5-Hydroxy-6-methoxy-7-phenyl-1H-phenalen-1-one

Details

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Internal ID dca4d643-5ec5-4081-a74c-2adef4840c51
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 5-hydroxy-6-methoxy-7-phenylphenalen-1-one
SMILES (Canonical) COC1=C(C=C2C=CC(=O)C3=C2C1=C(C=C3)C4=CC=CC=C4)O
SMILES (Isomeric) COC1=C(C=C2C=CC(=O)C3=C2C1=C(C=C3)C4=CC=CC=C4)O
InChI InChI=1S/C20H14O3/c1-23-20-17(22)11-13-7-10-16(21)15-9-8-14(19(20)18(13)15)12-5-3-2-4-6-12/h2-11,22H,1H3
InChI Key YBNVZTRILGRXEI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H14O3
Molecular Weight 302.30 g/mol
Exact Mass 302.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.43
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-6-methoxy-7-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 + 0.7772 77.72%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8414 84.14%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.9355 93.55%
OATP1B3 inhibitior + 0.9800 98.00%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8111 81.11%
P-glycoprotein inhibitior - 0.6504 65.04%
P-glycoprotein substrate - 0.8989 89.89%
CYP3A4 substrate + 0.5131 51.31%
CYP2C9 substrate - 0.6037 60.37%
CYP2D6 substrate - 0.7728 77.28%
CYP3A4 inhibition - 0.5986 59.86%
CYP2C9 inhibition + 0.8913 89.13%
CYP2C19 inhibition + 0.7622 76.22%
CYP2D6 inhibition - 0.9136 91.36%
CYP1A2 inhibition + 0.8505 85.05%
CYP2C8 inhibition - 0.6450 64.50%
CYP inhibitory promiscuity + 0.6944 69.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8773 87.73%
Carcinogenicity (trinary) Warning 0.3805 38.05%
Eye corrosion - 0.9728 97.28%
Eye irritation + 0.7424 74.24%
Skin irritation + 0.5693 56.93%
Skin corrosion - 0.9789 97.89%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7750 77.50%
Micronuclear + 0.7025 70.25%
Hepatotoxicity + 0.5878 58.78%
skin sensitisation - 0.8354 83.54%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.4500 45.00%
Acute Oral Toxicity (c) III 0.6311 63.11%
Estrogen receptor binding + 0.8722 87.22%
Androgen receptor binding + 0.8789 87.89%
Thyroid receptor binding + 0.5800 58.00%
Glucocorticoid receptor binding + 0.8211 82.11%
Aromatase binding + 0.8022 80.22%
PPAR gamma + 0.8461 84.61%
Honey bee toxicity - 0.9204 92.04%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9850 98.50%

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 98.93% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.67% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.47% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.65% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.73% 99.15%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 88.26% 96.67%
CHEMBL1951 P21397 Monoamine oxidase A 86.17% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.28% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 85.12% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.86% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.61% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.91% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.61% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.50% 95.50%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 82.17% 80.78%
CHEMBL2535 P11166 Glucose transporter 80.40% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.40% 93.99%
CHEMBL4208 P20618 Proteasome component C5 80.35% 90.00%

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
Strelitzia reginae
Tiliacora acuminata
Verbascum chaixii subsp. austriacum

Cross-Links

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PubChem 85730238
NPASS NPC3973
LOTUS LTS0110309
wikiData Q105345934