3,5-Dimethylcyclohex-2-en-1-one

Details

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Internal ID 66c08e55-3b70-497f-a65a-b9f1bb2265f7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 3,5-dimethylcyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H12O/c1-6-3-7(2)5-8(9)4-6/h4,7H,3,5H2,1-2H3
InChI Key NOQKKFBBAODEHN-UHFFFAOYSA-N
Popularity 31 references in papers

Physical and Chemical Properties

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Molecular Formula C8H12O
Molecular Weight 124.18 g/mol
Exact Mass 124.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.93
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1123-09-7
3,5-Dimethylcyclohex-2-en-1-one
2-Cyclohexen-1-one, 3,5-dimethyl-
EINECS 214-369-2
AI3-21772
DTXSID20870848
NSC 845
NSC 10113
RefChem:487025
DTXCID70818533
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-Dimethylcyclohex-2-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 + 0.9968 99.68%
Caco-2 + 0.9005 90.05%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.5733 57.33%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9552 95.52%
OATP1B3 inhibitior + 0.9623 96.23%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9099 90.99%
P-glycoprotein inhibitior - 0.9855 98.55%
P-glycoprotein substrate - 0.9458 94.58%
CYP3A4 substrate - 0.6516 65.16%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.8653 86.53%
CYP3A4 inhibition - 0.9313 93.13%
CYP2C9 inhibition - 0.9293 92.93%
CYP2C19 inhibition - 0.8554 85.54%
CYP2D6 inhibition - 0.9234 92.34%
CYP1A2 inhibition - 0.8408 84.08%
CYP2C8 inhibition - 0.9959 99.59%
CYP inhibitory promiscuity - 0.8426 84.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5946 59.46%
Carcinogenicity (trinary) Non-required 0.5229 52.29%
Eye corrosion + 0.5809 58.09%
Eye irritation + 0.9715 97.15%
Skin irritation + 0.6878 68.78%
Skin corrosion - 0.9213 92.13%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7973 79.73%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.8712 87.12%
skin sensitisation + 0.9578 95.78%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.7153 71.53%
Acute Oral Toxicity (c) III 0.7149 71.49%
Estrogen receptor binding - 0.9803 98.03%
Androgen receptor binding - 0.6429 64.29%
Thyroid receptor binding - 0.9210 92.10%
Glucocorticoid receptor binding - 0.8658 86.58%
Aromatase binding - 0.8337 83.37%
PPAR gamma - 0.9012 90.12%
Honey bee toxicity - 0.9396 93.96%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.8463 84.63%

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
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 94.94% 86.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.68% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.42% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.15% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.86% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.57% 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.
Chrysanthemum indicum

Cross-Links

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PubChem 14291
NPASS NPC187979