The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
27100031 |
85 |
A structural insight into the P1S1 binding mode of diaminoethylphosphonic and phosphinic acids, selective inhibitors of alanine aminopeptidases. |
Wroclaw University of Technology |
26629857 |
44 |
Novel leucine ureido derivatives as aminopeptidase N inhibitors. Design, synthesis and activity evaluation. |
Fudan University |
26463133 |
22 |
Influence of polar side chains modifications on the dual enkephalinase inhibitory activity and conformation of human opiorphin, a pain perception related peptide. |
Institute of Advanced Chemistry of Catalonia (Iqac-Csic) |
26241877 |
7 |
Modulation of disulfide dual ENKephalinase inhibitors (DENKIs) activity by a transient N-protection for pain alleviation by oral route. |
Pharmaleads |
25982416 |
43 |
Exploring S1 plasticity and probing S1' subsite of mammalian aminopeptidase N/CD13 with highly potent and selective aminobenzosuberone inhibitors. |
Universit£ |
25192493 |
57 |
Structure-guided, single-point modifications in the phosphinic dipeptide structure yield highly potent and selective inhibitors of neutral aminopeptidases. |
University of Athens |
24927250 |
18 |
New orally active dual enkephalinase inhibitors (DENKIs) for central and peripheral pain treatment. |
Pharmaleads |
23860593 |
17 |
Novelß-dicarbonyl derivatives as inhibitors of aminopeptidase N (APN). |
Shandong University |
23664876 |
1 |
Solid phase synthesis and biological evaluation of probestin as an angiogenesis inhibitor. |
The University of Oklahoma Health Sciences Center |
23528299 |
4 |
Discovery of a synthetic Aminopeptidase N inhibitor LB-4b as a potential anticancer agent. |
Shandong University |
23510562 |
30 |
Novel indoline-2,3-dione derivatives as inhibitors of aminopeptidase N (APN). |
Shandong University |
23428964 |
9 |
Selective aminopeptidase-N (CD13) inhibitors with relevance to cancer chemotherapy. |
Universit£ |
23453219 |
29 |
Novel leucine ureido derivatives as inhibitors of aminopeptidase N (APN). |
Shandong University |
19757839 |
26 |
The replacement of His(4) in angiotensin IV by conformationally constrained residues provides highly potent and selective analogues. |
Vrije Universiteit Brussel |
24900417 |
59 |
Development of Synthetic Aminopeptidase N/CD13 Inhibitors to Overcome Cancer Metastasis and Angiogenesis. |
TBA |
22796349 |
34 |
Rapid and efficient synthesis of a novel series of substituted aminobenzosuberone derivatives as potent, selective, non-peptidic neutral aminopeptidase inhibitors. |
Universit£ |
21780776 |
40 |
Remarkable potential of thea-aminophosphonate/phosphinate structural motif in medicinal chemistry. |
Wroclaw University of Technology |
22607877 |
38 |
Design, synthesis and biological evaluation of novel amino acid ureido derivatives as aminopeptidase N/CD13 inhibitors. |
Shandong University |
24900367 |
16 |
Proposed Bioactive Conformations of Opiorphin, an Endogenous Dual APN/NEP Inhibitor. |
TBA |
22224710 |
44 |
Structure-activity relationship study of opiorphin, a human dual ectopeptidase inhibitor with antinociceptive properties. |
Institute of Advanced Chemistry of Catalonia (Iqac-Csic) |
19822427 |
21 |
Inhibitors of bacterial N-succinyl-L,L-diaminopimelic acid desuccinylase (DapE) and demonstration of in vitro antimicrobial activity. |
Loyola University |
17331715 |
19 |
Synthesis, biological evaluation and structural determination of beta-aminoacyl-containing cyclic hydrazine derivatives as dipeptidyl peptidase IV (DPP-IV) inhibitors. |
Korea Research Institute of Chemical Technology |
15582436 |
7 |
N-hydroxy-2-(naphthalene-2-ylsulfanyl)-acetamide, a novel hydroxamic acid-based inhibitor of aminopeptidase N and its anti-angiogenic activity. |
Sejong University |
11585456 |
8 |
Long lasting antinociceptive properties of enkephalin degrading enzyme (NEP and APN) inhibitor prodrugs. |
University of Paris |
7909847 |
33 |
Investigation of the active site of aminopeptidase A using a series of new thiol-containing inhibitors. |
University of Paris |
