Genistin

Details

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Internal ID 35f72d95-a29c-4d7c-8d6f-0552a28734e9
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavonoid O-glycosides
IUPAC Name 5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
SMILES (Canonical) C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O
SMILES (Isomeric) C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O
InChI InChI=1S/C21H20O10/c22-7-15-18(26)19(27)20(28)21(31-15)30-11-5-13(24)16-14(6-11)29-8-12(17(16)25)9-1-3-10(23)4-2-9/h1-6,8,15,18-24,26-28H,7H2/t15-,18-,19+,20-,21-/m1/s1
InChI Key ZCOLJUOHXJRHDI-CMWLGVBASA-N
Popularity 1,248 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O10
Molecular Weight 432.40 g/mol
Exact Mass 432.10564683 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.05
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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Genistoside
529-59-9
Genistine
Genistein 7-glucoside
Genisteol 7-monoglucoside
Glucosyl-7-genistein
Genistein glucoside
Genistein 7-O-beta-D-glucoside
NSC 5112
Genistein-7-glucoside
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Genistin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5116 51.16%
Caco-2 - 0.9370 93.70%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.6068 60.68%
OATP2B1 inhibitior + 0.5888 58.88%
OATP1B1 inhibitior + 0.9521 95.21%
OATP1B3 inhibitior + 0.9265 92.65%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5394 53.94%
P-glycoprotein inhibitior - 0.8277 82.77%
P-glycoprotein substrate - 0.9175 91.75%
CYP3A4 substrate + 0.5951 59.51%
CYP2C9 substrate - 0.6762 67.62%
CYP2D6 substrate - 0.8575 85.75%
CYP3A4 inhibition - 0.9193 91.93%
CYP2C9 inhibition - 0.9296 92.96%
CYP2C19 inhibition - 0.9289 92.89%
CYP2D6 inhibition - 0.9513 95.13%
CYP1A2 inhibition - 0.9084 90.84%
CYP2C8 inhibition + 0.6652 66.52%
CYP inhibitory promiscuity - 0.7728 77.28%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7144 71.44%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.8281 82.81%
Skin irritation - 0.8036 80.36%
Skin corrosion - 0.9691 96.91%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5316 53.16%
Micronuclear + 0.6533 65.33%
Hepatotoxicity - 0.6946 69.46%
skin sensitisation - 0.9122 91.22%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.4741 47.41%
Acute Oral Toxicity (c) III 0.4045 40.45%
Estrogen receptor binding + 0.7238 72.38%
Androgen receptor binding + 0.7130 71.30%
Thyroid receptor binding + 0.6096 60.96%
Glucocorticoid receptor binding + 0.6300 63.00%
Aromatase binding + 0.6456 64.56%
PPAR gamma + 0.8322 83.22%
Honey bee toxicity - 0.7440 74.40%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5450 54.50%
Fish aquatic toxicity + 0.8218 82.18%

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 98.95% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.10% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.38% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.51% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.25% 99.15%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 91.75% 86.92%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 91.01% 96.21%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.86% 97.09%
CHEMBL242 Q92731 Estrogen receptor beta 88.57% 98.35%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 88.49% 95.78%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.85% 86.33%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 87.34% 95.64%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.04% 99.17%
CHEMBL3194 P02766 Transthyretin 85.31% 90.71%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.58% 91.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.09% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.45% 95.56%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.95% 97.28%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.32% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 80.87% 94.73%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 80.63% 95.83%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.12% 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.
Achillea pseudopectinata
Achlys triphylla
Adenocarpus complicatus
Aglaia australiensis
Allagopappus viscosissimus
Astragalus condensatus
Astragalus multiceps
Astragalus pterocephalus
Astragalus spinosus
Atuna excelsa subsp. racemosa
Barbarea verna
Berberis floribunda
Bertya dimerostigma
Bonamia spectabilis
Calicotome villosa
Camchaya loloana
Chaenomeles sinensis
Chamaecytisus supinus
Chenopodium foliosum
Cicer arietinum
Cymodocea nodosa
Dalbergia sissoo
Delphinium barbeyi
Dendrobium moniliforme
Diplacus longiflorus
Ducrosia ismaelis
Eriosema tuberosum
Erysimum siliculosum
Eschenbachia japonica
Euphrasia stricta
Ficus septica
Flemingia macrophylla
Flemingia paniculata
Fumaria densiflora
Genista ephedroides
Genista lydia
Genista morisii
Genista pichisermolliana
Genista sessilifolia
Glycine max
Grona styracifolia
Hibiscus schizopetalus
Hydrangea serrata
Hylodesmum podocarpum subsp. oxyphyllum
Hyoscyamus pusillus
Ipomoea muricata
Iris tectorum
Isoberlinia tomentosa
Jamesoniella colorata
Justicia adhatoda
Kaempferia rotunda
Lepidosperma ustulatum
Lespedeza davidii
Lunularia cruciata
Lupinus albus
Lupinus luteus
Lupinus polyphyllus
Lupinus pubescens
Maackia amurensis
Macadamia ternifolia
Magnolia coco
Mucuna birdwoodiana
Murraya exotica
Murraya paniculata
Ocimum basilicum
Oreomecon alpina
Orthocaulis attenuatus
Peltogyne paniculata subsp. pubescens
Pinus hartwegii
Piptanthus nepalensis
Prunus avium
Prunus cerasus
Pterocarpus indicus
Pterodon emarginatus
Pueraria montana var. lobata
Pulsatilla campanella
Punica granatum
Ranunculus peltatus
Retama sphaerocarpa
Rosulabryum capillare
Salvia miltiorrhiza
Saracha nigribaccata
Scabiosa pyrenaica
Selaginella sinensis
Sorbus cuspidata
Spatholobus suberectus
Styphnolobium japonicum
Styrax agrestis
Syzygium nervosum
Teucrium marum
Thermopsis alterniflora
Thermopsis dolichocarpa
Trifolium pratense
Trifolium resupinatum
Trifolium subterraneum
Urceola laevigata
Ziziphus jujuba var. spinosa

Cross-Links

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PubChem 5281377
NPASS NPC313163
LOTUS LTS0084994
wikiData Q5533221