D-Gluconic acid, potassium salt (1:1)

Details

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Internal ID f200bb87-e4cd-4f16-bd0e-ea58d8a1d670
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name potassium 2,3,4,5,6-pentahydroxyhexanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H12O7.K/c7-1-2(8)3(9)4(10)5(11)6(12)13;/h2-5,7-11H,1H2,(H,12,13);/q;+1/p-1
InChI Key HLCFGWHYROZGBI-UHFFFAOYSA-M
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11KO7
Molecular Weight 234.25 g/mol
Exact Mass 234.01418417 g/mol
Topological Polar Surface Area (TPSA) 141.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -7.82
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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RefChem:583743
35087-77-5
potassium;2,3,4,5,6-pentahydroxyhexanoate
kaliumgluconat
potassium hexonate
SCHEMBL25198892
DTXSID70956520
HLCFGWHYROZGBI-UHFFFAOYSA-M
potassium 2,3,4,5,6-pentahydroxyhexanoate
A829206
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of D-Gluconic acid, potassium salt (1:1)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7366 73.66%
Caco-2 - 0.9801 98.01%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6155 61.55%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9636 96.36%
OATP1B3 inhibitior + 0.9248 92.48%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9850 98.50%
P-glycoprotein inhibitior - 0.9863 98.63%
P-glycoprotein substrate - 0.9680 96.80%
CYP3A4 substrate - 0.7263 72.63%
CYP2C9 substrate - 0.8117 81.17%
CYP2D6 substrate - 0.8740 87.40%
CYP3A4 inhibition - 0.9374 93.74%
CYP2C9 inhibition - 0.9081 90.81%
CYP2C19 inhibition - 0.9132 91.32%
CYP2D6 inhibition - 0.9225 92.25%
CYP1A2 inhibition - 0.8420 84.20%
CYP2C8 inhibition - 0.9898 98.98%
CYP inhibitory promiscuity - 0.9781 97.81%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.7720 77.20%
Eye corrosion - 0.9838 98.38%
Eye irritation - 0.9278 92.78%
Skin irritation - 0.7012 70.12%
Skin corrosion - 0.9092 90.92%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8225 82.25%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.8625 86.25%
skin sensitisation - 0.9243 92.43%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.4554 45.54%
Acute Oral Toxicity (c) IV 0.4430 44.30%
Estrogen receptor binding - 0.8636 86.36%
Androgen receptor binding - 0.8005 80.05%
Thyroid receptor binding - 0.5749 57.49%
Glucocorticoid receptor binding + 0.5482 54.82%
Aromatase binding - 0.8933 89.33%
PPAR gamma - 0.7812 78.12%
Honey bee toxicity - 0.9640 96.40%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.9079 90.79%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.07% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.30% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.23% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.09% 99.17%

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 23679778
NPASS NPC73584