(6S,7R)-6-methyl-7-(3-oxobutyl)cyclohept-2-en-1-one

Details

Top
Internal ID 5bbe0338-db44-45e0-a479-e91d824bfdd7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name (6S,7R)-6-methyl-7-(3-oxobutyl)cyclohept-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H18O2/c1-9-5-3-4-6-12(14)11(9)8-7-10(2)13/h4,6,9,11H,3,5,7-8H2,1-2H3/t9-,11+/m0/s1
InChI Key PGQIQXCQGGDEBH-GXSJLCMTSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H18O2
Molecular Weight 194.27 g/mol
Exact Mass 194.130679813 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (6S,7R)-6-methyl-7-(3-oxobutyl)cyclohept-2-en-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.7965 79.65%
Blood Brain Barrier + 0.8330 83.30%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7267 72.67%
OATP2B1 inhibitior - 0.8508 85.08%
OATP1B1 inhibitior + 0.9379 93.79%
OATP1B3 inhibitior + 0.9393 93.93%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8891 88.91%
P-glycoprotein inhibitior - 0.9884 98.84%
P-glycoprotein substrate - 0.9098 90.98%
CYP3A4 substrate - 0.5651 56.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8733 87.33%
CYP3A4 inhibition - 0.9331 93.31%
CYP2C9 inhibition - 0.9212 92.12%
CYP2C19 inhibition - 0.9244 92.44%
CYP2D6 inhibition - 0.8964 89.64%
CYP1A2 inhibition - 0.6925 69.25%
CYP2C8 inhibition - 0.9599 95.99%
CYP inhibitory promiscuity - 0.9442 94.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.7260 72.60%
Eye corrosion - 0.5926 59.26%
Eye irritation + 0.6778 67.78%
Skin irritation + 0.6070 60.70%
Skin corrosion - 0.9257 92.57%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5801 58.01%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6255 62.55%
skin sensitisation + 0.7503 75.03%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.7275 72.75%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.6139 61.39%
Acute Oral Toxicity (c) III 0.8161 81.61%
Estrogen receptor binding - 0.9548 95.48%
Androgen receptor binding - 0.6317 63.17%
Thyroid receptor binding - 0.9107 91.07%
Glucocorticoid receptor binding - 0.7251 72.51%
Aromatase binding - 0.9080 90.80%
PPAR gamma - 0.9286 92.86%
Honey bee toxicity - 0.9433 94.33%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9534 95.34%

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 96.40% 83.82%
CHEMBL2581 P07339 Cathepsin D 94.45% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.69% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.67% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.96% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.52% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.89% 89.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.62% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.62% 100.00%

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 10465226
LOTUS LTS0174422
wikiData Q105208597