Pileotin A

Details

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Internal ID 9e4216ed-b2b6-44a4-a38f-15f54bc27f49
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name (2R,5R,6R,7S,9S,10R)-5,9-dihydroxy-2,10-dimethyl-5-prop-1-en-2-yl-14-pyridin-3-ylspiro[11,15-dioxatetracyclo[8.8.0.02,7.012,17]octadeca-1(18),12(17),13-triene-6,5'-oxane]-2',16-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H33NO7/c1-17(2)30(35)10-9-27(3)22-12-19-21(13-20(37-26(19)34)18-6-5-11-31-15-18)38-28(22,4)24(32)14-23(27)29(30)8-7-25(33)36-16-29/h5-6,11-13,15,23-24,32,35H,1,7-10,14,16H2,2-4H3/t23-,24-,27-,28+,29-,30+/m0/s1
InChI Key GHODSEBRMSIFPD-WKFBYQISSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H33NO7
Molecular Weight 519.60 g/mol
Exact Mass 519.22570239 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 4.05
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pileotin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9673 96.73%
Caco-2 - 0.7733 77.33%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7400 74.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8834 88.34%
OATP1B3 inhibitior + 0.8957 89.57%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7891 78.91%
BSEP inhibitior + 0.9879 98.79%
P-glycoprotein inhibitior + 0.7760 77.60%
P-glycoprotein substrate + 0.6671 66.71%
CYP3A4 substrate + 0.6905 69.05%
CYP2C9 substrate - 0.7986 79.86%
CYP2D6 substrate - 0.8502 85.02%
CYP3A4 inhibition - 0.6441 64.41%
CYP2C9 inhibition - 0.8118 81.18%
CYP2C19 inhibition - 0.8017 80.17%
CYP2D6 inhibition - 0.9278 92.78%
CYP1A2 inhibition + 0.5145 51.45%
CYP2C8 inhibition + 0.7961 79.61%
CYP inhibitory promiscuity - 0.8702 87.02%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5239 52.39%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.9264 92.64%
Skin irritation - 0.7338 73.38%
Skin corrosion - 0.9392 93.92%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8075 80.75%
Micronuclear - 0.5600 56.00%
Hepatotoxicity - 0.5134 51.34%
skin sensitisation - 0.8476 84.76%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.8338 83.38%
Acute Oral Toxicity (c) III 0.3968 39.68%
Estrogen receptor binding + 0.7809 78.09%
Androgen receptor binding + 0.7265 72.65%
Thyroid receptor binding + 0.6301 63.01%
Glucocorticoid receptor binding + 0.8094 80.94%
Aromatase binding + 0.7724 77.24%
PPAR gamma + 0.6462 64.62%
Honey bee toxicity - 0.6926 69.26%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9939 99.39%

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 98.39% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.03% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.82% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.97% 94.45%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 95.88% 85.30%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.57% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.36% 100.00%
CHEMBL1951 P21397 Monoamine oxidase A 92.11% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.43% 99.23%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 90.98% 88.84%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.84% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.97% 94.00%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 88.43% 96.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.12% 94.80%
CHEMBL2243 O00519 Anandamide amidohydrolase 85.48% 97.53%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 84.88% 80.96%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.85% 81.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.26% 97.09%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 82.60% 96.39%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.43% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.25% 96.77%
CHEMBL259 P32245 Melanocortin receptor 4 81.63% 95.38%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.71% 100.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.42% 96.67%

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 102488847
LOTUS LTS0073035
wikiData Q75069500