Salinipostin F

Details

Top
Internal ID ce8b8eb5-a142-4c68-9a6f-5b60000b99a5
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3R,8aS)-3-oxo-3-pentadecoxy-5-propyl-8,8a-dihydro-1H-furo[3,4-e][1,3,2]dioxaphosphepin-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H43O6P/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-18-28-31(26)29-20-21-19-27-24(25)23(21)22(30-31)17-4-2/h21H,3-20H2,1-2H3/t21-,31+/m0/s1
InChI Key CONVFBAOBJVKPP-JCOAXYOVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H43O6P
Molecular Weight 458.60 g/mol
Exact Mass 458.27972608 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 7.80
Atomic LogP (AlogP) 7.48
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 17

Synonyms

Top
(3R,8aS)-3-oxo-3-pentadecoxy-5-propyl-8,8a-dihydro-1H-furo[3,4-e][1,3,2]dioxaphosphepin-6-one

2D Structure

Top
2D Structure of Salinipostin F

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9819 98.19%
Caco-2 - 0.5844 58.44%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6107 61.07%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.9252 92.52%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8190 81.90%
P-glycoprotein inhibitior + 0.6043 60.43%
P-glycoprotein substrate - 0.5967 59.67%
CYP3A4 substrate + 0.6171 61.71%
CYP2C9 substrate + 0.5969 59.69%
CYP2D6 substrate - 0.8732 87.32%
CYP3A4 inhibition - 0.7191 71.91%
CYP2C9 inhibition - 0.7722 77.22%
CYP2C19 inhibition - 0.7313 73.13%
CYP2D6 inhibition - 0.8765 87.65%
CYP1A2 inhibition - 0.6956 69.56%
CYP2C8 inhibition - 0.6404 64.04%
CYP inhibitory promiscuity - 0.8576 85.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5212 52.12%
Eye corrosion - 0.9493 94.93%
Eye irritation + 0.5256 52.56%
Skin irritation - 0.7243 72.43%
Skin corrosion - 0.9130 91.30%
Ames mutagenesis - 0.7654 76.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5706 57.06%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.8578 85.78%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.7819 78.19%
Acute Oral Toxicity (c) III 0.4299 42.99%
Estrogen receptor binding + 0.5850 58.50%
Androgen receptor binding + 0.7324 73.24%
Thyroid receptor binding - 0.6205 62.05%
Glucocorticoid receptor binding - 0.6375 63.75%
Aromatase binding - 0.5419 54.19%
PPAR gamma + 0.5647 56.47%
Honey bee toxicity - 0.8788 87.88%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9936 99.36%

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 97.20% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.57% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 91.53% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.49% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.63% 97.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.31% 92.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.00% 86.33%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 86.38% 80.33%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 83.73% 85.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.56% 99.23%
CHEMBL255 P29275 Adenosine A2b receptor 83.31% 98.59%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.19% 91.11%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.95% 91.24%
CHEMBL3401 O75469 Pregnane X receptor 82.87% 94.73%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 82.25% 92.88%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.16% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.03% 96.09%

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 129903272
LOTUS LTS0244695
wikiData Q104967177