30 Results for "

asexual

" in MedChemExpress (MCE) Product Catalog:
Products (30)

30 Results for "asexual" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-131708A
CAS No.: 2641930-61-0
Purity:  98.00%
Target:  

HDAC Parasite

Research Areas:  

Infection

FNDR-20123 is a safe, first-in-class, and orally active anti-malarial HDAC inhibitor with IC50s of 31 nM and 3 nM for Plasmodium and human HDAC, respectively. FNDR-20123 exerts anti-malarial activity against Plasmodium falciparum asexual stage (IC50=41 nM) and sexual blood stage (IC50=190 nM for male gametocytes). FNDR-20123 inhibits HDAC1, HDAC2, HDAC3, HDAC6, and HDAC8 (IC50=25/29/2/11/282 nM, respectively.) and inhibits Class III HDAC isoforms at nanomolar concentrations .
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1
1 Cited Publications
Cat. No.: HY-111817
CAS No.: 1984890-99-4
Purity:  96.45%
Target:  

Parasite

Research Areas:  

Infection

ACT-451840 is an orally active, potent and low-toxicity compound, showing activity against sensitive and resistant plasmodium falciparum strains. ACT-451840 targets all asexual blood stages of the parasite, has a rapid onset of action. ACT-451840 behaves in a way similar to artemisinin derivatives, with very rapid onset of action and elimination of parasite. ACT-451840 can be used for the research of malarial .
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1
1 Cited Publications
Cat. No.: HY-163727
CAS No.: 2065197-82-0
Target:  

Parasite

Research Areas:  

Infection

MMV1557817 is an orally active and potent antimalarial compound. MMV1557817 is a selective, nanomolar inhibitor of both Plasmodium falciparum and Plasmodium vivax aminopeptidases M1 and M17, leading to inhibition of end-stage hemoglobin digestion in asexual parasites .
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Cat. No.: HY-108024A
CAS No.: 2751586-94-2
Purity:  97.19%
Synonyms: KAF156 hydrochloride; GNF156 hydrochloride
Target:  

Parasite

Research Areas:  

Infection

Ganaplacide (KAF156) hydrochloride is a first-in-class, orally active imidazolopiperazine antimalarial agent. Ganaplacide hydrochloride is active against a broad range of Plasmodium species, including drug-resistant parasites. Ganaplacide hydrochloride is parasiticidal against both asexual and sexual blood stages as well as the liver stages of the parasite .
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Cat. No.: HY-101000
CAS No.: 101831-36-1
Synonyms: R62690
Target:  

Parasite

Research Areas:  

Infection

Clazuril (R62690) has a coccidiocidal effect on the asexual and sexual developmental stages of both Eimeria species, resulting in a complete interruption of the life cycle .
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Cat. No.: HY-N15159
CAS No.: 146776-30-9
Cladophorol A is a cyclic GMP-AMP synthase (cGAS) inhibitor. Cladophorol A binds to the conserved adenosine nucleobase binding site within the cGAS active site to inhibit its catalytic activity. Cladophorol A effectively inhibits the overactivation of the cGAS-STING pathway with an IC50 of 370 nM. Cladophorol A inhibits asexual blood-stage Plasmodium falciparum with an EC50 of 0.7 μg/mL. Cladophorol A can be used for the researches of inflammatory disease and malaria .
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Cat. No.: HY-P10338
CAS No.: 1423743-97-8
LZ1 peptide acts as a Pyruvate kinase inhibitor, antimicrobial agent, and antimalarial agent. LZ1 peptide reduces ATP production and inhibits the malaria parasite Plasmodium falciparum. LZ1 peptide exhibits activity against Plasmodium berghei in mice and reduces parasitemia. LZ1 peptide shows favorable antimicrobial activity against pathogens associated with acne vulgaris. LZ1 peptide possesses anti-inflammatory effects. LZ1 peptide can be used in malaria-related research .
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Cat. No.: HY-136307S
Tizoxanide-d4 glucuronide is the deuterium labeled Tizoxanide glucuronide. Tizoxanide glucuronide is the metabolite of Nitazoxanide (HY-B0217) and is cell-permeable to inhibit asexual and sexual stages development of parasite C. parvum .
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Cat. No.: HY-108024
CAS No.: 1261113-96-5
Synonyms: KAF156; GNF156
Target:  

Parasite

Research Areas:  

