2,2-Dimethyl-3-hexanone

Details

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Internal ID 230cac04-6717-4b0d-bc7a-c3c26b5e7a97
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name 2,2-dimethylhexan-3-one
SMILES (Canonical) CCCC(=O)C(C)(C)C
SMILES (Isomeric) CCCC(=O)C(C)(C)C
InChI InChI=1S/C8H16O/c1-5-6-7(9)8(2,3)4/h5-6H2,1-4H3
InChI Key PYCHXHVFOZBVEY-UHFFFAOYSA-N
Popularity 16 references 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 2

Synonyms

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5405-79-8
2,2-dimethylhexan-3-one
3-Hexanone, 2,2-dimethyl-
tert-Butyl propyl ketone
2,2-dimethyl-hexan-3-one
NSC-5229
NSC5229
3-Hexanone,2-dimethyl-
2,2-Dimethy-3-hexanone
tert-Butyl n-propyl ketone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,2-Dimethyl-3-hexanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.8936 89.36%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4715 47.15%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.9433 94.33%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9359 93.59%
P-glycoprotein inhibitior - 0.9864 98.64%
P-glycoprotein substrate - 0.9437 94.37%
CYP3A4 substrate - 0.7200 72.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7863 78.63%
CYP3A4 inhibition - 0.9565 95.65%
CYP2C9 inhibition - 0.9068 90.68%
CYP2C19 inhibition - 0.9369 93.69%
CYP2D6 inhibition - 0.9441 94.41%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9818 98.18%
CYP inhibitory promiscuity - 0.8775 87.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6482 64.82%
Eye corrosion + 0.9451 94.51%
Eye irritation + 0.9934 99.34%
Skin irritation + 0.8170 81.70%
Skin corrosion - 0.9501 95.01%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7463 74.63%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6074 60.74%
skin sensitisation + 0.9407 94.07%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.4539 45.39%
Acute Oral Toxicity (c) III 0.6837 68.37%
Estrogen receptor binding - 0.9509 95.09%
Androgen receptor binding - 0.9464 94.64%
Thyroid receptor binding - 0.9032 90.32%
Glucocorticoid receptor binding - 0.9332 93.32%
Aromatase binding - 0.9323 93.23%
PPAR gamma - 0.9232 92.32%
Honey bee toxicity - 0.9788 97.88%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.7632 76.32%
Fish aquatic toxicity - 0.5809 58.09%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.10% 97.25%
CHEMBL2581 P07339 Cathepsin D 91.41% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.06% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.50% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.24% 100.00%

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.
Houttuynia cordata

Cross-Links

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PubChem 221168
NPASS NPC101820