(1E,5E,10R)-1,5,10-trimethyl-8-propan-2-ylidenecyclodeca-1,5-diene

Details

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Internal ID dec33f19-ccb5-42c5-8baf-366d0df4f8a6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name (1E,5E,10R)-1,5,10-trimethyl-8-propan-2-ylidenecyclodeca-1,5-diene
SMILES (Canonical) CC1CC(=C(C)C)CC=C(CCC=C1C)C
SMILES (Isomeric) C[C@@H]\1CC(=C(C)C)C/C=C(/CC/C=C1\C)\C
InChI InChI=1S/C16H26/c1-12(2)16-10-9-13(3)7-6-8-14(4)15(5)11-16/h8-9,15H,6-7,10-11H2,1-5H3/b13-9+,14-8+/t15-/m1/s1
InChI Key MBOZYHRSVMIYRG-HGMOOEGUSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H26
Molecular Weight 218.38 g/mol
Exact Mass 218.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 5.43
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 (1E,5E,10R)-1,5,10-trimethyl-8-propan-2-ylidenecyclodeca-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 + 0.9936 99.36%
Caco-2 + 0.9529 95.29%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.4692 46.92%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9539 95.39%
OATP1B3 inhibitior + 0.9110 91.10%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.6801 68.01%
P-glycoprotein inhibitior - 0.9448 94.48%
P-glycoprotein substrate - 0.8645 86.45%
CYP3A4 substrate - 0.5282 52.82%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.7625 76.25%
CYP3A4 inhibition - 0.9510 95.10%
CYP2C9 inhibition - 0.8641 86.41%
CYP2C19 inhibition - 0.8392 83.92%
CYP2D6 inhibition - 0.9474 94.74%
CYP1A2 inhibition - 0.6831 68.31%
CYP2C8 inhibition - 0.8835 88.35%
CYP inhibitory promiscuity - 0.6782 67.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Warning 0.4689 46.89%
Eye corrosion - 0.6640 66.40%
Eye irritation - 0.6772 67.72%
Skin irritation + 0.7035 70.35%
Skin corrosion - 0.9646 96.46%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7666 76.66%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.9162 91.62%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.4824 48.24%
Acute Oral Toxicity (c) III 0.5378 53.78%
Estrogen receptor binding - 0.9560 95.60%
Androgen receptor binding - 0.8031 80.31%
Thyroid receptor binding - 0.7516 75.16%
Glucocorticoid receptor binding - 0.8437 84.37%
Aromatase binding - 0.7661 76.61%
PPAR gamma - 0.7032 70.32%
Honey bee toxicity - 0.9304 93.04%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9970 99.70%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.76% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.69% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.33% 95.56%
CHEMBL2581 P07339 Cathepsin D 82.77% 98.95%

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.
There are no matching plants.

Cross-Links

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PubChem 10775218
LOTUS LTS0008728
wikiData Q105160878