
Antiparasitics
Found 695 products of "Antiparasitics"
GNF179
CAS:GNF179 is an optimized 8,8-dimethyl IP analog.Formula:C22H23ClFN5OPurity:98.9%Color and Shape:SolidMolecular weight:427.9Ref: TM-T15409
1mg109.00€2mg158.00€5mg260.00€10mg430.00€25mg710.00€50mg973.00€100mg1,333.00€1mL*10mM (DMSO)286.00€Quinoline, 7-chloro-4-[(4-diethylamino-1-methylbutyl)amino]-, diphosphate (6CI)
CAS:Formula:C18H30ClN3O7P2Purity:98%Color and Shape:SolidMolecular weight:497.8472Oxantel Pamoate
CAS:Oxantel Pamoate (Oxantel embonate) is used as an Antinematodal agent.Formula:C36H32N2O7Purity:99% - 99.89%Color and Shape:SolidMolecular weight:604.65Permethrin
CAS:Permethrin (NRDC-143) is a pyrethroid insecticide commonly used in the treatment of LICE INFESTATIONS and SCABIES.Formula:C21H20Cl2O3Purity:99.37% - 99.54%Color and Shape:Colorless Crystals To A Viscous Liquid; Color White To Pale Yellow Permethrin Is A Pale Brown Liquid Relatively Water Insoluble Used As An InsecticideMolecular weight:391.29Antiparasitic agent-22
Antiparasitic agent-22 (Compound 24) is a broad-spectrum antiparasitic compound that inhibits the procyclic form of T. brucei, L. infantum, and L. tropica with IC50 values of 2.41, 5.95, and 8.98 μM, respectively, and the amastigote form of L. infantum with an IC50 of 8.18 μM. It also shows inhibitory activity against the P. falciparum W2 strain with an IC50 of 0.155 μM. Additionally, Antiparasitic agent-22 exhibits low cytotoxicity in THP1 cells, with a CC50 of 64.16 μM.Formula:C18H20BrN3O3Molecular weight:405.0688Longestin
CAS:Longestin, a specific phosphodiesterase (phosphodiesterase) inhibitor with antitrypanosomal activity, is derived from Streptomyces argenteolus. It is under investigation for its potential use in anti-amnesic medications.Formula:C61H88O17Color and Shape:SolidMolecular weight:1093.34Dodecamethylpentasiloxane
CAS:Dodecamethylpentasiloxane can be used as a bed bug insecticide. Dodecamethylpentasiloxane is a component of siloxane and can be used as silicone oil.
Formula:C12H36O4Si5Purity:97.43%Color and Shape:SolidMolecular weight:384.84DXR-IN-1
DXR-IN-1 (Compound 13E) is an inhibitor of 1-deoxy-D-xylulose 5-phosphate reductoisomerase (DXR). It exhibits high selectivity for DXR of Plasmodium falciparum with an IC50 of 0.030 μM. DXR-IN-1 impedes the growth of Plasmodium by binding to the active site of DXR and inhibiting its catalytic activity.Formula:C19H24NO5PMolecular weight:377.13921TSO-13
TSO-13 is an inhibitor of the major cysteine protease Cruzipain found in Trypanosoma cruzi, with an IC50 of 2.2 μM. In Vero cells, TSO-13 also suppresses T. cruzi, exhibiting an IC50 of 1.9 μM.
