Goniopedaline

Details

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Internal ID 1fcbb21b-8c54-458a-9d3c-77d6b9307fd7
Taxonomy Alkaloids and derivatives > Aristolactams
IUPAC Name 14-hydroxy-13,15-dimethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2,4,6,8,12,14-heptaen-11-one
SMILES (Canonical) COC1=C(C(=C2C3=C1C4=CC=CC=C4C=C3NC2=O)OC)O
SMILES (Isomeric) COC1=C(C(=C2C3=C1C4=CC=CC=C4C=C3NC2=O)OC)O
InChI InChI=1S/C17H13NO4/c1-21-15-11-9-6-4-3-5-8(9)7-10-12(11)13(17(20)18-10)16(22-2)14(15)19/h3-7,19H,1-2H3,(H,18,20)
InChI Key UQUSUGQKCAHMQJ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H13NO4
Molecular Weight 295.29 g/mol
Exact Mass 295.08445790 g/mol
Topological Polar Surface Area (TPSA) 67.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.28
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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Aristolactam FII
Goniopetaline
112501-43-6
aristolactam F II
CHEMBL226655
DTXSID50150084
Dibenz(cd,f)indol-4(5H)-one, 2-hydroxy-1,3-dimethoxy-

2D Structure

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2D Structure of Goniopedaline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 + 0.8565 85.65%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.6344 63.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8878 88.78%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.5540 55.40%
P-glycoprotein inhibitior - 0.7380 73.80%
P-glycoprotein substrate - 0.8821 88.21%
CYP3A4 substrate + 0.5872 58.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8343 83.43%
CYP3A4 inhibition - 0.6989 69.89%
CYP2C9 inhibition - 0.9103 91.03%
CYP2C19 inhibition - 0.8398 83.98%
CYP2D6 inhibition - 0.8000 80.00%
CYP1A2 inhibition + 0.8258 82.58%
CYP2C8 inhibition + 0.5141 51.41%
CYP inhibitory promiscuity + 0.5463 54.63%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.4678 46.78%
Eye corrosion - 0.9935 99.35%
Eye irritation - 0.5186 51.86%
Skin irritation - 0.8534 85.34%
Skin corrosion - 0.9721 97.21%
Ames mutagenesis + 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7323 73.23%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.9388 93.88%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.7371 73.71%
Acute Oral Toxicity (c) III 0.4600 46.00%
Estrogen receptor binding + 0.7996 79.96%
Androgen receptor binding + 0.6677 66.77%
Thyroid receptor binding + 0.6693 66.93%
Glucocorticoid receptor binding + 0.8804 88.04%
Aromatase binding + 0.7432 74.32%
PPAR gamma + 0.8414 84.14%
Honey bee toxicity - 0.9399 93.99%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.7781 77.81%

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 99.75% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.76% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.10% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.65% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 90.36% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.59% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.47% 99.23%
CHEMBL4208 P20618 Proteasome component C5 88.28% 90.00%
CHEMBL1937 Q92769 Histone deacetylase 2 88.10% 94.75%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.57% 94.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.14% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.92% 99.15%
CHEMBL2535 P11166 Glucose transporter 86.59% 98.75%
CHEMBL2581 P07339 Cathepsin D 86.01% 98.95%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.59% 96.67%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.98% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.80% 92.62%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 81.46% 96.47%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 81.12% 94.23%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.05% 94.08%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.78% 89.00%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 80.01% 81.14%

Plants that contains it

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Cross-Links

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PubChem 183523
NPASS NPC22928
ChEMBL CHEMBL226655
LOTUS LTS0268895
wikiData Q83016017