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Cat. No. | Product Name | Target | Signaling Pathways |
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T78569 |
CPT2
Carnitine palmitoyltransferase 2 |
Apoptosis | Apoptosis |
CPT2 (Carnitine palmitoyltransferase 2) 是一种脂肪酸氧化过程中的酶,它在结直肠癌 (CRC) 预后评估中作为生物标志物。CPT2 通过过表达激活p-p53并增加p53蛋白水平,这有助于抑制肿瘤生长和促进细胞的凋亡。CPT2 缺乏是长链脂肪酸氧化障碍相关的常见遗传性疾病,并且CPT2 的表达降低与多种癌症的发展密切相关,因此,在癌症研究领域具有研究价值。 | |||
T4535 |
Etomoxir sodium salt
(R)-(+)-乙莫克舍钠盐,(R)-Etomoxir sodium salt,Na salt,Etomoxir |
Apoptosis; Others | Apoptosis; Others |
Etomoxir sodium salt ((R)-Etomoxir sodium salt) 是一种肉碱棕榈酰转移酶 1a (CPT-1a) 抑制剂,可以阻断脂肪酸合成。Etomoxir sodium salt 具有抗肿瘤活性。 | |||
T11978 |
McN3716
NSC359682,Methyl palmoxirate |
Mitochondrial Metabolism; CPT | Metabolism |
McN3716 是一种肉碱棕榈酰转移酶 I (CPT-1) 抑制剂,可用于研究代谢疾病。 | |||
T26308 |
Lipoxamycin hemisulfate
Lipoxamycin, sulfate (2:1),U-26146D,U26146D,U 26146D,Lipoxamycin |
Antifungal | Microbiology/Virology |
Lipoxamycin hemisulfate (Lipoxamycin) 是一种丝氨酸棕榈酰转移酶抑制剂 (IC50 = 21 nM),具有抗真菌活性。 | |||
T4535L |
Etomoxir
(R)-(+)-Etomoxir |
Antioxidant; CPT | Metabolism; oxidation-reduction |
Etomoxir 是肉碱棕榈酰转移酶 1a (CPT-1a) 抑制剂,通过抑制 CPT-1a 来抑制脂肪酸氧化,且抑制人、大鼠和豚鼠中棕榈酸酯的氧化。Etomoxir 对腺嘌呤核苷酸转位酶有抑制作用,可通过破坏CoA稳态来抑制巨噬细胞极化。 | |||
T35364 |
2-Bromohexadecanoic acid
2-BP,2-溴十六烷酸,2-bromopalmitate,2-Bromohexadecanoic acid |
Others | Others |
2-Bromohexadecanoic acid (2-BP) 是一种不可代谢的棕榈酸酯类似物,可用作棕榈酰化抑制剂。它直接且不可逆地抑制所有 DHHC (Asp-His-His-Cys) 蛋白的棕榈酰转移酶活性。 | |||
T26308L |
Lipoxamycin HCl
Lipoxamycin HCl(11075-87-9 Free base) |
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Lipoxamycin HCl 是一种高效的丝氨酸棕榈酰转移酶 (serine palmitoyltransferase) 抑制剂,具有抗真菌活性,抑制丝氨酸棕榈酰转移酶活性。 | |||
T68618 |
S-(-)-Etomoxir
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S-(-)-Etomoxir is an inhibitor of carnitine palmitoyltransferase A (CPT1) -- a molecule required for the oxidation of long-chain acyl CoA esters. | |||
T38685 |
C12-Sphingosine
C12-Sphingosine |
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C12-Sphingosine is a short-chain homologue of Sphingosine. It effectively inhibits the activity of serine palmitoyltransferase in primary cultured cerebellar cells. | |||
T68196 |
Aminocarnitine
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Aminocarnitine is an inhibitor of fatty acid oxidation that acts as a hypoglycemic and antiketogenic compound. It alters lipidic metabolism by inhibiting carnitine acetyltransferase (CAT) and carnitine palmitoyltransferase (CPT). | |||
T68445 |
Clomoxir
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Clomoxir is a carnitine palmitoyltransferase I inhibitor that was under development as an antiarrhythmic and antidiabetic. | |||
T37245 |
Palmitoyl-D-carnitine (chloride)
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Palmitoyl-D-carnitine is a long-chain acylcarnitine, an isomer of palmitoyl-L-carnitine , and the D enantiomer of palmitoyl-DL-carnitine . It inhibits carnitine palmitoyltransferase with a Ki value of 2.1 mM for 14C-palmitoylcarnitine synthesis by erythrocyte membranes. | |||
T71554 | ARN 14494 | ||
ARN 14494 is a potent serine palmitoyltransferase inhibitor (SPT; IC50 = 27.3 nM). ARN 14494 inhibits synthesis of long chain ceramides and dihydroceramides in an in vitro model of Alzheimer's diease. The compound prevents the synthesis of proinflammatory cytokines and the oxidative stress-related enzymes iNOS and COX-2 in mouse primary cortical astrocytes. ARN 14494 is neuroprotective against β-amyloid 1-42 induced neurotoxicity in primary cortical neurons co-cultured with astrocytes. | |||
T83767 |
4-Hydroxyphenylglyoxylic Acid
UK 22486 |
