2,5-Octanedione

Details

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Internal ID 1f25e859-4d7d-4752-8545-8e63e191a0d7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name octane-2,5-dione
SMILES (Canonical) CCCC(=O)CCC(=O)C
SMILES (Isomeric) CCCC(=O)CCC(=O)C
InChI InChI=1S/C8H14O2/c1-3-4-8(10)6-5-7(2)9/h3-6H2,1-2H3
InChI Key SPDFSSLYVRCMDZ-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O2
Molecular Weight 142.20 g/mol
Exact Mass 142.099379685 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 0.40
Atomic LogP (AlogP) 1.72
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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3214-41-3
octane-2,5-dione
2-Naphthaldehydeoxime
Octanedione, 2,5-
Octanedione, 2,7-
SCHEMBL4084926
SCHEMBL4084931
DTXSID101019346
AKOS006272909
BS-18935
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-Octanedione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.9542 95.42%
Blood Brain Barrier + 0.9580 95.80%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6417 64.17%
OATP2B1 inhibitior - 0.8370 83.70%
OATP1B1 inhibitior + 0.9439 94.39%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9325 93.25%
P-glycoprotein inhibitior - 0.9743 97.43%
P-glycoprotein substrate - 0.9489 94.89%
CYP3A4 substrate - 0.7197 71.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7622 76.22%
CYP3A4 inhibition - 0.9602 96.02%
CYP2C9 inhibition - 0.9204 92.04%
CYP2C19 inhibition - 0.9494 94.94%
CYP2D6 inhibition - 0.9322 93.22%
CYP1A2 inhibition + 0.5811 58.11%
CYP2C8 inhibition - 0.9813 98.13%
CYP inhibitory promiscuity - 0.9070 90.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.7755 77.55%
Eye corrosion + 0.9759 97.59%
Eye irritation + 0.9827 98.27%
Skin irritation + 0.5782 57.82%
Skin corrosion - 0.8672 86.72%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6360 63.60%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.6451 64.51%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9092 90.92%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8747 87.47%
Estrogen receptor binding - 0.9836 98.36%
Androgen receptor binding - 0.9502 95.02%
Thyroid receptor binding - 0.9120 91.20%
Glucocorticoid receptor binding - 0.9610 96.10%
Aromatase binding - 0.9247 92.47%
PPAR gamma - 0.8979 89.79%
Honey bee toxicity - 0.9750 97.50%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.7732 77.32%
Fish aquatic toxicity + 0.8480 84.80%

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
CHEMBL4040 P28482 MAP kinase ERK2 93.01% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.98% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.25% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.63% 99.17%
CHEMBL255 P29275 Adenosine A2b receptor 80.03% 98.59%

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.
Lobelia chinensis
Scleromitrion diffusum
Scutellaria barbata

Cross-Links

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PubChem 6420399
NPASS NPC192872