(7S)-hexadecane-1,7,16-triol

Details

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Internal ID 9869b509-131b-43c3-8ebc-a0afb06afb61
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (7S)-hexadecane-1,7,16-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H34O3/c17-14-10-6-3-1-2-4-8-12-16(19)13-9-5-7-11-15-18/h16-19H,1-15H2/t16-/m0/s1
InChI Key RKSTWDZUIGHKJJ-INIZCTEOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H34O3
Molecular Weight 274.44 g/mol
Exact Mass 274.25079494 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.40
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (7S)-hexadecane-1,7,16-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9235 92.35%
Caco-2 - 0.6236 62.36%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7804 78.04%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9703 97.03%
OATP1B3 inhibitior + 0.9540 95.40%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8461 84.61%
P-glycoprotein inhibitior - 0.9143 91.43%
P-glycoprotein substrate - 0.9589 95.89%
CYP3A4 substrate - 0.7236 72.36%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6778 67.78%
CYP3A4 inhibition - 0.9627 96.27%
CYP2C9 inhibition - 0.9060 90.60%
CYP2C19 inhibition - 0.9116 91.16%
CYP2D6 inhibition - 0.9623 96.23%
CYP1A2 inhibition - 0.9127 91.27%
CYP2C8 inhibition - 0.9872 98.72%
CYP inhibitory promiscuity - 0.9313 93.13%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.6653 66.53%
Eye corrosion + 0.7978 79.78%
Eye irritation + 0.9403 94.03%
Skin irritation - 0.7284 72.84%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation - 0.7726 77.26%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5507 55.07%
Acute Oral Toxicity (c) IV 0.5309 53.09%
Estrogen receptor binding - 0.7143 71.43%
Androgen receptor binding - 0.8363 83.63%
Thyroid receptor binding + 0.5293 52.93%
Glucocorticoid receptor binding - 0.5951 59.51%
Aromatase binding - 0.7076 70.76%
PPAR gamma + 0.5450 54.50%
Honey bee toxicity - 0.9437 94.37%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.8487 84.87%
Fish aquatic toxicity - 0.9205 92.05%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.44% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.73% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 90.30% 87.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.96% 91.11%
CHEMBL2581 P07339 Cathepsin D 82.46% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.86% 99.17%

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.
Arabidopsis thaliana

Cross-Links

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PubChem 163105830
LOTUS LTS0169054
wikiData Q105238823