2,4,6-Cycloheptatrien-1-one, 2-hydroxy-3-(1-methylethyl)-

Details

Top
Internal ID c1d74cc9-68dc-4e9b-b651-b742062a2189
Taxonomy Hydrocarbon derivatives > Tropones > Tropolones
IUPAC Name 2-hydroxy-3-propan-2-ylcyclohepta-2,4,6-trien-1-one
SMILES (Canonical) CC(C)C1=C(C(=O)C=CC=C1)O
SMILES (Isomeric) CC(C)C1=C(C(=O)C=CC=C1)O
InChI InChI=1S/C10H12O2/c1-7(2)8-5-3-4-6-9(11)10(8)12/h3-7H,1-2H3,(H,11,12)
InChI Key TUFYVOCKVJOUIR-UHFFFAOYSA-N
Popularity 16 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H12O2
Molecular Weight 164.20 g/mol
Exact Mass 164.083729621 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.88
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
1946-74-3
2,4,6-Cycloheptatrien-1-one, 2-hydroxy-3-(1-methylethyl)-
6TU33PGY8A
2-hydroxy-3-propan-2-ylcyclohepta-2,4,6-trien-1-one
CHEMBL1275969
2-hydroxy-3-isopropyl-2,4,6-cycloheptatrien-1-one
thujaplicin
.alpha.-Thujaplicin
3-Isopropyltropolone
D0A6ZK
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 2,4,6-Cycloheptatrien-1-one, 2-hydroxy-3-(1-methylethyl)-

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.8963 89.63%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.8908 89.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9351 93.51%
OATP1B3 inhibitior + 0.9632 96.32%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9131 91.31%
P-glycoprotein inhibitior - 0.9697 96.97%
P-glycoprotein substrate - 0.9704 97.04%
CYP3A4 substrate - 0.6532 65.32%
CYP2C9 substrate - 0.5701 57.01%
CYP2D6 substrate - 0.8073 80.73%
CYP3A4 inhibition - 0.9274 92.74%
CYP2C9 inhibition - 0.9145 91.45%
CYP2C19 inhibition - 0.8522 85.22%
CYP2D6 inhibition - 0.9010 90.10%
CYP1A2 inhibition + 0.5091 50.91%
CYP2C8 inhibition - 0.9674 96.74%
CYP inhibitory promiscuity - 0.9090 90.90%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7111 71.11%
Carcinogenicity (trinary) Non-required 0.7025 70.25%
Eye corrosion + 0.9292 92.92%
Eye irritation + 0.9122 91.22%
Skin irritation + 0.7996 79.96%
Skin corrosion + 0.9536 95.36%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8651 86.51%
Micronuclear - 0.6367 63.67%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.8506 85.06%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.5912 59.12%
Acute Oral Toxicity (c) III 0.8533 85.33%
Estrogen receptor binding - 0.9274 92.74%
Androgen receptor binding - 0.8870 88.70%
Thyroid receptor binding - 0.7555 75.55%
Glucocorticoid receptor binding - 0.8850 88.50%
Aromatase binding - 0.8580 85.80%
PPAR gamma - 0.8593 85.93%
Honey bee toxicity - 0.9450 94.50%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8145 81.45%

Targets

Top

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 97.23% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.83% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.54% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.93% 93.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.93% 99.15%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.88% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 82.32% 94.73%

Plants that contains it

Top
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.
Juniperus communis
Thuja occidentalis
Thuja plicata
Thujopsis dolabrata
Thymus vulgaris

Cross-Links

Top
PubChem 80297
NPASS NPC281195
ChEMBL CHEMBL1275969
LOTUS LTS0195291
wikiData Q83043198