32 Results for "

trypanosomes

" in MedChemExpress (MCE) Product Catalog:
Products (32)

32 Results for "trypanosomes" in MCE Product Catalog:

Cat. No.: HY-178326
Target:  

Parasite

Research Areas:  

Infection

NEU-5123 is a human kinase inhibitor with potent inhibitory activity to several kinases. NEU-5123 is a Trypanosome proliferation inhibitor. NEU-5123 can be used for the research of infection .
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Cat. No.: HY-DY2028
Research Areas:  

Others

Ready-to-Use Giemsa Staining Solution is a ready-to-use Romanowsky-type staining solution that can be used for staining blood and cell smears, bacteria, chromosome banding, parasites, and other specimens. Ready-to-Use Giemsa Staining Solution stains blood smears to reveal blood parasites including Plasmodium, microfilariae, and trypanosomes. Ready-to-Use Giemsa Staining Solution enables morphological identification of blood cells, and can also stain fixed cells to observe muscle cell nuclei, distinguish myotubes from myoblasts, and quantitatively analyze the differentiation status of myoblasts .
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Cat. No.: HY-184074
CAS No.: 2152662-88-7
Target:  

Parasite

Research Areas:  

Infection

Enfiborole is an oxaborolane ester inhibitor with trypanocidal activity against parasites. Enfiborole displays IC50 values ≤ 20 nM against Trypanosoma brucei and Trypanosoma cruzi, and its IC50 against replicating trypanosomes ranges from 21 to 999 nM. Enfiborole inhibits the growth of Trypanosoma brucei, suppresses hypoxanthine incorporation in replicating trypanosomes, and inhibits the growth of Trypanosoma cruzi amastigotes. Enfiborole can be used in studies related to trypanosome infections .
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Cat. No.: HY-180418
CAS No.: 602-52-8
Target:  

Parasite

Research Areas:  

Infection

Homidium chloride is a potent antiparasitic agent exhibiting activity against Trypanosoma rhodesiense and Trypanosoma congolense. Homidium chloride can reduce parasitaemia in murine models of infection. Homidium chloride can be used for trypanosomiasis research .
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Cat. No.: HY-W414557
CAS No.: 4143-00-4
Ethyl 2,4-dihydroxybenzoate is an ethyl ester derivative of 2,4-dihydroxybenzoate. The biological activities of Ethyl 2,4-dihydroxybenzoate are all mediated by its parent nucleus 2,4-dihydroxybenzoate .
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Cat. No.: HY-125188
CAS No.: 2306305-57-5
Research Areas:  

Infection

NEU-4438 is an antimalarial agent. NEU-4438 inhibits DNA synthesis, reduces AMPK-γ, and increases Clathrin heavy chain. NEU-4438 exhibits antiparasitic activity against Trypanosoma brucei. NEU-4438 reduces trypanosome tissue burden in a chronic HAT mouse model .
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Cat. No.: HY-183747
CAS No.: 1916476-01-1
Target:  

Parasite

Research Areas:  

Infection

Antitrypanosomal agent 32 is a antitrypanosomal agent with nanomolar potency against multiple Trypanosoma cruzi strains, including CL-Brener, Y, Dm28c-Luc and Tulahuen. Antitrypanosomal agent 32 sustains inhibition of parasite growth after washing and reduces parasitemia levels in BALB/c mice. Antitrypanosomal agent 32 can be used for the research of trypanosome infection .
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Cat. No.: HY-180158
CAS No.: 2413738-47-1
Research Areas:  

Infection Cancer

Antitrypanosomal agent 28 (Compound 2a) is a trypanocidal agent. Antitrypanosomal agent 28 effectively inhibits Trypanosoma cruzi by inducing the generation of ROS and mitochondrial damage, with an IC₅₀ of 49.4 μM. Antitrypanosomal agent 28 exhibits broad-spectrum anti-tumor activity against various tumor cell lines, especially being sensitive to leukemia, colon cancer, and breast cancer. Antitrypanosomal agent 28 can be used for research on anti-cancer and anti-trypanosome activities .
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Cat. No.: HY-187603
CAS No.: 211816-91-0
Target:  

Parasite

Research Areas:  

Infection

CGP 40215 is an S-adenosylmethionine decarboxylase inhibitor with an IC50 of 20.3 μM against Trypanosoma brucei brucei AdoMet decarboxylase. CGP 40215 blocks spermidine production and leads to putrescine accumulation. CGP 40215 inhibits polyamine biosynthesis in intact trypanosomes, acts synergistically with the ornithine decarboxylase inhibitor DFMO (HY-B0744) against CNS model infections, and ameliorates laboratory infections caused by multiple Trypanosoma brucei subspecies and Trypanosoma congolense isolates, including strains tolerant to standard trypanocides. CGP 40215 can be used for research on African trypanosomiasis and Chagas disease .
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Cat. No.: HY-183242
CAS No.: 120154-96-3
Target:  

Bacterial Parasite

Research Areas:  

Infection Neurological Disease Cancer

Eilatin is a seven-ring pyridoacridine marine alkaloid with anticancer, antibacterial, and antiparasitic activities. Eilatin acts as a DNA intercalator with selectivity for electron-deficient polycyclic purines; it can chelate Ni 2+ ions and cleave DNA via hydroxyl radical generation. Eilatin induces the SOS response in bacteria, inhibits cancer cell proliferation, and induces cancer cell differentiation and reversion of transformation. The IC50 of Eilatin against Trypanosoma brucei brucei is 1.33 μM. Eilatin can be used in research related to colon tumors, neuroblastoma, chronic myeloid leukemia, acute myeloid leukemia, and trypanosome infections .
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Cat. No.: HY-P11367
CAS No.: 118850-78-5
Boc-Ala-Gly-Pro-Arg-AMC is a synthetic fluorescent substrate, widely used for the detection of protease activity. Boc-Ala-Gly-Pro-Arg-AMC can be used to detect the activity of serine proteases and the oligopeptide enzyme B of Trypanosoma brucei .
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Cat. No.: HY-B0670S
Dihydroergotamine-d3 is the d3-labeled Dihydroergotamine (HY-B0670). Dihydroergotamine (DFN-19) is a blood-brain barrier-permeable semi-synthetic ergot alkaloid, acting as a full agonist of 5-HT1B/1D receptors (Ki values of 0.3 nM and 2.5 nM, respectively; functional IC50 values of 2 nM and 2.2 nM, respectively). Dihydroergotamine inhibits Forskolin (HY-15371)-stimulated cAMP accumulation, possesses α-adrenergic receptor antagonistic activity and weak dopaminergic agonistic activity. It mediates intracranial cerebrovascular contraction, inhibits the release of neuropeptides such as CGRP/substance P, and suppresses neurogenic inflammation by activating 5-HT1B/1D receptors in the trigeminovascular system. Dihydroergotamine binds to the catalytic site of Trypanosoma cruzi trypanothione reductase and exhibits trypanocidal activity in vitro. Dihydroergotamine can be used in studies related to migraine and trypanosome infections .
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