3,7,11-Trimethyl-14-prop-1-en-2-ylcyclotetradeca-2,6,10-trien-1-ol

Details

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Internal ID 4c5af42b-8d7b-448a-aa06-44aa65cd325a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Cembrane diterpenoids
IUPAC Name 3,7,11-trimethyl-14-prop-1-en-2-ylcyclotetradeca-2,6,10-trien-1-ol
SMILES (Canonical) CC1=CCCC(=CC(C(CCC(=CCC1)C)C(=C)C)O)C
SMILES (Isomeric) CC1=CCCC(=CC(C(CCC(=CCC1)C)C(=C)C)O)C
InChI InChI=1S/C20H32O/c1-15(2)19-13-12-17(4)10-6-8-16(3)9-7-11-18(5)14-20(19)21/h9-10,14,19-21H,1,6-8,11-13H2,2-5H3
InChI Key AZUVBPVDRHGGEP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O
Molecular Weight 288.50 g/mol
Exact Mass 288.245315640 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.73
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 3,7,11-Trimethyl-14-prop-1-en-2-ylcyclotetradeca-2,6,10-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 + 0.9933 99.33%
Caco-2 + 0.7872 78.72%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.4061 40.61%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.9650 96.50%
OATP1B3 inhibitior + 0.8977 89.77%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6308 63.08%
P-glycoprotein inhibitior - 0.6272 62.72%
P-glycoprotein substrate - 0.8997 89.97%
CYP3A4 substrate - 0.5598 55.98%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7021 70.21%
CYP3A4 inhibition - 0.7468 74.68%
CYP2C9 inhibition - 0.7786 77.86%
CYP2C19 inhibition - 0.7568 75.68%
CYP2D6 inhibition - 0.9057 90.57%
CYP1A2 inhibition - 0.5468 54.68%
CYP2C8 inhibition - 0.8181 81.81%
CYP inhibitory promiscuity - 0.7926 79.26%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.5997 59.97%
Eye corrosion - 0.8191 81.91%
Eye irritation - 0.7879 78.79%
Skin irritation + 0.6370 63.70%
Skin corrosion - 0.8703 87.03%
Ames mutagenesis - 0.8354 83.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3882 38.82%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.7698 76.98%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.4760 47.60%
Acute Oral Toxicity (c) III 0.6714 67.14%
Estrogen receptor binding - 0.6499 64.99%
Androgen receptor binding - 0.7706 77.06%
Thyroid receptor binding + 0.5153 51.53%
Glucocorticoid receptor binding - 0.5727 57.27%
Aromatase binding - 0.7686 76.86%
PPAR gamma + 0.6401 64.01%
Honey bee toxicity - 0.9022 90.22%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9914 99.14%

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 91.91% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.60% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.34% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.62% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.29% 97.25%
CHEMBL1871 P10275 Androgen Receptor 81.06% 96.43%

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.
Vernonia angustifolia

Cross-Links

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PubChem 72728641
LOTUS LTS0134718
wikiData Q105311922