Formula:C32H36N4O4S2Color and Shape:SolidMolecular weight:604.78β-Hederin
CAS:β-Hederin has antileishmanial activity. β-Hederin has apoptotic effect on cancer cells, it could be a promising candidate for chemotherapy of breast cancer.Formula:C41H66O11Purity:98%Color and Shape:SolidMolecular weight:734.96Antileishmanial agent-26
Antileishmanial agent-26 (Compound 69) is a guanidine-containing compound with activity against *Leishmania donovani*, exhibiting an IC50 value of 5.67 μM and a CC50 value of 3.79 μM in THP-1 cells. This compound is applicable for research in tropical diseases.Formula:C23H27FN4O2Molecular weight:410.2118NMT-IN-3
NMT-IN-3 is an inhibitor of N-myristoyltransferase (NMT), displaying an IC50 of 38 mM against Plasmodium vivax NMT.Formula:C26H32N6O4Molecular weight:492.2485Diarctigenin
Diarctigenin is a selective inhibitor of Leishmania major dihydrofolate reductase-thymidylate synthase (LmDHFR-TS), and it is applicable in the study of tropical diseases.Formula:C42H46O12Molecular weight:742.29893NPD-2975
NPD-2975 (compound 30) is an orally active antitrypanosomal agent effective against Human African Trypanosomiasis (HAT), demonstrating acceptable metabolicFormula:C14H13FN4OPurity:98%Color and Shape:SolidMolecular weight:272.28Antimalarial agent 33
Antimalarial agent 33 (compound 5g) exhibits antiplasmodial activity targeting both erythrocytic and hepatic stages of Plasmodium, with an effectivePurity:98%Color and Shape:Odour SolidAntitrypanosomal agent 13
Compound 4b (antitrypanosomal agent 13) is a potent antitrypanosomal with notable trypanocidal and cytotoxic activities, exhibiting GI50 values of 0.18 μMFormula:C47H81N2NaO10SPurity:98%Color and Shape:SolidMolecular weight:889.21Notrilobolide
CAS:Notrilobolide, an alkaloid with insecticidal properties, is isolated from sweet potatoes and impedes larval development in pests such as Tribolium castaneum.Formula:C26H36O10Purity:98%Color and Shape:SolidMolecular weight:508.56Anti-inflammatory agent 40
Anti-inflammatory agent 40 is a promising, orally-active compound with anti-malarial and anti-inflammatory properties.Formula:C30H24Cl2N2O4Purity:98%Color and Shape:SolidMolecular weight:547.43HAT-IN-8
HAT-IN-8 (Compound 38), a blood-brain barrier-permeable inhibitor of Trypanosoma brucei with an EC50 of 0.18 μM, is utilized in the study of Human AfricanFormula:C14H15F2N3O2SPurity:98%Color and Shape:SolidMolecular weight:327.35DCN-83
DCN-83, a potent anti-leishmanial compound, exhibits its highest efficacy against the amastigote form, achieving an IC50 value of 0.71 μM.Formula:C20H18BrN3SPurity:98%Color and Shape:SolidMolecular weight:412.35Antimalarial agent 31
Compound 31 (compound 7k) is an orally active inhibitor of Plasmodium falciparum aspartic protease, plasmepsin X (PMX), with antimalarial properties [1].Formula:C36H47N3O4Purity:98%Color and Shape:SolidMolecular weight:585.78Antitrypanosomal agent 23
Antitrypanosomal agent 23 is an antiparasitic compound effective against intracellular amastigotes of Trypanosoma cruzi in LLC-MK2 and C2C12 cells, demonstrating activity with IC50 values of 0.10 and 0.11 μM, respectively. It also acts as a weak inhibitor of recombinant Trypanosoma cruzi sialyltransferase (TcTS) with an IC50 of 1.1 mM.Formula:C14H16N4O7Color and Shape:SolidMolecular weight:352.1019Antitrypanosomal agent 17
Compound 17 (Compd 7a) exhibits potent antiamastigote activity, demonstrated by its IC50 value of 0.03 μM against the T. congolense strain IL3000 [1].Purity:98%Color and Shape:Odour SolidAntileishmanial agent-19
Compound F27 (Antileishmanial agent-19) is an antileishmanial compound effective against L.
