(3R)-3-hydroxy-3,5,5-trimethyl-7-propan-2-yl-2,4-dihydroinden-1-one

Details

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Internal ID 6d5a739a-8112-4787-be21-43f3267d349d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3R)-3-hydroxy-3,5,5-trimethyl-7-propan-2-yl-2,4-dihydroinden-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-9(2)10-6-14(3,4)7-11-13(10)12(16)8-15(11,5)17/h6,9,17H,7-8H2,1-5H3/t15-/m1/s1
InChI Key CDGJALSODSFJMM-OAHLLOKOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.80
Atomic LogP (AlogP) 3.02
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R)-3-hydroxy-3,5,5-trimethyl-7-propan-2-yl-2,4-dihydroinden-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 + 0.8769 87.69%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6561 65.61%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.9462 94.62%
OATP1B3 inhibitior + 0.9663 96.63%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9422 94.22%
P-glycoprotein inhibitior - 0.9280 92.80%
P-glycoprotein substrate - 0.9305 93.05%
CYP3A4 substrate - 0.5345 53.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8953 89.53%
CYP3A4 inhibition - 0.8978 89.78%
CYP2C9 inhibition - 0.8680 86.80%
CYP2C19 inhibition - 0.7944 79.44%
CYP2D6 inhibition - 0.9383 93.83%
CYP1A2 inhibition - 0.8823 88.23%
CYP2C8 inhibition - 0.9896 98.96%
CYP inhibitory promiscuity - 0.9206 92.06%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8932 89.32%
Carcinogenicity (trinary) Warning 0.4744 47.44%
Eye corrosion - 0.9668 96.68%
Eye irritation + 0.8776 87.76%
Skin irritation + 0.5541 55.41%
Skin corrosion - 0.9497 94.97%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4380 43.80%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.6169 61.69%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.8434 84.34%
Acute Oral Toxicity (c) III 0.4504 45.04%
Estrogen receptor binding - 0.7508 75.08%
Androgen receptor binding - 0.6543 65.43%
Thyroid receptor binding - 0.5410 54.10%
Glucocorticoid receptor binding - 0.7380 73.80%
Aromatase binding - 0.8259 82.59%
PPAR gamma - 0.8395 83.95%
Honey bee toxicity - 0.8975 89.75%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9660 96.60%

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 94.66% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.95% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.50% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.66% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.33% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 85.79% 90.17%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.55% 96.77%
CHEMBL1937 Q92769 Histone deacetylase 2 82.61% 94.75%

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 15690503
LOTUS LTS0259378
wikiData Q104954422