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4-Hydroxyphenylglyoxylic acid 是一种抑制剂,针对 carnitine palmitoyltransferase 1 (CPT1),同时也是前药 oxfenicine 的活性代谢物。在 200 至 1,000 µM 的浓度范围内,该化合物能够抑制离体大鼠肝线粒体中的 CPT1,并能够抑制离体大鼠肝细胞中的油酸氧化。 | |||
T73829 |
Malonyl CoA
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Malonyl CoA是脂肪酸生物合成的重要底物,同时也担任脂肪酸氧化过程中的抑制剂角色。此外,Malonyl CoA亦作为线粒体肉碱棕榈酰转移酶1(CPT1)的可逆性抑制剂。 | |||
T38214 |
1-Deoxysphingosine (m18:1(4E))
1-Deoxysphingosine (m18:1(4E)) |
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1-Deoxysphingosine (m18:1(4E)) is an atypical sphingolipid that contains a double bond at the 4E native position and is formed when serine palmitoyltransferase condenses palmitoyl-CoA with alanine instead of serine during sphingolipid synthesis.1,2 Plasma levels of 1-deoxysphingosine (m18:1(4E)) are increased in patients with chronic idiopathic axonal neuropathy (CIAP) and diabetic distal symmetrical polyneuropathy (DSPN).3 |1. Steiner, R., Saied, E.M., Othman, A., et al. Elucidating the chemica... | |||
T38284 |
C24 dihydro 1-Deoxyceramide (m18:0/24:0)
C24 dihydro 1-Deoxyceramide (m18:0/24:0) |
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C24 dihydro 1-Deoxyceramide (m18:0/24:0) is a very long-chain atypical ceramide containing a 1-deoxysphinganine backbone. 1-Deoxysphingolipids are formed when serine palmitoyltransferase condenses palmitoyl-CoA with alanine instead of serine during sphingolipid synthesis.1,2 C24 dihydro 1-Deoxyceramide (m18:0/24:0) has been found in mouse embryonic fibroblasts (MEFs) following application of 1-deoxysphinganine alkyne or 1-deoxysphinganine-d3.3 It has also been found in mouse brain, spinal cord, ... | |||
T38280 |
C22 dihydro 1-Deoxyceramide (m18:0/22:0)
C22 dihydro 1-Deoxyceramide (m18:0/22:0) |
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C22 dihydro 1-Deoxyceramide (m18:0/22:0) is a very long-chain atypical ceramide containing a 1-deoxysphinganine backbone. 1-Deoxysphingolipids are formed when serine palmitoyltransferase condenses palmitoyl-CoA with alanine instead of serine during sphingolipid synthesis.1,2 C22 dihydro 1-Deoxyceramide (m18:0/22:0) has been found in mouse embryonic fibroblasts (MEFs) following application of 1-deoxysphinganine alkyne or 1-deoxysphinganine-d3.3 It has also been found as the most prevalent dihydro... | |||
T69395 |
Nicotinamide-d4
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Nicotinamide-d4 is intended for use as an internal standard for the quantification of nicotinamide by GC- or LC-MS. Nicotinamide is an amide form of niacin, which is also known as vitamin B3, that can be biosynthesized in vivo or obtained through the diet. It is a precursor in the synthesis of the metabolic cofactor NAD+ and an inhibitor of sirtuin 1 (SIRT1; IC50 = <50 µM). Nicotinamide (10 µM) increases the activity of serine palmitoyltransferase (SPT) and the biosynthesis of ceramide, glucosyl... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T4785 |
Oxfenicine
4-羟基-L-苯甘氨酸,4-Hydroxy-L-phenylglycine |
Others | Others |
Oxfenicine (4-Hydroxy-L-phenylglycine) 是具有口服活性的肉碱棕榈酰转移酶-1 抑制剂。它在缺血期间保护心脏免受坏死组织的损害。它可抑制心脏中脂肪酸的氧化。 | |||
T36831 |
9-Oxononanoic Acid
9-ONA |
Phospholipase; CPT | Metabolism |
9-Oxononanoic Acid是一种氧化脂肪酸,由亚油酸自氧化形成,它能提高磷脂酶 A2(PLA2)的活性,并增加离体人体血浆中血栓素 B2 的生成。9-Oxononanoic Acid 能减少肝脏新脂肪酸的合成,并提高大鼠肝脏肉碱棕榈酰转移酶(β-氧化的标志物)的活性。 | |||
T16165 |
Myriocin
ISP-I,Thermozymocidin |
HCV Protease; Antifungal | Microbiology/Virology; Proteases/Proteasome |
Myriocin (Thermozymocidin) 是一种从 Myriococcum albomyces 中得到的代谢产物,是一种丝氨酸-棕榈酰转移酶 (SPT) 抑制剂,具有潜在的抗肿瘤抗癌和抗寄生虫活性,通过 PI3K/Akt/mTOR 通路调节巨噬细胞极化和功能来抑制肿瘤生长。Myriocin 抑制 HCV 感染,可用于研究神经病变和真菌感染。 |