Cyclocopacamphan-12-al

Details

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Internal ID 6c9f46cc-c4fb-4483-b902-272f3bf87ba3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-[(2R,6S,8S)-1,2-dimethyl-8-tetracyclo[4.4.0.02,4.03,7]decanyl]propanal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O/c1-8(7-16)9-4-5-14(2)10-6-11-13(12(9)10)15(11,14)3/h7-13H,4-6H2,1-3H3/t8?,9-,10+,11?,12?,13?,14?,15-/m1/s1
InChI Key JLHUXFWGEBRDST-AMQCQLRFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.14
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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JLHUXFWGEBRDST-AMQCQLRFSA-N

2D Structure

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2D Structure of Cyclocopacamphan-12-al

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 + 0.6564 65.64%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.6286 62.86%
OATP2B1 inhibitior - 0.8509 85.09%
OATP1B1 inhibitior + 0.8938 89.38%
OATP1B3 inhibitior + 0.9631 96.31%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8922 89.22%
P-glycoprotein inhibitior - 0.9196 91.96%
P-glycoprotein substrate - 0.8559 85.59%
CYP3A4 substrate + 0.5902 59.02%
CYP2C9 substrate - 0.6061 60.61%
CYP2D6 substrate - 0.7613 76.13%
CYP3A4 inhibition - 0.8734 87.34%
CYP2C9 inhibition - 0.7441 74.41%
CYP2C19 inhibition - 0.7813 78.13%
CYP2D6 inhibition - 0.9540 95.40%
CYP1A2 inhibition - 0.7195 71.95%
CYP2C8 inhibition - 0.9102 91.02%
CYP inhibitory promiscuity - 0.8143 81.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.5391 53.91%
Eye corrosion - 0.9307 93.07%
Eye irritation - 0.8519 85.19%
Skin irritation - 0.5609 56.09%
Skin corrosion - 0.9595 95.95%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6235 62.35%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6842 68.42%
skin sensitisation + 0.6583 65.83%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5667 56.67%
Acute Oral Toxicity (c) III 0.6271 62.71%
Estrogen receptor binding - 0.5119 51.19%
Androgen receptor binding + 0.6744 67.44%
Thyroid receptor binding - 0.5750 57.50%
Glucocorticoid receptor binding - 0.6806 68.06%
Aromatase binding - 0.6328 63.28%
PPAR gamma - 0.6852 68.52%
Honey bee toxicity - 0.6001 60.01%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9933 99.33%

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
CHEMBL4072 P07858 Cathepsin B 95.37% 93.67%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.83% 97.25%
CHEMBL3837 P07711 Cathepsin L 93.22% 96.61%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.92% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.55% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 90.20% 96.61%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 88.98% 95.71%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 86.80% 92.86%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.74% 95.56%
CHEMBL268 P43235 Cathepsin K 86.19% 96.85%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.01% 99.18%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.72% 96.77%
CHEMBL1937 Q92769 Histone deacetylase 2 83.72% 94.75%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.15% 89.50%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.51% 97.29%
CHEMBL4302 P08183 P-glycoprotein 1 82.48% 92.98%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.00% 96.47%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.91% 96.21%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.86% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.27% 100.00%
CHEMBL2094135 Q96BI3 Gamma-secretase 81.02% 98.05%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.60% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.16% 91.11%

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.
Chrysopogon zizanioides

Cross-Links

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PubChem 6428370
LOTUS LTS0253052
wikiData Q104667185