7-Tert-butyl-1,6-dimethyl-5-methylidenecyclononene

Details

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Internal ID c7176c9d-6fdc-4563-8272-6c3ce6621bd7
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 7-tert-butyl-1,6-dimethyl-5-methylidenecyclononene
SMILES (Canonical) CC1C(CCC(=CCCC1=C)C)C(C)(C)C
SMILES (Isomeric) CC1C(CCC(=CCCC1=C)C)C(C)(C)C
InChI InChI=1S/C16H28/c1-12-8-7-9-13(2)14(3)15(11-10-12)16(4,5)6/h8,14-15H,2,7,9-11H2,1,3-6H3
InChI Key VRTFVAUMJOGEOH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H28
Molecular Weight 220.39 g/mol
Exact Mass 220.219100893 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.10
Atomic LogP (AlogP) 5.36
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Tert-butyl-1,6-dimethyl-5-methylidenecyclononene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9892 98.92%
Caco-2 + 0.8117 81.17%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.6452 64.52%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.9687 96.87%
OATP1B3 inhibitior + 0.8196 81.96%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.7884 78.84%
P-glycoprotein inhibitior - 0.8610 86.10%
P-glycoprotein substrate - 0.9249 92.49%
CYP3A4 substrate - 0.5635 56.35%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7640 76.40%
CYP3A4 inhibition - 0.8968 89.68%
CYP2C9 inhibition - 0.7957 79.57%
CYP2C19 inhibition - 0.7617 76.17%
CYP2D6 inhibition - 0.9453 94.53%
CYP1A2 inhibition - 0.7562 75.62%
CYP2C8 inhibition - 0.7934 79.34%
CYP inhibitory promiscuity - 0.7305 73.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.4740 47.40%
Eye corrosion - 0.8116 81.16%
Eye irritation + 0.6447 64.47%
Skin irritation + 0.5797 57.97%
Skin corrosion - 0.9853 98.53%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6427 64.27%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.8704 87.04%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6555 65.55%
Acute Oral Toxicity (c) III 0.7467 74.67%
Estrogen receptor binding - 0.8851 88.51%
Androgen receptor binding - 0.7279 72.79%
Thyroid receptor binding - 0.8376 83.76%
Glucocorticoid receptor binding - 0.6022 60.22%
Aromatase binding - 0.8083 80.83%
PPAR gamma - 0.7211 72.11%
Honey bee toxicity - 0.9231 92.31%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 1.0000 100.00%

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 97.44% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.01% 91.11%
CHEMBL2581 P07339 Cathepsin D 85.95% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.41% 95.56%
CHEMBL1871 P10275 Androgen Receptor 83.89% 96.43%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.81% 86.00%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.09% 90.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.95% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.60% 97.09%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 80.05% 83.14%

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.
Silphium perfoliatum

Cross-Links

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PubChem 163043354
LOTUS LTS0040651
wikiData Q105291947