Formula:C22H18N4O3Purity:98%Color and Shape:SolidMolecular weight:386.4Norselic acid B
CAS:Norselic acid B is a naturally occurring compound that can be isolated from the sponge Crella sp. collected in Antarctica. It demonstrates activity against Leishmania parasites.Formula:C29H44O4Color and Shape:SolidMolecular weight:456.657Antiparasitic agent-20
Antiparasitic Agent-20 (Compound 1p) exhibits broad-spectrum activity as a parasitic inhibitor, demonstrating efficacy against T.Purity:98%Color and Shape:Odour SolidAntiparasitic agent-26
Antiparasitic agent-26 (Compound 8) is an antiparasitic compound that effectively inhibits the growth of Naegleria fowleri, with an IC50 of 22.87 μM (trophozoite stage) and 25.16 μM (cyst stage). It exerts its antiparasitic effects by inducing programmed cell death, which includes cytosolic calcium accumulation, mitochondrial membrane potential collapse, ATP synthesis inhibition, ROS accumulation, and chromatin condensation. Antiparasitic agent-26 can be utilized in research on primary amoebic meningoencephalitis (PAM).
Color and Shape:Odour SolidAntitrypanosomal agent 16
Antitrypanosomal agent 16 functions as a potent trypanocide, exhibiting an inhibitory concentration 50 (IC50) of 0.04μM against the T.Purity:98%Color and Shape:Odour SolidAnticancer agent 140
Compound 140 (Compd 3) exhibits potential anticancer and antiparasitic activities [1].Formula:C20H26N2OPurity:98%Color and Shape:SolidMolecular weight:310.43Antileishmanial agent-21
Antileishmanial agent-21 (compound 4e) functions as an inhibitor of Leishmania pteridine reductase 1 (Lm-PTR1), employing an anti-folate mechanism.Formula:C21H16N2O3Purity:98%Color and Shape:SolidMolecular weight:344.36Antimalarial agent 28
Antimalarial agent 28 (Compound 2i) acts as an antiplasmodial agent, exhibiting inhibition of P.
Formula:C27H25ClFN3O2Purity:98%Color and Shape:SolidMolecular weight:477.96Antiproliferative agent-56
Antiproliferative agent-56 (Compound 31) is an antimalarial agent that inhibits the Pf3D7 strain of the malaria parasite Plasmodium falciparum with an IC50 of >12.5 (48h) and 0.03 μM (98h), displaying slow-acting characteristics.Color and Shape:Odour SolidCysteine protease inhibitor-3
Cysteine protease inhibitor-3 (Compound 15), a cysteine protease inhibitor, exhibits anti-plasmodial activity, effectively inhibiting Pf3D7 (IC50 = 0.74 μM),Formula:C26H22ClF2N3OPurity:98%Color and Shape:SolidMolecular weight:465.92AAP4
AAP4 is a potent inhibitor of OfChi-h and OfHex1, exhibiting Ki values of 29.3 nM and 4.9 μM, respectively. It also demonstrates insecticidal activity against the lepidopteran pest Ostrinia furnacalis.Formula:C21H23BrClN7Color and Shape:SolidMolecular weight:488.811Nitroxynil
CAS:Nitroxynil is an anthelmintic for adult/immature parasites, mainly used in Fasciola hepatica studies.Formula:C7H3IN2O3Purity:99.76%Color and Shape:SolidMolecular weight:290.01Antileishmanial agent-20
Antileishmanial agent-20 exhibits selectivity against the Leishmania parasite, with IC50 values of 2.8 μM for L.Formula:C15H16N4O3Purity:98%Color and Shape:SolidMolecular weight:300.31CpNMT-IN-1
CpNMT-IN-1 (Compound 11e) is an inhibitor of N-myristoyltransferase (CpNMT) with an IC50 value of 2.5 μM. It also inhibits the growth of microsporidia, demonstrating an EC50 value of 6.9 μM.Formula:C25H25ClN4O4SColor and Shape:SolidMolecular weight:513.008LASSBio-1985
LASSBio-1985 is an inhibitor of NHLd (nucleoside hydrolase of Leishmania donovani), with a Ki of 79 μM and an IC50 of 84.6 μM. It exhibits selective toxicity against Leishmania parasites without affecting mammals, showing potential for research in infectious disease treatment.Formula:C18H22N2O7Color and Shape:SolidMolecular weight:378.38Antimalarial agent 43
