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Filtered Search Results
eMolecules 2117404-84-7 | Medchem Express | BAY-677 | 5mg | 446276260 | HY-111457 | 400.361 | C20H15F3N4O2
Ambeed | 5-Chloro-7-nitro-1H-indazole | 250mg | 600844352 | A622300 | 41926-18-5 | MFCD09027005 | 197.580 | C7H4ClN3O2
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5000739055 AZITHROMYCIN IMPURIT 10MG
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5000723905 CLARITHROMYCIN IMPUR 25MG
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5000738048 KANAMYCIN DISULFATE 1KG
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Medchemexpress LLC HY-B0970 1g , Diphenylpyraline (hydrochloride) 4-Diphenylmethoxy-1-methylpiperidine hydrochloride CAS:132-18-3 Purity:98%
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Medchemexpress, HY-B0970 1g Diphenylpyraline (hydrochloride) 4-Diphenylmethoxy-1-methylpiperidine hydrochloride CAS:132-18-3 Formula:C19H24ClNO Purity:98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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5000692321 CLINDAMYCIN HYDROCH 50MG
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5000693052 KASUGAMYCIN HYDROCH 5G
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5000723739 CLINDAMYCIN PALMITAT 25MG
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5000738859 CLINDAMYCIN PALMITAT 10MG
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5000738874 AZITHROMYCIN IMPURIT 10MG
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eMolecules Montelukast sodium hydrate | 151767-02-1 | | 10mg
Oakwood Chemicals | Montelukast sodium hydrate | 10mg | 480154829 | 103845 | | 151767-02-1 | | 627.190 | C35H38ClNNaO4S
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Apexbio Technology LLC Cefprozil hydrate 121123-17-9 5mg
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Cefprozil hydrate is a small-molecule inhibitor targeting bacterial penicillin-binding proteins (PBPs) It is designed to inhibit bacterial cell wall synthesis by blocking PBPs thereby disrupting peptidoglycan cross-linking and compromising cell wall integrity Cefprozil hydrate exerts its biological activity primarily through inhibition of PBPs leading to bacterial cell lysis and death In in vitro studies Cefprozil hydrate demonstrates antibacterial activity against both Gram-positive and Gram-negative microorganisms Based on these pharmacological properties Cefprozil hydrate holds research potential in antibacterial spectrum characterization bacterial resistance profiling comparator or control use in susceptibility testing and evaluation of novel antibacterial drug candidates
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Medchemexpress LLC HY-15971 5mg Medchemexpress, AMD 3465 (hexahydrobromide) CAS:185991-07-5 Purity:>98%
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Medchemexpress, HY-15971 5mg AMD 3465 (hexahydrobromide) CAS:185991-07-5 AMD 3465 hexahydrobromide (GENZ-644494 hexahydrobromide) is a potent antagonist of CXCR4, inhibits binding of 12G5 mAb and CXCL12AF647 to CXCR4, with IC50s of 0.75 nM and 18 nM in SupT1 cells; AMD 3465 also potently inhibits the replication of X4 HIV strains (IC50: 1-10 nM), but has no effect on CCR5-using (R5) viruses. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Mk-28 | 864388-65-8 | 99.88% | 396.44 | 100 MG
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MK-28 is a potent and selective PERK activator that demonstrates significant pharmacokinetic properties and high blood-brain barrier (BBB) penetration in mice. It has been shown to rescue cells from ER stress-induced apoptosis in vitro and improve systemic function and survival in R6/2 mice, an animal model for Huntington's disease. MK-28 also enhances motor and executive functions and delays the onset of death in R6/2 mice without causing toxicity.
- Potent and selective PERK activator
- Exhibits significant pharmacokinetic properties
- High blood-brain barrier (BBB) penetration in mice
- Rescues cells from ER stress-induced apoptosis in vitro
- Improves systemic function and survival in R6/2 mice
- Enhances motor and executive functions and delays death onset in R6/2 mice
- Activates EIF2AK4 (GCN2)
- Has little or no effect on EIF2AK1 (HRI) or EIF2AK2 (PKR)
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Apexbio Technology LLC Anisomycin 22862-76-6 50mg
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Anisomycin is an activator of c-Jun N-terminal kinase (JNK) a stress-activated protein kinase implicated in apoptotic signaling pathways regulating cell proliferation cell cycle progression and apoptosis It activates the JNK pathway at approximately 25 ng/ml concentration Experimental studies demonstrate anisomycin s capability to sensitize apoptosis-resistant cancer cell lines such as DU145 prostate carcinoma cells to Fas-mediated apoptosis as well as to induce apoptosis in leukemic HL-60 cells and primary mouse embryonic fibroblast cells by initiating JNK activation Anisomycin is thus widely utilized as a molecular tool in apoptosis-related research and insight into JNK-associated cell signaling
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