Fischeria A

Details

Top
Internal ID fdbec6e5-9dfc-404e-85ac-1230971ed6d6
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (1R,6R,10R,12R)-12-ethenyl-1,7,7,12-tetramethyl-5-oxatricyclo[8.4.0.02,6]tetradec-2-en-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H28O2/c1-6-18(4)9-10-19(5)13(12-18)7-8-17(2,3)16-14(19)11-15(20)21-16/h6,11,13,16H,1,7-10,12H2,2-5H3/t13-,16+,18-,19-/m1/s1
InChI Key HJTIEBXNTWYKEY-ZFKCKOODSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H28O2
Molecular Weight 288.40 g/mol
Exact Mass 288.208930132 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.66
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
221456-63-9
(1R,6R,10R,12R)-12-ethenyl-1,7,7,12-tetramethyl-5-oxatricyclo[8.4.0.02,6]tetradec-2-en-4-one
AKOS040761734
FS-8051
HY-133209
CS-0113346

2D Structure

Top
2D Structure of Fischeria A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.7986 79.86%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4664 46.64%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.8746 87.46%
OATP1B3 inhibitior + 0.9047 90.47%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.8622 86.22%
P-glycoprotein inhibitior - 0.8089 80.89%
P-glycoprotein substrate - 0.8608 86.08%
CYP3A4 substrate + 0.6011 60.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9102 91.02%
CYP3A4 inhibition - 0.8542 85.42%
CYP2C9 inhibition - 0.7647 76.47%
CYP2C19 inhibition + 0.6173 61.73%
CYP2D6 inhibition - 0.9136 91.36%
CYP1A2 inhibition + 0.6432 64.32%
CYP2C8 inhibition - 0.7238 72.38%
CYP inhibitory promiscuity - 0.8273 82.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5664 56.64%
Eye corrosion - 0.9589 95.89%
Eye irritation - 0.9055 90.55%
Skin irritation - 0.5290 52.90%
Skin corrosion - 0.9526 95.26%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8381 83.81%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.5874 58.74%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6025 60.25%
Acute Oral Toxicity (c) III 0.7316 73.16%
Estrogen receptor binding + 0.6243 62.43%
Androgen receptor binding - 0.5291 52.91%
Thyroid receptor binding + 0.5207 52.07%
Glucocorticoid receptor binding + 0.7743 77.43%
Aromatase binding + 0.6743 67.43%
PPAR gamma - 0.6838 68.38%
Honey bee toxicity - 0.7912 79.12%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9956 99.56%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.45% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.94% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.75% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.95% 97.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.88% 93.40%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.63% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.35% 95.89%
CHEMBL1871 P10275 Androgen Receptor 83.07% 96.43%
CHEMBL4588 P22894 Matrix metalloproteinase 8 82.87% 94.66%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.17% 94.80%
CHEMBL1937 Q92769 Histone deacetylase 2 81.42% 94.75%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.32% 97.25%
CHEMBL4530 P00488 Coagulation factor XIII 81.08% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.31% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.24% 89.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.11% 93.00%

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.
Euphorbia fischeriana

Cross-Links

Top
PubChem 15403260
LOTUS LTS0175863
wikiData Q105029442