5-(1,2-Dihydroxy-2,6,6-trimethylcyclohexyl)-3-methylpenta-2,4-dienoic acid

Details

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Internal ID 71b59af5-2b80-4057-b348-3b45cb90df3d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 5-(1,2-dihydroxy-2,6,6-trimethylcyclohexyl)-3-methylpenta-2,4-dienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O4/c1-11(10-12(16)17)6-9-15(19)13(2,3)7-5-8-14(15,4)18/h6,9-10,18-19H,5,7-8H2,1-4H3,(H,16,17)
InChI Key JJYFOQHXDGGLPW-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O4
Molecular Weight 268.35 g/mol
Exact Mass 268.16745924 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.27
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(1,2-Dihydroxy-2,6,6-trimethylcyclohexyl)-3-methylpenta-2,4-dienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9700 97.00%
Caco-2 + 0.6978 69.78%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8388 83.88%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.9182 91.82%
OATP1B3 inhibitior + 0.8881 88.81%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7528 75.28%
P-glycoprotein inhibitior - 0.9690 96.90%
P-glycoprotein substrate - 0.9066 90.66%
CYP3A4 substrate + 0.5627 56.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9078 90.78%
CYP3A4 inhibition - 0.9453 94.53%
CYP2C9 inhibition - 0.8606 86.06%
CYP2C19 inhibition - 0.8728 87.28%
CYP2D6 inhibition - 0.9348 93.48%
CYP1A2 inhibition - 0.8927 89.27%
CYP2C8 inhibition - 0.9465 94.65%
CYP inhibitory promiscuity - 0.9749 97.49%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6859 68.59%
Eye corrosion - 0.9908 99.08%
Eye irritation + 0.6069 60.69%
Skin irritation + 0.6043 60.43%
Skin corrosion - 0.9374 93.74%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7858 78.58%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.6608 66.08%
skin sensitisation + 0.5841 58.41%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6896 68.96%
Acute Oral Toxicity (c) III 0.6504 65.04%
Estrogen receptor binding + 0.6842 68.42%
Androgen receptor binding + 0.5668 56.68%
Thyroid receptor binding + 0.6598 65.98%
Glucocorticoid receptor binding + 0.6302 63.02%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6733 67.33%
Honey bee toxicity - 0.9050 90.50%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9743 97.43%

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
CHEMBL2061 P19793 Retinoid X receptor alpha 95.63% 91.67%
CHEMBL2004 P48443 Retinoid X receptor gamma 93.59% 100.00%
CHEMBL1870 P28702 Retinoid X receptor beta 93.00% 95.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.26% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 87.72% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.79% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 85.76% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.60% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.45% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 80.52% 91.19%

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 78384795
LOTUS LTS0236538
wikiData Q105130049