(6S,7E,9Z)-2,6,10-trimethyldodeca-2,7,9,11-tetraen-6-ol

Details

Top
Internal ID 30d3657d-8026-4706-8640-80f3bc6aa8e7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (6S,7E,9Z)-2,6,10-trimethyldodeca-2,7,9,11-tetraen-6-ol
SMILES (Canonical) CC(=CCCC(C)(C=CC=C(C)C=C)O)C
SMILES (Isomeric) CC(=CCC[C@@](C)(/C=C/C=C(/C)\C=C)O)C
InChI InChI=1S/C15H24O/c1-6-14(4)10-8-12-15(5,16)11-7-9-13(2)3/h6,8-10,12,16H,1,7,11H2,2-5H3/b12-8+,14-10-/t15-/m0/s1
InChI Key VJBVZYOKPWWGLN-QMNYXVAKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.17
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (6S,7E,9Z)-2,6,10-trimethyldodeca-2,7,9,11-tetraen-6-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9894 98.94%
Caco-2 + 0.9101 91.01%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.3689 36.89%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.8944 89.44%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6942 69.42%
P-glycoprotein inhibitior - 0.9778 97.78%
P-glycoprotein substrate - 0.9187 91.87%
CYP3A4 substrate - 0.5314 53.14%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.7761 77.61%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.8385 83.85%
CYP2C19 inhibition - 0.8080 80.80%
CYP2D6 inhibition - 0.9355 93.55%
CYP1A2 inhibition - 0.7566 75.66%
CYP2C8 inhibition - 0.9270 92.70%
CYP inhibitory promiscuity - 0.8199 81.99%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6315 63.15%
Eye corrosion - 0.7769 77.69%
Eye irritation + 0.9113 91.13%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.8784 87.84%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5430 54.30%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5968 59.68%
skin sensitisation + 0.9091 90.91%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6216 62.16%
Acute Oral Toxicity (c) III 0.8335 83.35%
Estrogen receptor binding - 0.7693 76.93%
Androgen receptor binding - 0.9322 93.22%
Thyroid receptor binding - 0.7054 70.54%
Glucocorticoid receptor binding - 0.5953 59.53%
Aromatase binding - 0.7635 76.35%
PPAR gamma - 0.5731 57.31%
Honey bee toxicity - 0.8434 84.34%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.7206 72.06%

Targets

Top

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
CHEMBL3401 O75469 Pregnane X receptor 90.89% 94.73%
CHEMBL2581 P07339 Cathepsin D 88.23% 98.95%
CHEMBL1977 P11473 Vitamin D receptor 85.42% 99.43%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.73% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.42% 97.21%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.78% 89.34%
CHEMBL2885 P07451 Carbonic anhydrase III 80.43% 87.45%

Plants that contains it

Top
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.
Ageratum fastigiatum

Cross-Links

Top
PubChem 162917793
LOTUS LTS0241013
wikiData Q105287150