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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T81471 | Phytoene desaturase-IN-2 | ||
PDS-IN-1为Oryza sativa中八氢番茄红素去饱和酶(OsPDS)的抑制剂,具备除草效能。 | |||
T74929 | Phytoene desaturase-IN-1 | ||
Phytoene desaturase-IN-1 是高效的PDS抑制剂(Kd: 65.9 μM),通过与Phe301残基形成π-π堆叠效应。该化合物显示出广谱的芽后除草活性,并能在白化病叶片中诱导PDS mRNA水平下降及八氢番茄红素与ROS累积,适用于农业生产。 | |||
T2650 |
MK-8245
|
Dehydrogenase; Stearoyl-CoA Desaturase (SCD) | Metabolism |
MK8245 是肝靶向的硬脂酰 -CoA 去饱和酶(SCD)抑制剂,对人 SCD1 和鼠 SCD1 的IC50值分别为 1 nM 和 3 nM,具有抗糖尿病和抗血脂异常的作用。 | |||
T10525 |
SCD1 inhibitor-4
|
Dehydrogenase; Stearoyl-CoA Desaturase (SCD) | Metabolism |
SCD1 inhibitor-4 是一种具有口服活性的 stearoylCoA desaturase-1 抑制剂,可用于研究糖尿病。 | |||
T16068 |
MF-438
|
Dehydrogenase; Stearoyl-CoA Desaturase (SCD) | Metabolism |
MF-438 是一种口服具有活力的 stearoyl-CoA desaturase 1 抑制剂,其对 rSCD1 的 EC50值为 2.3 nM。 | |||
T13356 |
XEN723
|
Dehydrogenase; Stearoyl-CoA Desaturase (SCD) | Metabolism |
XEN723 是新型的硬脂酰辅酶 A 去饱和酶的噻唑基咪唑烷酮抑制剂,能够抑制小鼠和 HepG2 细胞的活性,它们的 IC50值分别为 45 和 524 nM。 | |||
T6412 |
CVT-12012
|
Stearoyl-CoA Desaturase (SCD) | Metabolism |
CVT-12012 是口服具有活性的硬脂酰-CoA 去饱和酶抑制剂,能够抑制大鼠微粒体和人 HEPG2 的活性,它们的IC50值分别为 38 nM,6.1 nM。 | |||
T4515 |
A939572
|
Dehydrogenase; Stearoyl-CoA Desaturase (SCD) | Metabolism |
A939572 是口服具有活性的硬脂酰 CoA 去饱和酶 1SCD1抑制剂,对mSCD1和hSCD1的IC50分别为 <4 nM 和 37 nM。 | |||
T14878 |
CAY10566
|
Dehydrogenase; Stearoyl-CoA Desaturase (SCD) | Metabolism |
CAY10566 是选择性的、口服具有活性的硬脂酰辅酶 A 去饱和酶 1 抑制剂,在小鼠和人酶测定中IC50分别为 4.5 和 26 nM。它具有显著的细胞活性,可阻断 HepG2 细胞中饱和长链脂肪酸-CoAs (LCFA-CoAs) 向单不饱和 LCFA-CoAs 的转化 。 | |||
T9722 |
YTX-465
|
Stearoyl-CoA Desaturase (SCD) | Metabolism |
YTX-465 是有效的硬脂酰辅酶 A 去饱和酶 (Ole1/SCD) 抑制剂,抑制 Ole1 和 SCD1的IC50=分别为 0.039 μM 和 30.4 μM。YTX-465在帕金森病和其他突触核蛋白病领域有研究的价值。 | |||
T5427 |
GSK1940029
SCD inhibitor 1 |
Dehydrogenase; Stearoyl-CoA Desaturase (SCD) | Metabolism |
GSK1940029 (SCD inhibitor 1) 是酰基-辅酶A 去饱和酶 (SCD) 抑制剂。 | |||
T12856 |
SC-26196
ALPHA,ALPHA-二苯基-4-[(3-吡啶亚甲基)氨基]-1-吡嗪戊腈 |
Others | Others |
SC-26196 是一种 Delta6 去饱和酶 (D6D, FADS2) 抑制剂 (在大鼠肝微粒体中,IC50=0.2 µM),具有口服活性,具有抗炎作用。 | |||
T27061 |
CP-24879 hydrochloride
CP-24879 HCl |
Others | Others |
CP-24879 hydrochloride (CP-24879 HCl) 是选择性的 delta5D/delta6D 联合抑制剂。它能显著降低肝细胞内脂质积聚和炎症损伤。它在脂肪-1 和 ω-3 处理的肝细胞中表现出优越的抗脂肪变性和抗炎作用,可用于非酒精性脂肪性肝炎的研究。 | |||
T1869 |
PluriSIn 1
4-吡啶羧酸 2-苯基酰肼,NSC 14613,PluriSIn #1,PluriSln 1 |
Apoptosis; Dehydrogenase; Stearoyl-CoA Desaturase (SCD) | Apoptosis; Metabolism |
