16 Results for "

W2 strain

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

16 Results for "W2 strain" in MCE Product Catalog:

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1 Cited Publications
Cat. No.: HY-135855
CAS No.: 888958-25-6
Purity:  99.88%
Target:  

SARS-CoV Parasite

Research Areas:  

Infection

SARS-CoV-IN-1 is an effective inhibitor of SARS-CoV replication. SARS-CoV-IN-1 shows anti-Coronavirus activity with an EC50 of 4.9 μM in Vero cells. SARS-CoV-IN-1 inhibits the 3D7 and W2 strains of P. falciparum with IC50s of 15.4 and 133.2 nM; and IC90s of 25.7 and 459.1 nM; respectively. Antimalarial and antiviral activities .
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1
1 Cited Publications
Cat. No.: HY-135858
CAS No.: 888958-27-8
Purity:  99.36%
Target:  

SARS-CoV Parasite HIV

Research Areas:  

Infection

SARS-CoV-IN-3 is an effective inhibitor of SARS-CoV replication. SARS-CoV-IN-3 shows anti-Coronavirus activity with an EC50 of 3.6 μM in Vero cells. SARS-CoV-IN-3 inhibits the 3D7 and W2 strains of P. falciparum with IC50s of 11.7 and 20.4 nM; and IC90s of 29.19 and 56 nM; respectively. SARS-CoV-IN-3 reduces HIV-1-induced cytopathic effect with an EC50 of 10 μM in MT-4 cells .
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1 Cited Publications
Cat. No.: HY-135856
CAS No.: 888958-26-7
Purity:  98.66%
Target:  

SARS-CoV Parasite HIV

Research Areas:  

Infection

SARS-CoV-IN-2 is an effective inhibitor of SARS-CoV replication. SARS-CoV-IN-2 shows anti-Coronavirus activity with an EC50 of 1.9 μM in Vero cells. SARS-CoV-IN-2 inhibits the 3D7 and W2 strains of P. falciparum with IC50s of 21.5 and 30 nM; and IC90s of 51.0 and 99.9 nM; respectively. SARS-CoV-IN-2 reduces HIV-1-induced cytopathic effect with an EC50 of 2.9 μM in MT-4 cells. Antimalarial and Antiviral Activities .
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Cat. No.: HY-15975
CAS No.: 1261114-01-5
Target:  

Parasite

Research Areas:  

Infection

GNF179 is an optimized 8,8-dimethyl imidazolopiperazine analog that exhibits antimalarial potency (IC50 of 4.8 nM against the multidrug resistant strain W2). GNF179 is orally active .
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Cat. No.: HY-N6009
CAS No.: 33390-41-9
8-Deoxygartanin, a prenylated xanthones from G. mangostana, is a selective inhibitor of butyrylcholinesterase (BChE) . 8-Deoxygartanin exhibits antiplasmodial activity with an IC50 of 11.8 μM for the W2 strain of Plasmodium falciparum . 8-Deoxygartanin inhibits NF-κB (p65) activation with an IC50 of 11.3 μM .
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Cat. No.: HY-N11031
CAS No.: 111479-04-0
Z-Antiepilepsirine is an amide alkaloid that can be found in Piper capense L.f. Z-Antiepilepsirine shows antiplasmodial activity with an IC50 value of 27 µM for W2 strain of Plasmodium falciparum .
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Cat. No.: HY-186055
CAS No.: 1258387-05-1
Target:  

Parasite

Research Areas:  

Infection

Antimalarial agent 58 is a diaminoquinoline methanol compound with weak in vitro activity against Plasmodium falciparum strain D6, and no activity against Plasmodium falciparum strains W2, C235 and C2A .
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Cat. No.: HY-170840
Target:  

Parasite

Research Areas:  

Infection

Antimalarial agent 47 (compound F14) is an antimalarial compound, with an IC50 of 235 nM for the Plasmodium falciparum W2 strain .
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Cat. No.: HY-15980
CAS No.: 1310455-86-7
Target:  

Parasite

Research Areas:  

