Salinipostin C

Details

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Internal ID abfaa299-240e-4b14-8304-2e1c0eec4509
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3R,8aS)-5-butyl-3-oxo-3-tridecoxy-8,8a-dihydro-1H-furo[3,4-e][1,3,2]dioxaphosphepin-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H41O6P/c1-3-5-7-8-9-10-11-12-13-14-15-17-27-30(25)28-19-20-18-26-23(24)22(20)21(29-30)16-6-4-2/h20H,3-19H2,1-2H3/t20-,30+/m0/s1
InChI Key MXMZCWUTKKOBCT-WENCNXQZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H41O6P
Molecular Weight 444.50 g/mol
Exact Mass 444.26407602 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 7.20
Atomic LogP (AlogP) 7.09
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 16

Synonyms

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

2D Structure

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2D Structure of Salinipostin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9819 98.19%
Caco-2 - 0.5726 57.26%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6107 61.07%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9230 92.30%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8227 82.27%
P-glycoprotein inhibitior + 0.5797 57.97%
P-glycoprotein substrate - 0.5689 56.89%
CYP3A4 substrate + 0.6172 61.72%
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 - 0.6088 60.88%
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 - 0.5192 51.92%
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 - 0.4132 41.32%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8578 85.78%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.7599 75.99%
Acute Oral Toxicity (c) III 0.4299 42.99%
Estrogen receptor binding + 0.6388 63.88%
Androgen receptor binding + 0.7081 70.81%
Thyroid receptor binding - 0.5734 57.34%
Glucocorticoid receptor binding - 0.6060 60.60%
Aromatase binding - 0.5183 51.83%
PPAR gamma + 0.6014 60.14%
Honey bee toxicity - 0.8691 86.91%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9936 99.36%

Targets

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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 97.17% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 94.43% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.47% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.09% 97.25%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.41% 92.08%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.13% 97.09%
CHEMBL240 Q12809 HERG 86.85% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.49% 86.33%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 86.38% 80.33%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 85.20% 85.94%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.02% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.70% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.93% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 81.84% 94.73%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.54% 91.24%
CHEMBL255 P29275 Adenosine A2b receptor 81.42% 98.59%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.11% 92.88%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.94% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 129903221
LOTUS LTS0260846
wikiData Q77374891