Infection

Ganaplacide (KAF156) is a first-in-class, orally active imidazolopiperazine antimalarial agent. Ganaplacide is active against a broad range of Plasmodium species, including drug-resistant parasites. Ganaplacide is parasiticidal against both asexual and sexual blood stages as well as the liver stages of the parasite .
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Cat. No.: HY-121647
CAS No.: 128-50-7
Target:  

Parasite

Research Areas:  

Others

Nopol is a quinoline derivative based on nopol that has inhibitory activity against the asexual blood stage of Plasmodium falciparum. Derivatives with different structures have different activities against different Plasmodium strains, and some derivatives have submicromolar EC50 values in specific strains.
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Cat. No.: HY-W779377
CAS No.: 527-75-3
Category:  

Microorganisms Antibiotics

Target:  

Parasite

Erythromycin B has anti-malarial activity and effectively inhibits the asexual reproduction of Plasmodium falciparum .
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Cat. No.: HY-145912
CAS No.: 1801444-69-8
Purity:  98.28%
Target:  

Parasite

Research Areas:  

Infection Inflammation/Immunology

RYL-552S kills drug-resistant strains of Plasmodium falciparum. RYL-552S can efficiently kill asexual blood-stage parasites in vitro .
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Cat. No.: HY-116736
CAS No.: 2057420-00-3
Research Areas:  

Infection

BRD7539 is a PfDHODH inhibitor (IC50 = 0.033 μM). BRD7539 has potent activity against both multidrug-resistant asexual blood-stage (P. falciparum, Dd2 strain, EC50 = 0.010 μM) and liver-stage (P. berghei, EC50 = 0.015 μM) parasites .
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Cat. No.: HY-131708
CAS No.: 1267502-34-0
Target:  

HDAC Parasite

Research Areas:  

Infection

FNDR-20123 free base is a safe, first-in-class, and orally active anti-malarial HDAC inhibitor with IC50s of 31 nM and 3 nM for Plasmodium and human HDAC, respectively. FNDR-20123 free base exerts anti-malarial activity against Plasmodium falciparum asexual stage (IC50=41 nM) and sexual blood stage (IC50=190 nM for male gametocytes). FNDR-20123 free base inhibits HDAC1, HDAC2, HDAC3, HDAC6, and HDAC8 (IC50=25, 29, 2, 11, and 282 nM, respectively) and inhibits Class III HDAC isoforms at nanomolar concentrations .
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Cat. No.: HY-148178
CAS No.: 2260904-47-8
Purity:  99.50%
Target:  

Parasite

Research Areas:  

Infection

MMV688533 is an antimalarial agent. MMV688533 interferes with intracellular trafficking, lipid utilization, and endocytosis pathways in Plasmodium falciparum. MMV688533 rapidly kills asexual blood-stage Plasmodium falciparum and Plasmodium vivax parasites in vitro and reduces parasitemia in a Plasmodium falciparum NSG mouse model. MMV688533 can be used for the research of malaria .
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Cat. No.: HY-163997
Target:  

Parasite

Research Areas:  

Infection

Antimalarial agent 42 (Compound 2) is an antimalarial agent, that inhibits Plasmodium falciparum in the phase of asexual blood stages (IC50 <0.5μM) and gametocytes (IC50 is 0.14 μM) .
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Cat. No.: HY-N10190
CAS No.: 2378379-27-0
Asperaculane B is a fungal metabolite against P. falciparum transmission with an IC50 of 7.89 µM. Asperaculane B also inhibits the development of asexual P. falciparum with IC50 of 3 µM, and it is nontoxic to human cells .
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Cat. No.: HY-101000R
CAS No.: 101831-36-1
Synonyms: R62690 (Standard)
Research Areas:  

Infection

Clazuril (Standard) is the analytical standard of Clazuril. This product is intended for research and analytical applications. Clazuril (R62690) has a coccidiocidal effect on the asexual and sexual developmental stages of both Eimeria species, resulting in a complete interruption of the life cycle .
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Cat. No.: HY-N10197
CAS No.: 2826264-81-5
Pulixin prevents FREP1 from binding to P. falciparum-infected cell lysate. Pulixin blocks the transmission of the parasite to mosquitoes with an EC50 of 11 µM. Pulixin also inhibits the proliferation of asexual-stage P. falciparum with an EC50 of 47 nM .
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Cat. No.: HY-141837
CAS No.: 1820874-51-8
Target:  

Parasite

Research Areas:  

Infection

MMV674850 is potent against asexual stage parasites at 2.7 and 4.5 nM and preferentially targets early-stage gametocytes (early-stage gametocyte: IC50 4.5 ± 3.6 nM; late-stage gametocyte: IC50 28.7 ± 0.2 nM).
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