373 Results for "

parasite

" in MedChemExpress (MCE) Product Catalog:
Products (373)

373 Results for "parasite" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-13832
CAS No.: 95233-18-4
Purity:  99.75%
Synonyms: Atavaquone
Research Areas:  

Infection Cancer

Atovaquone (Atavaquone) is a potent, selective and orally active inhibitor of the parasite’s mitochondrial cytochrome bc1 complex. Atovaquone is against human and P. falciparum cytochrome bc1 activity with IC50 values of 460 nM and 2.0 nM, respectively. Atovaquone is an antimalarial agent and has the potential for the investigation of neumocystis pneumonia, toxoplasmosis, malaria, and babesia .
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4
4 Cited Publications
Cat. No.: HY-N0841
CAS No.: 25514-31-2
Synonyms: Dihydrobrusatol; NSC310616
Bruceine A (Dihydrobrusatol) is a natural quassinoid. Bruceine A is an inhibitor of parasites, NF-κB, and PFKFB4 (Kd: 44 nM). Bruceine A is an activator of P38α MAPK. Bruceine A has antiparasitic activity. Bruceine A has antitumor activity and inhibits cancer cell migration. Bruceine A blocks the cell cycle and induces apoptosis. Bruceine A can be used in parasites, pancreatic cancer, and breast cancer research .
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4
4 Cited Publications
Cat. No.: HY-B0291
CAS No.: 53716-50-0
Target:  

Parasite

Research Areas:  

Infection Cancer

Oxfendazole is a sulfoxide form of fenbendazole that is effective when taken orally. Oxfendazole fights parasites and has tumor-promoting activity .
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4
4 Cited Publications
Cat. No.: HY-14989
CAS No.: 502487-67-4
Purity:  98.24%
Synonyms: NSC 722041
Research Areas:  

Infection

SQ109 is a potent inhibitor of the trypomastigote form of the parasite, with IC50 for cell killing of 50±8 nM. SQ109, targets MmpL3, is an antitubercular agent.
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3
3 Cited Publications
Cat. No.: HY-B0175
CAS No.: 69004-03-1
Synonyms: BAY-i 9142
Target:  

Parasite Antibiotic

Research Areas:  

Infection

Toltrazuril (BAY-i 9142) is an antiprotozoal agent that acts upon Coccidia parasites.
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3
3 Cited Publications
Cat. No.: HY-101397
CAS No.: 16220-07-8
Purity:  99.05%
Allopurinol riboside, a metabolite of allopurinol, shows potent activities against parasites.
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3
3 Cited Publications
Cat. No.: HY-12785
CAS No.: 54029-12-8
Purity:  99.20%
Synonyms: Ricobendazole; Albendazole oxide
Target:  

Parasite

Research Areas:  

Infection

Albendazole sulfoxide (Ricobendazole), the main active metabolite of Albendazole, exhibits anti-parasite effect against Echinococcus multilocularis Metacestodes .
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3
3 Cited Publications
Cat. No.: HY-136065
CAS No.: 42494-73-5
Purity:  ≥98.0%
bpV(phen), a insulin-mimetic agent, is a potent protein tyrosine phosphatase (PTP) and PTEN inhibitor with IC50s of 38 nM, 343 nM and 920 nM for PTEN, PTP-β and PTP-1B, respectively. bpV(phen) inhibits proliferation of the protozoan parasite Leishmania in vitro. bpV(phen) strongly induces the secretion of a large number of chemokines and pro-inflammatory cytokines, and it activates a Th1-type pathway (IL-12, IFNγ). bpV(phen) can also induce cell apoptosis, and has anti-angiogenic and anti-tumor activity .
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3
3 Cited Publications
Cat. No.: HY-122818
CAS No.: 171202-16-7
Purity:  ≥98.0%
Synonyms: Bisperoxovanadium(phen) trihydrate
BpV(phen) trihydrate, a insulin-mimetic agent, is a potent protein tyrosine phosphatase (PTP) and PTEN inhibitor with IC50s of 38 nM, 343 nM and 920 nM for PTEN, PTP-β and PTP-1B, respectively. BpV(phen) trihydrate inhibits proliferation of the protozoan parasite Leishmania in vitro. bpV(phen) trihydrate strongly induces the secretion of a large number of chemokines and pro-inflammatory cytokines, and it activates a Th1-type pathway (IL-12, IFNγ). BpV(phen) trihydrate can also induce cell apoptosis, and has anti-angiogenic and anti-tumor activity .
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2
2 Cited Publications
Cat. No.: HY-B0148
CAS No.: 105462-24-6
Synonyms: Risedronate
Target:  

Parasite Apoptosis

Research Areas:  

Infection Metabolic Disease Cancer

Risedronic acid (Risedronate) is a bisphosphonate and potent antiresorptive agent. Risedronic acid induces Apoptosis. Risedronic acid inhibits the transfer of farnesyl pyrophosphate groups to parasite proteins. Risedronic acid inhibits osteoclast-mediated bone resorption and alters bone metabolism. Risedronic acid inhibits blood-stage Plasmodium falciparum (IC50 of 20.3 μM) .
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2
2 Cited Publications
Cat. No.: HY-17592A
CAS No.: 844-26-8
Target:  

