Phalarine

Details

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Internal ID 67ea83b8-37ed-405c-a158-4569f9aeb8bd
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Beta carbolines
IUPAC Name 1-(8-methoxy-21-methyl-11-oxa-6,19,21-triazahexacyclo[10.7.4.01,12.02,10.03,7.013,18]tricosa-2,4,7,9,13,15,17-heptaen-4-yl)-N,N-dimethylmethanamine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H28N4O2/c1-27(2)13-15-12-25-22-19(29-4)11-18-21(20(15)22)23-14-28(3)10-9-24(23,30-18)16-7-5-6-8-17(16)26-23/h5-8,11-12,25-26H,9-10,13-14H2,1-4H3
InChI Key ACLHIKYUUPINNW-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C24H28N4O2
Molecular Weight 404.50 g/mol
Exact Mass 404.22122615 g/mol
Topological Polar Surface Area (TPSA) 52.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Phalarine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9878 98.78%
Caco-2 + 0.6274 62.74%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.5454 54.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8748 87.48%
OATP1B3 inhibitior + 0.9375 93.75%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.6992 69.92%
P-glycoprotein inhibitior + 0.7907 79.07%
P-glycoprotein substrate + 0.6758 67.58%
CYP3A4 substrate + 0.6953 69.53%
CYP2C9 substrate + 0.6075 60.75%
CYP2D6 substrate + 0.6945 69.45%
CYP3A4 inhibition - 0.8612 86.12%
CYP2C9 inhibition - 0.8220 82.20%
CYP2C19 inhibition - 0.7494 74.94%
CYP2D6 inhibition - 0.6147 61.47%
CYP1A2 inhibition - 0.7749 77.49%
CYP2C8 inhibition + 0.4839 48.39%
CYP inhibitory promiscuity - 0.7570 75.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6135 61.35%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.9700 97.00%
Skin irritation - 0.7902 79.02%
Skin corrosion - 0.9317 93.17%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9145 91.45%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8613 86.13%
Respiratory toxicity + 0.9333 93.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.8841 88.41%
Acute Oral Toxicity (c) III 0.6261 62.61%
Estrogen receptor binding + 0.7695 76.95%
Androgen receptor binding + 0.7708 77.08%
Thyroid receptor binding + 0.7607 76.07%
Glucocorticoid receptor binding - 0.4635 46.35%
Aromatase binding + 0.6054 60.54%
PPAR gamma + 0.7485 74.85%
Honey bee toxicity - 0.7228 72.28%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.7420 74.20%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.58% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 98.54% 93.99%
CHEMBL228 P31645 Serotonin transporter 97.59% 95.51%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 95.44% 85.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.97% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.77% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.17% 91.11%
CHEMBL4208 P20618 Proteasome component C5 91.99% 90.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.57% 96.77%
CHEMBL204 P00734 Thrombin 91.29% 96.01%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.89% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.05% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.57% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.36% 95.89%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 88.20% 95.83%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 87.95% 89.44%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.77% 90.24%
CHEMBL255 P29275 Adenosine A2b receptor 87.26% 98.59%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 86.68% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.28% 94.45%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 85.17% 82.38%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.65% 97.14%
CHEMBL1937 Q92769 Histone deacetylase 2 83.96% 94.75%
CHEMBL2535 P11166 Glucose transporter 83.31% 98.75%
CHEMBL3310 Q96DB2 Histone deacetylase 11 82.25% 88.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.15% 90.08%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 80.50% 90.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.43% 96.00%

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.
Phalaris coerulescens

Cross-Links

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PubChem 73232188
LOTUS LTS0205852
wikiData Q104909167