4-Tridecanone

Details

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Internal ID c21cb6e5-7a8e-4e6b-8bf0-d74a25306ab9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name tridecan-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H26O/c1-3-5-6-7-8-9-10-12-13(14)11-4-2/h3-12H2,1-2H3
InChI Key JWSRUPAFLPWLNO-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C13H26O
Molecular Weight 198.34 g/mol
Exact Mass 198.198365449 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.50
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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Tridecan-4-one
n-Nonyl n-propyl ketone
EINECS 247-519-0
DTXSID80180854
NSC 158500
Tridecan4one
RefChem:100554
DTXCID20103345
247-519-0
JWSRUPAFLPWLNO-UHFFFAOYSA-N
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Tridecanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.9699 96.99%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.4585 45.85%
OATP2B1 inhibitior - 0.8404 84.04%
OATP1B1 inhibitior + 0.9339 93.39%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6598 65.98%
P-glycoprotein inhibitior - 0.9574 95.74%
P-glycoprotein substrate - 0.9238 92.38%
CYP3A4 substrate - 0.6912 69.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7622 76.22%
CYP3A4 inhibition - 0.9815 98.15%
CYP2C9 inhibition - 0.9433 94.33%
CYP2C19 inhibition - 0.9645 96.45%
CYP2D6 inhibition - 0.9502 95.02%
CYP1A2 inhibition + 0.6890 68.90%
CYP2C8 inhibition - 0.9518 95.18%
CYP inhibitory promiscuity - 0.8752 87.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.7622 76.22%
Eye corrosion + 0.9821 98.21%
Eye irritation + 0.9892 98.92%
Skin irritation + 0.7185 71.85%
Skin corrosion - 0.9333 93.33%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6162 61.62%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6404 64.04%
skin sensitisation + 0.9027 90.27%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9578 95.78%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.4600 46.00%
Acute Oral Toxicity (c) III 0.8455 84.55%
Estrogen receptor binding - 0.9391 93.91%
Androgen receptor binding - 0.9030 90.30%
Thyroid receptor binding - 0.7995 79.95%
Glucocorticoid receptor binding - 0.7904 79.04%
Aromatase binding - 0.8969 89.69%
PPAR gamma - 0.6041 60.41%
Honey bee toxicity - 0.9932 99.32%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity + 0.8268 82.68%
Fish aquatic toxicity + 0.8149 81.49%

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
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.60% 85.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.55% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.96% 92.08%
CHEMBL2581 P07339 Cathepsin D 91.78% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.27% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.96% 97.29%
CHEMBL230 P35354 Cyclooxygenase-2 89.48% 89.63%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.79% 91.81%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.35% 92.86%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.42% 91.11%

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.
Capillipedium parviflorum
Houttuynia cordata

Cross-Links

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PubChem 98673
NPASS NPC79887
LOTUS LTS0081096
wikiData Q83051468