Infection

GNF179 metabolite is the metabolite of GNF179, which is an optimized 8,8-dimethyl IP analog that exhibited the potency(4.8 nM against the multidrug resistant strain W2) in vitro metabolic stability and in vivo oral bioavailability.
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Cat. No.: HY-149937
CAS No.: 2299199-54-3
Target:  

Parasite

Research Areas:  

Infection

Antimalarial agent 24 (Compound 7) is an antimalarial agent in vitro. Antimalarial agent 24 inhibits P. falciparum W2 strain with an IC50 of 0.81 μM. Antimalarial agent 24 displays a CC50 higher than 200 μM against HepG2 cells .
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Cat. No.: HY-158379
Target:  

Parasite

Research Areas:  

Infection

Antiparasitic agent-22 (Compound 24) is a pan antiparasitic agent, that inhibits T. Brucei, L. infantum, L. tropica promastigotes (IC50 of 2.41, 5.95, 8.98 μM), L. infantum amastigotes (IC50 of 8.18 μM) and P. falciparum W2 strain (IC50 of 0.155 μM). Antiparasitic agent-22 exhibits low cytotoxicity against THP1, with CC50 of 64.16 μM .
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Cat. No.: HY-126914
CAS No.: 62574-06-5
Target:  

Parasite

Research Areas:  

Infection

Diacetylcercosporin is a perylenequinone produced by Cercospora and Septoria that has diverse biological activities. Diacetylcercosporin inhibits the growth of P. falciparum strains that are sensitive and resistant to chloroquine (IC50s=2.75 and 1.94 μM for D6 and W2 clones, respectively) and L. donovani parasites (IC50=3.1 μM) in vitro. Diacetylcercosporin exhibits cytotoxicity against SK-MEL, KB, BT549, and SKOV3 human cancer cell lines (IC50s=4.8-8.7 μM). Diacetylcercosporin is also a phytotoxin that inhibits the growth of lettuce and bentgrass at a concentration of 1.62 mM.
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Cat. No.: HY-N21530
CAS No.: 1295650-67-7
6,11,12,16-Tetrahydroxy-5,8,11,13-abitetetraen-7-one is an abietane diterpenoid with antimicrobial and antiparasitic activities. It exhibits IC50 values of 3.0 and 4.8 μg/mL against Plasmodium falciparum strains D6 and W2, respectively, and inhibits the growth of Leishmania donovani with an IC50 of 12 μg/mL and an IC90 of 22 μg/mL. 6,11,12,16-Tetrahydroxy-5,8,11,13-abitetetraen-7-one can be used in studies related to fungal infections, staphylococcal infections, malaria and leishmaniasis .
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Cat. No.: HY-183009
Target:  

Proteasome Parasite

Research Areas:  

Infection

Pf20S-IN-1 is a selective inhibitor of the 20S proteasome β5 subunit of Plasmodium falciparum. Pf20S-IN-1 exhibits antiparasitic activity against Plasmodium falciparum, with an EC50 of 20.1 nM against the Plasmodium falciparum W2 strain. Pf20S-IN-1 shows weak inhibitory effect on human 20S proteasome, has no obvious toxicity to human foreskin fibroblasts (HFF), and has a selectivity index > 25000. Pf20S-IN-1 can be used in malaria research .
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Cat. No.: HY-186053
CAS No.: 1220533-66-3
Target:  

Parasite

Research Areas:  

Infection

Antimalarial agent 56 is an orally active antimalarial agent. Antimalarial agent 56 inhibits the growth of both drug-sensitive and drug-resistant Plasmodium falciparum strains in vitro. Antimalarial agent 56 can be used in malaria research .
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Cat. No.: HY-181864
CAS No.: 2310304-72-2
Target:  

Parasite

Research Areas:  

Infection

Rac1-IN-6 (Compound 5e) is a selective Rac1 inhibitor and antimalarial agent. Rac1-IN-6 inhibits Rac1 activation induced by the Escherichia coli CNF1 toxin. Rac1-IN-6 suppresses the growth of chloroquine-sensitive Plasmodium falciparum D10 (IC50 = 76.0 nM) and chloroquine-resistant Plasmodium falciparum W2 (IC50 = 236.6 nM) .
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