5,5-Dimethyl-3-oxo-6-(3-oxobutyl)cyclohexene-1-carboxylic acid

Details

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Internal ID 8714e329-d578-4109-9d45-462580f3e880
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 5,5-dimethyl-3-oxo-6-(3-oxobutyl)cyclohexene-1-carboxylic acid
SMILES (Canonical) CC(=O)CCC1C(=CC(=O)CC1(C)C)C(=O)O
SMILES (Isomeric) CC(=O)CCC1C(=CC(=O)CC1(C)C)C(=O)O
InChI InChI=1S/C13H18O4/c1-8(14)4-5-11-10(12(16)17)6-9(15)7-13(11,2)3/h6,11H,4-5,7H2,1-3H3,(H,16,17)
InChI Key YHNGXQALPYIXQZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O4
Molecular Weight 238.28 g/mol
Exact Mass 238.12050905 g/mol
Topological Polar Surface Area (TPSA) 71.40 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.98
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,5-Dimethyl-3-oxo-6-(3-oxobutyl)cyclohexene-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 + 0.9741 97.41%
Caco-2 + 0.6619 66.19%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8968 89.68%
OATP2B1 inhibitior - 0.8508 85.08%
OATP1B1 inhibitior + 0.8943 89.43%
OATP1B3 inhibitior + 0.8400 84.00%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8810 88.10%
P-glycoprotein inhibitior - 0.9740 97.40%
P-glycoprotein substrate - 0.7909 79.09%
CYP3A4 substrate - 0.5524 55.24%
CYP2C9 substrate - 0.7627 76.27%
CYP2D6 substrate - 0.9143 91.43%
CYP3A4 inhibition - 0.7499 74.99%
CYP2C9 inhibition - 0.9003 90.03%
CYP2C19 inhibition - 0.9242 92.42%
CYP2D6 inhibition - 0.9052 90.52%
CYP1A2 inhibition - 0.8654 86.54%
CYP2C8 inhibition - 0.9275 92.75%
CYP inhibitory promiscuity - 0.9454 94.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8366 83.66%
Carcinogenicity (trinary) Non-required 0.7161 71.61%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.7237 72.37%
Skin irritation + 0.6240 62.40%
Skin corrosion - 0.9810 98.10%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6903 69.03%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6464 64.64%
skin sensitisation + 0.6110 61.10%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.5503 55.03%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.5606 56.06%
Acute Oral Toxicity (c) III 0.7012 70.12%
Estrogen receptor binding - 0.8052 80.52%
Androgen receptor binding - 0.7788 77.88%
Thyroid receptor binding - 0.8532 85.32%
Glucocorticoid receptor binding - 0.8161 81.61%
Aromatase binding - 0.8818 88.18%
PPAR gamma - 0.7643 76.43%
Honey bee toxicity - 0.9288 92.88%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9954 99.54%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.29% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.07% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.01% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.48% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.42% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 88.15% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.08% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.04% 99.23%

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 162992243
LOTUS LTS0198124
wikiData Q104201711