(3S)-3,6-dimethylheptane-2,4-dione

Details

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Internal ID 297d924b-f8c7-4bd8-b161-2325451169d5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > 1,3-dicarbonyl compounds > Beta-diketones
IUPAC Name (3S)-3,6-dimethylheptane-2,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H16O2/c1-6(2)5-9(11)7(3)8(4)10/h6-7H,5H2,1-4H3/t7-/m0/s1
InChI Key BEWPTSWPIROTRC-ZETCQYMHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16O2
Molecular Weight 156.22 g/mol
Exact Mass 156.115029749 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.83
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S)-3,6-dimethylheptane-2,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 - 0.5675 56.75%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6526 65.26%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9514 95.14%
OATP1B3 inhibitior + 0.9523 95.23%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9342 93.42%
P-glycoprotein inhibitior - 0.9784 97.84%
P-glycoprotein substrate - 0.9441 94.41%
CYP3A4 substrate - 0.7130 71.30%
CYP2C9 substrate + 0.5886 58.86%
CYP2D6 substrate - 0.7837 78.37%
CYP3A4 inhibition - 0.9458 94.58%
CYP2C9 inhibition - 0.9024 90.24%
CYP2C19 inhibition - 0.8777 87.77%
CYP2D6 inhibition - 0.9341 93.41%
CYP1A2 inhibition - 0.7859 78.59%
CYP2C8 inhibition - 0.9956 99.56%
CYP inhibitory promiscuity - 0.9391 93.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6929 69.29%
Eye corrosion + 0.9715 97.15%
Eye irritation + 0.9614 96.14%
Skin irritation + 0.5881 58.81%
Skin corrosion - 0.8984 89.84%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6386 63.86%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.7335 73.35%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6634 66.34%
Acute Oral Toxicity (c) III 0.4668 46.68%
Estrogen receptor binding - 0.9136 91.36%
Androgen receptor binding - 0.6587 65.87%
Thyroid receptor binding - 0.8376 83.76%
Glucocorticoid receptor binding - 0.8630 86.30%
Aromatase binding - 0.9056 90.56%
PPAR gamma - 0.9492 94.92%
Honey bee toxicity - 0.9557 95.57%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity - 0.5296 52.96%

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 93.63% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.56% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.91% 85.14%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 82.41% 83.10%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.01% 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 96356508
LOTUS LTS0020963
wikiData Q104933661