Campherenone

Details

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Internal ID 2b53b37c-8a97-47cc-9968-894205f6b45a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,7-dimethyl-7-(4-methylpent-3-enyl)bicyclo[2.2.1]heptan-2-one
SMILES (Canonical) CC(=CCCC1(C2CCC1(C(=O)C2)C)C)C
SMILES (Isomeric) CC(=CCCC1(C2CCC1(C(=O)C2)C)C)C
InChI InChI=1S/C15H24O/c1-11(2)6-5-8-14(3)12-7-9-15(14,4)13(16)10-12/h6,12H,5,7-10H2,1-4H3
InChI Key UTVLNNVHVYZXEC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.13
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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UTVLNNVHVYZXEC-UHFFFAOYSA-N

2D Structure

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2D Structure of Campherenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.8790 87.90%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5042 50.42%
OATP2B1 inhibitior - 0.8475 84.75%
OATP1B1 inhibitior + 0.8797 87.97%
OATP1B3 inhibitior + 0.8728 87.28%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7108 71.08%
P-glycoprotein inhibitior - 0.9757 97.57%
P-glycoprotein substrate - 0.8712 87.12%
CYP3A4 substrate + 0.5357 53.57%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8076 80.76%
CYP3A4 inhibition - 0.9268 92.68%
CYP2C9 inhibition - 0.9296 92.96%
CYP2C19 inhibition - 0.8935 89.35%
CYP2D6 inhibition - 0.9620 96.20%
CYP1A2 inhibition - 0.8589 85.89%
CYP2C8 inhibition - 0.9555 95.55%
CYP inhibitory promiscuity - 0.8211 82.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5273 52.73%
Eye corrosion - 0.9567 95.67%
Eye irritation + 0.8071 80.71%
Skin irritation + 0.7610 76.10%
Skin corrosion - 0.9812 98.12%
Ames mutagenesis - 0.8354 83.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4905 49.05%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5605 56.05%
skin sensitisation + 0.9142 91.42%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.6913 69.13%
Acute Oral Toxicity (c) III 0.6362 63.62%
Estrogen receptor binding - 0.8395 83.95%
Androgen receptor binding - 0.5303 53.03%
Thyroid receptor binding - 0.7225 72.25%
Glucocorticoid receptor binding - 0.7750 77.50%
Aromatase binding - 0.7288 72.88%
PPAR gamma - 0.6267 62.67%
Honey bee toxicity - 0.9013 90.13%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9818 98.18%

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 96.69% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 94.57% 94.75%
CHEMBL2581 P07339 Cathepsin D 90.41% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.34% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.41% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.28% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.20% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.06% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.54% 92.62%
CHEMBL221 P23219 Cyclooxygenase-1 81.18% 90.17%
CHEMBL1902 P62942 FK506-binding protein 1A 80.04% 97.05%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.00% 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.
Aloe vera
Cinnamomum camphora

Cross-Links

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PubChem 5315646
NPASS NPC108820