1-Methyl-7-methylidene-4-(propan-2-yl)cyclodeca-1,3-diene

Details

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Internal ID 88819cc1-fc92-4032-a02b-48b715f26710
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 1-methyl-7-methylidene-4-propan-2-ylcyclodeca-1,3-diene
SMILES (Canonical) CC1=CC=C(CCC(=C)CCC1)C(C)C
SMILES (Isomeric) CC1=CC=C(CCC(=C)CCC1)C(C)C
InChI InChI=1S/C15H24/c1-12(2)15-10-8-13(3)6-5-7-14(4)9-11-15/h9,11-12H,3,5-8,10H2,1-2,4H3
InChI Key BDDRMCBOHRMFIM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 5.04
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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DTXSID40825017
1-Methyl-7-methylidene-4-(propan-2-yl)cyclodeca-1,3-diene

2D Structure

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2D Structure of 1-Methyl-7-methylidene-4-(propan-2-yl)cyclodeca-1,3-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.9499 94.99%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Lysosomes 0.4651 46.51%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.9352 93.52%
OATP1B3 inhibitior + 0.9412 94.12%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8093 80.93%
P-glycoprotein inhibitior - 0.9434 94.34%
P-glycoprotein substrate - 0.9503 95.03%
CYP3A4 substrate - 0.6432 64.32%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7650 76.50%
CYP3A4 inhibition - 0.9422 94.22%
CYP2C9 inhibition - 0.8228 82.28%
CYP2C19 inhibition - 0.7961 79.61%
CYP2D6 inhibition - 0.9409 94.09%
CYP1A2 inhibition - 0.6853 68.53%
CYP2C8 inhibition - 0.9643 96.43%
CYP inhibitory promiscuity - 0.7758 77.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.5024 50.24%
Eye corrosion + 0.5274 52.74%
Eye irritation + 0.9267 92.67%
Skin irritation + 0.7425 74.25%
Skin corrosion - 0.9779 97.79%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6921 69.21%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.8987 89.87%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.6411 64.11%
Acute Oral Toxicity (c) III 0.8141 81.41%
Estrogen receptor binding - 0.9361 93.61%
Androgen receptor binding - 0.7697 76.97%
Thyroid receptor binding - 0.5756 57.56%
Glucocorticoid receptor binding - 0.7108 71.08%
Aromatase binding - 0.8177 81.77%
PPAR gamma - 0.7777 77.77%
Honey bee toxicity - 0.9365 93.65%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9974 99.74%

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
CHEMBL2581 P07339 Cathepsin D 90.60% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.35% 94.73%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.35% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.97% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.42% 93.56%
CHEMBL230 P35354 Cyclooxygenase-2 83.77% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.69% 91.11%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.58% 86.00%

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.
Ligularia thyrsoidea

Cross-Links

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PubChem 71404157
LOTUS LTS0086211
wikiData Q82808651