3-Methylheptan-4-one

Details

Top
Internal ID 019f5bc6-4528-4680-96e0-09aa0f6b56f1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name 3-methylheptan-4-one
SMILES (Canonical) CCCC(=O)C(C)CC
SMILES (Isomeric) CCCC(=O)C(C)CC
InChI InChI=1S/C8H16O/c1-4-6-8(9)7(3)5-2/h7H,4-6H2,1-3H3
InChI Key NHIMSNHOEAVUKE-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

Top
Molecular Formula C8H16O
Molecular Weight 128.21 g/mol
Exact Mass 128.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.40
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
3-METHYL-4-HEPTANONE
15726-15-5
4-Heptanone, 3-methyl-
sec-Butyl Propyl Ketone
EINECS 239-820-0
4-heptanone, 3-methyl
SCHEMBL105901
DTXSID00864629
NHIMSNHOEAVUKE-UHFFFAOYSA-N
LMFA12000026
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 3-Methylheptan-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.9153 91.53%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.4185 41.85%
OATP2B1 inhibitior - 0.8278 82.78%
OATP1B1 inhibitior + 0.8945 89.45%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9223 92.23%
P-glycoprotein inhibitior - 0.9886 98.86%
P-glycoprotein substrate - 0.9401 94.01%
CYP3A4 substrate - 0.7628 76.28%
CYP2C9 substrate - 0.6168 61.68%
CYP2D6 substrate - 0.7682 76.82%
CYP3A4 inhibition - 0.9763 97.63%
CYP2C9 inhibition - 0.9313 93.13%
CYP2C19 inhibition - 0.9556 95.56%
CYP2D6 inhibition - 0.9494 94.94%
CYP1A2 inhibition + 0.6354 63.54%
CYP2C8 inhibition - 0.9919 99.19%
CYP inhibitory promiscuity - 0.8654 86.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.7381 73.81%
Eye corrosion + 0.9685 96.85%
Eye irritation + 0.9850 98.50%
Skin irritation + 0.6545 65.45%
Skin corrosion - 0.9268 92.68%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6549 65.49%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6772 67.72%
skin sensitisation + 0.9015 90.15%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.9832 98.32%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.6974 69.74%
Acute Oral Toxicity (c) III 0.7838 78.38%
Estrogen receptor binding - 0.9575 95.75%
Androgen receptor binding - 0.9205 92.05%
Thyroid receptor binding - 0.8979 89.79%
Glucocorticoid receptor binding - 0.9512 95.12%
Aromatase binding - 0.9033 90.33%
PPAR gamma - 0.9374 93.74%
Honey bee toxicity - 0.9769 97.69%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.7995 79.95%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 94.53% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.41% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.24% 97.25%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.24% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.17% 94.45%

Plants that contains it

Top
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.
Thymus quinquecostatus
Thymus vulgaris

Cross-Links

Top
PubChem 27470
NPASS NPC36125