61
14
2
カタログ番号 | 製品名 | 別名 | ターゲット |
---|---|---|---|
TP2331 | Leishmania peptide 183 | Peptide 183,p183,Leishmania | |
Leishmania peptide 183 is an antigen. | |||
T12909 | SID 26681509 | Cysteine Protease , Parasite | |
T62330 | Antileishmanial agent-12 | ||
Antileishmanial agent-12 (compound 5a) is a potent anti-leishmanial agent with antibacterial activity against Leishmania brazilensis (IC50: 14.9 μM), Leishmania infantum (IC50: 21.3 μM) and T. cruzi (IC50. 9.3 μM). 9.3 μ... | |||
T63281 | Antileishmanial agent-11 | ||
Antileishmanial agent-11 is a potent antileishmanial agent that acts on Leishmania brazilensis (IC50: 28.3 μM), Leishmania infantum (IC50: 24.8 μM) and T. cruzi (IC50: 13.0 μM) with outstanding antiprotozoal effect. | |||
T61391 | Antileishmanial agent-3 | ||
Antileishmanial agent-3 (Compound 13) effectively inhibits the growth of Leishmania major [1]. | |||
T78963 | Antileishmanial agent-16 | Parasite | |
Antileishmanial agent-16 (compound 14c), an anti-Leishmania agent, exhibits potent activity against Leishmania major promastigotes (IC50 = 0.59 µM) and amastigotes (IC50 = 0.81 µM), while maintaining a favorable safety p... | |||
T61710 | Antileishmanial agent-7 | ||
Antileishmanial agent-7 (compound 23) exhibits strong antileishmanial activity against Leishmania donovani and L-6, with IC50 values of 6.89 and 259 μM, respectively [1]. | |||
T61416 | Antileishmanial agent-9 | ||
Antileishmanial agent-9 (compound 16c) exhibits potent and selective activity against Leishmania donovani (L. donovani) with an IC50 value of 4.01 μM. In addition, this compound demonstrates relatively low cytotoxicity i... | |||
T62574 | Antileishmanial agent-6 | ||
Antileishmanial agent-6 is a potent anti-leishmanial agent with anti-leishmanial activity (IC50: 0.54 μM) and cytotoxicity (IC50: 10.2 μM) against Leishmania donovani and L-6. | |||
T78680 | Antileishmanial agent-14 | Parasite | |
Antileishmanial agent-14, a sulfuretin analog, exhibits potential activity against Leishmania donovani promastigotes (IC 50 = 4.1 μM) and inhibits infection by L. donovani amastigotes (IC 50 = 11.1 μM) [1]. | |||
T60638 | Antileishmanial agent-8 | ||
Antileishmanial agent-8 (compound 18) shows potent and selective activity against Leishmania donovani ( L. donovani ) (IC50 = 5.64 μM) with relatively low cytotoxicity in L-6 cells (IC 50 =73.9 μM) [1]. | |||
T79471 | Antileishmanial agent-20 | Parasite | |
Antileishmanial agent-20 exhibits selectivity against the Leishmania parasite, with IC50 values of 2.8 μM for L. infantum and 0.2 μM for L. braziliensis. It is a potential research tool for studying these parasites [1]. | |||
T79390 | Antileishmanial agent-23 | Parasite | |
Antileishmanial agent-23 (compound G1/9), a potent and selective trypanothione reductase (TR) inhibitor, exhibits an IC50 of 2.24 ± 0.52 μM. It effectively inhibits the growth of Leishmania, Trypanosoma cruzi, and Trypan... | |||
T72260 | Antileishmanial agent-13 | ||
Antileishmanial agent-13, a quinoline-isatin hybrid, functions as an antileishmanial agent targeting the L. Major Leishmania strain through an anti-folate mechanism. This compound exhibits potent inhibition of both the p... | |||
T79632 | Antileishmanial agent-21 | Parasite | |
Antileishmanial agent-21 (compound 4e) functions as an inhibitor of Leishmania pteridine reductase 1 (Lm-PTR1), employing an anti-folate mechanism. Its antileishmanial effects can be negated by folic acid and leucovorin.... | |||
T79449 | Antileishmanial agent-19 | Parasite | |
Compound F27 (Antileishmanial agent-19) is an antileishmanial compound effective against L. donovani promastigotes, demonstrating an IC50 of 3.39 μM. It functions by inhibiting the Leishmania prolyl-tRNA synthetase and d... | |||
T79633 | Antileishmanial agent-22 | Parasite | |
Antileishmanial agent-22 (compound 15b) serves as an antiparasitic and antibacterial, exhibiting activities against Leishmania (IC50 = 0.408 μM), malaria, and tuberculosis. It operates on an antifolate mechanism, suppres... | |||
