2-Methyl-3-pentanone

Details

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Internal ID 79bb7813-6075-485e-8cfd-08fd6e5799f6
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name 2-methylpentan-3-one
SMILES (Canonical) CCC(=O)C(C)C
SMILES (Isomeric) CCC(=O)C(C)C
InChI InChI=1S/C6H12O/c1-4-6(7)5(2)3/h5H,4H2,1-3H3
InChI Key HYTRYEXINDDXJK-UHFFFAOYSA-N
Popularity 105 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12O
Molecular Weight 100.16 g/mol
Exact Mass 100.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.62
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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565-69-5
2-Methylpentan-3-one
Ethyl isopropyl ketone
3-Pentanone, 2-methyl-
4-Methyl-3-pentanone
Isopropyl ethyl ketone
2-Methyl-3-pentanal
iso-C3H7COC2H5
UNII-0R392X5X26
EINECS 209-288-4
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-Methyl-3-pentanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 - 0.5125 51.25%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6219 62.19%
OATP2B1 inhibitior - 0.8620 86.20%
OATP1B1 inhibitior + 0.9573 95.73%
OATP1B3 inhibitior + 0.9576 95.76%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9365 93.65%
P-glycoprotein inhibitior - 0.9861 98.61%
P-glycoprotein substrate - 0.9857 98.57%
CYP3A4 substrate - 0.7965 79.65%
CYP2C9 substrate - 0.6168 61.68%
CYP2D6 substrate - 0.7682 76.82%
CYP3A4 inhibition - 0.9782 97.82%
CYP2C9 inhibition - 0.9305 93.05%
CYP2C19 inhibition - 0.9260 92.60%
CYP2D6 inhibition - 0.9434 94.34%
CYP1A2 inhibition - 0.6553 65.53%
CYP2C8 inhibition - 0.9951 99.51%
CYP inhibitory promiscuity - 0.8733 87.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.7015 70.15%
Eye corrosion + 0.9847 98.47%
Eye irritation + 0.9953 99.53%
Skin irritation + 0.8064 80.64%
Skin corrosion - 0.9183 91.83%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7970 79.70%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5051 50.51%
skin sensitisation + 0.8539 85.39%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.5733 57.33%
Acute Oral Toxicity (c) III 0.8324 83.24%
Estrogen receptor binding - 0.9364 93.64%
Androgen receptor binding - 0.8844 88.44%
Thyroid receptor binding - 0.9144 91.44%
Glucocorticoid receptor binding - 0.9225 92.25%
Aromatase binding - 0.8672 86.72%
PPAR gamma - 0.8806 88.06%
Honey bee toxicity - 0.9638 96.38%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.6928 69.28%

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 92.83% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.65% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.26% 97.25%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.78% 96.47%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.18% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.59% 96.95%

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.
Santalum album
Zea mays

Cross-Links

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PubChem 11265
NPASS NPC246331
LOTUS LTS0213310
wikiData Q5404456