(-)-5-Methyl-3-heptanone

Details

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Internal ID 99c356ba-b28b-4b5c-86da-032db543059e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name (5R)-5-methylheptan-3-one
SMILES (Canonical) CCC(C)CC(=O)CC
SMILES (Isomeric) CC[C@@H](C)CC(=O)CC
InChI InChI=1S/C8H16O/c1-4-7(3)6-8(9)5-2/h7H,4-6H2,1-3H3/t7-/m1/s1
InChI Key PSBKJPTZCVYXSD-SSDOTTSWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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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

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5-Methyl-3-heptanone, (-)-
(R)-(-)-5-Methyl-3-heptanone
3-Heptanone, 5-methyl-, (5R)-
UNII-R1B57M585J
R1B57M585J
116003-10-2
SCHEMBL13283544
[R,(?)]-5-Methyl-3-heptanone
Q27287656

2D Structure

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2D Structure of (-)-5-Methyl-3-heptanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.9509 95.09%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.4656 46.56%
OATP2B1 inhibitior - 0.8419 84.19%
OATP1B1 inhibitior + 0.9291 92.91%
OATP1B3 inhibitior + 0.9450 94.50%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8970 89.70%
P-glycoprotein inhibitior - 0.9807 98.07%
P-glycoprotein substrate - 0.9522 95.22%
CYP3A4 substrate - 0.7325 73.25%
CYP2C9 substrate - 0.6168 61.68%
CYP2D6 substrate - 0.7682 76.82%
CYP3A4 inhibition - 0.9769 97.69%
CYP2C9 inhibition - 0.9374 93.74%
CYP2C19 inhibition - 0.9443 94.43%
CYP2D6 inhibition - 0.9411 94.11%
CYP1A2 inhibition - 0.6027 60.27%
CYP2C8 inhibition - 0.9911 99.11%
CYP inhibitory promiscuity - 0.8902 89.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.7219 72.19%
Eye corrosion + 0.9646 96.46%
Eye irritation + 0.9896 98.96%
Skin irritation + 0.7032 70.32%
Skin corrosion - 0.9168 91.68%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6879 68.79%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6324 63.24%
skin sensitisation + 0.8815 88.15%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5616 56.16%
Acute Oral Toxicity (c) III 0.7945 79.45%
Estrogen receptor binding - 0.9564 95.64%
Androgen receptor binding - 0.8219 82.19%
Thyroid receptor binding - 0.8857 88.57%
Glucocorticoid receptor binding - 0.9481 94.81%
Aromatase binding - 0.8182 81.82%
PPAR gamma - 0.8956 89.56%
Honey bee toxicity - 0.9732 97.32%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity + 0.6626 66.26%

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
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.48% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.44% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.19% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 91.04% 97.21%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.37% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.92% 96.47%

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.
Phyllanthus emblica
Thymus quinquecostatus
Thymus vulgaris

Cross-Links

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PubChem 6566014
NPASS NPC33909