1-Hydroxytridecan-2-one

Details

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Internal ID 3c10fb00-4602-4ac1-9a39-d5ea1c0b77eb
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name 1-hydroxytridecan-2-one
SMILES (Canonical) CCCCCCCCCCCC(=O)CO
SMILES (Isomeric) CCCCCCCCCCCC(=O)CO
InChI InChI=1S/C13H26O2/c1-2-3-4-5-6-7-8-9-10-11-13(15)12-14/h14H,2-12H2,1H3
InChI Key QTJBCXUJIXQYNP-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C13H26O2
Molecular Weight 214.34 g/mol
Exact Mass 214.193280068 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.47
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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1-hydroxy-2-tridecanone
99224-14-3
hydroxyl tridecanone
SCHEMBL9730057
DTXSID50540380
QTJBCXUJIXQYNP-UHFFFAOYSA-N

2D Structure

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2D Structure of 1-Hydroxytridecan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.7984 79.84%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6950 69.50%
OATP2B1 inhibitior - 0.8491 84.91%
OATP1B1 inhibitior + 0.9275 92.75%
OATP1B3 inhibitior + 0.8871 88.71%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.6292 62.92%
P-glycoprotein inhibitior - 0.9563 95.63%
P-glycoprotein substrate - 0.9388 93.88%
CYP3A4 substrate - 0.7046 70.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7863 78.63%
CYP3A4 inhibition - 0.9281 92.81%
CYP2C9 inhibition - 0.8266 82.66%
CYP2C19 inhibition - 0.8838 88.38%
CYP2D6 inhibition - 0.9031 90.31%
CYP1A2 inhibition + 0.6327 63.27%
CYP2C8 inhibition - 0.9676 96.76%
CYP inhibitory promiscuity - 0.8881 88.81%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.7160 71.60%
Eye corrosion + 0.7264 72.64%
Eye irritation + 0.9884 98.84%
Skin irritation - 0.5916 59.16%
Skin corrosion - 0.9642 96.42%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5479 54.79%
skin sensitisation + 0.7075 70.75%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.8612 86.12%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.5972 59.72%
Acute Oral Toxicity (c) III 0.5663 56.63%
Estrogen receptor binding - 0.8542 85.42%
Androgen receptor binding - 0.8759 87.59%
Thyroid receptor binding - 0.6504 65.04%
Glucocorticoid receptor binding - 0.7860 78.60%
Aromatase binding - 0.8199 81.99%
PPAR gamma - 0.5379 53.79%
Honey bee toxicity - 0.9918 99.18%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity + 0.7629 76.29%
Fish aquatic toxicity - 0.4070 40.70%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.46% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.18% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 94.10% 97.29%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.30% 92.08%
CHEMBL2581 P07339 Cathepsin D 92.01% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.19% 85.94%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.94% 91.81%
CHEMBL230 P35354 Cyclooxygenase-2 85.26% 89.63%
CHEMBL299 P17252 Protein kinase C alpha 85.26% 98.03%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.76% 92.86%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.80% 96.95%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.42% 100.00%
CHEMBL2885 P07451 Carbonic anhydrase III 80.08% 87.45%

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.
Pilocarpus trachylophus
Zanthoxylum gilletii

Cross-Links

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PubChem 13423645
LOTUS LTS0255418
wikiData Q82416378