5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[4-[3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-2-(hydroxymethyl)oxane-3,4-diol

Details

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Internal ID 42801d62-f439-4a48-9511-a64554e61a44
Taxonomy Lignans, neolignans and related compounds > Lignan glycosides
IUPAC Name 5-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[4-[3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-2-(hydroxymethyl)oxane-3,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H40O15/c1-39-20-7-14(3-5-18(20)34)25-16-10-42-26(17(16)11-41-25)15-4-6-19(21(8-15)40-2)44-29-27(24(36)23(35)22(9-32)45-29)46-30-28(37)31(38,12-33)13-43-30/h3-8,16-17,22-30,32-38H,9-13H2,1-2H3
InChI Key KUSSRNQTQUIBHR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H40O15
Molecular Weight 652.60 g/mol
Exact Mass 652.23672056 g/mol
Topological Polar Surface Area (TPSA) 215.00 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.87
H-Bond Acceptor 15
H-Bond Donor 7
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[4-[3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-2-(hydroxymethyl)oxane-3,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6351 63.51%
Caco-2 - 0.8781 87.81%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.6650 66.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8810 88.10%
OATP1B3 inhibitior + 0.9654 96.54%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6503 65.03%
P-glycoprotein inhibitior + 0.6121 61.21%
P-glycoprotein substrate - 0.6089 60.89%
CYP3A4 substrate + 0.6609 66.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8030 80.30%
CYP3A4 inhibition - 0.8906 89.06%
CYP2C9 inhibition - 0.9085 90.85%
CYP2C19 inhibition - 0.8141 81.41%
CYP2D6 inhibition - 0.8949 89.49%
CYP1A2 inhibition - 0.8862 88.62%
CYP2C8 inhibition + 0.6477 64.77%
CYP inhibitory promiscuity - 0.8031 80.31%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5668 56.68%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9220 92.20%
Skin irritation - 0.8199 81.99%
Skin corrosion - 0.9505 95.05%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7872 78.72%
Micronuclear + 0.5700 57.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.8834 88.34%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.8529 85.29%
Acute Oral Toxicity (c) III 0.5593 55.93%
Estrogen receptor binding + 0.7453 74.53%
Androgen receptor binding + 0.6557 65.57%
Thyroid receptor binding + 0.5666 56.66%
Glucocorticoid receptor binding + 0.5612 56.12%
Aromatase binding + 0.5635 56.35%
PPAR gamma + 0.6513 65.13%
Honey bee toxicity - 0.7648 76.48%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8681 86.81%

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 99.39% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.96% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 95.60% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.36% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.22% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.11% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 91.05% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.77% 89.00%
CHEMBL226 P30542 Adenosine A1 receptor 90.27% 95.93%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.14% 86.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.00% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.96% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.90% 95.89%
CHEMBL4208 P20618 Proteasome component C5 86.45% 90.00%
CHEMBL2581 P07339 Cathepsin D 86.18% 98.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.55% 97.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.25% 94.45%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.14% 97.36%
CHEMBL4581 P52732 Kinesin-like protein 1 81.54% 93.18%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.39% 85.49%

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.
Parsonsia alboflavescens

Cross-Links

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PubChem 14309782
LOTUS LTS0032477
wikiData Q105146344