(3S,6E)-3,11-dimethyldodeca-1,6,10-trien-3-ol

Details

Top
Internal ID 3038bc27-bf33-4bac-9177-287ae2d49407
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name (3S,6E)-3,11-dimethyldodeca-1,6,10-trien-3-ol
SMILES (Canonical) CC(=CCCC=CCCC(C)(C=C)O)C
SMILES (Isomeric) CC(=CCC/C=C/CC[C@@](C)(C=C)O)C
InChI InChI=1S/C14H24O/c1-5-14(4,15)12-10-8-6-7-9-11-13(2)3/h5-6,8,11,15H,1,7,9-10,12H2,2-4H3/b8-6+/t14-/m1/s1
InChI Key BLWFGFXUISFSJL-IZPAUZPXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H24O
Molecular Weight 208.34 g/mol
Exact Mass 208.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3S,6E)-3,11-dimethyldodeca-1,6,10-trien-3-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.7763 77.63%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.4009 40.09%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.8990 89.90%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6688 66.88%
P-glycoprotein inhibitior - 0.9725 97.25%
P-glycoprotein substrate - 0.9502 95.02%
CYP3A4 substrate - 0.5658 56.58%
CYP2C9 substrate - 0.7948 79.48%
CYP2D6 substrate - 0.7612 76.12%
CYP3A4 inhibition - 0.8586 85.86%
CYP2C9 inhibition - 0.8044 80.44%
CYP2C19 inhibition - 0.8324 83.24%
CYP2D6 inhibition - 0.9466 94.66%
CYP1A2 inhibition - 0.6869 68.69%
CYP2C8 inhibition - 0.9297 92.97%
CYP inhibitory promiscuity - 0.8513 85.13%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.6570 65.70%
Eye corrosion - 0.7964 79.64%
Eye irritation + 0.8908 89.08%
Skin irritation + 0.7483 74.83%
Skin corrosion - 0.9753 97.53%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5548 55.48%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6267 62.67%
skin sensitisation + 0.8831 88.31%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.8830 88.30%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.4720 47.20%
Acute Oral Toxicity (c) III 0.9000 90.00%
Estrogen receptor binding - 0.8809 88.09%
Androgen receptor binding - 0.8923 89.23%
Thyroid receptor binding - 0.6656 66.56%
Glucocorticoid receptor binding - 0.5704 57.04%
Aromatase binding - 0.8429 84.29%
PPAR gamma + 0.7139 71.39%
Honey bee toxicity - 0.7649 76.49%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9387 93.87%

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 88.45% 94.73%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 85.64% 90.93%
CHEMBL1977 P11473 Vitamin D receptor 85.05% 99.43%
CHEMBL2581 P07339 Cathepsin D 84.48% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.18% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.93% 97.21%

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.
Ursinia anethoides

Cross-Links

Top
PubChem 163190128
LOTUS LTS0153186
wikiData Q104938209