6-Hydroxy-2,5-dimethoxy-7-phenylphenalen-1-one

Details

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Internal ID 6c5297d2-edc7-4336-8b97-5efdbf7a2c80
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 6-hydroxy-2,5-dimethoxy-7-phenylphenalen-1-one
SMILES (Canonical) COC1=CC2=CC(=C(C3=C(C=CC(=C23)C1=O)C4=CC=CC=C4)O)OC
SMILES (Isomeric) COC1=CC2=CC(=C(C3=C(C=CC(=C23)C1=O)C4=CC=CC=C4)O)OC
InChI InChI=1S/C21H16O4/c1-24-16-10-13-11-17(25-2)21(23)19-14(12-6-4-3-5-7-12)8-9-15(18(13)19)20(16)22/h3-11,23H,1-2H3
InChI Key BVIDEWFIIVXACV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H16O4
Molecular Weight 332.30 g/mol
Exact Mass 332.10485899 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.40
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Hydroxy-2,5-dimethoxy-7-phenylphenalen-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 + 0.8792 87.92%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8531 85.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8968 89.68%
OATP1B3 inhibitior + 0.9673 96.73%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7347 73.47%
P-glycoprotein inhibitior + 0.7861 78.61%
P-glycoprotein substrate - 0.7737 77.37%
CYP3A4 substrate + 0.5130 51.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7244 72.44%
CYP3A4 inhibition + 0.7574 75.74%
CYP2C9 inhibition + 0.7645 76.45%
CYP2C19 inhibition + 0.8280 82.80%
CYP2D6 inhibition - 0.8373 83.73%
CYP1A2 inhibition + 0.8561 85.61%
CYP2C8 inhibition + 0.5797 57.97%
CYP inhibitory promiscuity + 0.8309 83.09%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8873 88.73%
Carcinogenicity (trinary) Non-required 0.4486 44.86%
Eye corrosion - 0.9884 98.84%
Eye irritation + 0.7308 73.08%
Skin irritation - 0.6085 60.85%
Skin corrosion - 0.9835 98.35%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6443 64.43%
Micronuclear + 0.7918 79.18%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8227 82.27%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.5465 54.65%
Acute Oral Toxicity (c) III 0.4645 46.45%
Estrogen receptor binding + 0.9349 93.49%
Androgen receptor binding + 0.8132 81.32%
Thyroid receptor binding + 0.6067 60.67%
Glucocorticoid receptor binding + 0.8382 83.82%
Aromatase binding + 0.6517 65.17%
PPAR gamma + 0.7347 73.47%
Honey bee toxicity - 0.8216 82.16%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5051 50.51%
Fish aquatic toxicity + 0.9930 99.30%

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 98.36% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.20% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.67% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.56% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 96.48% 91.49%
CHEMBL1255126 O15151 Protein Mdm4 90.13% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.93% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.53% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.89% 89.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 84.18% 96.67%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 83.41% 83.57%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.10% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.77% 85.14%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 82.76% 98.21%
CHEMBL2535 P11166 Glucose transporter 81.89% 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.
Haemodorum simplex
Xiphidium caeruleum

Cross-Links

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PubChem 162893020
LOTUS LTS0037399
wikiData Q104946582