3,5,5-Trimethylcyclohex-3-en-1-one

Details

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Internal ID e3ddc692-df6d-4f11-ba89-35923852d345
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 3,5,5-trimethylcyclohex-3-en-1-one
SMILES (Canonical) CC1=CC(CC(=O)C1)(C)C
SMILES (Isomeric) CC1=CC(CC(=O)C1)(C)C
InChI InChI=1S/C9H14O/c1-7-4-8(10)6-9(2,3)5-7/h5H,4,6H2,1-3H3
InChI Key LKOKKQDYMZUSCG-UHFFFAOYSA-N
Popularity 27 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O
Molecular Weight 138.21 g/mol
Exact Mass 138.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.32
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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3,5,5-Trimethylcyclohex-3-en-1-one
beta-Phorone
471-01-2
3,5,5-TRIMETHYL-3-CYCLOHEXEN-1-ONE
Crocusatin E
3-Cyclohexen-1-one, 3,5,5-trimethyl-
.beta.-Phorone
.beta.-Isophorone
EINECS 207-434-1
UNII-R817UQW62V
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,5,5-Trimethylcyclohex-3-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.9246 92.46%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.5982 59.82%
OATP2B1 inhibitior - 0.8636 86.36%
OATP1B1 inhibitior + 0.9622 96.22%
OATP1B3 inhibitior + 0.9506 95.06%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8516 85.16%
P-glycoprotein inhibitior - 0.9798 97.98%
P-glycoprotein substrate - 0.9815 98.15%
CYP3A4 substrate - 0.5862 58.62%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.8121 81.21%
CYP3A4 inhibition - 0.8979 89.79%
CYP2C9 inhibition - 0.8195 81.95%
CYP2C19 inhibition - 0.7521 75.21%
CYP2D6 inhibition - 0.9439 94.39%
CYP1A2 inhibition - 0.8760 87.60%
CYP2C8 inhibition - 0.9924 99.24%
CYP inhibitory promiscuity - 0.8593 85.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6336 63.36%
Carcinogenicity (trinary) Warning 0.5339 53.39%
Eye corrosion - 0.6292 62.92%
Eye irritation + 0.9752 97.52%
Skin irritation + 0.6706 67.06%
Skin corrosion - 0.9562 95.62%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7991 79.91%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.9559 95.59%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.8580 85.80%
Acute Oral Toxicity (c) III 0.8109 81.09%
Estrogen receptor binding - 0.9775 97.75%
Androgen receptor binding - 0.9431 94.31%
Thyroid receptor binding - 0.8847 88.47%
Glucocorticoid receptor binding - 0.9069 90.69%
Aromatase binding - 0.9017 90.17%
PPAR gamma - 0.8669 86.69%
Honey bee toxicity - 0.9387 93.87%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.8808 88.08%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.40% 95.56%
CHEMBL2581 P07339 Cathepsin D 85.52% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.93% 91.11%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 83.78% 85.30%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.37% 96.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.22% 86.00%
CHEMBL3401 O75469 Pregnane X receptor 80.87% 94.73%

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

Cross-Links

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PubChem 10108
NPASS NPC272765
LOTUS LTS0251396
wikiData Q27287939