T61199 | Antileishmanial agent-2 | ||
Antileishmanial agent-2 demonstrates potent submicromolar antileishmanial activity (IC50 = 0.29 μM) and a remarkable selectivity index against mammalian cells. | |||
T61560 | Antileishmanial agent-5 | ||
Antileishmanial agent-4 is a ribonucleoside analogue with potent activity against L.infantum and T.cruzi, having EC 50 values of 0.68 μM and 0.83 μM, respectively [1]. | |||
T78964 | Antileishmanial agent-17 | Parasite | |
Antileishmanial agent-17, a coumarin hybrid, exhibits potent antileishmanial activity (IC50 <0.78 μM) while proving non-toxic to normal VERO cells. It specifically interacts with the folate pathway enzymes pteridine redu... | |||
T61100 | Antileishmanial agent-4 | ||
Antileishmanial agent-4, a ribonucleoside analogue, functions as an antileishmanial agent [1]. | |||
T40117 | Antileishmanial agent-1 | ||
Antileishmanial agent-1 demonstrates activity against both L. amazonensis promastigotes (IC 50 = 15.52 μM) and intracellular amastigotes (IC 50 = 4.10 μM). | |||
T62210 | Antileishmanial agent-10 | ||
Antileishmanial agent-10 (Compound 7h) is an antiprotozoal agent. | |||
T83045 | Antileishmanial agent-25 | Parasite | |
Antileishmanial agent-25 (compound 24) exhibits selective activity against intracellular amastigotes, demonstrating an inhibitory concentration (IC50) of 6.63 μM [1]. | |||
T78962 | Antileishmanial agent-15 | Parasite | |
Antileishmanial agent-15 (compound 13c) exhibits potent activity against L. major promastigotes and amastigotes, demonstrating IC50 values of 0.78 μM for promastigotes and 0.99 μM for amastigotes, while also showing cyto... | |||
T79419 | Antileishmanial agent-24 | Parasite | |
Antileishmanial agent-24 (compound 33) exhibits antileishmanial activity, demonstrating an inhibitory concentration 50 (IC50) value of 5.39 μM against amastigotes [1]. | |||
T60531 | 2'-C-Methyladenosine | HCV Protease | |
2'-C-Methyladenosine is an inhibitor of hepatitis C virus (HCV) replication and a ribonucleoside diphosphate reductase inhibitor from Corynebacterium renalis.2'-C-Methyladenosine inhibits HCV replicon and NS5B-catalyzed ... | |||
T23132 | Pentamidine dihydrochloride | MP-601205 dihydrochloride | Phosphatase , Antibacterial , Antibiotic , Parasite , Antifungal |
Pentamidine dihydrochloride (MP-601205 dihydrochloride) is an aromatic diamidine agent with activity against a number of microorganisms including protozoa (Trypanosoma brucei, Leishmania spp., and Babesia spp.) and fungi... | |||
T16546 | PK 11195 | RP 52028 | Others |
PK 11195 is a ligand of translocator protein. It targets Leishmania chemotherapy (IC50s of 14.2 μM, 8.2 μM, 3.5 μM for L. amazonensis, L. major and L. braziliensis, respectively). | |||
T60092 | CHEMBL1276927 | N-[3-(1H-benzimidazol-2-yl)phenyl]-3-methylbenzamide,N-(3-(1H-benzo[d]imidazol-2-yl)phenyl)-3-methylbenzamide | Antibacterial , Parasite |
CHEMBL1276927 (N-(3-(1H-benzo[d]imidazol-2-yl)phenyl)-3-methylbenzamide) shows antibacterial and antiparasitic activities against Chlamydia pneumoniae and Leishmania donovani. | |||
T1654 | Pentamidine isethionate | Pentamidine isethionate salt,Pentamidine diisethionate | Phosphatase , Antibacterial , Antibiotic , Parasite , Antifungal |
Pentamidine isethionate (Pentamidine diisethionate) is a synthetic amidine derivative, Pentamidine Isethionate is an antiprotozoal and antifungal agent. | |||
T39746 | DNDI-6148 | Parasite | |
DNDI-6148 has anti-experimental cutaneous leishmaniasis activity and can be used to study visceral leishmaniasis by inhibiting Leishmania protozoa cleavage and polyadenylation-specific factor (CPSF3) endonuclease. | |||
T9858 | 5-(3-bromo-4,5-dihydroisoxazol-5-yl)-3-(4-(tert-butyl)phenyl)-1,2,4-oxadiazole | Parasite | |
Antileishmanial agent-2 is a 3-Br-isoxazoline-Based Inhibitors against Plasmodium falciparum (D10 and W2 strains) and Leishmania spp. (L. infantum and L. tropica) Promastigotes with IC50s of 0.035, 0.058, 3.5 and 7.5 μM. | |||
