13-Hydroxy-tricho-2(12),9(10)-diene-3-one

Details

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Internal ID a79a53e0-78df-4e5a-8d43-3d2aa1c006c5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name (4R)-4-[(1S)-1,4-dimethylcyclohex-3-en-1-yl]-3-(hydroxymethyl)-4-methylcyclopent-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-11-4-6-14(2,7-5-11)15(3)9-13(17)8-12(15)10-16/h4,8,16H,5-7,9-10H2,1-3H3/t14-,15+/m1/s1
InChI Key FBSYQYBRVWGYEB-CABCVRRESA-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 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 13-Hydroxy-tricho-2(12),9(10)-diene-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.9585 95.85%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7728 77.28%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.8794 87.94%
OATP1B3 inhibitior + 0.9243 92.43%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.5296 52.96%
P-glycoprotein inhibitior - 0.9755 97.55%
P-glycoprotein substrate - 0.8886 88.86%
CYP3A4 substrate + 0.5270 52.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8785 87.85%
CYP3A4 inhibition - 0.8259 82.59%
CYP2C9 inhibition - 0.8599 85.99%
CYP2C19 inhibition - 0.8549 85.49%
CYP2D6 inhibition - 0.8864 88.64%
CYP1A2 inhibition - 0.7172 71.72%
CYP2C8 inhibition - 0.8694 86.94%
CYP inhibitory promiscuity - 0.7849 78.49%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8728 87.28%
Carcinogenicity (trinary) Non-required 0.5951 59.51%
Eye corrosion - 0.9799 97.99%
Eye irritation + 0.5462 54.62%
Skin irritation - 0.5529 55.29%
Skin corrosion - 0.9830 98.30%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5181 51.81%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.6138 61.38%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5173 51.73%
Acute Oral Toxicity (c) III 0.8210 82.10%
Estrogen receptor binding - 0.8616 86.16%
Androgen receptor binding + 0.5839 58.39%
Thyroid receptor binding - 0.6643 66.43%
Glucocorticoid receptor binding - 0.5398 53.98%
Aromatase binding - 0.6770 67.70%
PPAR gamma - 0.6982 69.82%
Honey bee toxicity - 0.9008 90.08%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9497 94.97%

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 95.71% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.18% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.55% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.81% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.60% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.90% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.75% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.54% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.42% 100.00%
CHEMBL4208 P20618 Proteasome component C5 82.46% 90.00%
CHEMBL1937 Q92769 Histone deacetylase 2 80.17% 94.75%

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.
There are no matching plants.

Cross-Links

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PubChem 139584005
LOTUS LTS0253913
wikiData Q77278421