3-(1,4-Dihydroxy-2,2,6-trimethylcyclohexyl)prop-2-enoic acid

Details

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Internal ID 48e24296-af63-4bce-a76c-4da0888d4aa2
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols > Cyclohexanols
IUPAC Name 3-(1,4-dihydroxy-2,2,6-trimethylcyclohexyl)prop-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H20O4/c1-8-6-9(13)7-11(2,3)12(8,16)5-4-10(14)15/h4-5,8-9,13,16H,6-7H2,1-3H3,(H,14,15)
InChI Key XQMQNQUWBFJLCF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O4
Molecular Weight 228.28 g/mol
Exact Mass 228.13615911 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.18
H-Bond Acceptor 3
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 3-(1,4-Dihydroxy-2,2,6-trimethylcyclohexyl)prop-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9850 98.50%
Caco-2 + 0.6889 68.89%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8512 85.12%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.9440 94.40%
OATP1B3 inhibitior + 0.9593 95.93%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9166 91.66%
P-glycoprotein inhibitior - 0.9786 97.86%
P-glycoprotein substrate - 0.7676 76.76%
CYP3A4 substrate + 0.5556 55.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9037 90.37%
CYP3A4 inhibition - 0.9206 92.06%
CYP2C9 inhibition - 0.9257 92.57%
CYP2C19 inhibition - 0.9467 94.67%
CYP2D6 inhibition - 0.9680 96.80%
CYP1A2 inhibition - 0.9611 96.11%
CYP2C8 inhibition - 0.9449 94.49%
CYP inhibitory promiscuity - 0.9837 98.37%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8256 82.56%
Carcinogenicity (trinary) Non-required 0.6632 66.32%
Eye corrosion - 0.9692 96.92%
Eye irritation - 0.6414 64.14%
Skin irritation - 0.5817 58.17%
Skin corrosion - 0.9392 93.92%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8928 89.28%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.6207 62.07%
skin sensitisation + 0.6706 67.06%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.8041 80.41%
Acute Oral Toxicity (c) III 0.7104 71.04%
Estrogen receptor binding - 0.6436 64.36%
Androgen receptor binding - 0.5795 57.95%
Thyroid receptor binding - 0.5801 58.01%
Glucocorticoid receptor binding - 0.4903 49.03%
Aromatase binding - 0.7515 75.15%
PPAR gamma - 0.7472 74.72%
Honey bee toxicity - 0.8463 84.63%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9586 95.86%

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 94.85% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.58% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 90.91% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 90.21% 90.17%
CHEMBL206 P03372 Estrogen receptor alpha 88.40% 97.64%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.05% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 85.44% 91.19%
CHEMBL284 P27487 Dipeptidyl peptidase IV 84.90% 95.69%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.54% 96.95%
CHEMBL2179 P04062 Beta-glucocerebrosidase 80.20% 85.31%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.20% 95.56%

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.
Glycosmis pentaphylla

Cross-Links

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PubChem 85195576
LOTUS LTS0264300
wikiData Q105339884