Methyl 1,3,4,5-tetrahydroxycyclohexane-1-carboxylate

Details

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Internal ID 30a52a42-498a-4a63-96f8-54e8d7c36400
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclitols and derivatives > Quinic acids and derivatives
IUPAC Name methyl 1,3,4,5-tetrahydroxycyclohexane-1-carboxylate
SMILES (Canonical) COC(=O)C1(CC(C(C(C1)O)O)O)O
SMILES (Isomeric) COC(=O)C1(CC(C(C(C1)O)O)O)O
InChI InChI=1S/C8H14O6/c1-14-7(12)8(13)2-4(9)6(11)5(10)3-8/h4-6,9-11,13H,2-3H2,1H3
InChI Key GBNSPDJKJDIAFT-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C8H14O6
Molecular Weight 206.19 g/mol
Exact Mass 206.07903816 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP -2.00
Atomic LogP (AlogP) -2.23
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 1,3,4,5-tetrahydroxycyclohexane-1-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6304 63.04%
Caco-2 - 0.8874 88.74%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8124 81.24%
OATP2B1 inhibitior - 0.8499 84.99%
OATP1B1 inhibitior + 0.9802 98.02%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9074 90.74%
P-glycoprotein inhibitior - 0.9808 98.08%
P-glycoprotein substrate - 0.9186 91.86%
CYP3A4 substrate - 0.5224 52.24%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.7995 79.95%
CYP3A4 inhibition - 0.9640 96.40%
CYP2C9 inhibition - 0.9276 92.76%
CYP2C19 inhibition - 0.9249 92.49%
CYP2D6 inhibition - 0.9563 95.63%
CYP1A2 inhibition - 0.9325 93.25%
CYP2C8 inhibition - 0.9892 98.92%
CYP inhibitory promiscuity - 0.9922 99.22%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6658 66.58%
Eye corrosion - 0.9790 97.90%
Eye irritation - 0.9342 93.42%
Skin irritation - 0.6191 61.91%
Skin corrosion - 0.8748 87.48%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6411 64.11%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.6019 60.19%
skin sensitisation - 0.7957 79.57%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6108 61.08%
Acute Oral Toxicity (c) III 0.7070 70.70%
Estrogen receptor binding - 0.7875 78.75%
Androgen receptor binding - 0.7383 73.83%
Thyroid receptor binding - 0.6502 65.02%
Glucocorticoid receptor binding - 0.6507 65.07%
Aromatase binding - 0.8649 86.49%
PPAR gamma - 0.8211 82.11%
Honey bee toxicity - 0.8198 81.98%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.5630 56.30%

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 96.91% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.09% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.53% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 92.16% 83.82%
CHEMBL340 P08684 Cytochrome P450 3A4 86.78% 91.19%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.52% 94.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.60% 94.45%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 84.67% 95.71%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.48% 96.77%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.66% 91.07%
CHEMBL3437 Q16853 Amine oxidase, copper containing 80.48% 94.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 80.44% 91.24%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Spiraea formosana

Cross-Links

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PubChem 14314247
LOTUS LTS0095759
wikiData Q105005977