Antimalarial agent 43 (compound 16c) is an antimalarial compound that exhibits an IC50 value of 0.0151 μM against the 3D7 strain.Color and Shape:Odour SolidEmoquine-1
Emoquine-1 is a potent orally active antimalarial agent effective against various drug-resistant Plasmodium strains, including artemisinin-resistant dormant parasites. It demonstrates efficacy against proliferative malignant Plasmodium with an IC50 value ranging from 20 to 55 nM. Emoquine-1 holds potential for treating Plasmodium strains resistant to artemisinin combination therapy (ACT), with the capability to eradicate persistent parasites.Formula:C30H28ClN3O6Color and Shape:SolidMolecular weight:562.0138304-vs
8304-vs is a macrocyclic anti-Plasmodial compound that irreversibly binds to and inhibits the Plasmodium proteasome, effectively halting the growth ofFormula:C35H53N5O8SPurity:98%Color and Shape:SolidMolecular weight:703.89Antileishmanial agent-24
Antileishmanial agent-24 (compound 33) exhibits antileishmanial activity, demonstrating an inhibitory concentration 50 (IC50) value of 5.39 μM againstFormula:C34H29Cl4N3O2Purity:98%Color and Shape:SolidMolecular weight:653.42Antimalarial agent 47
Antimalarial agent 47 (compound F14) is a chemical compound effective against Plasmodium falciparum, specifically targeting the W2 strain with an IC50 value of 235 nM.Formula:C16H14ClF2NOColor and Shape:SolidMolecular weight:309.74Antimalarial agent 27
Antimalarial agent 27 (compound 11a) potently inhibits P.Formula:C10H11NNaO5PPurity:98%Color and Shape:SolidMolecular weight:279.16Antileishmanial agent-25
Antileishmanial agent-25 (compound 24) exhibits selective activity against intracellular amastigotes, demonstrating an inhibitory concentration (IC50) of 6.63Purity:98%Color and Shape:Odour SolidAlkaline tryptase-IN-1
Alkaline tryptase-IN-1 (compound H-13) is an insecticide that targets alkaline trypsin-like enzymes. It has lethal concentration (LC50) values of 8.72, 13.77, 14.17, 12.96, and 12.35 μg/mL against Schizaphis graminum, Sitobion avenae, Brevicoryne brassicae, Aphis gossypii, Aphis spiraecola, and Myzus persicae, respectively.Formula:C29H33BrN2O2SColor and Shape:SolidMolecular weight:553.55Antitrypanosomal agent 12
Antitrypanosomal agent 12, a C20-phenylthiourea, exhibits trypanocidal and cytotoxic activities, demonstrating antitrypanosomal activity with GI50 values of 0.Formula:C49H77N2NaO10SPurity:98%Color and Shape:SolidMolecular weight:909.2Amprolium
CAS:Amprolium is a veterinary coccidiostat that interferes with THIAMINE metabolism.Formula:C14H19N4·ClPurity:98%Color and Shape:SolidMolecular weight:278.79CpCDPK1/TgCDPK1-IN-2
CAS:CpCDPK1/TgCDPK1-IN-2 is a dual inhibitor of CpCDPK1 and TgCDPK1 with IC50 values of 12 and 5 nM for CpCDPK1 and TgCDPK1, respectively.CpCDPK1/TgCDPK1-IN-2 can
Formula:C20H21N5OPurity:99.12%Color and Shape:SoildMolecular weight:347.41Se2h
Se2h is a cruzain inhibitor exhibiting potent activity against intracellular amastigotes of Trypanosoma cruzi (EC50< 1 μM, SI> 10), with an inhibitory effect on cruzain of IC50< 100 nM (SI> 5.55). Compared to Benznidazole and cruzain inhibitor K777, Se2h shows superior selectivity and inhibition while its selenazole structure reduces selenium-related toxicity. Se2h demonstrates antiparasitic activity and holds promise for Chagas disease research.Formula:C12H13ClN4O2SeColor and Shape:SolidMolecular weight:359.67Anti-Trypanosoma cruzi agent-6
