15 Results for "

serine palmitoyltransferase

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "serine palmitoyltransferase" in MCE Product Catalog:

Cat. No.: HY-116073
CAS No.: 1113-41-3
Target:  

Acyltransferase

Research Areas:  

Infection Cancer

L-Penicillamine is an orally active serine palmitoyltransferase (SPT) inhibitor. L-Penicillamine inactivates the PLP cofactor by forming adducts, thereby inhibiting SPT activity and reducing sphingolipid biosynthesis. L-Penicillamine not only blocks tumor access to vitamin B6, but also stabilizes the human papillomavirus 16 E6 oncoprotein monomer and inhibits its polymerization, exhibiting a unique anticancer mechanism. L-Penicillamine effectively delays the growth of Sarcoma-180, induces tumor necrosis and prolongs survival (though long-term use may lead to Pyridoxine (HY-B1328) deficiency and weight loss) .
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Cat. No.: HY-170794
CAS No.: 2035010-37-6
Research Areas:  

Metabolic Disease

ALT-007 is an orally active serine palmitoyltransferase (SPT) inhibitor that selectively reduces the levels of toxic very-long-chain deoxysphingolipids to enhance protein homeostasis. ALT-007 restores aging-related loss of muscle mass in a mouse model of sarcopenia. ALT-007 enhances protein homeostasis in both mouse and C. elegans models of aging and disease. ALT-007 can be used for age-related neuromuscular diseases research .
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Cat. No.: HY-W688565
CAS No.: 18944-28-0
Target:  

Ceramidase

Research Areas:  

Metabolic Disease

(2S)-2-Amino-1-hydroxyoctadecan-3-one is the product generated by the decarboxylative condensation of L-serine and palmitoyl-CoA catalyzed by serine palmitoyltransferase (SPT) .
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Cat. No.: HY-119759A
CAS No.: 11075-87-9
Purity:  99.96%
Target:  

Antibiotic Fungal

Research Areas:  

Infection

Lipoxamycin hemisulfate is an antifungal antibiotic and a potent serine palmitoyltransferase inhibitor with an IC50 of 21 nM .
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Cat. No.: HY-115498
CAS No.: 1037837-27-6
Purity:  99.08%
ARN14494 is a potent and selective serine palmitoyltransferase (SPT) inhibitor, with an IC50 of 27.3 nM. ARN14494 affects the CNS in terms of anti-inflammation and neuroprotection. ARN14494 protects neurons from β-amyloid 1-42-induced neurotoxicity through a variety of mechanisms, including anti-oxidation, anti-apoptosis, and anti-inflammation. ARN14494 can be used for Alzheimer’s disease research .
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Cat. No.: HY-139097
CAS No.: 128427-86-1
Purity:  98.0%
Target:  

Acyltransferase

Research Areas:  

Others

C12-Sphingosine is a short-chain Sphingosine homologue. C12-Sphingosine inhibits serine palmitoyltransferase activity in primary cultured cerebellar cells .
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Cat. No.: HY-119759
CAS No.: 32886-15-0
Lipoxamycin is an antifungal antibiotic and a potent serine palmitoyltransferase inhibitor with an IC50 of 21 nM .
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Cat. No.: HY-119759AR
CAS No.: 11075-87-9
Research Areas:  

Infection

Lipoxamycin (hemisulfate) (Standard) is the analytical standard of Lipoxamycin (hemisulfate). This product is intended for research and analytical applications. Lipoxamycin hemisulfate is an antifungal antibiotic and a potent serine palmitoyltransferase inhibitor with an IC50 of 21 nM[1][2].
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Cat. No.: HY-W745771
D-Penicillamine-d6 is the deuterium labeled L-Penicillamine (HY-116073). L-Penicillamine is a mechanism-based inhibitor of serine palmitoyltransferase by forming a pyridoxal-5 '-phosphate-thiazolidine adduct. L-Penicillamine is a metal chelating agent of intermediate strength .
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Cat. No.: HY-N20677
CAS No.: 1151683-53-2
9''-Methyl lithospermic acid is a serine palmitoyltransferase (SPT) activator. 9''-Methyl lithospermic acid increases the levels of SPT1 and SPT2 in human keratinocytes. 9''-Methyl lithospermic acid maintains epidermal permeability barrier function by promoting SPT expression .
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Cat. No.: HY-181943
CAS No.: 2035011-97-1
Target:  

Acyltransferase

Research Areas:  

Cancer

SPT-IN-2 is an orally active serine palmitoyltransferase (SPT) inhibitor (with an IC50 of 0.71 nM against human SPT2). SPT-IN-2 inhibits ceramide synthesis, suppresses cancer cell growth, and exhibits in vivo anti-tumor activity, favorable metabolic stability and cell membrane permeability in xenograft mouse models. SPT-IN-2 blocks the de novo sphingolipid synthesis pathway, significantly reducing intracellular ceramide levels and the levels of 3-ketodihydrosphingosine (3-KDS), the immediate downstream product of SPT. SPT-IN-2 can be used in research related to lung adenocarcinoma, acute promyelocytic leukemia and breast cancer .
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Cat. No.: HY-P811111
Synonyms: LCB1, SPTLC1, serine palmitoyltransferase 1, Long chain base biosynthesis protein 1, serine-palmitoyl-CoA transferase 1, LCB 1, SPT 1, SPT1

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P812048
Synonyms: LCB1, SPTLC1, serine palmitoyltransferase 1, Long chain base biosynthesis protein 1, serine-palmitoyl-CoA transferase 1, LCB 1, SPT 1, SPT1

Host:  

Mouse

Application:  

WB, FC

Reactivity:  

Human

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Cat. No.: HY-P812048A
Synonyms: LCB1, SPTLC1, serine palmitoyltransferase 1, Long chain base biosynthesis protein 1, serine-palmitoyl-CoA transferase 1, LCB 1, SPT 1, SPT1

Host:  

Mouse

Application:  

WB, FC

Reactivity:  

Human

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Cat. No.: HY-16342
CAS No.: 827034-92-4
NA808 is an Serine Palmitoyltransferase (SPT) inhibitor. NA808 reduces sphingomyelin synthesis, inhibits its activation in hepatic stellate cells, and decreases the expression of α-SMA protein and mRNA, as well as collagen 1A1 mRNA (IC50 0.16, 0.12, and 0.11 μM, respectively). NA808 inhibits HCV replication and reduces NS3 and RdRp protein expression in HCV replicon cells without significant cytotoxicity and exhibits almost no immunosuppressive effect at effective concentrations. NA808 demonstrates broad-spectrum antiviral activity in humanized chimeric liver mice infected with various HCV genotypes, and dose-dependently reduces serum and hepatic HCV RNA levels. NA808 can be used for research on non-alcoholic steatohepatitis and hepatitis C virus infection .
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