T2112 | Fexinidazole | HOE 239 | Others , Parasite |
Fexinidazole (HOE 239) is an antiparasitic agent. It has activity against Trypanosoma cruzi, Tritrichomonas foetus, Trichomonas vaginalis, Entamoeba histolytica, Trypanosoma brucei, and Leishmania donovani. The biologica... | |||
T15095 | Dehydroemetine | Others , Parasite | |
Dehydroemetine is an effective antigenic insecticide, which is a synthetic analogue of Emetine dihydrochloride. It can be used to prevent and treat amoeba infections and diseases. It has the effect of treating leishmania... | |||
T68109 | Moxipraquine | Antibiotic | |
Moxipraquine is a novel 8-aminoquinolone compound with anti-infective activity against Trypanosoma cruzi. Moxipraquine effectively inhibited parasitemia but did not eradicate infections in mice or guinea pigs. Moxipraqui... | |||
T15546 | ICA | N-[4-(2-Pyridinyl)-2-thiazolyl]-2-pyridinamine | Potassium Channel , Parasite |
ICA (N-[4-(2-Pyridinyl)-2-thiazolyl]-2-pyridinamine) is a SK channel inhibitor and exhibits antileishmanial activity (IC50: 2.1 µM). | |||
T23133 | Pentamidine | Phosphatase , Antibacterial , Antibiotic , Parasite , Antifungal | |
Pentamidine is an antifungal and antiprotozoal agent, interacting directly with the pathogen genome by binding to AT-rich regions of duplex DNA and the minor groove of DNA, thereby interfering with DNA replication. | |||
T15110 | DHQZ 36 | Others | |
DHQZ 36 is a potent retrograde trafficking inhibitor. It has potent anti-parasite activity. DHQZ 36 inhibits Leishmania amazonensis infection in macrophages (EC50: 13.63 μM). | |||
T69891 | CGP 40215 | ||
CGP 40215 is a specific S-adenosylmethionine decarboxylase (AdoMetDC) inhibitor that was found to inhibit the growth of Leishmania donovani promastigotes | |||
T20303 | Dibenzalacetone | AI3-00896,AI3 00896,AI300896 | |
Dibenzylideneacetone is a synthetic curcumin analog. It leads to apoptotic cell death in Leishmania donovani. | |||
T69511 | Diospyrin | ||
Diospyrin is a plant product that has significant inhibitory effect on the growth of Leishmania donovani promastigotes. | |||
T61364 | LmCPB-IN-1 | ||
LmCPB-IN-1 (compound 35) is a highly effective and reversible covalent inhibitor of Leishmania mexicana cysteine protease B (LmCPB). It exhibits a strong binding affinity with a pK i value of 9.7 [1]. | |||
T72925 | Naloxonazine | ||
Naloxonazine, a potent, selective opiate mu-1 (μ1) antagonist, also influences leishmania through the modulation of host coding function. | |||
T40652 | Meclizine | Meclozine | Histamine Receptor |
Meclizine, also known as Meclozine, is a piperazine class H1 antagonist with antihistamine properties that inhibits the interaction of histamine at H1 receptors reversibly. It serves as an effective anti-motion sickness ... | |||
T83025 | Antiparasitic agent-19 | ||
Antiparasitic Agent-19 (Compound 40) is a broad-spectrum antiparasitic with minimal toxicity to Trypanosoma brucei, Leishmania infantum, and Trypanosoma cruzi [1]. | |||
T61245 | Antiparasitic agent-7 | ||
Antiparasitic agent-7 (compound 5d) displays specific antiparasitic activity against Leishmania infantum (L. infantum), exhibiting an IC50 value of 2.85 μM. Additionally, Antiparasitic agent-7 demonstrates cytotoxicity a... | |||
T63831 | SID 26681509 quarterhydrate | ||
SID 26681509 quarterhydrate is a reversible, potent, selective, competitive inhibitor of human cathepsin L (IC50: 56 nM). SID 26681509 inhibits in vitro propagation of Plasmodium falciparum (IC50: 15.4 μM) and inhibits L... | |||
T61641 | Antiparasitic agent-5 | ||
Antiparasitic agent-5 (compound 8h) exhibits potent selectivity as an antiparasitic agent against Leishmania infantum (L. infantum), with an IC50 value of 2.50 μM. Additionally, this compound displays cytotoxic effects o... | |||
T80648 | Eugenitin | Parasite | |
Eugenitin, a polyketide from Mycoleptodiscus indicus, exhibits inhibitory activity against Leishmania major with an LD50 of 39.9 μM and demonstrates low cytotoxicity (IC50 >131 μM) in various human cancer cell lines [1]. |
