3,4,5-Trimethyl-2-cyclopenten-1-one

Details

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Internal ID ef8c08c7-6e8a-4201-82fc-ff1ce7ac6de9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 3,4,5-trimethylcyclopent-2-en-1-one
SMILES (Canonical) CC1C(C(=O)C=C1C)C
SMILES (Isomeric) CC1C(C(=O)C=C1C)C
InChI InChI=1S/C8H12O/c1-5-4-8(9)7(3)6(5)2/h4,6-7H,1-3H3
InChI Key LPBXNOSWWUFYQN-UHFFFAOYSA-N
Popularity 5 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 1.40
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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55683-21-1
2-Cyclopenten-1-one, 3,4,5-trimethyl-
3,4,5-trimethylcyclopent-2-en-1-one
SCHEMBL6895210
SCHEMBL20962958
DTXSID20971041
LPBXNOSWWUFYQN-UHFFFAOYSA-N
3,4,5-Trimethyl-2-cyclopenten-1-one #

2D Structure

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2D Structure of 3,4,5-Trimethyl-2-cyclopenten-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 + 0.9967 99.67%
Caco-2 + 0.7271 72.71%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.9286 92.86%
Subcellular localzation Mitochondria 0.5334 53.34%
OATP2B1 inhibitior - 0.8698 86.98%
OATP1B1 inhibitior + 0.9447 94.47%
OATP1B3 inhibitior + 0.9631 96.31%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9133 91.33%
P-glycoprotein inhibitior - 0.9761 97.61%
P-glycoprotein substrate - 0.9637 96.37%
CYP3A4 substrate - 0.6766 67.66%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8805 88.05%
CYP3A4 inhibition - 0.9161 91.61%
CYP2C9 inhibition - 0.9267 92.67%
CYP2C19 inhibition - 0.7797 77.97%
CYP2D6 inhibition - 0.9112 91.12%
CYP1A2 inhibition - 0.7322 73.22%
CYP2C8 inhibition - 0.9939 99.39%
CYP inhibitory promiscuity - 0.6464 64.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7017 70.17%
Carcinogenicity (trinary) Non-required 0.4603 46.03%
Eye corrosion + 0.6951 69.51%
Eye irritation + 0.9579 95.79%
Skin irritation + 0.7660 76.60%
Skin corrosion - 0.7166 71.66%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7639 76.39%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.8783 87.83%
skin sensitisation + 0.9145 91.45%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.4833 48.33%
Acute Oral Toxicity (c) II 0.4806 48.06%
Estrogen receptor binding - 0.9523 95.23%
Androgen receptor binding - 0.7075 70.75%
Thyroid receptor binding - 0.8367 83.67%
Glucocorticoid receptor binding - 0.8564 85.64%
Aromatase binding - 0.8454 84.54%
PPAR gamma - 0.9223 92.23%
Honey bee toxicity - 0.9140 91.40%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.7465 74.65%

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
CHEMBL2581 P07339 Cathepsin D 91.17% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.63% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.06% 97.25%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.16% 86.00%

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.
Curcuma longa

Cross-Links

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PubChem 41520
NPASS NPC39347