Longicamphenylone

Details

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Internal ID 61a057d3-dde6-4731-9350-e09037d597ba
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids
IUPAC Name 2,3,3,7-tetramethyltricyclo[5.4.0.02,9]undecan-8-one
SMILES (Canonical) CC1(CCCC2(C3C1(C(C2=O)CC3)C)C)C
SMILES (Isomeric) CC1(CCCC2(C3C1(C(C2=O)CC3)C)C)C
InChI InChI=1S/C15H24O/c1-13(2)8-5-9-14(3)11-7-6-10(12(14)16)15(11,13)4/h10-11H,5-9H2,1-4H3
InChI Key VMYWIJUHQAMXNC-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 4.10
Atomic LogP (AlogP) 3.82
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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CHEBI:190813
VMYWIJUHQAMXNC-UHFFFAOYSA-N
Q67879993
2,3,3,7-tetramethyltricyclo[5.4.0.02,9]undecan-8-one

2D Structure

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2D Structure of Longicamphenylone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.8631 86.31%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.5245 52.45%
OATP2B1 inhibitior - 0.8359 83.59%
OATP1B1 inhibitior + 0.9236 92.36%
OATP1B3 inhibitior + 0.9692 96.92%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8132 81.32%
P-glycoprotein inhibitior - 0.9389 93.89%
P-glycoprotein substrate - 0.9436 94.36%
CYP3A4 substrate + 0.5132 51.32%
CYP2C9 substrate - 0.7483 74.83%
CYP2D6 substrate - 0.7683 76.83%
CYP3A4 inhibition - 0.9450 94.50%
CYP2C9 inhibition - 0.8226 82.26%
CYP2C19 inhibition - 0.8948 89.48%
CYP2D6 inhibition - 0.9607 96.07%
CYP1A2 inhibition - 0.7554 75.54%
CYP2C8 inhibition - 0.9638 96.38%
CYP inhibitory promiscuity - 0.9466 94.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6136 61.36%
Eye corrosion - 0.8877 88.77%
Eye irritation + 0.7193 71.93%
Skin irritation + 0.7123 71.23%
Skin corrosion - 0.9397 93.97%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6623 66.23%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.8567 85.67%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.6879 68.79%
Acute Oral Toxicity (c) III 0.5170 51.70%
Estrogen receptor binding - 0.7988 79.88%
Androgen receptor binding + 0.5817 58.17%
Thyroid receptor binding - 0.7683 76.83%
Glucocorticoid receptor binding - 0.8309 83.09%
Aromatase binding - 0.6314 63.14%
PPAR gamma - 0.6817 68.17%
Honey bee toxicity - 0.8987 89.87%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9766 97.66%

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
CHEMBL1937 Q92769 Histone deacetylase 2 93.15% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.70% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.49% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.10% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.00% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.17% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.09% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.08% 95.89%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.04% 93.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.97% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.87% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.63% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.06% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.00% 93.04%
CHEMBL3012 Q13946 Phosphodiesterase 7A 81.18% 99.29%
CHEMBL1902 P62942 FK506-binding protein 1A 81.16% 97.05%
CHEMBL259 P32245 Melanocortin receptor 4 81.09% 95.38%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.47% 94.78%

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.
Artemisia capillaris
Halocarpus bidwillii

Cross-Links

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PubChem 91747202
NPASS NPC223574
LOTUS LTS0191995
wikiData Q67879993