11 Results for "

dehydropeptidase-I

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "dehydropeptidase-I" in MCE Product Catalog:

7
7 Publications Verification
Cat. No.: HY-A0166
CAS No.: 82009-34-5
Synonyms: MK0791
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Cilastatin (MK0791) is a reversible, competitive renal dehydropeptidase I inhibitor with an IC50 of 0.1 μM. Cilastatin inhibits the bacterial metallob-lactamase enzyme CphA with an IC50 of 178 μM. Cilastatin is an antibacterial adjunct .
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7
7 Publications Verification
Cat. No.: HY-A0166A
CAS No.: 81129-83-1
Synonyms: MK0791 sodium
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Cilastatin sodium (MK0791 sodium) is a reversible, competitive renal dehydropeptidase I inhibitor with an IC50 of 0.1 μM. Cilastatin sodium inhibits the bacterial metallob-lactamase enzyme CphA with an IC50 of 178 μM. Cilastatin sodium is an antibacterial adjunct .
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Cat. No.: HY-B1127
CAS No.: 3440-28-6
Synonyms: N-Benzoyl-β-alanine
Target:  

Antibiotic Bacterial

Research Areas:  

Infection Endocrinology

Betamipron (N-benzoyl-β-alanine) is a carbapenem β-lactam antibiotic with antibacterial activity against most Gram-positive and Gram-negative aerobic and anaerobic bacteria. Betamipron can target and inhibit renal organic anion transporters, alleviate renal injury caused by Cisplatin (HY-17394), without interfering with the biological activity of cisplatin. Betamipron is often used in combination with panipenem, which can attenuate the renal effects induced by panipenem and slightly promote the proliferation of Clostridium difficile in the cecum. Betamipron can be used in studies related to renal injury and bacterial infection .
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Cat. No.: HY-A0166S
CAS No.: 2738376-83-3
Synonyms: MK0791-15N,d3
Cilastatin- 15N,d3 is a 15N-labeled and deuterium labeled Cilastatin. Cilastatin (MK0791) is a reversible, competitive renal dehydropeptidase I inhibitor with an IC50 of 0.1 μM. Cilastatin inhibits the bacterial metallob-lactamase enzyme CphA with an IC50 of 178 μM. Cilastatin is an antibacterial adjunct .
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Cat. No.: HY-P3820
[Dehydro-Pro4] Substance P (4-11) is a peptide fragment of Substance P. Substance P is a peptide mainly secreted by neurons. Substance P takes part in many biological processes, including nociception, inflammation and immunity .
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Cat. No.: HY-P81486
Synonyms: DPEP1; MDP; RDP; Dipeptidase 1; dehydropeptidase-I; Microsomal dipeptidase; Renal dipeptidase

Host:  

Rabbit

Application:  

IHC-P

Reactivity:  

Human

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Cat. No.: HY-P81486A
Synonyms: DPEP1; MDP; RDP; Dipeptidase 1; dehydropeptidase-I; Microsomal dipeptidase; Renal dipeptidase

Host:  

Rabbit

Application:  

IHC-P

Reactivity:  

Human

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Cat. No.: HY-A0166R
CAS No.: 82009-34-5
Synonyms: MK0791 (Standard)
Research Areas:  

Infection

Cilastatin (Standard) is the analytical standard of Cilastatin. This product is intended for research and analytical applications. Cilastatin (MK0791) is a reversible, competitive renal dehydropeptidase I inhibitor with an IC50 of 0.1 μM. Cilastatin inhibits the bacterial metallob-lactamase enzyme CphA with an IC50 of 178 μM. Cilastatin is an antibacterial adjunct .
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Cat. No.: HY-A0166AR
CAS No.: 81129-83-1
Synonyms: MK0791 sodium (Standard)
Research Areas:  

Infection

Cilastatin (sodium) (Standard) is the analytical standard of Cilastatin (sodium). This product is intended for research and analytical applications. Cilastatin sodium (MK0791 sodium) is a reversible, competitive renal dehydropeptidase I inhibitor with an IC50 of 0.1 μM. Cilastatin sodium inhibits the bacterial metallob-lactamase enzyme CphA with an IC50 of 178 μM. Cilastatin sodium is an antibacterial adjunct[1][2][3].
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Cat. No.: HY-P70003
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: DPEP1; HRDP; Dipeptidase 1; MDP; Microsomal Dipeptidase; RDP; Dipeptidase 1 (Renal); Testicular Tissue Protein Li 57; dehydropeptidase-I; Dipeptidase; Renal Dipeptidase; MBD1; Beta-Lactamase
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-111282
CAS No.: 85394-14-5
Target:  

Dipeptidyl Peptidase

Research Areas:  

Endocrinology

MK-789 is a competitive reversible inhibitor of dehydropeptidase I (DHP-I). MK-789 competitively blocks the entry of N-formimidoylthienamycin into proximal tubular cells, thereby inhibiting its renal metabolism. MK-789 shifts the renal excretion pathway of N-formimidoylthienamycin to glomerular filtration only, increasing its urinary recovery rate and renal clearance. MK-789 is applicable to studies on renal metabolism and pharmacokinetics .
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