Paecilomycone B

Details

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Internal ID d4bd9ae9-9c1c-48ae-8f59-4f33c5b5d0e7
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 4,9-dihydroxy-6-methoxy-7-methylphenalene-1,2,3-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H10O6/c1-5-3-6(16)10-12-9(5)8(21-2)4-7(17)11(12)14(19)15(20)13(10)18/h3-4,16-17H,1-2H3
InChI Key CMDRFERFCZVBIH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10O6
Molecular Weight 286.24 g/mol
Exact Mass 286.04773803 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 0.68
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Paecilomycone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9867 98.67%
Caco-2 + 0.6305 63.05%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8309 83.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9571 95.71%
OATP1B3 inhibitior + 0.9329 93.29%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9334 93.34%
P-glycoprotein inhibitior - 0.8995 89.95%
P-glycoprotein substrate - 0.9579 95.79%
CYP3A4 substrate - 0.5856 58.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7976 79.76%
CYP3A4 inhibition - 0.8346 83.46%
CYP2C9 inhibition + 0.5067 50.67%
CYP2C19 inhibition - 0.6468 64.68%
CYP2D6 inhibition - 0.7472 74.72%
CYP1A2 inhibition + 0.9109 91.09%
CYP2C8 inhibition - 0.8676 86.76%
CYP inhibitory promiscuity - 0.6522 65.22%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8795 87.95%
Carcinogenicity (trinary) Non-required 0.5355 53.55%
Eye corrosion - 0.9806 98.06%
Eye irritation + 0.8973 89.73%
Skin irritation - 0.5600 56.00%
Skin corrosion - 0.9405 94.05%
Ames mutagenesis - 0.6764 67.64%
Human Ether-a-go-go-Related Gene inhibition - 0.5861 58.61%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8987 89.87%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5288 52.88%
Acute Oral Toxicity (c) II 0.5323 53.23%
Estrogen receptor binding + 0.8082 80.82%
Androgen receptor binding - 0.5349 53.49%
Thyroid receptor binding - 0.7006 70.06%
Glucocorticoid receptor binding + 0.6570 65.70%
Aromatase binding + 0.5186 51.86%
PPAR gamma - 0.6060 60.60%
Honey bee toxicity - 0.9166 91.66%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9767 97.67%

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 94.31% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.54% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.58% 94.00%
CHEMBL2581 P07339 Cathepsin D 86.32% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.15% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.30% 93.99%
CHEMBL4208 P20618 Proteasome component C5 85.18% 90.00%
CHEMBL2535 P11166 Glucose transporter 82.21% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.20% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.44% 99.15%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.90% 93.65%

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 101899578
LOTUS LTS0173359
wikiData Q77506332