YN250314 Narasin 55134-13-9

Narasin is a cationic ionophore and coccidiostat agent. Narasin inhibitsNF-κBsignaling and induces tumor cellsapoptosis. Narasin has antimicrobial and anticancer activity.

YN250036 Davercin 55224-05-0

Erythromycin Cyclocarbonate, derivative of Erythromycin, inhibits protein synthesis of bacteria by binding to the 50S ribosome.

YN251273 Cefuroxime 55268-75-2

Cefuroxime is an orally active second-generation cephalosporinantibioticwith increased stability toβ-lactamase. Cefuroxime has a broad spectrum activity against Gram-positive and Gram-negative bacteria.

YN251397 Tiamulin 55297-95-5

Tiamulin is a semisynthetic pleuromutilin antibiotic that binds to the ribosomal peptidyl transferase centre and inhibits protein synthesis.

YN251398 Tiamulin fumarate 55297-96-6

Tiamulin fumarate is a semisynthetic pleuromutilin antibiotic that binds to the ribosomal peptidyl transferase centre and inhibits protein synthesis.

YN250726 Salinomycin sodium salt 55721-31-8

Salinomycin sodium salt (Salinomycin sodium), an antibiotic potassium ionophore, is a potent inhibitor ofWnt/β-cateninsignaling. Salinomycin sodium salt (Salinomycin sodium) acts on the Wnt/Fzd/LRP complex, blocks Wnt-induced L...

YN250480 Ionomycin calcium 56092-82-1

Ionomycin calcium (SQ23377 calcium) is a potent, selectivecalcium ionophore and an antibiotic produced byStreptomyces conglobatus. Ionomycin calcium (SQ23377 calcium) is highly specific for divalent cations (Ca>Mg>Sr=Ba). Ionom...

YN250562 d-Atabrine dihydrochloride 56100-41-5

d-Atabrine dihydrochloride is an active enantiomer of quinacrine which displays antiprion activity.

YN250561 l-Atabrine dihydrochloride 56100-42-6

l-Atabrine dihydrochloride is a less active enantiomer of quinacrine which displays antiprion activity.

YN250309 Cefazedone 56187-47-4

Cefazedone is a semisynthetic first-generation cephalosporin with antibacterial activity.

YN251272 Cefuroxime sodium 56238-63-2

Cefuroxime Sodium is a cephalosporin effective against gram-positive and gram-negative bacteria with resistance to β-lactamase.

YN250145 Nosiheptide 56377-79-8

Nosiheptide (Multhiomycin), a thiopeptide antibiotic produced byStreptomyces actuosus, inhibitsbacterialprotein synthesis and bears a unique indole side ring system and regiospecific hydroxyl groups on the characteristic macrocyclic ...

YN250861 Netilmicin sulfate 56391-57-2

Netilmicin Sulfate is a member of the aminoglycoside family of antibiotics.

YN251274 Cefmetazole sodium 56796-39-5

Cefmetazole sodium is a semisynthetic cephamycin antibiotic with a broad spectrum of activity against both gram-positive and gram-negative microorganisms. It has a high rate of efficacy in many types of infection and to date no severe sid...

YN251395 Tolclofos-methyl 57018-04-9

Tolclofos-methyl is a broad-spectrum aromatic hydrocarbon fungicide that is used as a see treatment for protection against soil-borne and seed borne fungal pathogens that caused seed decay and seedling blights.

YN250212 Kanosamine hydrochloride 57649-10-2

Kanosamine hydrochloride is an antibiotic which inhibits the growth of plant-pathogenic oomycetes, certainfungi and a fewbacterialspecies. Kanosamine inhibitsPhytophthora medicaginisM2913 and Aphanomyces euteichesWI-98 withMICs ...

YN251737 (-)-Corynoxidine 57906-85-1

(-)-Corynoxidine is anacetylcholinesteraseinhibitor with an IC50 value of 89.0μM, isolated from the aerial parts ofCorydalis speciosa. (-)-Corynoxidine exhibits antibacterial activities against Staphylococcus aureus and methicilli...

YN251760 Clindamycin hydrochloride mon... 58207-19-5

Clindamycin alcoholate is a crystallizable compound of Clindamycin with alcohol. Clindamycin is a semisynthetic lincosamide antibiotic that inhibits bacterial protein synthesis by binding to bacterial 50S ribosomal subunits.

YN251793 Lehmannine 58480-54-9

Lehmannine is a quinolizidinebioalkaloidisolated fromS. alopecuroides L, has antibacterial, anti-inflammatory and anti-tumor activities.

YN250923 Bestatin 58970-76-6

Bestatin is a potent aminopeptidase-B and leukotriene (LT) A4 hydrolase inhibitor, used in the treatment of acute myelocytic leukemia.