12873488 |
11 |
Design, synthesis and antimalarial activity of novel, quinoline-based, zinc metallo-aminopeptidase inhibitors. |
Universit£ |
10098663 |
81 |
Nonpeptide small-molecular inhibitors of dipeptidyl peptidase IV: N-phenylphthalimide analogs. |
University of Tokyo |
| 40 |
Pseudopeptide inhibitors of aminopeptidases containing the [CH(CN)NH] surrogate as a transition-state MIMIC |
TBA |
21911297 |
40 |
Design, synthesis and biological evaluation of novel 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives as aminopeptidase N/CD13 inhibitors. |
Shandong University |
21802307 |
64 |
Novel aminopeptidase N (APN/CD13) inhibitors derived from chloramphenicol amine. |
Shandong University |
21476495 |
31 |
Potent macrocyclic inhibitors of insulin-regulated aminopeptidase (IRAP) by olefin ring-closing metathesis. |
Uppsala University |
21306895 |
46 |
Discovery ofß-aminoacyl containing thiazolidine derivatives as potent and selective dipeptidyl peptidase IV inhibitors. |
Korea Research Institute of Chemical Technology |
21292493 |
23 |
Amino-benzosuberone: a novel warhead for selective inhibition of human aminopeptidase-N/CD13. |
Merck Sharpe and Dohme |
21047126 |
51 |
Disulfide cyclized tripeptide analogues of angiotensin IV as potent and selective inhibitors of insulin-regulated aminopeptidase (IRAP). |
Uppsala University |
20129718 |
32 |
Novel cyclic-imide peptidomimetics as aminopeptidase N inhibitors. Structure-based design, chemistry and activity evaluation. II. |
Shandong University |
20347318 |
49 |
New aromatic monoesters of alpha-aminoaralkylphosphonic acids as inhibitors of aminopeptidase N/CD13. |
Wroclaw University of Technology |
18718763 |
50 |
Synthesis of new sulfonyl pyrrolidine derivatives as matrix metalloproteinase inhibitors. |
Shandong University |
18556208 |
48 |
Ligands to the (IRAP)/AT4 receptor encompassing a 4-hydroxydiphenylmethane scaffold replacing Tyr2. |
Uppsala University |
18440232 |
38 |
Design, synthesis and evaluation of novel sulfonyl pyrrolidine derivatives as matrix metalloproteinase inhibitors. |
Shandong University |
18362041 |
59 |
Design, synthesis and preliminary evaluation of novel pyrrolidine derivatives as matrix metalloproteinase inhibitors. |
Shandong University |
17270439 |
23 |
Novel hydroxamic acid-related phosphinates: inhibition of neutral aminopeptidase N (APN). |
Wroclaw University of Technology |
31251594 |
57 |
Novel Human Aminopeptidase N Inhibitors: Discovery and Optimization of Subsite Binding Interactions. |
Monash University |
10090787 |
25 |
Structure-activity relationship of diaryl phosphonate esters as potent irreversible dipeptidyl peptidase IV inhibitors. |
University of Antwerp (Uia) |
30537832 |
7 |
Hydroxamic Acid Inhibitors Provide Cross-Species Inhibition of Plasmodium M1 and M17 Aminopeptidases. |
Monash University |
30737134 |
52 |
Leucine ureido derivatives as aminopeptidase N inhibitors using click chemistry. Part II. |
Shandong University |
22707871 |
12 |
Kinetic studies of novel inhibitors of endomorphin degrading enzymes. |
TBA |
18386881 |
38 |
Beta-homo-amino acid scan of angiotensin IV. |
Vrije Universiteit Brussel |
9464355 |
59 |
Novel potent nonpeptide aminopeptidase N inhibitors with a cyclic imide skeleton. |
University of Tokyo |
29630364 |
63 |
Design of Aminopeptidase N Inhibitors as Anti-cancer Agents. |
Jadavpur University |
29202398 |
17 |
Synthesis and biological characterization of ubenimex-fluorouracil conjugates for anti-cancer therapy. |
Shandong University |
28803047 |
20 |
Puromycin based inhibitors of aminopeptidases for the potential treatment of hematologic malignancies. |
University of Minnesota |
29859750 |
56 |
Novel leucine ureido derivatives as aminopeptidase N inhibitors using click chemistry. |
Shandong University |
1738140 |
26 |
alpha-Keto amide inhibitors of aminopeptidases. |
University of Wisconsin-Madison |
28442252 |
62 |
Approaches towards the development of chimeric DPP4/ACE inhibitors for treating metabolic syndrome. |
Ranbaxy Laboratories |