2-Cyclohexylbut-2-enoic acid

Details

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Internal ID 64c68034-cead-42b0-8936-be06703d98d9
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Unsaturated fatty acids
IUPAC Name 2-cyclohexylbut-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O2/c1-2-9(10(11)12)8-6-4-3-5-7-8/h2,8H,3-7H2,1H3,(H,11,12)
InChI Key ZVSYQDMZYPEEGJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O2
Molecular Weight 168.23 g/mol
Exact Mass 168.115029749 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Cyclohexylbut-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 + 0.9921 99.21%
Caco-2 + 0.8187 81.87%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.5305 53.05%
OATP2B1 inhibitior - 0.8360 83.60%
OATP1B1 inhibitior + 0.9378 93.78%
OATP1B3 inhibitior + 0.8968 89.68%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9259 92.59%
P-glycoprotein inhibitior - 0.9785 97.85%
P-glycoprotein substrate - 0.9828 98.28%
CYP3A4 substrate - 0.6699 66.99%
CYP2C9 substrate + 0.8284 82.84%
CYP2D6 substrate - 0.9201 92.01%
CYP3A4 inhibition - 0.9323 93.23%
CYP2C9 inhibition - 0.9300 93.00%
CYP2C19 inhibition - 0.9497 94.97%
CYP2D6 inhibition - 0.9572 95.72%
CYP1A2 inhibition - 0.8998 89.98%
CYP2C8 inhibition - 0.9669 96.69%
CYP inhibitory promiscuity - 0.9108 91.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7463 74.63%
Carcinogenicity (trinary) Non-required 0.6199 61.99%
Eye corrosion + 0.8253 82.53%
Eye irritation + 0.9641 96.41%
Skin irritation + 0.6711 67.11%
Skin corrosion - 0.9681 96.81%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6481 64.81%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.8273 82.73%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6722 67.22%
Acute Oral Toxicity (c) III 0.8818 88.18%
Estrogen receptor binding - 0.7775 77.75%
Androgen receptor binding - 0.8099 80.99%
Thyroid receptor binding - 0.7716 77.16%
Glucocorticoid receptor binding - 0.7583 75.83%
Aromatase binding - 0.7869 78.69%
PPAR gamma - 0.8381 83.81%
Honey bee toxicity - 0.9895 98.95%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9634 96.34%

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
CHEMBL340 P08684 Cytochrome P450 3A4 85.04% 91.19%
CHEMBL2581 P07339 Cathepsin D 84.51% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.26% 95.56%
CHEMBL5255 O00206 Toll-like receptor 4 80.54% 92.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.34% 93.56%

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.
Pelargonium quercifolium

Cross-Links

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PubChem 67419349
LOTUS LTS0205573
wikiData Q105384576