188 Results for "

SPPS

" in MedChemExpress (MCE) Product Catalog:
Products (188)

188 Results for "SPPS" in MCE Product Catalog:

20
20 Publications Verification
Cat. No.: HY-W009168
CAS No.: 89785-84-2
Target:  

Bacterial Antibiotic

Research Areas:  

Infection Cancer

Tazobactam sodium is an antibiotic of the beta-lactamase inhibitor class. Ceftolozane combines with Tazobactam, extends the activity of ceftolozane against many ESBL-producing Enterobacteriaceae and some Bacteroides spp..
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12
12 Cited Publications
Cat. No.: HY-16911
CAS No.: 620175-39-5
Synonyms: API-1252; Debio 1452
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

AFN-1252 is an orally active and selective inhibitor of FabI, an essential enzyme in fatty acid biosynthesis in Staphylococcus spp. AFN-1252 exhibits exquisite and highly selective activity against Staphylococcus spp. AFN-1252 exhibits typical MIC90 values of ⩽0.015 μg/ml against diverse clinical isolates of S. aureus. AFN-1252 is efficacious in a mouse model of septicemia providing 100% protection from an otherwise lethal peritoneal infection of S. aureus Smith .
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11
11 Cited Publications
Cat. No.: HY-12177
CAS No.: 173334-58-2
Purity:  99.62%
Synonyms: CGP 60536 hemifumarate; CGP60536B hemifumarate; SPP 100 hemifumarate
Target:  

Renin Autophagy

Research Areas:  

Cardiovascular Disease Cancer

Aliskiren (CGP 60536; CGP60536B; SPP 100) hemifumarate is an orally active and selective renin inhibitor, with IC50 of 1.5 nM. Aliskiren hemifumarate can be used for the research of hypertension, cardiovascular diseases and cancer cachexia .
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4
4 Cited Publications
Cat. No.: HY-108009A
CAS No.: 1631754-41-0
Purity:  99.84%
Synonyms: Biafungin acetate; CD101 acetate; SP-3025 acetate
Target:  

Fungal

Research Areas:  

Infection

Rezafungin acetate (Biafungin acetate) is a next-generation, broad-spectrum, and long-lasting echinocandin. Rezafungin acetate shows potent antifungal activity against Candida spp., Aspergillus spp., and Pneumocystis spp. .
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4
4 Cited Publications
Cat. No.: HY-12136
CAS No.: 569-77-7
Purity:  96.87%
Purpurogallin is a naturally phenol extracted from the plants of Quercus spp, has potent xanthine oxidase (XO) inhibitory activity with an IC50 of 0.2 μM. Purpurogallin has antioxidant and anti-inflammatory effects .
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4
4 Cited Publications
Cat. No.: HY-N8461
CAS No.: 2134-29-4
Synonyms: 3-Hydroxypropionaldehyde; 3-Hydroxypropanal
Reuterin is a broad-spectrum antimicrobial agent active against Gram positive and Gram negative bacteria, as well as yeasts, moulds and protozoa. Reuterin is produced by specific strains of Lactobacillus reuteri during anaerobic metabolism of glycerol. Reuterin also demonstrates potent antimicrobial activity against a broad panel of human and poultry meat campylobacter spp. Isolates .
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3
3 Cited Publications
Cat. No.: HY-P0123
CAS No.: 1621717-95-0
Target:  

Peptides

Research Areas:  

Others

SPACE peptide is a skin penetrating peptide (SPPs). SPACE peptide can enhance topical delivery of a macromolecule, hyaluronic acid .
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3
3 Cited Publications
Cat. No.: HY-B0398
CAS No.: 389-08-2
Nalidixic acid, a quinolone antibiotic, is effective against both gram-positive and gram-negative bacteria. Nalidixic acid acts in a bacteriostatic manner in lower concentrations and is bactericidal in higher concentrations. Nalidixic acid inhibits a subunit of DNA gyrase and topoisomerase IV and reversibly blocks DNA replication in susceptible bacteria .
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3
3 Cited Publications
Cat. No.: HY-B0398A
CAS No.: 3374-05-8
Research Areas:  

Infection

Nalidixic acid sodium salt, a quinolone antibiotic, is effective against both gram-positive and gram-negative bacteria. Nalidixic acid acts in a bacteriostatic manner in lower concentrations and is bactericidal in higher concentrations. Nalidixic acid inhibits a subunit of DNA gyrase and topoisomerase IV and reversibly blocks DNA replication in susceptible bacteria .
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2
2 Cited Publications
Cat. No.: HY-105048
CAS No.: 204248-78-2
Purity:  98.64%
Target:  

Bacterial

Research Areas:  

