5-(2-methoxyethyl)-1,2,4,6-tetramethyl-3H-indene-1,2,7-triol

Details

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Internal ID f007689a-fa30-4c5e-96e9-5c82f77c1154
Taxonomy Benzenoids > Indanes
IUPAC Name 5-(2-methoxyethyl)-1,2,4,6-tetramethyl-3H-indene-1,2,7-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H24O4/c1-9-11(6-7-20-5)10(2)14(17)13-12(9)8-15(3,18)16(13,4)19/h17-19H,6-8H2,1-5H3
InChI Key FUGLZGQQRWICTH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H24O4
Molecular Weight 280.36 g/mol
Exact Mass 280.16745924 g/mol
Topological Polar Surface Area (TPSA) 69.90 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.71
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(2-methoxyethyl)-1,2,4,6-tetramethyl-3H-indene-1,2,7-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9717 97.17%
Caco-2 + 0.7744 77.44%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6492 64.92%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.8844 88.44%
OATP1B3 inhibitior + 0.9090 90.90%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6584 65.84%
P-glycoprotein inhibitior - 0.8842 88.42%
P-glycoprotein substrate - 0.7245 72.45%
CYP3A4 substrate + 0.6209 62.09%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate + 0.3512 35.12%
CYP3A4 inhibition - 0.8975 89.75%
CYP2C9 inhibition - 0.8056 80.56%
CYP2C19 inhibition - 0.8295 82.95%
CYP2D6 inhibition - 0.9480 94.80%
CYP1A2 inhibition + 0.5958 59.58%
CYP2C8 inhibition - 0.5749 57.49%
CYP inhibitory promiscuity - 0.9573 95.73%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.6549 65.49%
Eye corrosion - 0.9906 99.06%
Eye irritation + 0.8677 86.77%
Skin irritation - 0.6884 68.84%
Skin corrosion - 0.9410 94.10%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5428 54.28%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.6466 64.66%
skin sensitisation - 0.7876 78.76%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7218 72.18%
Acute Oral Toxicity (c) III 0.5628 56.28%
Estrogen receptor binding + 0.5729 57.29%
Androgen receptor binding - 0.5135 51.35%
Thyroid receptor binding + 0.5886 58.86%
Glucocorticoid receptor binding - 0.4762 47.62%
Aromatase binding - 0.5408 54.08%
PPAR gamma - 0.4881 48.81%
Honey bee toxicity - 0.8964 89.64%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8404 84.04%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.64% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.16% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.90% 95.17%
CHEMBL240 Q12809 HERG 85.56% 89.76%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 85.55% 92.68%
CHEMBL221 P23219 Cyclooxygenase-1 84.81% 90.17%
CHEMBL1907 P15144 Aminopeptidase N 83.93% 93.31%
CHEMBL206 P03372 Estrogen receptor alpha 83.76% 97.64%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.21% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.53% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139586272
LOTUS LTS0243871
wikiData Q77502803