2-(Hydroxymethyl)-6-(2,5,6-trihydroxycyclohex-3-en-1-yl)oxyoxane-3,4,5-triol

Details

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Internal ID ee1effef-4612-4d47-8393-58a4362e8420
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name 2-(hydroxymethyl)-6-(2,5,6-trihydroxycyclohex-3-en-1-yl)oxyoxane-3,4,5-triol
SMILES (Canonical) C1=CC(C(C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O)O
SMILES (Isomeric) C1=CC(C(C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O)O
InChI InChI=1S/C12H20O9/c13-3-6-8(17)9(18)10(19)12(20-6)21-11-5(15)2-1-4(14)7(11)16/h1-2,4-19H,3H2
InChI Key ILKCZSIFTWFKAX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O9
Molecular Weight 308.28 g/mol
Exact Mass 308.11073221 g/mol
Topological Polar Surface Area (TPSA) 160.00 Ų
XlogP -3.70
Atomic LogP (AlogP) -4.18
H-Bond Acceptor 9
H-Bond Donor 7
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(Hydroxymethyl)-6-(2,5,6-trihydroxycyclohex-3-en-1-yl)oxyoxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8915 89.15%
Caco-2 - 0.9302 93.02%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.6860 68.60%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.9229 92.29%
OATP1B3 inhibitior + 0.9615 96.15%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9869 98.69%
P-glycoprotein inhibitior - 0.9147 91.47%
P-glycoprotein substrate - 0.9858 98.58%
CYP3A4 substrate - 0.5732 57.32%
CYP2C9 substrate - 0.8055 80.55%
CYP2D6 substrate - 0.8331 83.31%
CYP3A4 inhibition - 0.9106 91.06%
CYP2C9 inhibition - 0.9289 92.89%
CYP2C19 inhibition - 0.8797 87.97%
CYP2D6 inhibition - 0.9343 93.43%
CYP1A2 inhibition - 0.9476 94.76%
CYP2C8 inhibition - 0.9383 93.83%
CYP inhibitory promiscuity - 0.7729 77.29%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7064 70.64%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9733 97.33%
Skin irritation - 0.8731 87.31%
Skin corrosion - 0.9671 96.71%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5486 54.86%
Micronuclear - 0.7341 73.41%
Hepatotoxicity - 0.8750 87.50%
skin sensitisation - 0.8965 89.65%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.5616 56.16%
Acute Oral Toxicity (c) IV 0.4988 49.88%
Estrogen receptor binding - 0.8252 82.52%
Androgen receptor binding - 0.7473 74.73%
Thyroid receptor binding - 0.5631 56.31%
Glucocorticoid receptor binding - 0.7482 74.82%
Aromatase binding - 0.5562 55.62%
PPAR gamma - 0.5511 55.11%
Honey bee toxicity - 0.6275 62.75%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.6548 65.48%

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 93.51% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.00% 96.09%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 86.49% 83.57%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.83% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 81.99% 94.73%
CHEMBL3589 P55263 Adenosine kinase 81.95% 98.05%

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 85240801
LOTUS LTS0232169
wikiData Q105115234