5,6,7-Trimethoxy-1-indanone

Details

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Internal ID 1d74503e-088f-4611-8ed7-a9243fdbb472
Taxonomy Benzenoids > Indanes > Indanones
IUPAC Name 5,6,7-trimethoxy-2,3-dihydroinden-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H14O4/c1-14-9-6-7-4-5-8(13)10(7)12(16-3)11(9)15-2/h6H,4-5H2,1-3H3
InChI Key GQMRLYSXCICRFW-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O4
Molecular Weight 222.24 g/mol
Exact Mass 222.08920892 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.84
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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5,6,7-trimethoxy-2,3-dihydroinden-1-one
Maybridge1_004149
MLS000859046
5,6,7-trimethoxyindan-1-one
SCHEMBL6378725
CHEMBL1892020
HMS553E15
HMS2781J12
AKOS010641412
CCG-252036
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5,6,7-Trimethoxy-1-indanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.8857 88.57%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.7927 79.27%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9469 94.69%
OATP1B3 inhibitior + 0.9791 97.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9208 92.08%
P-glycoprotein inhibitior - 0.9168 91.68%
P-glycoprotein substrate - 0.9523 95.23%
CYP3A4 substrate - 0.5268 52.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7023 70.23%
CYP3A4 inhibition - 0.8020 80.20%
CYP2C9 inhibition - 0.9074 90.74%
CYP2C19 inhibition - 0.5111 51.11%
CYP2D6 inhibition - 0.9551 95.51%
CYP1A2 inhibition + 0.8705 87.05%
CYP2C8 inhibition - 0.8501 85.01%
CYP inhibitory promiscuity - 0.7381 73.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8920 89.20%
Carcinogenicity (trinary) Non-required 0.5480 54.80%
Eye corrosion - 0.8842 88.42%
Eye irritation + 0.9499 94.99%
Skin irritation - 0.6988 69.88%
Skin corrosion - 0.9631 96.31%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5518 55.18%
Micronuclear - 0.6341 63.41%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.8042 80.42%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5957 59.57%
Acute Oral Toxicity (c) III 0.5417 54.17%
Estrogen receptor binding - 0.6188 61.88%
Androgen receptor binding - 0.7173 71.73%
Thyroid receptor binding - 0.7010 70.10%
Glucocorticoid receptor binding - 0.8031 80.31%
Aromatase binding - 0.7661 76.61%
PPAR gamma - 0.7642 76.42%
Honey bee toxicity - 0.9103 91.03%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.7072 70.72%

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 92.88% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.46% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.93% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.30% 86.33%
CHEMBL2535 P11166 Glucose transporter 86.77% 98.75%
CHEMBL2581 P07339 Cathepsin D 85.97% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.24% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.58% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.13% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.87% 85.14%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 82.65% 96.86%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 80.82% 92.38%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.80% 99.17%
CHEMBL4208 P20618 Proteasome component C5 80.11% 90.00%

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.
Ficus carica

Cross-Links

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PubChem 610210
NPASS NPC46947