(1Z,5Z,9E)-1,5,9-trimethyl-12-propan-2-ylidenecyclotetradeca-1,5,9-triene

Details

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Internal ID 5a89f03b-e7c3-4bba-9aa3-1ba013497062
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1Z,5Z,9E)-1,5,9-trimethyl-12-propan-2-ylidenecyclotetradeca-1,5,9-triene
SMILES (Canonical)
SMILES (Isomeric)
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/h8,11-12H,6-7,9-10,13-15H2,1-5H3/b17-8-,18-12+,19-11-
InChI Key SHVZFTWRFOQOFU-ZEXQNBDISA-N
Popularity 6 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 5.40
Atomic LogP (AlogP) 6.91
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,5Z,9E)-1,5,9-trimethyl-12-propan-2-ylidenecyclotetradeca-1,5,9-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.9635 96.35%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.4255 42.55%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9642 96.42%
OATP1B3 inhibitior + 0.9557 95.57%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.4686 46.86%
P-glycoprotein inhibitior - 0.7236 72.36%
P-glycoprotein substrate - 0.9643 96.43%
CYP3A4 substrate - 0.6160 61.60%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.7601 76.01%
CYP3A4 inhibition - 0.9515 95.15%
CYP2C9 inhibition - 0.8556 85.56%
CYP2C19 inhibition - 0.8447 84.47%
CYP2D6 inhibition - 0.9427 94.27%
CYP1A2 inhibition - 0.7131 71.31%
CYP2C8 inhibition - 0.9384 93.84%
CYP inhibitory promiscuity - 0.7471 74.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Warning 0.4922 49.22%
Eye corrosion + 0.5247 52.47%
Eye irritation + 0.7772 77.72%
Skin irritation + 0.7729 77.29%
Skin corrosion - 0.9586 95.86%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8469 84.69%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation + 0.9263 92.63%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.5282 52.82%
Acute Oral Toxicity (c) III 0.7428 74.28%
Estrogen receptor binding - 0.8072 80.72%
Androgen receptor binding - 0.6982 69.82%
Thyroid receptor binding - 0.5961 59.61%
Glucocorticoid receptor binding - 0.7261 72.61%
Aromatase binding - 0.7130 71.30%
PPAR gamma + 0.7396 73.96%
Honey bee toxicity - 0.9610 96.10%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9944 99.44%

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 90.28% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.24% 96.09%
CHEMBL4208 P20618 Proteasome component C5 84.41% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.23% 95.56%
CHEMBL2581 P07339 Cathepsin D 80.82% 98.95%

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 90658459
LOTUS LTS0222695
wikiData Q104251755