カタログ番号 | 製品名 | 別名 | ターゲット |
---|---|---|---|
TN1961 | Myricetin 3-O-glucoside | Myricetin 3-O-beta-D-glucopyranoside | Immunology/Inflammation related |
Myricetin 3-O-glucoside (Myricetin 3-O-beta-D-glucopyranoside) is a flavonol extracted from Tibouchina paratropica. Myricetin 3-O-glucoside has many activities, including anti-leishmania, anti-inflammatory and antibacter... | |||
T4861 | Trans-Aconitic acid | ATPase , Endogenous Metabolite | |
Trans-Aconitic acid is normally present in normal human urine, and it has been suggested that is present in larger amounts with Reye's syndrome and organic aciduria. trans-Aconitic acid is a substrate of enzyme trans-aco... | |||
TN2101 | Primin | Antifection | |
Primin has antimycobacterial, and strong antineoplastic actions. | |||
T19876 | Simiarenol | UNII-6OU4M247SJ,Simiaren-3beta-ol,beta-Simiarenol | |
Simiarenol may have leishmanicidal activity against Leishmania donovani promastigotes in vitro. | |||
TN5092 | Tagitinin F | Antifection | |
Tagitinin F possesses antileukemic activity; it also shows in vitro leishmanicidal activities against Leishmania braziliensis promastigotes and amastigotes. | |||
TN5872 | Phebalosin | Alosin | |
Phebalosin displays 50% effective concentrations (EC(50)) of 14.1 microg/mL against axenic amastigote forms of Leishmania panamensis. It also displays cytotoxicity (IC(50)) at concentrations of 20.7 microg/mL on human pr... | |||
TN4653 | Niazinin | Antifection | |
Niazinin shows antileishmanial activity against promastigotes of Leishmania donavani, with an IC50 value of 5.25 microM. | |||
TN2697 | 2,3-Dihydrohinokiflavone | MMP , Parasite , Antifection | |
TN4733 | Pancixanthone A | Antifection | |
Pancixanthone A may have antimalarial activity, it also shows a significant antileishmanial activity against the promastigote forms of Leishmania mexicana and L. infantum and against the amastigote forms of L. infantum. | |||
TN3721 | Cryptofolione | Antifection | |
Z-Cryptofolione and Cryptomoscatone D2 as highly efficacious inhibitors of the G(2) checkpoint, G(2) checkpoint inhibitors can force cells arrested in G(2) phase by DNA damage to enter mitosis. Cryptofolione shows modera... | |||
T72234 | 3β-Hydroxy-hop-22(29)-ene | ||
3β-Hydroxy-hop-22(29)-ene is a potent antiparasitic compound demonstrating moderate efficacy against Trypanosoma cruzi and Leishmania mexicana. | |||
T73949 | Isatropolone A | ||
Isatropolone A, a natural product with a 1,5-diketone moiety, has been reisolated from Streptomyces Gö66. This compound exhibits potent anti-Leishmania donovani activity, evidenced by an IC50 value of 0.5 μM [1]. | |||
TN4683 | Nyasol | ERK , IL Receptor , IκB/IKK , NOS , NF-κB , Akt , Antifection | |
Nyasol may have potential to be developed as medicines for the treatment of allergies by inhibiting the activation of mast cells. Nyasol shows anti-inflammatory properties by inhibiting iNOS expression; it also has antif... | |||
TN4778 | Physalin H | gp120/CD4 , Antifection , Autophagy | |
Physalin H is an Hh signaling inhibitor blocks GLI1-DNA-complex formation, it also strong quinone reductase induction activity with IR (Induction ratio, QR induction activity) value of 3.74±0.02. Physalin H shows immunos... |
カタログ番号 | 製品名 | Species | Expression System |
---|---|---|---|
TMPH-02403 | JBP1 Protein, Leishmania infantum, Recombinant (His & V5) | Leishmania infantum | E. coli |
JBP1 Protein, Leishmania infantum, Recombinant (His & V5) is expressed in E. coli expression system with N-10xHis-V5 tag. The predicted molecular weight is 53.4 kDa and the accession number is A4HU70. | |||
TMPY-02929 | ENTPD2 Protein, Human, Recombinant (aa 29-460, His) | Human | Baculovirus Insect Cells |
NTPDase 2, also known as ENTPD2, belongs to the ecto-nucleoside triphosphate diphosphohydrolase family (E-NTPDase). Members of E-NTPDase family are nucleotidases able to hydrolyze 5′-nucleoside tri- and/or diphosphates; ... |