(6Z,12S)-12-methyl-1-oxacyclododec-6-en-2-one

Details

Top
Internal ID 96bdc5ae-b93c-4126-bf1f-1b895e9b4af7
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (6Z,12S)-12-methyl-1-oxacyclododec-6-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H20O2/c1-11-9-7-5-3-2-4-6-8-10-12(13)14-11/h2,4,11H,3,5-10H2,1H3/b4-2-/t11-/m0/s1
InChI Key LDWZVYJMOWTMFA-MORRKMRCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H20O2
Molecular Weight 196.29 g/mol
Exact Mass 196.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.22
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (6Z,12S)-12-methyl-1-oxacyclododec-6-en-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.8973 89.73%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Plasma membrane 0.6402 64.02%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.9088 90.88%
OATP1B3 inhibitior + 0.9574 95.74%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8409 84.09%
P-glycoprotein inhibitior - 0.9751 97.51%
P-glycoprotein substrate - 0.9715 97.15%
CYP3A4 substrate - 0.5985 59.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8641 86.41%
CYP3A4 inhibition - 0.9195 91.95%
CYP2C9 inhibition - 0.9345 93.45%
CYP2C19 inhibition - 0.7578 75.78%
CYP2D6 inhibition - 0.9679 96.79%
CYP1A2 inhibition + 0.5875 58.75%
CYP2C8 inhibition - 0.9812 98.12%
CYP inhibitory promiscuity - 0.9558 95.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8428 84.28%
Carcinogenicity (trinary) Non-required 0.6037 60.37%
Eye corrosion + 0.7525 75.25%
Eye irritation + 0.9276 92.76%
Skin irritation + 0.7260 72.60%
Skin corrosion - 0.9429 94.29%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7074 70.74%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.7355 73.55%
skin sensitisation + 0.6482 64.82%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.4602 46.02%
Acute Oral Toxicity (c) III 0.5566 55.66%
Estrogen receptor binding - 0.8578 85.78%
Androgen receptor binding - 0.8717 87.17%
Thyroid receptor binding - 0.8628 86.28%
Glucocorticoid receptor binding - 0.7247 72.47%
Aromatase binding - 0.8537 85.37%
PPAR gamma - 0.7294 72.94%
Honey bee toxicity - 0.9477 94.77%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.8682 86.82%

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 91.64% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.57% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.28% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.49% 91.11%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.85% 93.04%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.56% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.34% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.10% 89.00%

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 163188101
LOTUS LTS0274494
wikiData Q105150424