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

Details

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Internal ID 80f95dfc-bf01-4909-ba3f-7bfc3d399856
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavonoid O-glycosides
IUPAC Name (3S)-5,7-dihydroxy-3-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one
SMILES (Canonical) C1C(C(=O)C2=C(C=C(C=C2O1)O)O)C3=C(C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O
SMILES (Isomeric) C1[C@@H](C(=O)C2=C(C=C(C=C2O1)O)O)C3=C(C=C(C=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O
InChI InChI=1S/C21H22O11/c22-6-15-18(27)19(28)20(29)21(32-15)31-9-1-2-10(12(24)5-9)11-7-30-14-4-8(23)3-13(25)16(14)17(11)26/h1-5,11,15,18-25,27-29H,6-7H2/t11-,15-,18-,19+,20-,21-/m1/s1
InChI Key SLPFAONKVXHOCP-XREQLKKTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O11
Molecular Weight 450.40 g/mol
Exact Mass 450.11621151 g/mol
Topological Polar Surface Area (TPSA) 186.00 Ų
XlogP 0.40
Atomic LogP (AlogP) -0.66
H-Bond Acceptor 11
H-Bond Donor 7
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S)-5,7-dihydroxy-3-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-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 - 0.5736 57.36%
Caco-2 - 0.9250 92.50%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.5848 58.48%
OATP2B1 inhibitior - 0.5652 56.52%
OATP1B1 inhibitior + 0.9338 93.38%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5657 56.57%
P-glycoprotein inhibitior - 0.7499 74.99%
P-glycoprotein substrate - 0.7981 79.81%
CYP3A4 substrate + 0.6170 61.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8517 85.17%
CYP3A4 inhibition - 0.9390 93.90%
CYP2C9 inhibition - 0.9315 93.15%
CYP2C19 inhibition - 0.9047 90.47%
CYP2D6 inhibition - 0.9458 94.58%
CYP1A2 inhibition - 0.9180 91.80%
CYP2C8 inhibition + 0.4543 45.43%
CYP inhibitory promiscuity - 0.7526 75.26%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6848 68.48%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.8359 83.59%
Skin irritation - 0.8255 82.55%
Skin corrosion - 0.9691 96.91%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5440 54.40%
Micronuclear + 0.6433 64.33%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.9132 91.32%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6286 62.86%
Acute Oral Toxicity (c) IV 0.4763 47.63%
Estrogen receptor binding + 0.8085 80.85%
Androgen receptor binding + 0.6348 63.48%
Thyroid receptor binding + 0.6005 60.05%
Glucocorticoid receptor binding + 0.5719 57.19%
Aromatase binding - 0.4859 48.59%
PPAR gamma + 0.7568 75.68%
Honey bee toxicity - 0.7675 76.75%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5650 56.50%
Fish aquatic toxicity + 0.7958 79.58%

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 99.52% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 97.90% 95.93%
CHEMBL2581 P07339 Cathepsin D 96.78% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.87% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.08% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.23% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.16% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.89% 95.56%
CHEMBL220 P22303 Acetylcholinesterase 90.93% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.78% 95.89%
CHEMBL4208 P20618 Proteasome component C5 90.47% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.83% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.45% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.31% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 88.79% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.61% 99.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.41% 100.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.90% 94.80%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.83% 99.23%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.76% 93.40%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.14% 86.92%

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.
Ormosia monosperma

Cross-Links

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PubChem 162842591
LOTUS LTS0220036
wikiData Q105255486