Musanolone E

Details

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Internal ID 51edc8cf-afe7-47b2-ad1a-807618b13f64
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 2,3-dihydroxy-9-(4-hydroxyphenyl)phenalen-1-one
SMILES (Canonical) C1=CC2=C3C(=C1)C(=C(C(=O)C3=C(C=C2)C4=CC=C(C=C4)O)O)O
SMILES (Isomeric) C1=CC2=C3C(=C1)C(=C(C(=O)C3=C(C=C2)C4=CC=C(C=C4)O)O)O
InChI InChI=1S/C19H12O4/c20-12-7-4-10(5-8-12)13-9-6-11-2-1-3-14-15(11)16(13)18(22)19(23)17(14)21/h1-9,20-21,23H
InChI Key CFIUGIYVJPSAET-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H12O4
Molecular Weight 304.30 g/mol
Exact Mass 304.07355886 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.19
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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2,3-dihydroxy-9-(4-hydroxyphenyl)-1H-phenalen-1-one
2,3-dihydroxy-9-(4-hydroxyphenyl)phenalen-1-one
CHEBI:174909
DTXSID101317904
173560-65-1

2D Structure

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2D Structure of Musanolone E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 - 0.5635 56.35%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7472 74.72%
OATP2B1 inhibitior - 0.6708 67.08%
OATP1B1 inhibitior + 0.8591 85.91%
OATP1B3 inhibitior + 0.9653 96.53%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6037 60.37%
P-glycoprotein inhibitior - 0.8947 89.47%
P-glycoprotein substrate - 0.9004 90.04%
CYP3A4 substrate - 0.5347 53.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8526 85.26%
CYP3A4 inhibition - 0.6953 69.53%
CYP2C9 inhibition + 0.8648 86.48%
CYP2C19 inhibition - 0.7142 71.42%
CYP2D6 inhibition - 0.9101 91.01%
CYP1A2 inhibition + 0.9208 92.08%
CYP2C8 inhibition + 0.6179 61.79%
CYP inhibitory promiscuity + 0.7309 73.09%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Warning 0.4774 47.74%
Eye corrosion - 0.9922 99.22%
Eye irritation + 0.9825 98.25%
Skin irritation + 0.6503 65.03%
Skin corrosion - 0.9530 95.30%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8219 82.19%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.6265 62.65%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.8680 86.80%
Acute Oral Toxicity (c) III 0.3694 36.94%
Estrogen receptor binding + 0.8653 86.53%
Androgen receptor binding + 0.8531 85.31%
Thyroid receptor binding + 0.6211 62.11%
Glucocorticoid receptor binding + 0.9336 93.36%
Aromatase binding + 0.7951 79.51%
PPAR gamma + 0.9421 94.21%
Honey bee toxicity - 0.8563 85.63%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9956 99.56%

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
CHEMBL2581 P07339 Cathepsin D 97.57% 98.95%
CHEMBL242 Q92731 Estrogen receptor beta 93.42% 98.35%
CHEMBL1951 P21397 Monoamine oxidase A 93.33% 91.49%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 91.80% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.72% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.13% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 89.96% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.49% 99.23%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.99% 91.71%
CHEMBL230 P35354 Cyclooxygenase-2 87.66% 89.63%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.89% 99.15%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 86.70% 96.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.17% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 84.89% 93.31%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.53% 94.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.22% 93.10%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.18% 82.69%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.05% 89.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.88% 93.03%
CHEMBL2535 P11166 Glucose transporter 80.86% 98.75%

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.
Musa acuminata

Cross-Links

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PubChem 10733280
LOTUS LTS0038674
wikiData Q104956622