(1E,4E,8E,12Z)-2,6,6,9,13-pentamethylcyclopentadeca-1,4,8,12-tetraene

Details

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Internal ID b0e40c4b-2620-462d-bca8-e1d456d31934
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (1E,4E,8E,12Z)-2,6,6,9,13-pentamethylcyclopentadeca-1,4,8,12-tetraene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32/c1-17-9-6-11-18(2)13-8-15-20(4,5)16-14-19(3)12-7-10-17/h8,10-11,14-15H,6-7,9,12-13,16H2,1-5H3/b15-8+,17-10-,18-11+,19-14+
InChI Key SPMBDLTUBLYRCT-QIXATTRFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32
Molecular Weight 272.50 g/mol
Exact Mass 272.250401021 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 6.76
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,4E,8E,12Z)-2,6,6,9,13-pentamethylcyclopentadeca-1,4,8,12-tetraene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9865 98.65%
Caco-2 + 0.9728 97.28%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.5618 56.18%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.9636 96.36%
OATP1B3 inhibitior + 0.9127 91.27%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6799 67.99%
P-glycoprotein inhibitior - 0.7920 79.20%
P-glycoprotein substrate - 0.9444 94.44%
CYP3A4 substrate - 0.5518 55.18%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.9419 94.19%
CYP2C9 inhibition - 0.8482 84.82%
CYP2C19 inhibition - 0.8653 86.53%
CYP2D6 inhibition - 0.9503 95.03%
CYP1A2 inhibition - 0.8469 84.69%
CYP2C8 inhibition - 0.8842 88.42%
CYP inhibitory promiscuity - 0.8220 82.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Warning 0.5247 52.47%
Eye corrosion + 0.4717 47.17%
Eye irritation + 0.6502 65.02%
Skin irritation + 0.7804 78.04%
Skin corrosion - 0.9840 98.40%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8274 82.74%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.9186 91.86%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.6272 62.72%
Acute Oral Toxicity (c) III 0.7252 72.52%
Estrogen receptor binding - 0.6799 67.99%
Androgen receptor binding - 0.8979 89.79%
Thyroid receptor binding - 0.5066 50.66%
Glucocorticoid receptor binding - 0.6240 62.40%
Aromatase binding - 0.4874 48.74%
PPAR gamma + 0.6336 63.36%
Honey bee toxicity - 0.9286 92.86%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9935 99.35%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.62% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.17% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.76% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.03% 97.25%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 5824184
LOTUS LTS0177254
wikiData Q105257455