9-Heptadecanone

Details

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Internal ID 074970dd-0cc3-40b9-922b-47558f31031d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name heptadecan-9-one
SMILES (Canonical) CCCCCCCCC(=O)CCCCCCCC
SMILES (Isomeric) CCCCCCCCC(=O)CCCCCCCC
InChI InChI=1S/C17H34O/c1-3-5-7-9-11-13-15-17(18)16-14-12-10-8-6-4-2/h3-16H2,1-2H3
InChI Key WTJKUFMLQFLJOT-UHFFFAOYSA-N
Popularity 151 references in papers

Physical and Chemical Properties

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Molecular Formula C17H34O
Molecular Weight 254.50 g/mol
Exact Mass 254.260965704 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 7.00
Atomic LogP (AlogP) 6.06
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

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Heptadecan-9-one
540-08-9
Pelargone
Di-n-octyl ketone
Dioctyl ketone
Dioctylketone
Octyl ketone
9-Oxoheptadecane
C17H34O
NSC 7336
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 9-Heptadecanone

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 + 0.9676 96.76%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4585 45.85%
OATP2B1 inhibitior - 0.8408 84.08%
OATP1B1 inhibitior + 0.9370 93.70%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6463 64.63%
P-glycoprotein inhibitior - 0.8651 86.51%
P-glycoprotein substrate - 0.9463 94.63%
CYP3A4 substrate - 0.7331 73.31%
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 - 0.9711 97.11%
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 + 0.9919 99.19%
Skin irritation + 0.7185 71.85%
Skin corrosion - 0.9333 93.33%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4581 45.81%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7478 74.78%
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 + 0.5450 54.50%
Acute Oral Toxicity (c) III 0.8455 84.55%
Estrogen receptor binding - 0.8942 89.42%
Androgen receptor binding - 0.8963 89.63%
Thyroid receptor binding - 0.7145 71.45%
Glucocorticoid receptor binding - 0.9116 91.16%
Aromatase binding - 0.8303 83.03%
PPAR gamma - 0.5226 52.26%
Honey bee toxicity - 0.9951 99.51%
Biodegradation + 0.9250 92.50%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.78% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.55% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.18% 92.08%
CHEMBL2581 P07339 Cathepsin D 91.92% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 91.68% 85.94%
CHEMBL230 P35354 Cyclooxygenase-2 91.67% 89.63%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.97% 97.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.93% 96.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.47% 91.81%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.16% 92.86%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.13% 95.17%
CHEMBL299 P17252 Protein kinase C alpha 80.97% 98.03%

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.
Heteroplexis microcephala
Terminalia chebula
Tridax procumbens

Cross-Links

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PubChem 10887
NPASS NPC225318
LOTUS LTS0181921
wikiData Q104962948