(3E,7R,10S)-2,10-dimethyl-6-methylidenedodeca-3,11-diene-2,7,10-triol

Details

Top
Internal ID 4b9e9aa8-8708-489a-907f-21889ae7e22f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3E,7R,10S)-2,10-dimethyl-6-methylidenedodeca-3,11-diene-2,7,10-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O3/c1-6-15(5,18)11-9-13(16)12(2)8-7-10-14(3,4)17/h6-7,10,13,16-18H,1-2,8-9,11H2,3-5H3/b10-7+/t13-,15-/m1/s1
InChI Key FCMJFKBUUKKQQA-VINFDWDVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H26O3
Molecular Weight 254.36 g/mol
Exact Mass 254.18819469 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.34
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3E,7R,10S)-2,10-dimethyl-6-methylidenedodeca-3,11-diene-2,7,10-triol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9819 98.19%
Caco-2 - 0.5459 54.59%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5280 52.80%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.8895 88.95%
OATP1B3 inhibitior + 0.9612 96.12%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7708 77.08%
P-glycoprotein inhibitior - 0.9308 93.08%
P-glycoprotein substrate - 0.9062 90.62%
CYP3A4 substrate - 0.5171 51.71%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate - 0.7496 74.96%
CYP3A4 inhibition - 0.7632 76.32%
CYP2C9 inhibition - 0.7950 79.50%
CYP2C19 inhibition - 0.7852 78.52%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.7449 74.49%
CYP2C8 inhibition - 0.8756 87.56%
CYP inhibitory promiscuity - 0.7764 77.64%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.6859 68.59%
Eye corrosion - 0.8851 88.51%
Eye irritation - 0.7215 72.15%
Skin irritation + 0.5369 53.69%
Skin corrosion - 0.9773 97.73%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5491 54.91%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.7576 75.76%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.7941 79.41%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.6302 63.02%
Acute Oral Toxicity (c) III 0.7698 76.98%
Estrogen receptor binding - 0.6300 63.00%
Androgen receptor binding - 0.8232 82.32%
Thyroid receptor binding - 0.5679 56.79%
Glucocorticoid receptor binding + 0.6255 62.55%
Aromatase binding - 0.6495 64.95%
PPAR gamma + 0.5439 54.39%
Honey bee toxicity - 0.8655 86.55%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9606 96.06%

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
CHEMBL2885 P07451 Carbonic anhydrase III 88.19% 87.45%
CHEMBL2581 P07339 Cathepsin D 86.87% 98.95%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 86.65% 90.93%
CHEMBL3401 O75469 Pregnane X receptor 86.62% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.76% 97.25%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.82% 96.47%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.74% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.58% 91.11%
CHEMBL1907 P15144 Aminopeptidase N 80.10% 93.31%

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.
Schistostephium crataegifolium

Cross-Links

Top
PubChem 163018619
LOTUS LTS0224057
wikiData Q104993221