Biochanin A 7-O-xylosyl-(1->6)-glucoside

Details

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Internal ID 17cd3d46-6ffe-4e88-96b7-a89311a9ff2b
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavonoid O-glycosides
IUPAC Name 5-hydroxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H30O14/c1-36-12-4-2-11(3-5-12)14-8-37-17-7-13(6-15(28)19(17)20(14)30)40-27-25(35)23(33)22(32)18(41-27)10-39-26-24(34)21(31)16(29)9-38-26/h2-8,16,18,21-29,31-35H,9-10H2,1H3/t16-,18-,21+,22-,23+,24-,25-,26+,27-/m1/s1
InChI Key ODHKRSFJWQEWGG-HWGSVKNTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H30O14
Molecular Weight 578.50 g/mol
Exact Mass 578.16355563 g/mol
Topological Polar Surface Area (TPSA) 214.00 Ų
XlogP -0.90
Atomic LogP (AlogP) -1.18
H-Bond Acceptor 14
H-Bond Donor 7
Rotatable Bonds 7

Synonyms

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Biochanin A 7-O-xylosyl-(1->6)-glucoside
5-hydroxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one
5-hydroxy-3-(4-methoxyphenyl)-7-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(((2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl)oxymethyl)oxan-2-yl)oxychromen-4-one
RefChem:119844
Kakkanin
orb1690393
HY-N9375
LMPK12050222
AKOS040758251
CS-0159570
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Biochanin A 7-O-xylosyl-(1->6)-glucoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5869 58.69%
Caco-2 - 0.8904 89.04%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.6520 65.20%
OATP2B1 inhibitior - 0.8417 84.17%
OATP1B1 inhibitior + 0.9279 92.79%
OATP1B3 inhibitior + 0.9536 95.36%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7277 72.77%
P-glycoprotein inhibitior - 0.6168 61.68%
P-glycoprotein substrate - 0.6231 62.31%
CYP3A4 substrate + 0.6653 66.53%
CYP2C9 substrate - 0.8664 86.64%
CYP2D6 substrate - 0.8478 84.78%
CYP3A4 inhibition - 0.9412 94.12%
CYP2C9 inhibition - 0.9439 94.39%
CYP2C19 inhibition - 0.8989 89.89%
CYP2D6 inhibition - 0.9172 91.72%
CYP1A2 inhibition - 0.9037 90.37%
CYP2C8 inhibition + 0.6164 61.64%
CYP inhibitory promiscuity - 0.8756 87.56%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6679 66.79%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9220 92.20%
Skin irritation - 0.8291 82.91%
Skin corrosion - 0.9599 95.99%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7525 75.25%
Micronuclear + 0.6074 60.74%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.9195 91.95%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.8772 87.72%
Acute Oral Toxicity (c) III 0.6736 67.36%
Estrogen receptor binding + 0.8098 80.98%
Androgen receptor binding + 0.6471 64.71%
Thyroid receptor binding + 0.5180 51.80%
Glucocorticoid receptor binding - 0.4662 46.62%
Aromatase binding + 0.5608 56.08%
PPAR gamma + 0.7355 73.55%
Honey bee toxicity - 0.8093 80.93%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.8179 81.79%

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 99.61% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.04% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.16% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.07% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.81% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.55% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.23% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.14% 99.15%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 92.93% 86.92%
CHEMBL226 P30542 Adenosine A1 receptor 92.58% 95.93%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.69% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.67% 95.56%
CHEMBL4208 P20618 Proteasome component C5 90.11% 90.00%
CHEMBL1907 P15144 Aminopeptidase N 86.92% 93.31%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.24% 95.89%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 85.28% 95.53%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.98% 99.17%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.23% 96.77%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.35% 97.28%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 82.79% 95.83%
CHEMBL1951 P21397 Monoamine oxidase A 82.43% 91.49%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.23% 92.62%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.08% 96.21%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.75% 90.71%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 80.66% 95.64%

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.
Heliotropium hirsutissimum
Inulanthera calva
Nicotiana raimondii
Scolopia chinensis
Trollius europaeus

Cross-Links

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PubChem 44257291
NPASS NPC182729