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.89% 85.14%
CHEMBL245 P20309 Muscarinic acetylcholine receptor M3 80.55% 97.53%
CHEMBL3038469 P24941 CDK2/Cyclin A 80.22% 91.38%

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.
Zingiber spectabile
Zingiber zerumbet

Cross-Links

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PubChem 11203112
NPASS NPC48093
LOTUS LTS0233954
wikiData Q104935878