(2R,3R,4S,5S)-2,4-bis(4-hydroxyphenyl)-3,5-dihydroxy-tetrahydropyran

Details

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Internal ID 737bdc67-fa6e-4490-adac-35e098f536d1
Taxonomy Lignans, neolignans and related compounds
IUPAC Name (2R,3R,4S,5S)-2,4-bis(4-hydroxyphenyl)oxane-3,5-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H18O5/c18-12-5-1-10(2-6-12)15-14(20)9-22-17(16(15)21)11-3-7-13(19)8-4-11/h1-8,14-21H,9H2/t14-,15+,16-,17-/m1/s1
InChI Key NMAKNUBSPANVCK-YYIAUSFCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H18O5
Molecular Weight 302.32 g/mol
Exact Mass 302.11542367 g/mol
Topological Polar Surface Area (TPSA) 90.20 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.67
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R,4S,5S)-2,4-bis(4-hydroxyphenyl)-3,5-dihydroxy-tetrahydropyran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7066 70.66%
Caco-2 + 0.5568 55.68%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6584 65.84%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.8254 82.54%
OATP1B3 inhibitior + 0.8776 87.76%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8786 87.86%
P-glycoprotein inhibitior - 0.7649 76.49%
P-glycoprotein substrate - 0.9112 91.12%
CYP3A4 substrate - 0.5787 57.87%
CYP2C9 substrate - 0.7752 77.52%
CYP2D6 substrate + 0.3587 35.87%
CYP3A4 inhibition - 0.7081 70.81%
CYP2C9 inhibition - 0.7543 75.43%
CYP2C19 inhibition - 0.8388 83.88%
CYP2D6 inhibition - 0.9117 91.17%
CYP1A2 inhibition - 0.8574 85.74%
CYP2C8 inhibition - 0.7281 72.81%
CYP inhibitory promiscuity - 0.5110 51.10%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5888 58.88%
Eye corrosion - 0.9918 99.18%
Eye irritation + 0.8734 87.34%
Skin irritation - 0.7328 73.28%
Skin corrosion - 0.9311 93.11%
Ames mutagenesis + 0.6363 63.63%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.5759 57.59%
Hepatotoxicity - 0.7073 70.73%
skin sensitisation - 0.8501 85.01%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.6093 60.93%
Acute Oral Toxicity (c) III 0.6972 69.72%
Estrogen receptor binding - 0.4891 48.91%
Androgen receptor binding + 0.7232 72.32%
Thyroid receptor binding + 0.5253 52.53%
Glucocorticoid receptor binding - 0.6026 60.26%
Aromatase binding - 0.5547 55.47%
PPAR gamma + 0.6109 61.09%
Honey bee toxicity - 0.8893 88.93%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity - 0.4549 45.49%

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 97.17% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 95.55% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.92% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 90.34% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.49% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.38% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.44% 95.56%
CHEMBL2581 P07339 Cathepsin D 80.47% 98.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 155803404
LOTUS LTS0211955
wikiData Q105181667