16 Results for "

5 nucleotidase Inhibitors

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "5 nucleotidase Inhibitors" in MCE Product Catalog:

24
24 Publications Verification
Cat. No.: HY-125286
CAS No.: 2105904-82-1
Purity:  99.71%
Target:  

CD73

Research Areas:  

Cancer

AB-680 is a highly potent, reversible and selective inhibitor of CD73 (an ecto-nucleotidase), with a Ki of 4.9 pM for hCD73, displays >10,000-fold selectivity over related ecto-nucleotidases CD39. Anti-tumor activity .
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5
5 Cited Publications
Cat. No.: HY-100747
CAS No.: 1802226-78-3
Purity:  98.08%
Target:  

CD73

Research Areas:  

Cancer

PSB-12379, a nucleotide analogue, is a potent Ecto-5'-Nucleotidase (CD73) inhibitor with Kis of 9.03 nM (rat) and 2.21 nM (human) .
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Cat. No.: HY-125539
CAS No.: 16891-85-3
Roridin E is a glucose-6-phosphatase (G6Pase) inhibitor and antibiotic, and is a metabolic byproduct of Roridin A (HY-N9599). Roridin E induces significant oxidative stress, characterized by depletion of glutathione in vivo, induction of hepatic lipid peroxidation, and inhibition of renal superoxide dismutase activity. Roridin E reduces blood glucose levels in rats, but exhibits acute toxicity (which is enhanced when co-administered with linoleic acid (HY-N0729)) and causes hepatotoxicity in male albino mice. Roridin E induces a decrease in total blood protein and increases in the levels of total lipids, γ-glutamyltransferase, alkaline phosphatase, and 5'-nucleotidase. Roridin E can be isolated from molds, and possesses cytostatic and antifungal activities similar to those of Verrucarin A (HY-107426) and Roridin A. Roridin E exhibits in vivo activity in rodents and is commonly used in hepatotoxicity-related studies .
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Cat. No.: HY-100130
CAS No.: 95523-13-0
Purity:  98.06%
Target:  

Adenosine Receptor

Research Areas:  

Neurological Disease

N-[(4-Aminophenyl)methyl]adenosine is a adenosine receptor inhibitor, with Ki of 29 nM for Rat ecto-5′-Nucleotidase.
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Cat. No.: HY-122524S
Purity:  98.54%
7-Methylguanosine-d3 is the deuterium labeled 7-Methylguanosine . 7-Methylguanosine is a novel cNIIIB nucleotidase inhibitor with IC50 value of 87.8 ± 7.5 μM .
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Cat. No.: HY-167710
CAS No.: 941185-83-7
Target:  

Endogenous Metabolite

Research Areas:  

Cancer

CRCD2 is a small molecule NT5C2 nucleotidase inhibitor with enhanced 6-mercaptopurine cytotoxic activity. CRCD2 can effectively reverse 6-mercaptopurine resistance caused by mutations in the NT5C2 gene or non-genetic activation mechanisms. CRCD2 combined with 6-mercaptopurine can enhance its cytotoxic activity in NT5C2 wild-type leukemia, showing its potential in the treatment of acute lymphoblastic leukemia .
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Cat. No.: HY-125286A
Target:  

CD73

Research Areas:  

Cancer

AB-680 ammonium is a highly potent, reversible and selective inhibitor of CD73 (an ecto-nucleotidase), with a Ki of 4.9 pM for hCD73, displays >10,000-fold selectivity over related ecto-nucleotidases CD39. Anti-tumor activity .
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Cat. No.: HY-W095633
CAS No.: 89-02-1
Target:  

CD73

Research Areas:  

Cancer

2,4-Dinitrobenzenesulfonic acid (Compound 3) is a ecto-5'-Nucleotidase (CD73) inhibitor with a Ki value of 63 μM for human and 144 μM for rat. 2,4-Dinitrobenzenesulfonic acid can inhibit the hydrolysis of adenosine monophosphate (AMP) to generate adenosine. 2,4-Dinitrobenzenesulfonic acid can be used for the research of cancer .
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Cat. No.: HY-171805
CAS No.: 1213268-73-5
Target:  

CD73

Research Areas:  

Cancer

PSB-0963 is a selective and competitive ecto-5'-nucleotidase (eN/CD73) inhibitor with a Ki of 150 nM for rat ecto-5'-nucleotidase. PSB-0963 shows high selectivity over other ectonucleotidases (NTPDases 1-3) and P2Y receptors. PSB-0963 can be used for the study of cancer .
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Cat. No.: HY-100747A
Target:  

CD73

Research Areas:  

Cancer

PSB-12379 disodium, a nucleotide analogue, is a potent Ecto-5'-Nucleotidase (CD73) inhibitor with Kis of 9.03 nM (rat) and 2.21 nM (human) .
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Cat. No.: HY-169189
CAS No.: 3037968-61-6
Target:  

CD73

Research Areas:  

Cancer

CD73-IN-18 (compound 35j) is an orally available inhibitor of extracellular 5-nucleotidase (CD73). CD73-IN-18 can be used in anti-cancer research .
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Cat. No.: HY-137717A
Target:  

CD73

Research Areas:  

Cancer

COPCP trisodium (Compound 7a) is a potent and selective ecto-5'-nucleotidase CD73 inhibitor. COPCP trisodium blocks CD73-mediated adenosine production, reducing the inhibitory effect of adenosine on immune cells. COPCP trisodium is promising for research of cancers .
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Cat. No.: HY-175319
Target:  

CD73

Research Areas:  

Cancer

CD73-IN-21 (Compound 12f) is an Ecto-5′-nucleotidase (CD73) inhibitor with Kis of 20 and 302  nM for hCD73 and mCD73, respectively. CD73-IN-21 can be used for cancers like breast cancer research .
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Cat. No.: HY-172801
Target:  

CD73

Research Areas:  

Cancer

PSB-24000 (Compound 27) is a selective ecto-5'-nucleotidase (CD73) inhibitor with a Ki value of 563 nM against human CD73 (Ki= 481 nM at membrane-bound CD73 in triple-negative breast cancer cells). PSB-24000 interferes with CD73's recognition and action on the substrate AMP, and prevents the generation of immunosuppressive and cancer-promoting adenosine from AMP. PSB-24000 is promising for research of cancers .
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Cat. No.: HY-137404
CAS No.: 93839-85-1
Adenosine 5'-O-thiomonophosphate dilithium is a compound that inhibits phosphohydrolase activity and can also serve as a substrate for 5'-nucleotidase.
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Cat. No.: HY-100747R
CAS No.: 1802226-78-3
Research Areas:  

Cancer

PSB-12379 (Standard) is the analytical standard of PSB-12379 (HY-100747). This product is intended for research and analytical applications. PSB-12379, a nucleotide analogue, is a potent Ecto-5'-Nucleotidase (CD73) inhibitor with Kis of 9.03 nM (rat) and 2.21 nM (human) .
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