Hex(?1-3)Hex-O-Ph(4-OH)

Details

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Internal ID 8d9cae40-74cd-4815-bd9e-90c5ead6fce5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 2-[3,5-dihydroxy-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H26O12/c19-5-9-11(22)13(24)14(25)17(28-9)30-16-12(23)10(6-20)29-18(15(16)26)27-8-3-1-7(21)2-4-8/h1-4,9-26H,5-6H2
InChI Key VSYANFBIFILLON-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H26O12
Molecular Weight 434.40 g/mol
Exact Mass 434.14242626 g/mol
Topological Polar Surface Area (TPSA) 199.00 Ų
XlogP -2.30
Atomic LogP (AlogP) -3.60
H-Bond Acceptor 12
H-Bond Donor 8
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hex(?1-3)Hex-O-Ph(4-OH)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9196 91.96%
Caco-2 - 0.8819 88.19%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.8857 88.57%
Subcellular localzation Mitochondria 0.6469 64.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9392 93.92%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8955 89.55%
P-glycoprotein inhibitior - 0.8483 84.83%
P-glycoprotein substrate - 0.9546 95.46%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8139 81.39%
CYP3A4 inhibition - 0.9445 94.45%
CYP2C9 inhibition - 0.9180 91.80%
CYP2C19 inhibition - 0.8982 89.82%
CYP2D6 inhibition - 0.9269 92.69%
CYP1A2 inhibition - 0.9529 95.29%
CYP2C8 inhibition - 0.6065 60.65%
CYP inhibitory promiscuity - 0.7839 78.39%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5680 56.80%
Eye corrosion - 0.9934 99.34%
Eye irritation - 0.9225 92.25%
Skin irritation - 0.8480 84.80%
Skin corrosion - 0.9726 97.26%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4606 46.06%
Micronuclear - 0.6641 66.41%
Hepatotoxicity - 0.9500 95.00%
skin sensitisation - 0.8841 88.41%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.6053 60.53%
Acute Oral Toxicity (c) III 0.5316 53.16%
Estrogen receptor binding - 0.5555 55.55%
Androgen receptor binding - 0.4830 48.30%
Thyroid receptor binding + 0.5812 58.12%
Glucocorticoid receptor binding - 0.6820 68.20%
Aromatase binding + 0.5973 59.73%
PPAR gamma + 0.7363 73.63%
Honey bee toxicity - 0.7871 78.71%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6250 62.50%
Fish aquatic toxicity - 0.6266 62.66%

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 98.54% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 91.41% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.21% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.48% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.29% 96.09%
CHEMBL242 Q92731 Estrogen receptor beta 87.95% 98.35%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 85.79% 83.57%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.99% 95.89%
CHEMBL4208 P20618 Proteasome component C5 84.20% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.18% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.56% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 83.03% 94.73%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 82.25% 94.97%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.29% 86.92%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 80.16% 85.00%

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 162953445
LOTUS LTS0094823
wikiData Q105292593