Falconensin M

Details

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Internal ID 84a675d0-e4b2-42d3-ad3f-0a02dc8c979e
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] 3,5-dichloro-4-hydroxy-2-methoxy-6-methylbenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H22Cl2O7/c1-5-6-12-7-11-8-14(25)22(3,20(27)13(11)9-30-12)31-21(28)15-10(2)16(23)18(26)17(24)19(15)29-4/h5-8,13,20,26-27H,9H2,1-4H3/b6-5+/t13-,20+,22+/m1/s1
InChI Key ABDSGQRCBJROHY-PISAZCMYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H22Cl2O7
Molecular Weight 469.30 g/mol
Exact Mass 468.0742584 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.91
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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C22H22Cl2O7

2D Structure

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2D Structure of Falconensin M

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 - 0.6350 63.50%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7330 73.30%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7445 74.45%
OATP1B3 inhibitior + 0.8737 87.37%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9409 94.09%
P-glycoprotein inhibitior - 0.4497 44.97%
P-glycoprotein substrate - 0.5726 57.26%
CYP3A4 substrate + 0.7186 71.86%
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 + 0.6558 65.58%
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 - 0.9497 94.97%
Skin irritation - 0.7106 71.06%
Skin corrosion - 0.9323 93.23%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6926 69.26%
Micronuclear + 0.5459 54.59%
Hepatotoxicity + 0.5784 57.84%
skin sensitisation - 0.7866 78.66%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8464 84.64%
Acute Oral Toxicity (c) III 0.5537 55.37%
Estrogen receptor binding + 0.8568 85.68%
Androgen receptor binding + 0.6664 66.64%
Thyroid receptor binding + 0.6834 68.34%
Glucocorticoid receptor binding + 0.8306 83.06%
Aromatase binding + 0.5196 51.96%
PPAR gamma + 0.7806 78.06%
Honey bee toxicity - 0.7673 76.73%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6200 62.00%
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 99.09% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.86% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.52% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.89% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.90% 96.09%
CHEMBL1871 P10275 Androgen Receptor 89.56% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.89% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.23% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.19% 86.92%
CHEMBL340 P08684 Cytochrome P450 3A4 86.24% 91.19%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.34% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.74% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.70% 97.25%
CHEMBL4208 P20618 Proteasome component C5 84.37% 90.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.35% 90.24%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.76% 89.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.68% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 81.67% 94.73%

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 10695634
LOTUS LTS0046000
wikiData Q77497230