Infection

Omiganan is a cationic antimicrobial peptide. Omiganan as an analogue of indolicidin shows activity against gram-positive and gram-negative bacteria but also Candida spp. isolates. Omiganan can be used for the research of alcohol nose and acne .
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2
2 Cited Publications
Cat. No.: HY-110193
CAS No.: 1357349-91-7
Purity:  99.71%
Target:  

RET

Research Areas:  

Cancer

SPP-86 is a potent and selective cell permeable inhibitor of RET tyrosine kinase, with an IC50 of 8 nM. SPP-86 inhibits RET-induced phosphatidylinositide 3-kinases (PI3K)/Akt and MAPK signaling, also inhibits RET-induced estrogen receptorα (ERα) phosphorylation in MCF7 cells . SPP-86 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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2
2 Cited Publications
Cat. No.: HY-B0293A
CAS No.: 64872-76-0
Target:  

Fungal

Research Areas:  

Infection

Butoconazole, an imidazole antifungal agent, is active against Candida spp. and effective against vaginal infections due to Candida albicans. Butoconazole is presumed to function as other imidazole derivatives via inhibition of steroid synthesis .
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2
2 Cited Publications
Cat. No.: HY-B0293
CAS No.: 64872-77-1
Synonyms: RS 35887
Target:  

Fungal

Research Areas:  

Infection

Butoconazole nitrate (RS 35887), an imidazole antifungal agent, is active against Candida spp. and effective against vaginal infections due to Candida albicans. Butoconazole nitrate is presumed to function as other imidazole derivatives via inhibition of steroid synthesis .
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2
2 Cited Publications
Cat. No.: HY-N7071A
CAS No.: 84878-61-5
Synonyms: Maduramycin ammonium
Maduramicin ammonium (Maduramycin ammonium) is isolated from the actinomycete Actinomadura rubra. Maduramicin ammonium (Maduramycin ammonium) is an anticoccidial agent for the the treatment of Eimeria spp., E. adenoeides, E. gallopavonis, and E. dispersa infection . Maduramicin ammonium (Maduramycin ammonium) induces cell apoptosis in chicken myocardial cells via intrinsic and extrinsic pathways .
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2
2 Cited Publications
Cat. No.: HY-15275
CAS No.: 582315-72-8
Purity:  99.59%
BMS-265246 is a potent and selective cyclin-dependent kinase CDK1 and CDK2 inhibitor, with IC50 values of 6 and 9 nM, respectively. BMS-265246 inhibits CHI3L1 (chitinase 3-like-1) stimulation of ACE2 (angiotensin converting enzyme 2) and SPP (viral spike protein priming proteases). BMS-265246 can be used for ovarian cancer and COVID-19 research .
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1
1 Cited Publications
Cat. No.: HY-B2060A
CAS No.: 55297-96-6
Synonyms: Thiamutilin fumarate
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Tiamulin (Thiamutilin) fumarate is a diterpenic antibiotic that is widely used in pigs and poultry for the control of infectious diseases. Tiamulin fumarate is effectively used in the study of airsacculitis, which is primarily caused by Mycoplasma spp .
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1
1 Cited Publications
Cat. No.: HY-B2060
CAS No.: 55297-95-5
Synonyms: Thiamutilin
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Tiamulin (Thiamutilin) is a diterpenic antibiotic that is widely used in pigs and poultry for the control of infectious diseases. Tiamulin is effectively used in the study of airsacculitis, which is primarily caused by Mycoplasma spp .
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1
1 Cited Publications
Cat. No.: HY-128926
CAS No.: 341498-08-6
Purity:  97.65%
Synonyms: N-succinimidyl 4-(2-pyridyldithio) pentanoate
Target:  

ADC Linkers

Research Areas:  

Cancer

SPP (N-succinimidyl 4-(2-pyridyldithio) pentanoate) is a cleavable disulfide linker, can be used to form cytotoxic compound- linker conjugate .
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1
1 Cited Publications
Cat. No.: HY-B0643
CAS No.: 62013-04-1
Synonyms: LY237216
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Dirithromycin (LY237216), a derivative of Erythromycin, is a potent and orally active semi-synthetic macrolide antibiotic. Dirithromycin is active against gram-positive bacteria, Legionella spp., Helicobacter pylori, and Chlamydia trachomatis .
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1
1 Cited Publications
Cat. No.: HY-111360
CAS No.: 2195361-33-0
Purity:  99.94%
Target:  

γ-secretase

Research Areas:  

Inflammation/Immunology

SPL-707 is an orally active, selective signal peptide peptidase-like 2a (SPPL2a) inhibitor with an IC50 of 77 nM for hSPPL2a. SPL-707 inhibits γ-secretase (IC50=6.1 μM) and SPP (IC50=3.7 μM). SPL-707 has the potential for autoimmune diseases research by targeting B cells and dendritic cells .
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