(5S,S)-5-methyl-3-(7-methylnonyl)furan-2(5H)-one

Details

Top
Internal ID e83357a6-89aa-465f-b4b6-4be5893f1406
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Annonaceous acetogenins
IUPAC Name (2S)-2-methyl-4-[(7S)-7-methylnonyl]-2H-furan-5-one
SMILES (Canonical) CCC(C)CCCCCCC1=CC(OC1=O)C
SMILES (Isomeric) CC[C@H](C)CCCCCCC1=C[C@@H](OC1=O)C
InChI InChI=1S/C15H26O2/c1-4-12(2)9-7-5-6-8-10-14-11-13(3)17-15(14)16/h11-13H,4-10H2,1-3H3/t12-,13-/m0/s1
InChI Key GGPPVFPMDTYVJM-STQMWFEESA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.24
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (5S,S)-5-methyl-3-(7-methylnonyl)furan-2(5H)-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.9275 92.75%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4503 45.03%
OATP2B1 inhibitior - 0.8471 84.71%
OATP1B1 inhibitior + 0.8927 89.27%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.6870 68.70%
P-glycoprotein inhibitior - 0.8866 88.66%
P-glycoprotein substrate - 0.7544 75.44%
CYP3A4 substrate + 0.5113 51.13%
CYP2C9 substrate - 0.5814 58.14%
CYP2D6 substrate - 0.8888 88.88%
CYP3A4 inhibition - 0.6864 68.64%
CYP2C9 inhibition - 0.8450 84.50%
CYP2C19 inhibition - 0.5517 55.17%
CYP2D6 inhibition - 0.8997 89.97%
CYP1A2 inhibition + 0.6301 63.01%
CYP2C8 inhibition - 0.9336 93.36%
CYP inhibitory promiscuity - 0.5106 51.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5675 56.75%
Eye corrosion - 0.8992 89.92%
Eye irritation + 0.8422 84.22%
Skin irritation + 0.6190 61.90%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.5619 56.19%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.5706 57.06%
Acute Oral Toxicity (c) III 0.6989 69.89%
Estrogen receptor binding - 0.7250 72.50%
Androgen receptor binding - 0.7777 77.77%
Thyroid receptor binding - 0.5341 53.41%
Glucocorticoid receptor binding - 0.7709 77.09%
Aromatase binding - 0.7760 77.60%
PPAR gamma - 0.6663 66.63%
Honey bee toxicity - 0.9249 92.49%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9893 98.93%

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 93.99% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.70% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 89.42% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.31% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.95% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.61% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.85% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.49% 86.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.13% 93.56%
CHEMBL2996 Q05655 Protein kinase C delta 81.42% 97.79%

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 16090231
LOTUS LTS0023795
wikiData Q77491285