Amaroridine

Details

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Internal ID ae3893c4-f507-4e1f-bb44-969bd23793ec
Taxonomy Alkaloids and derivatives > Indolonaphthyridine alkaloids
IUPAC Name 11-methoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one
SMILES (Canonical) COC1=CC=CC2=C1C3=C4N2C(=O)C=CC4=NC=C3
SMILES (Isomeric) COC1=CC=CC2=C1C3=C4N2C(=O)C=CC4=NC=C3
InChI InChI=1S/C15H10N2O2/c1-19-12-4-2-3-11-14(12)9-7-8-16-10-5-6-13(18)17(11)15(9)10/h2-8H,1H3
InChI Key CJMWTIHSXJKZRH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H10N2O2
Molecular Weight 250.25 g/mol
Exact Mass 250.074227566 g/mol
Topological Polar Surface Area (TPSA) 44.10 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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CHEMBL513557

2D Structure

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2D Structure of Amaroridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.5969 59.69%
Blood Brain Barrier + 0.8946 89.46%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8241 82.41%
OATP2B1 inhibitior - 0.8657 86.57%
OATP1B1 inhibitior + 0.9571 95.71%
OATP1B3 inhibitior + 0.9585 95.85%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8348 83.48%
BSEP inhibitior - 0.5752 57.52%
P-glycoprotein inhibitior - 0.8354 83.54%
P-glycoprotein substrate - 0.6820 68.20%
CYP3A4 substrate + 0.5765 57.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8321 83.21%
CYP3A4 inhibition + 0.5957 59.57%
CYP2C9 inhibition - 0.8179 81.79%
CYP2C19 inhibition + 0.5729 57.29%
CYP2D6 inhibition - 0.7633 76.33%
CYP1A2 inhibition + 0.9586 95.86%
CYP2C8 inhibition + 0.5913 59.13%
CYP inhibitory promiscuity + 0.5282 52.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9423 94.23%
Carcinogenicity (trinary) Non-required 0.4569 45.69%
Eye corrosion - 0.9836 98.36%
Eye irritation + 0.5313 53.13%
Skin irritation - 0.8452 84.52%
Skin corrosion - 0.9716 97.16%
Ames mutagenesis + 0.6846 68.46%
Human Ether-a-go-go-Related Gene inhibition - 0.5870 58.70%
Micronuclear + 0.8200 82.00%
Hepatotoxicity - 0.6341 63.41%
skin sensitisation - 0.9028 90.28%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.6577 65.77%
Acute Oral Toxicity (c) III 0.4689 46.89%
Estrogen receptor binding + 0.8069 80.69%
Androgen receptor binding - 0.5176 51.76%
Thyroid receptor binding + 0.7092 70.92%
Glucocorticoid receptor binding + 0.8278 82.78%
Aromatase binding + 0.8439 84.39%
PPAR gamma - 0.5103 51.03%
Honey bee toxicity - 0.8890 88.90%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity - 0.7401 74.01%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.27% 85.14%
CHEMBL2581 P07339 Cathepsin D 95.19% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.16% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.28% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.13% 95.56%
CHEMBL2535 P11166 Glucose transporter 94.04% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.79% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.28% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.05% 93.99%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.44% 96.00%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 88.51% 96.47%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.79% 99.23%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.90% 97.36%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.12% 94.03%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.60% 100.00%
CHEMBL1907 P15144 Aminopeptidase N 81.93% 93.31%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.99% 96.67%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.65% 89.62%

Plants that contains it

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Cross-Links

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PubChem 14463028
NPASS NPC174672
LOTUS LTS0079269
wikiData Q104391951