1,5,9-Cyclotetradecatriene, 1,5,9-trimethyl-12-(1-methylethenyl)-

Details

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Internal ID 4c8db401-4213-43d6-9c04-c6ac935a1eaa
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Cembrane diterpenoids
IUPAC Name 1,5,9-trimethyl-12-prop-1-en-2-ylcyclotetradeca-1,5,9-triene
SMILES (Canonical) CC1=CCCC(=CCC(CCC(=CCC1)C)C(=C)C)C
SMILES (Isomeric) CC1=CCCC(=CCC(CCC(=CCC1)C)C(=C)C)C
InChI InChI=1S/C20H32/c1-16(2)20-14-12-18(4)10-6-8-17(3)9-7-11-19(5)13-15-20/h8,11-12,20H,1,6-7,9-10,13-15H2,2-5H3
InChI Key VWSPQDDPRITBAM-UHFFFAOYSA-N
Popularity 1 reference 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 5.90
Atomic LogP (AlogP) 6.76
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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139492-81-2
DTXSID40316990

2D Structure

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2D Structure of 1,5,9-Cyclotetradecatriene, 1,5,9-trimethyl-12-(1-methylethenyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.8916 89.16%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.5878 58.78%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9771 97.71%
OATP1B3 inhibitior + 0.9473 94.73%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6288 62.88%
P-glycoprotein inhibitior - 0.6556 65.56%
P-glycoprotein substrate - 0.9171 91.71%
CYP3A4 substrate - 0.5944 59.44%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9207 92.07%
CYP2C9 inhibition - 0.8613 86.13%
CYP2C19 inhibition - 0.8203 82.03%
CYP2D6 inhibition - 0.9379 93.79%
CYP1A2 inhibition - 0.6699 66.99%
CYP2C8 inhibition - 0.8562 85.62%
CYP inhibitory promiscuity - 0.7682 76.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Warning 0.4978 49.78%
Eye corrosion + 0.5909 59.09%
Eye irritation + 0.5572 55.72%
Skin irritation + 0.7468 74.68%
Skin corrosion - 0.9749 97.49%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8329 83.29%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8923 89.23%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.5376 53.76%
Acute Oral Toxicity (c) III 0.8499 84.99%
Estrogen receptor binding - 0.7568 75.68%
Androgen receptor binding - 0.7954 79.54%
Thyroid receptor binding - 0.5951 59.51%
Glucocorticoid receptor binding - 0.6463 64.63%
Aromatase binding - 0.7377 73.77%
PPAR gamma + 0.6369 63.69%
Honey bee toxicity - 0.9391 93.91%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9965 99.65%

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 94.63% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.70% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.75% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.28% 97.21%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.44% 100.00%
CHEMBL2581 P07339 Cathepsin D 82.04% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.72% 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.
Cedrela odorata
Ixora chinensis
Picea obovata
Pinus heldreichii
Stillingia sanguinolenta

Cross-Links

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PubChem 328947
NPASS NPC51936
LOTUS LTS0098244
wikiData Q82071259