5-Hydroxy-4-(hydroxymethyl)-2-methyl-1,3-dioxane-2-carboxylic acid

Details

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Internal ID 322aecad-bd37-4b63-86bd-375080db8f11
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals > Ketals
IUPAC Name 5-hydroxy-4-(hydroxymethyl)-2-methyl-1,3-dioxane-2-carboxylic acid
SMILES (Canonical) CC1(OCC(C(O1)CO)O)C(=O)O
SMILES (Isomeric) CC1(OCC(C(O1)CO)O)C(=O)O
InChI InChI=1S/C7H12O6/c1-7(6(10)11)12-3-4(9)5(2-8)13-7/h4-5,8-9H,2-3H2,1H3,(H,10,11)
InChI Key WRIRJVDXCHWRSC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H12O6
Molecular Weight 192.17 g/mol
Exact Mass 192.06338810 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP -1.10
Atomic LogP (AlogP) -1.44
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-4-(hydroxymethyl)-2-methyl-1,3-dioxane-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8349 83.49%
Caco-2 - 0.7885 78.85%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7475 74.75%
OATP2B1 inhibitior - 0.8456 84.56%
OATP1B1 inhibitior + 0.9154 91.54%
OATP1B3 inhibitior + 0.9396 93.96%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9768 97.68%
P-glycoprotein inhibitior - 0.9845 98.45%
P-glycoprotein substrate - 0.8611 86.11%
CYP3A4 substrate - 0.5303 53.03%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8924 89.24%
CYP3A4 inhibition - 0.9652 96.52%
CYP2C9 inhibition - 0.9575 95.75%
CYP2C19 inhibition - 0.9482 94.82%
CYP2D6 inhibition - 0.9579 95.79%
CYP1A2 inhibition - 0.9645 96.45%
CYP2C8 inhibition - 0.9701 97.01%
CYP inhibitory promiscuity - 0.9866 98.66%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6800 68.00%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.8291 82.91%
Skin irritation - 0.8099 80.99%
Skin corrosion - 0.9360 93.60%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7636 76.36%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.6898 68.98%
skin sensitisation - 0.9213 92.13%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.6501 65.01%
Acute Oral Toxicity (c) III 0.5660 56.60%
Estrogen receptor binding - 0.8156 81.56%
Androgen receptor binding - 0.7074 70.74%
Thyroid receptor binding - 0.7780 77.80%
Glucocorticoid receptor binding - 0.7654 76.54%
Aromatase binding - 0.9051 90.51%
PPAR gamma - 0.8685 86.85%
Honey bee toxicity - 0.9034 90.34%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity - 0.7730 77.30%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.37% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.63% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.18% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 88.36% 91.19%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.54% 96.61%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.57% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.92% 97.09%

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 129995022
LOTUS LTS0045330
wikiData Q105311328