(1Z,4Z,8Z)-1,3,3,8-tetramethylcycloundeca-1,4,8-triene

Details

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Internal ID f40634ea-72b6-4575-9f33-3d6e5725c5f5
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (1Z,4Z,8Z)-1,3,3,8-tetramethylcycloundeca-1,4,8-triene
SMILES (Canonical) CC1=CCCC(=CC(C=CCC1)(C)C)C
SMILES (Isomeric) C/C/1=C/CC/C(=C\C(/C=C\CC1)(C)C)/C
InChI InChI=1S/C15H24/c1-13-8-5-6-11-15(3,4)12-14(2)10-7-9-13/h6,9,11-12H,5,7-8,10H2,1-4H3/b11-6-,13-9-,14-12-
InChI Key RTIZXJCGCGLKCH-JGKOJNDLSA-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 4.50
Atomic LogP (AlogP) 5.04
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 (1Z,4Z,8Z)-1,3,3,8-tetramethylcycloundeca-1,4,8-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.9767 97.67%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Lysosomes 0.5788 57.88%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.9662 96.62%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6614 66.14%
P-glycoprotein inhibitior - 0.9720 97.20%
P-glycoprotein substrate - 0.9194 91.94%
CYP3A4 substrate - 0.5800 58.00%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.9106 91.06%
CYP2C9 inhibition - 0.7994 79.94%
CYP2C19 inhibition - 0.7952 79.52%
CYP2D6 inhibition - 0.9406 94.06%
CYP1A2 inhibition - 0.8014 80.14%
CYP2C8 inhibition - 0.9019 90.19%
CYP inhibitory promiscuity - 0.7646 76.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Warning 0.5028 50.28%
Eye corrosion - 0.6888 68.88%
Eye irritation + 0.8217 82.17%
Skin irritation + 0.6995 69.95%
Skin corrosion - 0.9762 97.62%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7655 76.55%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.9074 90.74%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.6576 65.76%
Acute Oral Toxicity (c) III 0.6889 68.89%
Estrogen receptor binding - 0.9329 93.29%
Androgen receptor binding - 0.8659 86.59%
Thyroid receptor binding - 0.6726 67.26%
Glucocorticoid receptor binding - 0.7250 72.50%
Aromatase binding - 0.7297 72.97%
PPAR gamma - 0.7173 71.73%
Honey bee toxicity - 0.9418 94.18%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9940 99.40%

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 93.25% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.17% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 88.31% 89.63%
CHEMBL4208 P20618 Proteasome component C5 85.05% 90.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.37% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.90% 95.56%

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.
Saccogyna viticulosa

Cross-Links

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PubChem 101349815
LOTUS LTS0188445
wikiData Q105245176