(2R,3S,6S)-3-methyl-2-(3-oxobutyl)-6-prop-1-en-2-ylcycloheptan-1-one

Details

Top
Internal ID ef127414-7e60-4046-8072-08a3384b7510
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2R,3S,6S)-3-methyl-2-(3-oxobutyl)-6-prop-1-en-2-ylcycloheptan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O2/c1-10(2)13-7-5-11(3)14(15(17)9-13)8-6-12(4)16/h11,13-14H,1,5-9H2,2-4H3/t11-,13-,14+/m0/s1
InChI Key CGLWYEZJKQTMLC-FPMFFAJLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.55
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (2R,3S,6S)-3-methyl-2-(3-oxobutyl)-6-prop-1-en-2-ylcycloheptan-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.8331 83.31%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6237 62.37%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.9447 94.47%
OATP1B3 inhibitior + 0.8908 89.08%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7916 79.16%
P-glycoprotein inhibitior - 0.8787 87.87%
P-glycoprotein substrate - 0.8079 80.79%
CYP3A4 substrate - 0.5339 53.39%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.7855 78.55%
CYP3A4 inhibition - 0.8347 83.47%
CYP2C9 inhibition - 0.8643 86.43%
CYP2C19 inhibition - 0.7842 78.42%
CYP2D6 inhibition - 0.9009 90.09%
CYP1A2 inhibition - 0.6298 62.98%
CYP2C8 inhibition - 0.9213 92.13%
CYP inhibitory promiscuity - 0.8992 89.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.6368 63.68%
Eye corrosion - 0.8730 87.30%
Eye irritation + 0.8129 81.29%
Skin irritation + 0.5337 53.37%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis - 0.8128 81.28%
Human Ether-a-go-go-Related Gene inhibition - 0.5908 59.08%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7930 79.30%
skin sensitisation + 0.7055 70.55%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.6941 69.41%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6961 69.61%
Estrogen receptor binding - 0.9067 90.67%
Androgen receptor binding - 0.5754 57.54%
Thyroid receptor binding - 0.6902 69.02%
Glucocorticoid receptor binding - 0.6554 65.54%
Aromatase binding - 0.8574 85.74%
PPAR gamma - 0.8375 83.75%
Honey bee toxicity - 0.9275 92.75%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9840 98.40%

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
CHEMBL4040 P28482 MAP kinase ERK2 95.06% 83.82%
CHEMBL2581 P07339 Cathepsin D 94.77% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.28% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.72% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.15% 97.25%
CHEMBL340 P08684 Cytochrome P450 3A4 83.72% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.15% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.55% 97.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.65% 96.95%

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.
There are no matching plants.

Cross-Links

Top
PubChem 46177449
LOTUS LTS0039148
wikiData Q104957852