Neoamphimedine

Details

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Internal ID 9bd900c6-b41e-4b0c-8b0c-54966f1bca2e
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Pyridoacridines > Pyrido[2,3,4-kl]acridines
IUPAC Name 5-methyl-5,10,20-triazapentacyclo[11.7.1.02,7.09,21.014,19]henicosa-1(20),2(7),3,9,11,13(21),14,16,18-nonaene-6,8-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H11N3O2/c1-22-9-7-12-15(19(22)24)18(23)17-14-11(6-8-20-17)10-4-2-3-5-13(10)21-16(12)14/h2-9H,1H3
InChI Key HHTUKGISODJJKH-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C19H11N3O2
Molecular Weight 313.30 g/mol
Exact Mass 313.085126602 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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neoamphimidine
CHEMBL216600
SCHEMBL14952449
NSC759023
NSC-759023
5-methyl-5,10,20-triazapentacyclo[11.7.1.02,7.09,21.014,19]henicosa-1(20),2(7),3,9,11,13(21),14,16,18-nonaene-6,8-dione

2D Structure

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2D Structure of Neoamphimedine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9829 98.29%
Caco-2 + 0.7631 76.31%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.8620 86.20%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.9387 93.87%
OATP1B3 inhibitior + 0.9596 95.96%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7830 78.30%
P-glycoprotein inhibitior - 0.7753 77.53%
P-glycoprotein substrate - 0.8574 85.74%
CYP3A4 substrate + 0.5997 59.97%
CYP2C9 substrate + 0.5905 59.05%
CYP2D6 substrate - 0.8620 86.20%
CYP3A4 inhibition - 0.8268 82.68%
CYP2C9 inhibition - 0.7999 79.99%
CYP2C19 inhibition - 0.5530 55.30%
CYP2D6 inhibition - 0.9609 96.09%
CYP1A2 inhibition + 0.5090 50.90%
CYP2C8 inhibition + 0.6146 61.46%
CYP inhibitory promiscuity - 0.6105 61.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6046 60.46%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9458 94.58%
Skin irritation - 0.8653 86.53%
Skin corrosion - 0.9649 96.49%
Ames mutagenesis + 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7223 72.23%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.8375 83.75%
skin sensitisation - 0.9303 93.03%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.5918 59.18%
Acute Oral Toxicity (c) III 0.5733 57.33%
Estrogen receptor binding + 0.8794 87.94%
Androgen receptor binding + 0.8410 84.10%
Thyroid receptor binding + 0.6862 68.62%
Glucocorticoid receptor binding + 0.9065 90.65%
Aromatase binding + 0.8064 80.64%
PPAR gamma + 0.7298 72.98%
Honey bee toxicity - 0.9002 90.02%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity - 0.7940 79.40%

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 97.52% 85.14%
CHEMBL2581 P07339 Cathepsin D 96.94% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 96.82% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.04% 89.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 95.89% 96.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 95.47% 99.23%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 95.08% 96.47%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.23% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.01% 86.33%
CHEMBL1781 P11387 DNA topoisomerase I 91.20% 97.00%
CHEMBL2094121 P14867 GABA-A receptor; alpha-1/beta-3/gamma-2 88.92% 95.50%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.95% 85.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.48% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.58% 96.09%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 84.81% 92.67%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.63% 94.42%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 84.04% 95.83%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.68% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.15% 96.00%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 81.58% 100.00%
CHEMBL4040 P28482 MAP kinase ERK2 81.23% 83.82%
CHEMBL240 Q12809 HERG 81.02% 89.76%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.78% 96.25%
CHEMBL255 P29275 Adenosine A2b receptor 80.71% 98.59%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.40% 96.00%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.26% 80.78%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.05% 93.10%

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.
There are no matching plants.

Cross-Links

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PubChem 10041259
LOTUS LTS0208532
wikiData Q105028569