(2R,3R,4R,5S)-4-(hydroxymethyl)oxane-2,3,4,5-tetrol

Details

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Internal ID b0d37023-0da4-494f-8100-78bca5fc8bc9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides
IUPAC Name (2R,3R,4R,5S)-4-(hydroxymethyl)oxane-2,3,4,5-tetrol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H12O6/c7-2-6(11)3(8)1-12-5(10)4(6)9/h3-5,7-11H,1-2H2/t3-,4-,5+,6+/m0/s1
InChI Key XULYGFMRZJHJSA-UNTFVMJOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12O6
Molecular Weight 180.16 g/mol
Exact Mass 180.06338810 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP -2.80
Atomic LogP (AlogP) -3.22
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R,4R,5S)-4-(hydroxymethyl)oxane-2,3,4,5-tetrol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9243 92.43%
Caco-2 - 0.9684 96.84%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6999 69.99%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9558 95.58%
OATP1B3 inhibitior + 0.9538 95.38%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9644 96.44%
P-glycoprotein inhibitior - 0.9743 97.43%
P-glycoprotein substrate - 0.9433 94.33%
CYP3A4 substrate - 0.6079 60.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8395 83.95%
CYP3A4 inhibition - 0.9743 97.43%
CYP2C9 inhibition - 0.9518 95.18%
CYP2C19 inhibition - 0.9195 91.95%
CYP2D6 inhibition - 0.9563 95.63%
CYP1A2 inhibition - 0.9605 96.05%
CYP2C8 inhibition - 0.9686 96.86%
CYP inhibitory promiscuity - 0.9844 98.44%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6103 61.03%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.9253 92.53%
Skin irritation - 0.8538 85.38%
Skin corrosion - 0.9475 94.75%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6377 63.77%
Micronuclear - 0.8341 83.41%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.9076 90.76%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.6063 60.63%
Acute Oral Toxicity (c) IV 0.5146 51.46%
Estrogen receptor binding - 0.8151 81.51%
Androgen receptor binding - 0.7399 73.99%
Thyroid receptor binding - 0.6963 69.63%
Glucocorticoid receptor binding - 0.7982 79.82%
Aromatase binding - 0.8037 80.37%
PPAR gamma - 0.8137 81.37%
Honey bee toxicity - 0.8876 88.76%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.9033 90.33%

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 93.75% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 90.22% 95.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.72% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.58% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.44% 96.09%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.24% 95.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.29% 100.00%

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 130758902
LOTUS LTS0111772
wikiData Q105342395