(5Z,7Z,10Z)-1,7,11-trimethyl-4-propan-2-ylcyclotetradeca-5,7,10-trien-1-ol

Details

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Internal ID d8f4c7c5-a2bf-45ce-be4c-1b803dc62b0e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Cembrane diterpenoids
IUPAC Name (5Z,7Z,10Z)-1,7,11-trimethyl-4-propan-2-ylcyclotetradeca-5,7,10-trien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H34O/c1-16(2)19-12-11-18(4)9-6-8-17(3)10-7-14-20(5,21)15-13-19/h8-9,11-12,16,19,21H,6-7,10,13-15H2,1-5H3/b12-11-,17-8-,18-9-
InChI Key WKQKVJFYCDGSFS-QYNRSAJESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O
Molecular Weight 290.50 g/mol
Exact Mass 290.260965704 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.20
Atomic LogP (AlogP) 5.81
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5Z,7Z,10Z)-1,7,11-trimethyl-4-propan-2-ylcyclotetradeca-5,7,10-trien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.9100 91.00%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.4277 42.77%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9014 90.14%
OATP1B3 inhibitior + 0.9655 96.55%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.4912 49.12%
P-glycoprotein inhibitior - 0.8704 87.04%
P-glycoprotein substrate - 0.7660 76.60%
CYP3A4 substrate + 0.5404 54.04%
CYP2C9 substrate - 0.7880 78.80%
CYP2D6 substrate - 0.7952 79.52%
CYP3A4 inhibition - 0.8700 87.00%
CYP2C9 inhibition - 0.7162 71.62%
CYP2C19 inhibition - 0.7231 72.31%
CYP2D6 inhibition - 0.9398 93.98%
CYP1A2 inhibition - 0.7191 71.91%
CYP2C8 inhibition - 0.8367 83.67%
CYP inhibitory promiscuity - 0.8773 87.73%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.5939 59.39%
Eye corrosion - 0.9150 91.50%
Eye irritation - 0.9115 91.15%
Skin irritation + 0.7873 78.73%
Skin corrosion - 0.9461 94.61%
Ames mutagenesis - 0.7070 70.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7651 76.51%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5284 52.84%
skin sensitisation + 0.7894 78.94%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.7017 70.17%
Acute Oral Toxicity (c) III 0.7917 79.17%
Estrogen receptor binding - 0.6499 64.99%
Androgen receptor binding - 0.7822 78.22%
Thyroid receptor binding + 0.7264 72.64%
Glucocorticoid receptor binding + 0.5536 55.36%
Aromatase binding - 0.6999 69.99%
PPAR gamma + 0.5282 52.82%
Honey bee toxicity - 0.9305 93.05%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9106 91.06%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.89% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.94% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.09% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.03% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.74% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.65% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.26% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.34% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 83.76% 94.75%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.41% 93.56%
CHEMBL1871 P10275 Androgen Receptor 82.85% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.46% 100.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.70% 93.99%
CHEMBL4073 P09237 Matrix metalloproteinase 7 81.31% 97.56%

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.
Pinus heldreichii

Cross-Links

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PubChem 101670433
LOTUS LTS0270087
wikiData Q104375892