Falconensin J

Details

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Internal ID bb8c9ffc-de29-487a-907b-ff562fec2329
Taxonomy Organoheterocyclic compounds > Azaphilones
IUPAC Name [(7R,8S,8aS)-8-hydroxy-7-methyl-6-oxo-3-propyl-8,8a-dihydro-1H-isochromen-7-yl] 4-hydroxy-2-methoxy-6-methylbenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H26O7/c1-5-6-15-8-13-9-18(24)22(3,20(25)16(13)11-28-15)29-21(26)19-12(2)7-14(23)10-17(19)27-4/h7-10,16,20,23,25H,5-6,11H2,1-4H3/t16-,20+,22+/m1/s1
InChI Key YAJWDUVDBNRHLD-BUVFEPMLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O7
Molecular Weight 402.40 g/mol
Exact Mass 402.16785316 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Falconensin J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9803 98.03%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8560 85.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8492 84.92%
OATP1B3 inhibitior + 0.8816 88.16%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.7438 74.38%
P-glycoprotein inhibitior + 0.6323 63.23%
P-glycoprotein substrate + 0.5089 50.89%
CYP3A4 substrate + 0.6906 69.06%
CYP2C9 substrate - 0.6019 60.19%
CYP2D6 substrate - 0.8599 85.99%
CYP3A4 inhibition - 0.7101 71.01%
CYP2C9 inhibition - 0.7904 79.04%
CYP2C19 inhibition - 0.6184 61.84%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition + 0.5291 52.91%
CYP2C8 inhibition + 0.7209 72.09%
CYP inhibitory promiscuity - 0.7059 70.59%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6557 65.57%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9421 94.21%
Skin irritation - 0.7612 76.12%
Skin corrosion - 0.9591 95.91%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5771 57.71%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8646 86.46%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6580 65.80%
Acute Oral Toxicity (c) III 0.4021 40.21%
Estrogen receptor binding + 0.7811 78.11%
Androgen receptor binding + 0.6683 66.83%
Thyroid receptor binding - 0.5070 50.70%
Glucocorticoid receptor binding + 0.7332 73.32%
Aromatase binding - 0.5416 54.16%
PPAR gamma + 0.6903 69.03%
Honey bee toxicity - 0.8395 83.95%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9921 99.21%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.69% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.77% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.09% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.83% 94.45%
CHEMBL2581 P07339 Cathepsin D 93.64% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.04% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.02% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.94% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.83% 99.17%
CHEMBL4208 P20618 Proteasome component C5 87.78% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.51% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.70% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.43% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.37% 90.71%
CHEMBL340 P08684 Cytochrome P450 3A4 84.10% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.02% 92.94%
CHEMBL3401 O75469 Pregnane X receptor 83.98% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.73% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.05% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.56% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.52% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 81.40% 95.93%
CHEMBL1871 P10275 Androgen Receptor 80.72% 96.43%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.22% 92.62%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.21% 94.33%

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 10692475
LOTUS LTS0010753
wikiData Q77497593