3-Methyl-2-penten-4-one

Details

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Internal ID daa5e5e1-b8db-4802-9574-f7ef5fbb7785
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Alpha-branched alpha,beta-unsaturated ketones
IUPAC Name (E)-3-methylpent-3-en-2-one
SMILES (Canonical) CC=C(C)C(=O)C
SMILES (Isomeric) C/C=C(\C)/C(=O)C
InChI InChI=1S/C6H10O/c1-4-5(2)6(3)7/h4H,1-3H3/b5-4+
InChI Key ZAMCMCQRTZKGDX-SNAWJCMRSA-N
Popularity 29 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 1.10
Atomic LogP (AlogP) 1.54
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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3-Methyl-3-penten-2-one
(E)-3-methyl-3-penten-2-one
565-62-8
1567-73-3
3-Methyl-pent-3-en-2-one
JBR4O01DB2
3-Methyl-2-penten-4-one
3-Penten-2-one, 3-methyl-
3-Methyl-3-penten-2-one, (3E)-
3-Penten-2-one, 3-methyl-, (E)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Methyl-2-penten-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.7858 78.58%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4398 43.98%
OATP2B1 inhibitior - 0.8774 87.74%
OATP1B1 inhibitior + 0.9358 93.58%
OATP1B3 inhibitior + 0.9624 96.24%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8755 87.55%
P-glycoprotein inhibitior - 0.9841 98.41%
P-glycoprotein substrate - 0.9928 99.28%
CYP3A4 substrate - 0.7422 74.22%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.8740 87.40%
CYP3A4 inhibition - 0.9338 93.38%
CYP2C9 inhibition - 0.9360 93.60%
CYP2C19 inhibition - 0.8456 84.56%
CYP2D6 inhibition - 0.9333 93.33%
CYP1A2 inhibition - 0.8225 82.25%
CYP2C8 inhibition - 0.9963 99.63%
CYP inhibitory promiscuity - 0.6535 65.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6383 63.83%
Carcinogenicity (trinary) Non-required 0.5260 52.60%
Eye corrosion + 0.9502 95.02%
Eye irritation + 0.9901 99.01%
Skin irritation + 0.8973 89.73%
Skin corrosion + 0.7292 72.92%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7863 78.63%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.8250 82.50%
skin sensitisation + 0.9416 94.16%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.6370 63.70%
Acute Oral Toxicity (c) III 0.7463 74.63%
Estrogen receptor binding - 0.9757 97.57%
Androgen receptor binding - 0.9041 90.41%
Thyroid receptor binding - 0.8718 87.18%
Glucocorticoid receptor binding - 0.9359 93.59%
Aromatase binding - 0.8549 85.49%
PPAR gamma - 0.9559 95.59%
Honey bee toxicity - 0.9136 91.36%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity - 0.5000 50.00%

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 85.23% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 81.86% 91.19%
CHEMBL4040 P28482 MAP kinase ERK2 80.78% 83.82%

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.
Terminalia chebula

Cross-Links

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PubChem 5364579
NPASS NPC269641