6''-(4-Carboxy-3-hydroxy-3-methylbutanoyl)hyperin

Details

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Internal ID 569d20dd-990e-4379-9e02-ec1a68f91d54
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name 5-[[6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-hydroxy-3-methyl-5-oxopentanoic acid
SMILES (Canonical) CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O)O
SMILES (Isomeric) CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O)O
InChI InChI=1S/C27H28O16/c1-27(39,7-17(32)33)8-18(34)40-9-16-20(35)22(37)23(38)26(42-16)43-25-21(36)19-14(31)5-11(28)6-15(19)41-24(25)10-2-3-12(29)13(30)4-10/h2-6,16,20,22-23,26,28-31,35,37-39H,7-9H2,1H3,(H,32,33)
InChI Key FMMBDZGNMFRGMV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H28O16
Molecular Weight 608.50 g/mol
Exact Mass 608.13773480 g/mol
Topological Polar Surface Area (TPSA) 270.00 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.37
H-Bond Acceptor 15
H-Bond Donor 9
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6''-(4-Carboxy-3-hydroxy-3-methylbutanoyl)hyperin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6471 64.71%
Caco-2 - 0.8947 89.47%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7011 70.11%
OATP2B1 inhibitior - 0.5713 57.13%
OATP1B1 inhibitior + 0.8766 87.66%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6102 61.02%
P-glycoprotein inhibitior + 0.6215 62.15%
P-glycoprotein substrate - 0.5729 57.29%
CYP3A4 substrate + 0.6826 68.26%
CYP2C9 substrate - 0.6235 62.35%
CYP2D6 substrate - 0.8751 87.51%
CYP3A4 inhibition - 0.8834 88.34%
CYP2C9 inhibition - 0.9273 92.73%
CYP2C19 inhibition - 0.8901 89.01%
CYP2D6 inhibition - 0.9443 94.43%
CYP1A2 inhibition - 0.8872 88.72%
CYP2C8 inhibition + 0.8734 87.34%
CYP inhibitory promiscuity - 0.9482 94.82%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5992 59.92%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9115 91.15%
Skin irritation - 0.8145 81.45%
Skin corrosion - 0.9444 94.44%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7416 74.16%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.9116 91.16%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.9391 93.91%
Acute Oral Toxicity (c) III 0.5689 56.89%
Estrogen receptor binding + 0.7376 73.76%
Androgen receptor binding + 0.7234 72.34%
Thyroid receptor binding - 0.5236 52.36%
Glucocorticoid receptor binding + 0.6943 69.43%
Aromatase binding + 0.6646 66.46%
PPAR gamma + 0.6599 65.99%
Honey bee toxicity - 0.7783 77.83%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9754 97.54%

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 99.42% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.53% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.25% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.67% 85.14%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 95.34% 95.64%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.93% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 94.53% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.49% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.32% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.98% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 91.57% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.21% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.75% 95.56%
CHEMBL220 P22303 Acetylcholinesterase 86.51% 94.45%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 86.33% 80.78%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.80% 99.23%
CHEMBL3194 P02766 Transthyretin 82.31% 90.71%

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.
Euphorbia ebracteolata

Cross-Links

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PubChem 73829993
LOTUS LTS0270803
wikiData Q104997904