Pterolinus K

Details

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Internal ID 7c6b00bb-5a5e-490b-b7f0-46a309e52cd7
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 7-hydroxy-9-(3-hydroxy-4-methoxyphenyl)-3,6-dimethoxyphenanthrene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H18O7/c1-28-19-5-4-11(6-17(19)25)12-7-15-16(24)10-21(30-3)23(27)22(15)14-9-20(29-2)18(26)8-13(12)14/h4-10,25-26H,1-3H3
InChI Key GKGJEHWLTNMFNY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H18O7
Molecular Weight 406.40 g/mol
Exact Mass 406.10525291 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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RefChem:177117
7-hydroxy-9-(3-hydroxy-4-methoxyphenyl)-3,6-dimethoxyphenanthrene-1,4-dione
CHEMBL1829656

2D Structure

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2D Structure of Pterolinus K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.6627 66.27%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.8104 81.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9265 92.65%
OATP1B3 inhibitior + 0.8417 84.17%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8398 83.98%
P-glycoprotein inhibitior + 0.7344 73.44%
P-glycoprotein substrate - 0.7774 77.74%
CYP3A4 substrate + 0.5567 55.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7787 77.87%
CYP3A4 inhibition - 0.6599 65.99%
CYP2C9 inhibition + 0.5520 55.20%
CYP2C19 inhibition - 0.5338 53.38%
CYP2D6 inhibition - 0.8471 84.71%
CYP1A2 inhibition + 0.8132 81.32%
CYP2C8 inhibition + 0.8126 81.26%
CYP inhibitory promiscuity + 0.6921 69.21%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9038 90.38%
Carcinogenicity (trinary) Non-required 0.4768 47.68%
Eye corrosion - 0.9931 99.31%
Eye irritation - 0.6401 64.01%
Skin irritation - 0.7157 71.57%
Skin corrosion - 0.9635 96.35%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6848 68.48%
Micronuclear + 0.8200 82.00%
Hepatotoxicity - 0.5217 52.17%
skin sensitisation - 0.8632 86.32%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5055 50.55%
Acute Oral Toxicity (c) II 0.4792 47.92%
Estrogen receptor binding + 0.8932 89.32%
Androgen receptor binding + 0.7750 77.50%
Thyroid receptor binding - 0.5690 56.90%
Glucocorticoid receptor binding + 0.7275 72.75%
Aromatase binding - 0.5627 56.27%
PPAR gamma + 0.7471 74.71%
Honey bee toxicity - 0.7974 79.74%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6249 62.49%
Fish aquatic toxicity + 0.9948 99.48%

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
CHEMBL1951 P21397 Monoamine oxidase A 97.82% 91.49%
CHEMBL2581 P07339 Cathepsin D 97.07% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.04% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.84% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.72% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.20% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.54% 94.00%
CHEMBL1907 P15144 Aminopeptidase N 90.83% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.49% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 90.09% 90.20%
CHEMBL2535 P11166 Glucose transporter 89.76% 98.75%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.04% 92.94%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.44% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.09% 96.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 86.90% 92.68%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 86.22% 96.67%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 85.87% 80.78%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.84% 93.03%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.96% 99.15%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.12% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.13% 99.17%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 81.89% 95.53%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.00% 97.28%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.50% 95.89%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 80.31% 92.38%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.23% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 80.22% 94.75%

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.
Pterocarpus santalinus

Cross-Links

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PubChem 53388317
NPASS NPC295977
ChEMBL CHEMBL1829656
LOTUS LTS0093960
wikiData Q105009932