4-Hydroxy-3,5-dimethoxycyclohexane-1-carboxylic acid

Details

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Internal ID 6d3a5581-bbdc-4a27-92c1-58716ae4b3c2
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols > Cyclohexanols
IUPAC Name 4-hydroxy-3,5-dimethoxycyclohexane-1-carboxylic acid
SMILES (Canonical) COC1CC(CC(C1O)OC)C(=O)O
SMILES (Isomeric) COC1CC(CC(C1O)OC)C(=O)O
InChI InChI=1S/C9H16O5/c1-13-6-3-5(9(11)12)4-7(14-2)8(6)10/h5-8,10H,3-4H2,1-2H3,(H,11,12)
InChI Key YUPTUNNQGRXCIO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16O5
Molecular Weight 204.22 g/mol
Exact Mass 204.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP -0.50
Atomic LogP (AlogP) -0.13
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-3,5-dimethoxycyclohexane-1-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 + 0.9590 95.90%
Caco-2 - 0.6010 60.10%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8938 89.38%
OATP2B1 inhibitior - 0.8447 84.47%
OATP1B1 inhibitior + 0.9682 96.82%
OATP1B3 inhibitior + 0.9472 94.72%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9789 97.89%
P-glycoprotein inhibitior - 0.9519 95.19%
P-glycoprotein substrate - 0.9636 96.36%
CYP3A4 substrate - 0.5770 57.70%
CYP2C9 substrate + 0.6015 60.15%
CYP2D6 substrate - 0.8362 83.62%
CYP3A4 inhibition - 0.9790 97.90%
CYP2C9 inhibition - 0.9662 96.62%
CYP2C19 inhibition - 0.9397 93.97%
CYP2D6 inhibition - 0.9378 93.78%
CYP1A2 inhibition - 0.9550 95.50%
CYP2C8 inhibition - 0.9679 96.79%
CYP inhibitory promiscuity - 0.9848 98.48%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8558 85.58%
Carcinogenicity (trinary) Non-required 0.7699 76.99%
Eye corrosion - 0.8598 85.98%
Eye irritation + 0.7929 79.29%
Skin irritation - 0.6561 65.61%
Skin corrosion - 0.9493 94.93%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6259 62.59%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8778 87.78%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.5874 58.74%
Acute Oral Toxicity (c) III 0.5443 54.43%
Estrogen receptor binding + 0.6221 62.21%
Androgen receptor binding - 0.6498 64.98%
Thyroid receptor binding - 0.6562 65.62%
Glucocorticoid receptor binding - 0.7101 71.01%
Aromatase binding - 0.8933 89.33%
PPAR gamma - 0.8659 86.59%
Honey bee toxicity - 0.8667 86.67%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6255 62.55%
Fish aquatic toxicity + 0.7348 73.48%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.89% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.65% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.55% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 82.98% 90.17%
CHEMBL340 P08684 Cytochrome P450 3A4 81.60% 91.19%

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.
Moringa oleifera

Cross-Links

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PubChem 149428703
LOTUS LTS0135111
wikiData Q105364363