2,3-Heptanedione

Details

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Internal ID 140d40ba-75eb-448b-bdfe-48074814f7a0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones > Alpha-diketones
IUPAC Name heptane-2,3-dione
SMILES (Canonical) CCCCC(=O)C(=O)C
SMILES (Isomeric) CCCCC(=O)C(=O)C
InChI InChI=1S/C7H12O2/c1-3-4-5-7(9)6(2)8/h3-5H2,1-2H3
InChI Key FJPGAMCQJNLTJC-UHFFFAOYSA-N
Popularity 44 references in papers

Physical and Chemical Properties

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Molecular Formula C7H12O2
Molecular Weight 128.17 g/mol
Exact Mass 128.083729621 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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96-04-8
Heptane-2,3-dione
Acetyl valeryl
Valerylacetyl
Acetyl pentanoyl
Acetylvaleryl
FEMA No. 2543
DK55DDE86P
CHEBI:88623
NSC-31668
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,3-Heptanedione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9893 98.93%
Caco-2 + 0.9231 92.31%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6058 60.58%
OATP2B1 inhibitior - 0.8348 83.48%
OATP1B1 inhibitior + 0.9164 91.64%
OATP1B3 inhibitior + 0.9440 94.40%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9209 92.09%
P-glycoprotein inhibitior - 0.9806 98.06%
P-glycoprotein substrate - 0.9547 95.47%
CYP3A4 substrate - 0.7034 70.34%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.7760 77.60%
CYP3A4 inhibition - 0.9740 97.40%
CYP2C9 inhibition - 0.9200 92.00%
CYP2C19 inhibition - 0.9138 91.38%
CYP2D6 inhibition - 0.9311 93.11%
CYP1A2 inhibition - 0.5122 51.22%
CYP2C8 inhibition - 0.9745 97.45%
CYP inhibitory promiscuity - 0.9153 91.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.7415 74.15%
Eye corrosion + 0.9684 96.84%
Eye irritation + 0.9799 97.99%
Skin irritation + 0.7755 77.55%
Skin corrosion - 0.7466 74.66%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6836 68.36%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5291 52.91%
skin sensitisation + 0.7717 77.17%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.8087 80.87%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6264 62.64%
Acute Oral Toxicity (c) III 0.8223 82.23%
Estrogen receptor binding - 0.9729 97.29%
Androgen receptor binding - 0.8326 83.26%
Thyroid receptor binding - 0.8931 89.31%
Glucocorticoid receptor binding - 0.9495 94.95%
Aromatase binding - 0.9238 92.38%
PPAR gamma - 0.9359 93.59%
Honey bee toxicity - 0.9888 98.88%
Biodegradation + 0.9750 97.50%
Crustacea aquatic toxicity - 0.6032 60.32%
Fish aquatic toxicity - 0.6412 64.12%

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
CHEMBL2581 P07339 Cathepsin D 93.89% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.87% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.61% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.08% 96.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.95% 97.25%

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.
There are no matching plants.

Cross-Links

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PubChem 60983
LOTUS LTS0241400
wikiData Q26841270