Anti-Trypanosoma cruzi agent-6 (Compound 8) exhibits inhibitory activity against Trypanosoma cruzi. It effectively suppresses the epimastigote, trypomastigote, and amastigote forms of T. cruzi, with IC50 values of 24.7 µM, 1.8 µM, and 1.6 µM, respectively.Formula:C19H20N2O5Color and Shape:SolidMolecular weight:356.374-(2-Aminoethyl)amino-7-chloroquinoline
CAS:4-(2-Aminoethyl)amino-7-chloroquinoline (N1-(7-Chloroquinolin-4-yl)ethane-1,2-diamine) has potential anthelmintic and antitumor activity for the study ofFormula:C11H12ClN3Purity:98.53%Color and Shape:SolidMolecular weight:221.69MCG-02
MCG-02 is an inhibitor of cruzain (CRZ) and cathepsin L-like protease (CATL), capable of inhibiting CRZ in Trypanosoma cruzi and CATL in Trypanosoma brucei, with IC50 values of 0.2 μM and 0.02 μM, respectively.Formula:C13H13N3O2SColor and Shape:SolidMolecular weight:275.33Cordysinin C/D
CAS:Cordysinin C/D (compound 9) is a potential antimalarial agent that effectively inhibits the Plasmodium falciparum 3D7 strain.Formula:C13H12N2OColor and Shape:SolidMolecular weight:212.25Sulfadiazine
CAS:Sulfadiazine, a short-acting sulfonamide, blocks bacterial folic acid synthesis; used with pyrimethamine to treat toxoplasmosis in AIDS, newborns.Formula:C10H10N4O2SPurity:99.32%Color and Shape:White To Slightly Yellow Crystalline PowderMolecular weight:250.28Antileishmanial agent-31
CAS:Antileishmanial agent-31 (Compound p1) is a pyrazole derivative exhibiting antileishmanial activity with an IC50 of 35.53 μg/mL. Furthermore, Antileishmanial agent-31 demonstrates high stability and is applicable in studies focused on leishmaniasis treatment.Formula:C11H11ClN2Color and Shape:SolidMolecular weight:206.67Methylclonazepam
CAS:Methylclonazepam is a benzodiazepine with anxiolytic properties. It inhibits the uptake of 5-hydroxytryptamine by Schistosoma mansoni, and its derivatives exhibit anti-Schistosoma mansoni activity.Formula:C16H12ClN3O3Color and Shape:SolidMolecular weight:329.74Antiparasitic agent-17
Antiparasitic Agent-17 (compound 5u), an orally active antiparasitic, demonstrates inhibition against both Chloroquine-sensitive (Pf3D7) and Chloroquine-Formula:C32H30N2O4Purity:98%Color and Shape:SolidMolecular weight:506.59Eflornithine
CAS:Eflornithine blocks ornithine decarboxylase, treating African trypanosomiasis and female facial hair.Formula:C6H12F2N2O2Purity:99.44% - 99.84%Color and Shape:SolidMolecular weight:182.17Sarolaner
CAS:Sarolaner (PF-6450567) is an orally active and broad-spectrum ectoparasiticide (LC80: 0.3 μg/mL against C. felis and an LC100: 0.003 μg/mL against O. turicata).Formula:C23H18Cl2F4N2O5SPurity:99.54% - 99.65%Color and Shape:SolidMolecular weight:581.36ACT-451840
CAS:ACT-451840 eliminates both sensitive and resistant strains of Plasmodium falciparum and has the advantages of oral, potency, low toxicity, rapid.Formula:C47H54N6O3Purity:96.07%Color and Shape:SolidMolecular weight:750.97Ref: TM-T203012
1mg108.00€5mg229.00€10mg366.00€25mg701.00€50mg1,123.00€100mg1,700.00€1mL*10mM (DMSO)239.00€Antileishmanial agent-30
Compound 17k, also known as Antileishmanial agent-30, effectively inhibits Leishmania with an IC50 of 0.2 μM for L. donovani. It exhibits a CC50 of >100 μM and an SI of >500, indicating significant selectivity and potency.Formula:C23H21N5O2Color and Shape:SolidMolecular weight:399.45PfSUB1-IN-1
PfSUB1-IN-1 (compound 4c) is an inhibitor of Plasmodium falciparum subtilisin-like serine protease 1 (PfSUB1), exhibiting potent activity with an IC50 value of 15 nM. PfSUB1 is a key target in antimalarial research. PfSUB1-IN-1 demonstrates a 13-fold greater inhibitory effect on the growth of transgenic Plasmodium falciparum strains (expressing lower levels of PfSUB1 compared to the wild-type) than on wild-type parasite strains.
