2,3-Dimethoxy-4-phenyl-1H-phenalen-1-one

Details

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Internal ID 1ee46160-c394-4390-b776-2ec779499be1
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 2,3-dimethoxy-4-phenylphenalen-1-one
SMILES (Canonical) COC1=C(C(=O)C2=CC=CC3=C2C1=C(C=C3)C4=CC=CC=C4)OC
SMILES (Isomeric) COC1=C(C(=O)C2=CC=CC3=C2C1=C(C=C3)C4=CC=CC=C4)OC
InChI InChI=1S/C21H16O3/c1-23-20-18-15(13-7-4-3-5-8-13)12-11-14-9-6-10-16(17(14)18)19(22)21(20)24-2/h3-12H,1-2H3
InChI Key NUGBKGKAXZOPHR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H16O3
Molecular Weight 316.30 g/mol
Exact Mass 316.109944368 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.66
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,3-Dimethoxy-4-phenyl-1H-phenalen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8776 87.76%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.8303 83.03%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9447 94.47%
OATP1B3 inhibitior + 0.9841 98.41%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8594 85.94%
P-glycoprotein inhibitior - 0.4344 43.44%
P-glycoprotein substrate - 0.8896 88.96%
CYP3A4 substrate - 0.5636 56.36%
CYP2C9 substrate - 0.8221 82.21%
CYP2D6 substrate - 0.7749 77.49%
CYP3A4 inhibition - 0.5264 52.64%
CYP2C9 inhibition + 0.6106 61.06%
CYP2C19 inhibition + 0.7867 78.67%
CYP2D6 inhibition - 0.9268 92.68%
CYP1A2 inhibition + 0.9165 91.65%
CYP2C8 inhibition - 0.6473 64.73%
CYP inhibitory promiscuity + 0.9108 91.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8863 88.63%
Carcinogenicity (trinary) Non-required 0.4821 48.21%
Eye corrosion - 0.9807 98.07%
Eye irritation + 0.6795 67.95%
Skin irritation - 0.6792 67.92%
Skin corrosion - 0.9864 98.64%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5839 58.39%
Micronuclear + 0.6759 67.59%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.7155 71.55%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.8567 85.67%
Acute Oral Toxicity (c) III 0.4012 40.12%
Estrogen receptor binding + 0.9366 93.66%
Androgen receptor binding + 0.8554 85.54%
Thyroid receptor binding + 0.6737 67.37%
Glucocorticoid receptor binding + 0.7385 73.85%
Aromatase binding + 0.7555 75.55%
PPAR gamma + 0.6884 68.84%
Honey bee toxicity - 0.8603 86.03%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9885 98.85%

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 97.43% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.11% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 93.51% 93.31%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 92.60% 96.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.17% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 91.43% 94.75%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 91.09% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.01% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.86% 82.69%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 85.79% 95.72%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.32% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.12% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.07% 94.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.65% 93.03%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.61% 92.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.59% 96.00%
CHEMBL2535 P11166 Glucose transporter 80.06% 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.
Aesculus hippocastanum
Andrographis viscosula
Anigozanthos preissii
Cyphanthera albicans
Diospyros canaliculata
Euclea crispa
Lindera obtusiloba
Senna spectabilis
Tiliacora acuminata
Verbascum chaixii subsp. austriacum

Cross-Links

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PubChem 85730244
NPASS NPC152331
LOTUS LTS0012214
wikiData Q105185858