6-(2-Hydroxyethyl)-2,5,7-trimethylinden-1-one

Details

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Internal ID 5b234d66-05bf-4a99-b776-908c04f4bd69
Taxonomy Benzenoids > Indenes and isoindenes
IUPAC Name 6-(2-hydroxyethyl)-2,5,7-trimethylinden-1-one
SMILES (Canonical) CC1=CC2=C(C(=C1CCO)C)C(=O)C(=C2)C
SMILES (Isomeric) CC1=CC2=C(C(=C1CCO)C)C(=O)C(=C2)C
InChI InChI=1S/C14H16O2/c1-8-6-11-7-9(2)14(16)13(11)10(3)12(8)4-5-15/h6-7,15H,4-5H2,1-3H3
InChI Key LLPPZAOWAGVIIJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O2
Molecular Weight 216.27 g/mol
Exact Mass 216.115029749 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.44
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(2-Hydroxyethyl)-2,5,7-trimethylinden-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 + 1.0000 100.00%
Caco-2 + 0.9160 91.60%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6439 64.39%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.8393 83.93%
OATP1B3 inhibitior + 0.9536 95.36%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.7937 79.37%
P-glycoprotein inhibitior - 0.9628 96.28%
P-glycoprotein substrate - 0.8724 87.24%
CYP3A4 substrate - 0.5859 58.59%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.8117 81.17%
CYP3A4 inhibition - 0.8143 81.43%
CYP2C9 inhibition - 0.8607 86.07%
CYP2C19 inhibition - 0.6095 60.95%
CYP2D6 inhibition - 0.8099 80.99%
CYP1A2 inhibition + 0.7589 75.89%
CYP2C8 inhibition - 0.9140 91.40%
CYP inhibitory promiscuity - 0.6870 68.70%
UGT catelyzed - 0.5638 56.38%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6828 68.28%
Eye corrosion - 0.9833 98.33%
Eye irritation + 0.9518 95.18%
Skin irritation - 0.5153 51.53%
Skin corrosion - 0.9482 94.82%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6294 62.94%
Micronuclear - 0.8541 85.41%
Hepatotoxicity - 0.5160 51.60%
skin sensitisation + 0.6481 64.81%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.6096 60.96%
Acute Oral Toxicity (c) III 0.7615 76.15%
Estrogen receptor binding - 0.5643 56.43%
Androgen receptor binding - 0.6215 62.15%
Thyroid receptor binding - 0.7160 71.60%
Glucocorticoid receptor binding - 0.5282 52.82%
Aromatase binding - 0.7368 73.68%
PPAR gamma - 0.6104 61.04%
Honey bee toxicity - 0.9289 92.89%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity + 0.7708 77.08%

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
CHEMBL2581 P07339 Cathepsin D 94.63% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.17% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.36% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 85.91% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.78% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.63% 89.00%
CHEMBL2664 P23526 Adenosylhomocysteinase 80.87% 86.67%

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.
Pteris multifida
Pteris wallichiana
Swietenia mahagoni

Cross-Links

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PubChem 15674624
NPASS NPC48999
LOTUS LTS0243887
wikiData Q105153635