Falconensin K

Details

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Internal ID e3c8f5b7-d139-4d77-8f17-6561c6d765f9
Taxonomy Organoheterocyclic compounds > Azaphilones
IUPAC Name [(7R,8S,8aS)-8-hydroxy-7-methyl-6-oxo-3-[(E)-prop-1-enyl]-8,8a-dihydro-1H-isochromen-7-yl] 3-chloro-4-hydroxy-6-methoxy-2-methylbenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H23ClO7/c1-5-6-13-7-12-8-17(25)22(3,20(26)14(12)10-29-13)30-21(27)18-11(2)19(23)15(24)9-16(18)28-4/h5-9,14,20,24,26H,10H2,1-4H3/b6-5+/t14-,20+,22+/m1/s1
InChI Key ZXTNKQJBZVFQFX-LHOLRKRRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H23ClO7
Molecular Weight 434.90 g/mol
Exact Mass 434.1132308 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.25
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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C22H23ClO7

2D Structure

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2D Structure of Falconensin K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9832 98.32%
Caco-2 - 0.6192 61.92%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.7330 73.30%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7904 79.04%
OATP1B3 inhibitior + 0.8737 87.37%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9142 91.42%
P-glycoprotein inhibitior + 0.5944 59.44%
P-glycoprotein substrate - 0.5206 52.06%
CYP3A4 substrate + 0.7110 71.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8790 87.90%
CYP3A4 inhibition - 0.8741 87.41%
CYP2C9 inhibition - 0.5309 53.09%
CYP2C19 inhibition - 0.5525 55.25%
CYP2D6 inhibition - 0.8694 86.94%
CYP1A2 inhibition - 0.5291 52.91%
CYP2C8 inhibition + 0.6866 68.66%
CYP inhibitory promiscuity - 0.5656 56.56%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8828 88.28%
Carcinogenicity (trinary) Danger 0.4559 45.59%
Eye corrosion - 0.9858 98.58%
Eye irritation - 0.9616 96.16%
Skin irritation - 0.7106 71.06%
Skin corrosion - 0.9323 93.23%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7934 79.34%
Micronuclear + 0.5459 54.59%
Hepatotoxicity + 0.5659 56.59%
skin sensitisation - 0.7866 78.66%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7089 70.89%
Acute Oral Toxicity (c) III 0.5537 55.37%
Estrogen receptor binding + 0.8621 86.21%
Androgen receptor binding + 0.7409 74.09%
Thyroid receptor binding + 0.6690 66.90%
Glucocorticoid receptor binding + 0.8171 81.71%
Aromatase binding + 0.5446 54.46%
PPAR gamma + 0.7657 76.57%
Honey bee toxicity - 0.7346 73.46%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9901 99.01%

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 98.99% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.18% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.58% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.66% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.46% 96.09%
CHEMBL4208 P20618 Proteasome component C5 90.29% 90.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.81% 86.92%
CHEMBL3194 P02766 Transthyretin 88.95% 90.71%
CHEMBL3492 P49721 Proteasome Macropain subunit 88.42% 90.24%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.19% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.51% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.96% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 86.75% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.38% 92.94%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.12% 97.14%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.76% 96.77%
CHEMBL2581 P07339 Cathepsin D 84.61% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.81% 92.62%
CHEMBL1937 Q92769 Histone deacetylase 2 82.42% 94.75%
CHEMBL1871 P10275 Androgen Receptor 82.34% 96.43%
CHEMBL3401 O75469 Pregnane X receptor 81.86% 94.73%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.91% 95.89%
CHEMBL2535 P11166 Glucose transporter 80.71% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.44% 96.00%

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 10670510
LOTUS LTS0161154
wikiData Q77379322