2-Hydroxy-3,5,5-trimethylcyclohex-2-ene-1,4-dione

Details

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Internal ID 2011d698-fbc1-48f3-9678-2d218aea3417
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 2-hydroxy-3,5,5-trimethylcyclohex-2-ene-1,4-dione
SMILES (Canonical) CC1=C(C(=O)CC(C1=O)(C)C)O
SMILES (Isomeric) CC1=C(C(=O)CC(C1=O)(C)C)O
InChI InChI=1S/C9H12O3/c1-5-7(11)6(10)4-9(2,3)8(5)12/h11H,4H2,1-3H3
InChI Key BSRFZJMVFOPNKR-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O3
Molecular Weight 168.19 g/mol
Exact Mass 168.078644241 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.39
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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35692-98-9
2-hydroxy-3,5,5-trimethylcyclohex-2-ene-1,4-dione
2-Hydroxy-4-oxoisophorone
SCHEMBL3154825
DTXSID40189207
BSRFZJMVFOPNKR-UHFFFAOYSA-N
1,5,5-Trimethyl-2-hydroxycyclohexene-3,6-dione
2-Hydroxy-3,5,5-trimethyl-2-cyclohexen-1,4-dione
4-Hydroxy-1,1,3-trimethyl-3-cyclohexen-2,5-dione
3,5,5-trimethyl-2-hydroxy-1,4-cyclohexadion-2-ene
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-Hydroxy-3,5,5-trimethylcyclohex-2-ene-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.6425 64.25%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.8499 84.99%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.8945 89.45%
OATP1B3 inhibitior + 0.9638 96.38%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9149 91.49%
P-glycoprotein inhibitior - 0.9651 96.51%
P-glycoprotein substrate - 0.9776 97.76%
CYP3A4 substrate - 0.5816 58.16%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.8657 86.57%
CYP3A4 inhibition - 0.8226 82.26%
CYP2C9 inhibition - 0.8677 86.77%
CYP2C19 inhibition - 0.8639 86.39%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.8924 89.24%
CYP2C8 inhibition - 0.9852 98.52%
CYP inhibitory promiscuity - 0.9317 93.17%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8093 80.93%
Carcinogenicity (trinary) Non-required 0.4830 48.30%
Eye corrosion - 0.9437 94.37%
Eye irritation + 0.9479 94.79%
Skin irritation - 0.5543 55.43%
Skin corrosion - 0.9245 92.45%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7249 72.49%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5658 56.58%
skin sensitisation + 0.7917 79.17%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.8143 81.43%
Acute Oral Toxicity (c) III 0.5892 58.92%
Estrogen receptor binding - 0.9168 91.68%
Androgen receptor binding - 0.7579 75.79%
Thyroid receptor binding - 0.7647 76.47%
Glucocorticoid receptor binding - 0.8620 86.20%
Aromatase binding - 0.8428 84.28%
PPAR gamma - 0.8459 84.59%
Honey bee toxicity - 0.9370 93.70%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9097 90.97%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.55% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.35% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 86.69% 94.75%
CHEMBL2581 P07339 Cathepsin D 84.20% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.39% 99.23%

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 37246
NPASS NPC17295
LOTUS LTS0125799
wikiData Q83061190