5-Methyl-8-(3-oxoprop-1-en-2-yl)cyclodeca-1,5-diene-1-carbaldehyde

Details

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Internal ID 087fb602-0126-4af5-aea8-cb848c0249ee
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 5-methyl-8-(3-oxoprop-1-en-2-yl)cyclodeca-1,5-diene-1-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O2/c1-12-4-3-5-14(11-17)7-9-15(8-6-12)13(2)10-16/h5-6,10-11,15H,2-4,7-9H2,1H3
InChI Key DWSDJKIPKRTYMJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O2
Molecular Weight 232.32 g/mol
Exact Mass 232.146329876 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.39
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Methyl-8-(3-oxoprop-1-en-2-yl)cyclodeca-1,5-diene-1-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.7574 75.74%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.3810 38.10%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.9279 92.79%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.6438 64.38%
P-glycoprotein inhibitior - 0.9094 90.94%
P-glycoprotein substrate - 0.9260 92.60%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8385 83.85%
CYP3A4 inhibition - 0.9271 92.71%
CYP2C9 inhibition - 0.8797 87.97%
CYP2C19 inhibition - 0.8288 82.88%
CYP2D6 inhibition - 0.9341 93.41%
CYP1A2 inhibition - 0.6116 61.16%
CYP2C8 inhibition - 0.7805 78.05%
CYP inhibitory promiscuity - 0.8525 85.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.6171 61.71%
Eye corrosion + 0.8424 84.24%
Eye irritation + 0.5470 54.70%
Skin irritation + 0.6735 67.35%
Skin corrosion - 0.8501 85.01%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6719 67.19%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5560 55.60%
skin sensitisation + 0.8575 85.75%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5454 54.54%
Acute Oral Toxicity (c) III 0.8320 83.20%
Estrogen receptor binding - 0.5745 57.45%
Androgen receptor binding - 0.7335 73.35%
Thyroid receptor binding - 0.7377 73.77%
Glucocorticoid receptor binding + 0.5694 56.94%
Aromatase binding - 0.6104 61.04%
PPAR gamma - 0.5136 51.36%
Honey bee toxicity - 0.9395 93.95%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9931 99.31%

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
CHEMBL1951 P21397 Monoamine oxidase A 92.27% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.36% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.65% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.27% 91.11%
CHEMBL2581 P07339 Cathepsin D 84.13% 98.95%
CHEMBL1871 P10275 Androgen Receptor 82.45% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.98% 100.00%
CHEMBL4208 P20618 Proteasome component C5 80.95% 90.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.48% 93.03%

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.
Cassinia uncata

Cross-Links

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PubChem 163085772
LOTUS LTS0252241
wikiData Q104990718