7-Methyl-3-methylidene-10-propan-2-ylcyclodeca-1,5-diene

Details

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Internal ID dd6142a5-0d0d-4e3b-af32-a2c00ba07744
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 7-methyl-3-methylidene-10-propan-2-ylcyclodeca-1,5-diene
SMILES (Canonical) CC1CCC(C=CC(=C)CC=C1)C(C)C
SMILES (Isomeric) CC1CCC(C=CC(=C)CC=C1)C(C)C
InChI InChI=1S/C15H24/c1-12(2)15-10-8-13(3)6-5-7-14(4)9-11-15/h5,7-8,10,12,14-15H,3,6,9,11H2,1-2,4H3
InChI Key KVMPFZSAJWHCMX-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 5.40
Atomic LogP (AlogP) 4.75
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Methyl-3-methylidene-10-propan-2-ylcyclodeca-1,5-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.8910 89.10%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.4305 43.05%
OATP2B1 inhibitior - 0.8626 86.26%
OATP1B1 inhibitior + 0.9267 92.67%
OATP1B3 inhibitior + 0.9148 91.48%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7390 73.90%
P-glycoprotein inhibitior - 0.9600 96.00%
P-glycoprotein substrate - 0.8207 82.07%
CYP3A4 substrate - 0.5571 55.71%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7751 77.51%
CYP3A4 inhibition - 0.9621 96.21%
CYP2C9 inhibition - 0.8618 86.18%
CYP2C19 inhibition - 0.8285 82.85%
CYP2D6 inhibition - 0.9359 93.59%
CYP1A2 inhibition - 0.7419 74.19%
CYP2C8 inhibition - 0.9423 94.23%
CYP inhibitory promiscuity - 0.8058 80.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Warning 0.4938 49.38%
Eye corrosion + 0.5252 52.52%
Eye irritation - 0.5498 54.98%
Skin irritation + 0.7600 76.00%
Skin corrosion - 0.9616 96.16%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4091 40.91%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7450 74.50%
skin sensitisation + 0.9030 90.30%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.7518 75.18%
Acute Oral Toxicity (c) III 0.8180 81.80%
Estrogen receptor binding - 0.9049 90.49%
Androgen receptor binding - 0.9050 90.50%
Thyroid receptor binding - 0.6624 66.24%
Glucocorticoid receptor binding - 0.7450 74.50%
Aromatase binding - 0.8456 84.56%
PPAR gamma - 0.8881 88.81%
Honey bee toxicity - 0.8280 82.80%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9927 99.27%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.12% 97.25%
CHEMBL2581 P07339 Cathepsin D 87.07% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.24% 91.11%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.57% 86.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.00% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.50% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.30% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.18% 93.56%

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.
Cyrtocymura scorpioides
Senecio crassissimus

Cross-Links

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PubChem 162992916
LOTUS LTS0007675
wikiData Q105146618