Color and Shape:Odour SolidAmitraz
CAS:Amitraz (NSC 324552): white monoclinic crystals, mp 86-87°C, water-insoluble, used as acaricide and in canine demodectic mange.Formula:C19H23N3Purity:99.88%Color and Shape:White/Pale Yellow Crystalline SolidMolecular weight:293.41ML251
CAS:ML251, potent inhibitor, targets T. brucei PFK (IC50=0.37μM) & T. cruzi PFK (IC50=0.13μM), aids parasite research.Formula:C17H13Cl2N3O4SPurity:99.87%Color and Shape:SolidMolecular weight:426.27Ref: TM-T64320
1mg115.00€5mg274.00€10mg432.00€25mg715.00€50mg1,008.00€100mg1,359.00€200mg1,825.00€1mL*10mM (DMSO)301.00€Antimalarial agent 42
Compound 42 (Compound 2), an antimalarial agent, effectively inhibits Plasmodium falciparum during the asexual blood stages (IC 50 <0.5μM) and gametocytes (IC 50 is 0.14 μM).Formula:C24H42N2Color and Shape:SolidMolecular weight:358.63-Deoxyaphidicolin
CAS:3-Deoxyaphidicolin is a phytotoxin that inhibits root growth in lettuce seedlings. Additionally, 3-Deoxyaphidicolin exhibits inhibitory activity against the protozoan parasites Leishmania major and Leishmania braziliensis.Formula:C20H34O3Color and Shape:SolidMolecular weight:322.48LL-37 FK-13 TFA
LL-37 FK-13 TFA, the TFA salt form of LL-37 FK-13, is an antimicrobial agent that inhibits Trichomonas vaginalis. It exhibits minimal hemolytic effects on human red blood cells and shows slight cytotoxicity towards human fibroblasts.Color and Shape:Odour SolidMMV1634566
MMV1634566 is an effective antimalarial agent that can inhibit Plasmodium falciparum and exhibits cytotoxicity.Color and Shape:Odour SolidAChE-IN-66
Nematicidal Agent 1 is an effective nematicide that binds to the pocket of acetylcholinesterase (AChE).Color and Shape:Odour SolidBitoscanate
CAS:Bitoscanate (PDITC) is used in the treatment of hookworms.Formula:C8H4N2S2Purity:98.32%Color and Shape:Colorless Needles Bitoscanate Is An Odorless Colorless Crystals Melting Point 132°CMolecular weight:192.26SpdSyn binder-1
CAS:SpdSyn binder-1 weakly inhibits malaria by binding to Plasmodium falciparum's spermidine synthase. Used for research.Formula:C21H22N4OPurity:99.5%Color and Shape:SolidMolecular weight:346.43Insecticidal agent 24
Insecticidal agent 24 is an orally active pyridinyl spiroindoline lead compound. It demonstrates antimalarial activity with Pf NF54IC50 of 0.08 μM. Insecticidal agent 24 also inhibits hERG activity with an IC50 of 6.5 μM. In a humanized immunodeficient NSG mouse model of malaria infection, it effectively reduces parasitemia.Formula:C26H29N3O2Color and Shape:SolidMolecular weight:415.22598JC-229
CAS:JC-229 is a potent and selective TbRPA1 inhibitor that can inhibit RPA1 in Trypanosoma brucei. JC-229 can be used to study human African Trypanosomiasis (HAT).Formula:C20H14Cl4N2O3SPurity:97.13%Color and Shape:SolidMolecular weight:504.21pCDPK1/TgCDPK1-IN-3
CAS:CpCDPK1/TgCDPK1-IN-3 inhibits Cp/TgCDPK1; IC50: 0.003/0.0036 µM. It's used to research Toxoplasma, Cryptosporidium diseases.Formula:C17H18N6Purity:98.13%Color and Shape:SoildMolecular weight:306.36Antimalarial agent 13
