2,5-Heptanedione

Details

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Internal ID 6585e86e-0bf6-420c-bdff-dc5ede1fb719
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name heptane-2,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H12O2/c1-3-7(9)5-4-6(2)8/h3-5H2,1-2H3
InChI Key HGRGPAAXHOTBAM-UHFFFAOYSA-N
Popularity 38 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 0.00
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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2,5-HEPTANEDIONE
1703-51-1
Heptan-2,5-dione
UP8A88O1MS
3,6-Heptanedione
2,5-Heptanedione #
UNII-UP8A88O1MS
SCHEMBL588863
DTXSID7073272
CHEBI:179466
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,5-Heptanedione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 + 0.9294 92.94%
Blood Brain Barrier + 0.9580 95.80%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6485 64.85%
OATP2B1 inhibitior - 0.8454 84.54%
OATP1B1 inhibitior + 0.9454 94.54%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9346 93.46%
P-glycoprotein inhibitior - 0.9810 98.10%
P-glycoprotein substrate - 0.9643 96.43%
CYP3A4 substrate - 0.7397 73.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7622 76.22%
CYP3A4 inhibition - 0.9600 96.00%
CYP2C9 inhibition - 0.9221 92.21%
CYP2C19 inhibition - 0.9372 93.72%
CYP2D6 inhibition - 0.9270 92.70%
CYP1A2 inhibition + 0.5863 58.63%
CYP2C8 inhibition - 0.9803 98.03%
CYP inhibitory promiscuity - 0.8915 89.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.7513 75.13%
Eye corrosion + 0.9736 97.36%
Eye irritation + 0.9707 97.07%
Skin irritation + 0.6994 69.94%
Skin corrosion - 0.8395 83.95%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6438 64.38%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.6683 66.83%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.8516 85.16%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5184 51.84%
Acute Oral Toxicity (c) III 0.8484 84.84%
Estrogen receptor binding - 0.9729 97.29%
Androgen receptor binding - 0.9411 94.11%
Thyroid receptor binding - 0.9198 91.98%
Glucocorticoid receptor binding - 0.9555 95.55%
Aromatase binding - 0.9385 93.85%
PPAR gamma - 0.9102 91.02%
Honey bee toxicity - 0.9620 96.20%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.6965 69.65%

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 93.17% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 87.67% 83.82%
CHEMBL2581 P07339 Cathepsin D 86.81% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.86% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.45% 99.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.38% 97.21%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 15559
LOTUS LTS0242443
wikiData Q77512728