1,18-Octadecanediol

Details

Top
Internal ID ac349b2e-e061-42ab-93db-dd79fac951ad
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name octadecane-1,18-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H38O2/c19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18-20/h19-20H,1-18H2
InChI Key LUUFSCNUZAYHAT-UHFFFAOYSA-N
Popularity 17 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H38O2
Molecular Weight 286.50 g/mol
Exact Mass 286.287180451 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 6.80
Atomic LogP (AlogP) 5.21
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 17

Synonyms

Top
octadecane-1,18-diol
3155-43-9
1,18-octadecane-diol
ST454BM3B9
C18H38O2
1,18- Octadecandiol
UNII-ST454BM3B9
SCHEMBL93355
AMY036
DTXSID30334385
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 1,18-Octadecanediol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9461 94.61%
Caco-2 - 0.5423 54.23%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5544 55.44%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.9655 96.55%
OATP1B3 inhibitior + 0.9463 94.63%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8743 87.43%
P-glycoprotein inhibitior - 0.9128 91.28%
P-glycoprotein substrate - 0.9900 99.00%
CYP3A4 substrate - 0.8031 80.31%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6902 69.02%
CYP3A4 inhibition - 0.9700 97.00%
CYP2C9 inhibition - 0.8980 89.80%
CYP2C19 inhibition - 0.9491 94.91%
CYP2D6 inhibition - 0.9706 97.06%
CYP1A2 inhibition - 0.8671 86.71%
CYP2C8 inhibition - 0.9866 98.66%
CYP inhibitory promiscuity - 0.9440 94.40%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6204 62.04%
Eye corrosion + 0.9714 97.14%
Eye irritation + 0.9800 98.00%
Skin irritation - 0.5374 53.74%
Skin corrosion - 0.9481 94.81%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4513 45.13%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5368 53.68%
skin sensitisation + 0.5129 51.29%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.5955 59.55%
Acute Oral Toxicity (c) III 0.8566 85.66%
Estrogen receptor binding - 0.7963 79.63%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.6818 68.18%
Glucocorticoid receptor binding - 0.6576 65.76%
Aromatase binding - 0.7127 71.27%
PPAR gamma - 0.6440 64.40%
Honey bee toxicity - 0.9729 97.29%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8284 82.84%
Fish aquatic toxicity - 0.9040 90.40%

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 89.13% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.76% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.48% 97.29%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.38% 91.11%

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.
Arabidopsis thaliana

Cross-Links

Top
PubChem 520529
LOTUS LTS0000367
wikiData Q72497050