6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydro-1H-indene-4-carboxylic acid

Details

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Internal ID a76521cc-d0e8-49c7-a910-7a603e560f5a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name 6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroindene-4-carboxylic acid
SMILES (Canonical) CCC1CC2C(CCC2=O)C(=C1)C(=O)O
SMILES (Isomeric) CCC1CC2C(CCC2=O)C(=C1)C(=O)O
InChI InChI=1S/C12H16O3/c1-2-7-5-9-8(3-4-11(9)13)10(6-7)12(14)15/h6-9H,2-5H2,1H3,(H,14,15)
InChI Key ONMAUQRMJXNSCG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O3
Molecular Weight 208.25 g/mol
Exact Mass 208.109944368 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.02
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydro-1H-indene-4-carboxylic acid
EN300-296300
6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydro-1H-indene-4-carboxylicacid

2D Structure

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2D Structure of 6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydro-1H-indene-4-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.5564 55.64%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6671 66.71%
OATP2B1 inhibitior - 0.8509 85.09%
OATP1B1 inhibitior + 0.8579 85.79%
OATP1B3 inhibitior + 0.9680 96.80%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9206 92.06%
P-glycoprotein inhibitior - 0.9672 96.72%
P-glycoprotein substrate - 0.8849 88.49%
CYP3A4 substrate - 0.5875 58.75%
CYP2C9 substrate - 0.7627 76.27%
CYP2D6 substrate - 0.9063 90.63%
CYP3A4 inhibition - 0.8767 87.67%
CYP2C9 inhibition - 0.8930 89.30%
CYP2C19 inhibition - 0.8575 85.75%
CYP2D6 inhibition - 0.8778 87.78%
CYP1A2 inhibition - 0.7473 74.73%
CYP2C8 inhibition - 0.8657 86.57%
CYP inhibitory promiscuity - 0.8598 85.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6393 63.93%
Eye corrosion - 0.9473 94.73%
Eye irritation + 0.6732 67.32%
Skin irritation - 0.5956 59.56%
Skin corrosion - 0.9416 94.16%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6218 62.18%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.6898 68.98%
skin sensitisation + 0.5403 54.03%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7610 76.10%
Acute Oral Toxicity (c) III 0.6532 65.32%
Estrogen receptor binding - 0.6166 61.66%
Androgen receptor binding - 0.5545 55.45%
Thyroid receptor binding - 0.8091 80.91%
Glucocorticoid receptor binding - 0.8098 80.98%
Aromatase binding - 0.8619 86.19%
PPAR gamma - 0.9269 92.69%
Honey bee toxicity - 0.9546 95.46%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9794 97.94%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.67% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.56% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.88% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.69% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.45% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.25% 91.11%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.91% 93.00%

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.
Musa × paradisiaca

Cross-Links

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PubChem 13676357
LOTUS LTS0197589
wikiData Q105183531