CAS:Antimalarial agent 13 (N2-(3-chlorophenyl)-N4-(furan-2-ylmethyl)quinazoline-2,4-diamine) is a potent antimalarial agent.Formula:C19H15ClN4OPurity:99.15%Color and Shape:SolidMolecular weight:350.8Ref: TM-T9984
1mg85.00€5mg170.00€10mg245.00€25mg371.00€50mg522.00€100mg700.00€200mg928.00€1mL*10mM (DMSO)173.00€1,2-Dimethyl-1H-benzo[d]imidazole
CAS:1,2-Dimethyl-1H-benzo[d]imidazole has antibacterial activity against Entamoeba histolytica and Giardia lamblia,Formula:C9H10N2Purity:99.86%Color and Shape:SolidMolecular weight:146.19N-Methyl-1,3-benzoxazol-2-amine
CAS:N-Methyl-1,3-benzoxazol-2-amine, with CAS No. 19776-98-8, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. N-Methyl-1,3-benzoxazol-2-amine provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.Formula:C8H8N2OColor and Shape:SoildMolecular weight:148.1616Antileishmanial agent-33
Antileishmanial agent-33 (4e) is a hybrid compound of grandisin and machilin G, demonstrating moderate activity against promastigotes with an IC50 of 38.1 μM. In studies of cutaneous leishmaniasis (CL), Antileishmanial agent-33 (4e) has shown potential as an antileishmanial agent.Color and Shape:Odour SolidDoxycycline monohydrate
CAS:Doxycycline monohydrate is an inhibitor of metalloproteinase (MMP)Formula:C22H26N2O9Purity:99.97%Color and Shape:SolidMolecular weight:462.4Biotin-PEG3-Mal
CAS:Biotin-PEG3-Mal (Biotin-PEG3-NH-Mal) is a biotin-labeled PROTAC linker belonging to the PEG class that can be used to synthesize PROTAC molecules.Formula:C25H39N5O8SPurity:99.5%Color and Shape:SolidMolecular weight:569.67Morantel tartrate
CAS:Morantel tartrate (CP-12009-18 tartrate) is an antinematodal agent used mainly for livestock.Formula:C16H22N2O6SPurity:98.08%Color and Shape:White Or Pale Yellow Crystalline PowderMolecular weight:370.42Cardol triene
CAS:Cardol triene, Phenolic compound, competitively inhibits mushroom tyrosinase (IC50=22.5 μM) and S. mansoni, for dibenzoxazine synthesis.Formula:C21H30O2Color and Shape:SolidMolecular weight:314.46Pyronaridine tetraphosphate
CAS:Pyronaridine tetraphosphate is a DNA topoisomerase 2 inhibitor with antimalarial and antitumor activity for the treatment of P. falciparum infection.Formula:C29H44ClN5O18P4Purity:99.82%Color and Shape:SolidMolecular weight:910.03Modoflaner
CAS:Modoflaner is an antiparasitic (veterinary use).Formula:C23H10F12IN3O2Purity:98.78%Color and Shape:SolidMolecular weight:715.23Ile-AMS TFA
Ile-AMS TFA exhibits activity against P. falciparum, with an ABSIC50 value of 1.19 nM.Formula:C18H27F3N8O8SColor and Shape:SolidMolecular weight:572.52Urethane
CAS:Urethane (Ethylurethane) was an antineoplastic agent .Now is used for other medicinal purposes.Formula:C3H7NO2Purity:99.01%Color and Shape:SoildMolecular weight:89.09Febrifugine dihydrochloride
CAS:Febrifugine dihydrochloride (Propyldazine hydrochloride) is a biochemical with therapeutic activity regarding malaria, cancer, fibrosis and inflammatoryFormula:C16H21Cl2N3O3Purity:98.27% - 99.85%Color and Shape:SolidMolecular weight:374.26Azlocillin sodium salt
