(1Z,5E)-1,5-dimethyl-8-prop-1-en-2-ylcyclodeca-1,5-diene

Details

Top
Internal ID 3c369f64-48a8-4a1d-81e8-78cc9d2f1646
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name (1Z,5E)-1,5-dimethyl-8-prop-1-en-2-ylcyclodeca-1,5-diene
SMILES (Canonical) CC1=CCCC(=CCC(CC1)C(=C)C)C
SMILES (Isomeric) C/C/1=C/CC/C(=C/CC(CC1)C(=C)C)/C
InChI InChI=1S/C15H24/c1-12(2)15-10-8-13(3)6-5-7-14(4)9-11-15/h6,9,15H,1,5,7-8,10-11H2,2-4H3/b13-6-,14-9+
InChI Key XMRKUJJDDKYUHV-LBJJKJHXSA-N
Popularity 35 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.04
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
(1Z,5E)-1,5-dimethyl-8-prop-1-en-2-ylcyclodeca-1,5-diene

2D Structure

Top
2D Structure of (1Z,5E)-1,5-dimethyl-8-prop-1-en-2-ylcyclodeca-1,5-diene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.9529 95.29%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.5878 58.78%
OATP2B1 inhibitior - 0.8483 84.83%
OATP1B1 inhibitior + 0.9771 97.71%
OATP1B3 inhibitior + 0.9473 94.73%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7585 75.85%
P-glycoprotein inhibitior - 0.9428 94.28%
P-glycoprotein substrate - 0.9171 91.71%
CYP3A4 substrate - 0.5944 59.44%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9207 92.07%
CYP2C9 inhibition - 0.8613 86.13%
CYP2C19 inhibition - 0.8203 82.03%
CYP2D6 inhibition - 0.9379 93.79%
CYP1A2 inhibition - 0.6699 66.99%
CYP2C8 inhibition - 0.8562 85.62%
CYP inhibitory promiscuity - 0.7682 76.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Warning 0.4978 49.78%
Eye corrosion + 0.5909 59.09%
Eye irritation + 0.7499 74.99%
Skin irritation + 0.7468 74.68%
Skin corrosion - 0.9749 97.49%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7064 70.64%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8923 89.23%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.5376 53.76%
Acute Oral Toxicity (c) III 0.8499 84.99%
Estrogen receptor binding - 0.9144 91.44%
Androgen receptor binding - 0.8100 81.00%
Thyroid receptor binding - 0.8156 81.56%
Glucocorticoid receptor binding - 0.7659 76.59%
Aromatase binding - 0.7733 77.33%
PPAR gamma - 0.7847 78.47%
Honey bee toxicity - 0.9391 93.91%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9965 99.65%

Targets

Top

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 94.63% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.70% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.75% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.28% 97.21%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.44% 100.00%
CHEMBL2581 P07339 Cathepsin D 82.04% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.72% 95.56%

Plants that contains it

Top
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.
Cichorium intybus
Cichorium pumilum
Inula helenium
Lindera aggregata
Litsea cubeba
Piper cubeba

Cross-Links

Top
PubChem 5463084
NPASS NPC198586