5,7-dihydroxy-6-methoxy-3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]chromen-4-one

Details

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Internal ID 775647c1-5ae6-4a57-bbd4-be78c19c8a95
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavonoid O-glycosides
IUPAC Name 5,7-dihydroxy-6-methoxy-3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H34O17/c1-40-14-5-10(11-8-42-15-6-12(31)27(41-2)22(35)18(15)19(11)32)3-4-13(14)44-29-26(39)24(37)21(34)17(46-29)9-43-28-25(38)23(36)20(33)16(7-30)45-28/h3-6,8,16-17,20-21,23-26,28-31,33-39H,7,9H2,1-2H3/t16-,17-,20-,21-,23+,24+,25-,26-,28-,29-/m1/s1
InChI Key IFSJVHMZFISVOZ-SFMJQTNTSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H34O17
Molecular Weight 654.60 g/mol
Exact Mass 654.17959961 g/mol
Topological Polar Surface Area (TPSA) 264.00 Ų
XlogP -1.30
Atomic LogP (AlogP) -2.11
H-Bond Acceptor 17
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 5,7-dihydroxy-6-methoxy-3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]chromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5623 56.23%
Caco-2 - 0.8956 89.56%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.5984 59.84%
OATP2B1 inhibitior - 0.7143 71.43%
OATP1B1 inhibitior + 0.8919 89.19%
OATP1B3 inhibitior + 0.9748 97.48%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6500 65.00%
P-glycoprotein inhibitior - 0.5218 52.18%
P-glycoprotein substrate - 0.6305 63.05%
CYP3A4 substrate + 0.6507 65.07%
CYP2C9 substrate - 0.8485 84.85%
CYP2D6 substrate - 0.8501 85.01%
CYP3A4 inhibition - 0.9284 92.84%
CYP2C9 inhibition - 0.9208 92.08%
CYP2C19 inhibition - 0.9124 91.24%
CYP2D6 inhibition - 0.9531 95.31%
CYP1A2 inhibition - 0.9232 92.32%
CYP2C8 inhibition + 0.7559 75.59%
CYP inhibitory promiscuity - 0.7113 71.13%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7032 70.32%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9164 91.64%
Skin irritation - 0.8442 84.42%
Skin corrosion - 0.9614 96.14%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4408 44.08%
Micronuclear + 0.6633 66.33%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.9340 93.40%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.8184 81.84%
Acute Oral Toxicity (c) III 0.7041 70.41%
Estrogen receptor binding + 0.8062 80.62%
Androgen receptor binding - 0.5070 50.70%
Thyroid receptor binding - 0.5149 51.49%
Glucocorticoid receptor binding + 0.5691 56.91%
Aromatase binding + 0.5758 57.58%
PPAR gamma + 0.6918 69.18%
Honey bee toxicity - 0.7233 72.33%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6349 63.49%
Fish aquatic toxicity + 0.7167 71.67%

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 98.00% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.63% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.21% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.91% 89.00%
CHEMBL4302 P08183 P-glycoprotein 1 94.74% 92.98%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.37% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.57% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.32% 85.14%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 91.00% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.22% 99.17%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.70% 96.21%
CHEMBL1937 Q92769 Histone deacetylase 2 87.39% 94.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.37% 96.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.18% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.91% 95.56%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 83.82% 95.78%
CHEMBL5747 Q92793 CREB-binding protein 82.57% 95.12%
CHEMBL3194 P02766 Transthyretin 82.12% 90.71%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.30% 94.03%

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.
Iris spuria

Cross-Links

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PubChem 102034324
LOTUS LTS0055812
wikiData Q105112346