Target Poor or Non Binder(s) Information
Target General Information | Top | ||||
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Target ID | T15610 | Target Info | |||
Target Name | Puromycin-sensitive aminopeptidase (NPEPPS) | ||||
Synonyms |
NPEPPS
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Target Type | Clinical trial Target | ||||
Gene Name | NPEPPS | ||||
Biochemical Class | Peptidase | ||||
UniProt ID |
Poor Binders of This Target (in total, 8 binders) | Download | Top | |||
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Compound Name |
Chembl4161744
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Investigative | Compound Info | ||
Synonyms |
BDBM50277150
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Activity |
IC50 = 53000 nM
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[1] | |||
Compound Name |
Chembl4173240
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Investigative | Compound Info | ||
Synonyms |
BDBM50277157
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Activity |
IC50 = 53000 nM
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[1] | |||
Compound Name |
Methyl 4-anilino-2,6-bis(4-nitrophenyl)-1-phenyl-3,6-dihydro-2H-pyridine-5-carboxylate
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Investigative | Compound Info | ||
Synonyms |
CHEMBL3740158; BDBM50499704
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Activity |
IC50 = 68810 nM
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[2] | |||
Compound Name |
Ethyl 4-anilino-2-(4-bromophenyl)-1-phenyl-6-thiophen-2-yl-3,6-dihydro-2H-pyridine-5-carboxylate
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Investigative | Compound Info | ||
Synonyms |
CHEMBL3741344; BDBM50499713
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Activity |
IC50 = 80970 nM
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[2] | |||
Compound Name |
Ethyl 4-anilino-1-phenyl-2,6-dipyridin-2-yl-3,6-dihydro-2H-pyridine-5-carboxylate
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Investigative | Compound Info | ||
Synonyms |
CHEMBL3741701; BDBM50499701
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Activity |
IC50 = 92510 nM
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[2] | |||
Compound Name |
Ethyl 4-oxo-1-phenyl-2,6-dipyridin-2-ylpiperidine-3-carboxylate
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Investigative | Compound Info | ||
Synonyms |
CHEMBL3740862; BDBM50499703
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Activity |
IC50 = 92870 nM
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[2] | |||
Compound Name |
Ethyl 4-anilino-2-(4-chlorophenyl)-1-phenyl-6-pyridin-3-yl-3,6-dihydro-2H-pyridine-5-carboxylate
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Investigative | Compound Info | ||
Synonyms |
CHEMBL3741419; BDBM50499711
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Activity |
IC50 = 98190 nM
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[2] | |||
Compound Name |
Chembl4169814
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Investigative | Compound Info | ||
Synonyms |
BDBM50277159
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Activity |
IC50 ~ 100000 nM
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[1] | |||
Click to Show/Hide the Information of All Poor Binders |
References | Top | ||||
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REF 1 | Puromycin based inhibitors of aminopeptidases for the potential treatment of hematologic malignancies. Eur J Med Chem. 2017 Oct 20;139:325-336. | ||||
REF 2 | Highly functionalized tetrahydropyridines are cytotoxic and selective inhibitors of human puromycin sensitive aminopeptidase. Eur J Med Chem. 2015 Dec 1;106:26-33. |
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