CAS:Azlocillin sodium, an acylampicillin, is a broad-spectrum antibioticsFormula:C20H22N5NaO6SPurity:97.63% - 98.302%Color and Shape:SolidMolecular weight:483.47Dixanthogen
CAS:Dixanthogen (Auligen) is an ectoparasiticide. Dixanthogen is a thiocarbonyl compound.Formula:C6H10O2S4Purity:95% - 98%Color and Shape:SolidMolecular weight:242.4WJM280
WJM280 is an orally active antimalarial compound with an EC50 of 0.04 μM against the parasite P. falciparum 3D7.Formula:C22H25F3N2OColor and Shape:SolidMolecular weight:390.44Nanaomycin A
CAS:Nanaomycin A, a quinone antibiotic, reactivates cancer suppressor genes and inhibits DNMT3B (IC50=500nM).Formula:C16H14O6Purity:98%Color and Shape:SolidMolecular weight:302.28Antitrypanosomal agent 15
Antitrypanosomal Agent 15 (Compound 26) is an orally active, brain-penetrant, selective inhibitor of the Trypanosoma cruzi proteasome, exhibiting a pIC50 of 7.4Formula:C21H19FN4O4Purity:98%Color and Shape:SolidMolecular weight:410.4Proteasome-IN-6
Proteasome-IN-6 (Compound J-80) inhibits the β5 catalytic subunit of the Trypanosoma brucei 20S proteasome, effectively blocking T. b. brucei, T. b. gambiense, and T. b. rhodesiense with EC50 values of 157 nM, 220 nM, and 156 nM, respectively. Additionally, Proteasome-IN-6 has demonstrated antitrypanosomal activity in a mouse model.Formula:C35H45F3N4O6Color and Shape:SolidMolecular weight:674.75Antimalarial agent 45
Antimalarial agent 45 (compound 8I) is an antimalarial with activity against Plasmodium parasites, exhibiting an IC50 of 0.21 μM. It is used in the study of malaria.Formula:C33H34N4O3Color and Shape:SolidMolecular weight:534.654-(Trifluoromethyl)nicotinic acid
CAS:Compound FL0181, with CAS No. 158063-66-2, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Compound FL0181 provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.Formula:C7H4F3NO2Purity:98%Molecular weight:191.11Antimalarial agent 46
CAS:Antimalarial agent 46 (Compound 42a) is a compound with antimalarial activity, effective in inhibiting P. falciparum lines.Formula:C21H17Cl3N4OColor and Shape:SolidMolecular weight:447.75Cinchonidine
CAS:Cinchonidine (L-Cinchonidine) is an alkaloid extracted from Cinchona officinalis. It is a pseudo-enantiomer and stereoisomer of cinchonine.Formula:C19H22N2OPurity:94.96% - 99.87%Color and Shape:White PowderMolecular weight:294.39Human α-defensin 5
Human α-defensin 5 is an antiviral peptide that inhibits the infection of non-enveloped viruses such as AdV, HPV, and polyomaviruses, with an IC50 range of 0.6-Formula:C144H238N50O45S6Purity:98%Color and Shape:SolidMolecular weight:3582.13Antiparasitic agent-25
Antiparasitic agent-25 (Compounds 11) is an orally active antiparasitic compound. It inhibits the invasion and replication capabilities of parasites and has an irreversible effect on Toxoplasma gondii. The agent significantly reduces the replication rate of Toxoplasma gondii, with an IC50 value of 6.33 μM, and exhibits low cytotoxicity, having a CC50 value of 285 μM.Color and Shape:Odour Solid


