Psorofebrin

Details

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Internal ID 38692670-457d-4652-98d5-18636640f2a1
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name (3S,6R,7R)-6,18-dihydroxy-11-methoxy-6-methyl-4,8,20-trioxapentacyclo[10.8.0.02,9.03,7.014,19]icosa-1,9,11,14(19),15,17-hexaen-13-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H16O7/c1-19(22)7-24-17-13-11(25-18(17)19)6-10(23-2)12-14(21)8-4-3-5-9(20)15(8)26-16(12)13/h3-6,17-18,20,22H,7H2,1-2H3/t17-,18+,19+/m0/s1
InChI Key ZDHCSGNLOGAREA-IPMKNSEASA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C19H16O7
Molecular Weight 356.30 g/mol
Exact Mass 356.08960285 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.24
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEMBL518565

2D Structure

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2D Structure of Psorofebrin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9837 98.37%
Caco-2 - 0.6019 60.19%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7558 75.58%
OATP2B1 inhibitior - 0.5732 57.32%
OATP1B1 inhibitior + 0.9340 93.40%
OATP1B3 inhibitior + 0.9206 92.06%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7215 72.15%
P-glycoprotein inhibitior + 0.6667 66.67%
P-glycoprotein substrate - 0.5442 54.42%
CYP3A4 substrate + 0.6702 67.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8088 80.88%
CYP3A4 inhibition - 0.5822 58.22%
CYP2C9 inhibition - 0.7530 75.30%
CYP2C19 inhibition - 0.5794 57.94%
CYP2D6 inhibition - 0.5473 54.73%
CYP1A2 inhibition - 0.5235 52.35%
CYP2C8 inhibition + 0.5366 53.66%
CYP inhibitory promiscuity - 0.7397 73.97%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4751 47.51%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.7336 73.36%
Skin irritation - 0.8163 81.63%
Skin corrosion - 0.9604 96.04%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8030 80.30%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.5052 50.52%
skin sensitisation - 0.7541 75.41%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8723 87.23%
Acute Oral Toxicity (c) III 0.7039 70.39%
Estrogen receptor binding + 0.9171 91.71%
Androgen receptor binding + 0.7191 71.91%
Thyroid receptor binding + 0.5755 57.55%
Glucocorticoid receptor binding + 0.8355 83.55%
Aromatase binding + 0.8422 84.22%
PPAR gamma + 0.9150 91.50%
Honey bee toxicity - 0.7830 78.30%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5449 54.49%
Fish aquatic toxicity + 0.6992 69.92%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.55% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.10% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.33% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.11% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 94.71% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.34% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 94.31% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.30% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.74% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.08% 86.33%
CHEMBL2535 P11166 Glucose transporter 91.92% 98.75%
CHEMBL2581 P07339 Cathepsin D 90.31% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.78% 92.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.33% 97.14%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 86.56% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.63% 96.09%
CHEMBL2803 P43403 Tyrosine-protein kinase ZAP-70 84.43% 82.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.18% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.21% 97.09%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 82.03% 85.30%

Plants that contains it

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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.
Psorospermum febrifugum

Cross-Links

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PubChem 14352929
LOTUS LTS0047955
wikiData Q105372188