Goniothalactam

Details

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Internal ID e21ac836-c460-446e-ae70-7d9141f1f061
Taxonomy Alkaloids and derivatives > Aristolactams
IUPAC Name 4-hydroxy-14,15-dimethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one
SMILES (Canonical) COC1=C(C2=C3C=C(C=CC3=CC4=C2C(=C1)C(=O)N4)O)OC
SMILES (Isomeric) COC1=C(C2=C3C=C(C=CC3=CC4=C2C(=C1)C(=O)N4)O)OC
InChI InChI=1S/C17H13NO4/c1-21-13-7-11-14-12(18-17(11)20)5-8-3-4-9(19)6-10(8)15(14)16(13)22-2/h3-7,19H,1-2H3,(H,18,20)
InChI Key UDPCZNQWXHKYPJ-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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CHEMBL228081
204975-46-2

2D Structure

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2D Structure of Goniothalactam

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 + 0.7418 74.18%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6242 62.42%
OATP2B1 inhibitior - 0.8621 86.21%
OATP1B1 inhibitior + 0.8813 88.13%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6070 60.70%
P-glycoprotein inhibitior - 0.7560 75.60%
P-glycoprotein substrate - 0.6224 62.24%
CYP3A4 substrate + 0.5836 58.36%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.8230 82.30%
CYP3A4 inhibition - 0.5561 55.61%
CYP2C9 inhibition - 0.7615 76.15%
CYP2C19 inhibition - 0.8844 88.44%
CYP2D6 inhibition - 0.8127 81.27%
CYP1A2 inhibition + 0.8938 89.38%
CYP2C8 inhibition + 0.6114 61.14%
CYP inhibitory promiscuity + 0.6085 60.85%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4510 45.10%
Eye corrosion - 0.9939 99.39%
Eye irritation + 0.5726 57.26%
Skin irritation - 0.8234 82.34%
Skin corrosion - 0.9730 97.30%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5734 57.34%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.9427 94.27%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.7151 71.51%
Acute Oral Toxicity (c) III 0.4534 45.34%
Estrogen receptor binding + 0.8145 81.45%
Androgen receptor binding + 0.7298 72.98%
Thyroid receptor binding + 0.6662 66.62%
Glucocorticoid receptor binding + 0.8771 87.71%
Aromatase binding + 0.7560 75.60%
PPAR gamma + 0.7947 79.47%
Honey bee toxicity - 0.8739 87.39%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5451 54.51%
Fish aquatic toxicity + 0.8196 81.96%

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 97.96% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 95.15% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.78% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.05% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.45% 94.45%
CHEMBL2535 P11166 Glucose transporter 92.40% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.51% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.52% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.56% 98.95%
CHEMBL4208 P20618 Proteasome component C5 86.22% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 85.72% 90.20%
CHEMBL213 P08588 Beta-1 adrenergic receptor 85.59% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 85.38% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.06% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.66% 99.15%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.89% 89.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.54% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.10% 89.00%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.09% 80.78%

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.
Annona squamosa
Curcuma zedoaria
Fissistigma balansae
Fissistigma glaucescens
Fissistigma oldhamii
Goniothalamus borneensis
Piper macropiper

Cross-Links

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PubChem 10447198
NPASS NPC215747
LOTUS LTS0178227
wikiData Q105270476