11-Dodecanolide

Details

Top
Internal ID 8f6bd40f-f80a-4fd6-bea9-b106645ddf05
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 12-methyl-oxacyclododecan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H22O2/c1-11-9-7-5-3-2-4-6-8-10-12(13)14-11/h11H,2-10H2,1H3
InChI Key IBLSRZGJYAOPLB-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H22O2
Molecular Weight 198.30 g/mol
Exact Mass 198.161979940 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.44
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
12-methyl-oxacyclododecan-2-one
95338-31-1
SCHEMBL15656167
DTXSID40337584
CHEBI:179197
IBLSRZGJYAOPLB-UHFFFAOYSA-N
12-Methyl-oxa-cyclododecan-2-one
LMFA07040038

2D Structure

Top
2D Structure of 11-Dodecanolide

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.9091 90.91%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Plasma membrane 0.4043 40.43%
OATP2B1 inhibitior - 0.8446 84.46%
OATP1B1 inhibitior + 0.9425 94.25%
OATP1B3 inhibitior + 0.9655 96.55%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8991 89.91%
P-glycoprotein inhibitior - 0.9537 95.37%
P-glycoprotein substrate - 0.9734 97.34%
CYP3A4 substrate - 0.6194 61.94%
CYP2C9 substrate - 0.7965 79.65%
CYP2D6 substrate - 0.8634 86.34%
CYP3A4 inhibition - 0.9412 94.12%
CYP2C9 inhibition - 0.9184 91.84%
CYP2C19 inhibition - 0.8137 81.37%
CYP2D6 inhibition - 0.9698 96.98%
CYP1A2 inhibition - 0.5161 51.61%
CYP2C8 inhibition - 0.9912 99.12%
CYP inhibitory promiscuity - 0.9801 98.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6309 63.09%
Eye corrosion + 0.8464 84.64%
Eye irritation + 0.9095 90.95%
Skin irritation + 0.7350 73.50%
Skin corrosion - 0.7530 75.30%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7015 70.15%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.7355 73.55%
skin sensitisation - 0.5608 56.08%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.8037 80.37%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.6075 60.75%
Acute Oral Toxicity (c) III 0.6271 62.71%
Estrogen receptor binding - 0.8795 87.95%
Androgen receptor binding - 0.8797 87.97%
Thyroid receptor binding - 0.8108 81.08%
Glucocorticoid receptor binding - 0.8489 84.89%
Aromatase binding - 0.8371 83.71%
PPAR gamma - 0.8433 84.33%
Honey bee toxicity - 0.9598 95.98%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.7150 71.50%

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 93.18% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.18% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.27% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.25% 97.09%
CHEMBL3012 Q13946 Phosphodiesterase 7A 84.85% 99.29%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.60% 93.04%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.16% 96.38%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.07% 94.78%

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 543499
LOTUS LTS0260855
wikiData Q82105462