4-(Hydroxymethyl)hexadec-15-yne-1,2,6-triol

Details

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Internal ID 9c029f9d-13c7-4d0f-9b33-83fc587d284b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name 4-(hydroxymethyl)hexadec-15-yne-1,2,6-triol
SMILES (Canonical) C#CCCCCCCCCC(CC(CC(CO)O)CO)O
SMILES (Isomeric) C#CCCCCCCCCC(CC(CC(CO)O)CO)O
InChI InChI=1S/C17H32O4/c1-2-3-4-5-6-7-8-9-10-16(20)11-15(13-18)12-17(21)14-19/h1,15-21H,3-14H2
InChI Key WZFKQOQODVEDIE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H32O4
Molecular Weight 300.40 g/mol
Exact Mass 300.23005950 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.84
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(Hydroxymethyl)hexadec-15-yne-1,2,6-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6203 62.03%
Caco-2 - 0.7363 73.63%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7680 76.80%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9541 95.41%
OATP1B3 inhibitior + 0.9508 95.08%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7889 78.89%
P-glycoprotein inhibitior - 0.9177 91.77%
P-glycoprotein substrate - 0.8809 88.09%
CYP3A4 substrate - 0.5372 53.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7333 73.33%
CYP3A4 inhibition - 0.9103 91.03%
CYP2C9 inhibition - 0.8541 85.41%
CYP2C19 inhibition - 0.8824 88.24%
CYP2D6 inhibition - 0.9531 95.31%
CYP1A2 inhibition - 0.8481 84.81%
CYP2C8 inhibition - 0.9400 94.00%
CYP inhibitory promiscuity - 0.9515 95.15%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6947 69.47%
Eye corrosion - 0.8255 82.55%
Eye irritation - 0.8281 82.81%
Skin irritation - 0.7904 79.04%
Skin corrosion - 0.9455 94.55%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3736 37.36%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6304 63.04%
skin sensitisation - 0.7234 72.34%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.4661 46.61%
Acute Oral Toxicity (c) IV 0.4665 46.65%
Estrogen receptor binding - 0.5851 58.51%
Androgen receptor binding - 0.8667 86.67%
Thyroid receptor binding + 0.6124 61.24%
Glucocorticoid receptor binding + 0.7344 73.44%
Aromatase binding - 0.6074 60.74%
PPAR gamma - 0.6030 60.30%
Honey bee toxicity - 0.7675 76.75%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6683 66.83%
Fish aquatic toxicity - 0.8670 86.70%

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 93.22% 97.29%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.69% 91.11%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.14% 92.86%
CHEMBL2581 P07339 Cathepsin D 87.65% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 87.63% 89.63%
CHEMBL242 Q92731 Estrogen receptor beta 87.60% 98.35%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.87% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.03% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 82.64% 87.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.23% 100.00%

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.
Sextonia rubra

Cross-Links

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PubChem 162820200
LOTUS LTS0180902
wikiData Q104200763