4-Penten-2-one, 4-methyl-

Details

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Internal ID 8ed471a1-5fcc-4de4-b01e-38de172d03e6
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name 4-methylpent-4-en-2-one
SMILES (Canonical) CC(=C)CC(=O)C
SMILES (Isomeric) CC(=C)CC(=O)C
InChI InChI=1S/C6H10O/c1-5(2)4-6(3)7/h1,4H2,2-3H3
InChI Key VADUDTKCGJKNDY-UHFFFAOYSA-N
Popularity 20 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O
Molecular Weight 98.14 g/mol
Exact Mass 98.073164938 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.54
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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4-Penten-2-one, 4-methyl-
3744-02-3
4-Methyl-4-penten-2-one
ISOMESITYL OXIDE
Isopropenyl acetone
P549RW6459
Isopropenylacetone
3-Acetylisobutene
2-Methylene-4-pentanal
4-methyl-pent-4-en-2-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Penten-2-one, 4-methyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 + 0.7687 76.87%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4138 41.38%
OATP2B1 inhibitior - 0.8686 86.86%
OATP1B1 inhibitior + 0.9549 95.49%
OATP1B3 inhibitior + 0.9495 94.95%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9332 93.32%
P-glycoprotein inhibitior - 0.9772 97.72%
P-glycoprotein substrate - 0.9682 96.82%
CYP3A4 substrate - 0.7223 72.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7774 77.74%
CYP3A4 inhibition - 0.8745 87.45%
CYP2C9 inhibition - 0.9310 93.10%
CYP2C19 inhibition - 0.7878 78.78%
CYP2D6 inhibition - 0.9305 93.05%
CYP1A2 inhibition - 0.7299 72.99%
CYP2C8 inhibition - 0.9956 99.56%
CYP inhibitory promiscuity - 0.7318 73.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6483 64.83%
Carcinogenicity (trinary) Non-required 0.5657 56.57%
Eye corrosion + 0.9378 93.78%
Eye irritation + 0.9912 99.12%
Skin irritation + 0.7541 75.41%
Skin corrosion - 0.6582 65.82%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8106 81.06%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.9350 93.50%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.7356 73.56%
Acute Oral Toxicity (c) II 0.5534 55.34%
Estrogen receptor binding - 0.9687 96.87%
Androgen receptor binding - 0.9679 96.79%
Thyroid receptor binding - 0.8365 83.65%
Glucocorticoid receptor binding - 0.9311 93.11%
Aromatase binding - 0.8281 82.81%
PPAR gamma - 0.9129 91.29%
Honey bee toxicity - 0.9354 93.54%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.9600 96.00%
Fish aquatic toxicity + 0.6970 69.70%

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 99.03% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.09% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.47% 98.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.26% 94.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.18% 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.
Crocus sativus
Cryptotaenia japonica
Murraya paniculata

Cross-Links

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PubChem 19543
NPASS NPC125090