Parasite

Research Areas:  

Infection

Bithionol sulfoxide is an anti-infection agent for parasites. Bithionol sulfoxide has mutagenic activity. Bithionol sulfoxide can be used in the research of parasite infection, such as paragonimiasis, flukes andcestodes infection .
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2
2 Cited Publications
Cat. No.: HY-P990212
Anti-Mouse IL-6 Antibody (MP5-20F3) is an anti-mouse IL-6 IgG1 monoclonal antibody. Anti-Mouse IL-6 Antibody (MP5-20F3) reshapes the tumor microenvironment by blocking IL-6. Anti-Mouse IL-6 Antibody (MP5-20F3) can inhibit the STAT3 pathway and enhance T cell infiltration. Anti-Mouse IL-6 Antibody (MP5-20F3) can be used for researches on inflammation and infection conditions such as malignant pleural effusion (MPE) .
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2
2 Cited Publications
Cat. No.: HY-100184
CAS No.: 1282041-94-4
Purity:  99.92%
Research Areas:  

Infection

DSM265 is a long-duration inhibitor of P. falciparum dihydroorotate dehydrogenase (PfDHODH) with an IC50 of 8.9 nM. DSM265 can also inhibit the growth of Pf3D7 parasites with an EC50 of 4.3 nM .
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2
2 Cited Publications
Cat. No.: HY-B1916
CAS No.: 24916-51-6
Synonyms: Spiramycin B; Spiramycin II; Foromacidin B
Research Areas:  

Infection

Acetylspiramycin (Spiramycin B) is an effective oral macrolide antibiotic produced by Streptomyces, It can inhibit the splenic lymphocyte transformation induced by phytohemagglutinin (PHA), LPS (HY-D1056) and antigen, reduce the procoagulant activity of macrophages, have good antibacterial effect on gram-positive bacteria, and is also an effective antigenic insect agent, which can be used to fight parasitic infection .
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2
2 Cited Publications
Cat. No.: HY-119046
CAS No.: 1073969-18-2
Purity:  99.12%
Target:  

HSP Parasite

Research Areas:  

Infection

SNX-0723 is a potent Hsp90 Inhibitor with anti-Plasmodium activity. SNX-0723 shows high binding affinity for HsHsp90 and PfHsp90 with Kis of 4.4 and 47 nM, respectively. SNX-0723 inhibits liver-stage P. berghei ANKA parasites with the EC50 of 3.3 μM .
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2
2 Cited Publications
Cat. No.: HY-B0119
CAS No.: 115436-72-1
Synonyms: Risedronate sodium
Target:  

Parasite Apoptosis

Research Areas:  

Infection Metabolic Disease Cancer

Risedronic acid (Risedronate) sodium, a bisphosphonate, is a potent anti-resorption agent that inhibits osteoclast-mediated bone resorption and changes the bone metabolism. Risedronic acid sodium suppresses osteoblast differentiation and induced caspase- and isoprenoid depletion-dependent apoptosis. Risedronic acid sodium inhibits blood stages of Plasmodium falciparum (IC50 of 20.3 μM). Risedronic acid sodium inhibits the transfer of the farnesyl pyrophosphate group to parasite proteins .
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2
2 Cited Publications
Cat. No.: HY-B1212
CAS No.: 521-74-4
Synonyms: Dibromohydroxyquinoline; 5,7-Dibromo-8-hydroxyquinoline
Research Areas:  

Infection

Broxyquinoline (Dibromohydroxyquinoline) is an effective inhibitor of severe fever with thrombocytopenia syndrome virus (SFTSV) with an IC50 of 5.8 µM. Additionally, Broxyquinoline is an inhibitor of CpACBP1 with an IC50 of 64.9 μM. CpACBP1 is a fatty acyl-CoA binding protein of Cryptosporidium parvum, thus Broxyquinoline has the potential to inhibit parasite growth. Broxyquinoline shows promise for research in the field of infectious diseases .
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1
1 Cited Publications
Cat. No.: HY-107496
CAS No.: 55750-06-6
Purity:  99.07%
Target:  

Parasite Antibiotic

Research Areas:  

Infection

Imidocarb dipropionate is a potent antiprotozoal agent. Imidocarb dipropionate is active against the parasite B. bovis with an IC50 of 87 μg/mL .
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1
1 Cited Publications
Cat. No.: HY-135611
CAS No.: 27885-92-3
Purity:  98.21%
Target:  

Parasite Antibiotic

Research Areas:  

Infection

Imidocarb is a potent antiprotozoal agent. Imidocarb is active against the parasite B. bovis with an IC50 of 87 μg/mL .
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1
1 Cited Publications
Cat. No.: HY-12607
CAS No.: 1486482-16-9
Purity:  99.62%
Target:  

Parasite

Research Areas:  

Infection

ML251, a potent nanomolar T. brucei and T. cruzi phosphofructokinase (PFK) inhibitor, inhibits T. brucei PFK (IC50=0.37 μM) and T. cruzi PFK (IC50=0.13 μM). ML251 can be used for the research of parasite .
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