PluriSIn 1 (NSC 14613) 是一种酰基-辅酶 A 去饱和酶抑制剂,是一种多能细胞特异性的抑制剂。 | |||
T9003 |
CVT-11127
N-[2-[6-[[(3,4-二氯苯基)甲基]氨基]-2-(4-甲氧基苯基)-3-氧代-3,4-二氢吡啶并[2,3-B]吡嗪-4-基]乙基]乙酰胺 |
Dehydrogenase | Metabolism |
CVT-11127 是 SCD 抑制剂。它将细胞周期阻滞在 G1/S 期,诱导细胞凋亡。它可用于肺癌的研究。 | |||
T21012 |
Diflufenican
M&B 38544,吡氟草胺 |
Others | Others |
Diflufenican (M&B 38544) 是一种选择性除草剂,用于专门防治某些阔叶杂草。 | |||
T20950 |
MK-8245 analog
MK-8245-analog,MK 8245 analog |
Others | Others |
MK-8245 analog 是 MK-8245 的类似物,MK-8245 是一种肝脏靶向的硬脂酰辅酶 A 去饱和酶 (SCD) 抑制剂。它可用于治疗血脂异常和糖尿病。 | |||
T9859 |
SW209049
|
Dehydrogenase | Metabolism |
SW209049 是一种硬脂酰辅酶A 9-去饱和酶抑制剂。 SW209049 对H2122细胞表现出有效的活性,IC50为0.13uM。 | |||
T28903 |
T-3364366
T 3364366,T3364366 |
Others | Others |
T-3364366 是一种噻吩并嘧啶酮 delta-5 去饱和酶 (Δ5D) 抑制剂,在 HepG2 和 RLN-10 细胞中的 IC50 分别为 1.9 nM 和 2.1 nM。 | |||
T60952 |
Fluridone
EL-171 |
Others | Others |
Fluridone (EL-171) 是 一种有效的合成脱落酸 (ABA) 的抑制剂,抑制 AchnFAR 和 TF 基因的表达,减少伯醇的形成。Fluridone 常作为水生除草剂用于控制入侵植物,也被用来控制水螅和欧亚水螅等物种。 | |||
T28892 |
SW208108
SW 208108,SW-208108 |
||
SW208108 is a tumor-specific irreversible inhibitor of stearoyl CoA desaturase (SCD). | |||
T19796 | Beflubutamid | ||
Beflubutamid is an herbicide. It works by inhibiting phytoene-desaturase. | |||
T13054 |
T-3764518
|
Dehydrogenase | Metabolism |
T-3764518 is a novel and potent inhibitor of stearoyl coenzyme A desaturase (SCD)(IC50 of 4.7 nM). | |||
T68939 |
GT11
|
||
GT-11 is an inhibitor of dihydroceramides (DHCer) desaturase activity. | |||
T12863 |
SCD1 inhibitor-1
|
Others | Others |
SCD1 inhibitor-1 is a potent and liver-selective inhibitor of stearoyl-CoA desaturase-1 (SCD1). | |||
T71745 |
XEN103
|
||
XEN103 is a potent and selective Stearoyl-CoA Desaturase-1 inhibitor. | |||
T60308 | N'-(2-Fluorophenyl)pyrazine-2-carbohydrazide | ||
N'-(2-Fluorophenyl)pyrazine-2-carbohydrazide 是Ole1p 去饱和酶抑制剂,也是一种抗真菌剂。 | |||
T10167 |
5-Dehydroepisterol
|
Others | Others |
5-Dehydroepisterol is an episterol derivative with anti-fungal activities. It can be formed by C-5 sterol desaturase and converted into 24-methylenecholesterol by 7-dehydrocholesterol reductase. | |||
T79262 | SSI-4 | Stearoyl-CoA Desaturase (SCD) | Metabolism |
SSI-4为SCD1 (硬脂酰辅酶A去饱和酶1) 抑制剂,能够通过11C标记,用于SCD1体内小动物PET/CT成像的配体。 | |||
T15043 | D5D-IN-326 | Others | Others |
D5D-IN-326 is an orally active delta-5 desaturase (D5D) inhibitor (IC50s: 72 and 22 nM for rat and human D5D in enzymic and cell-based assays). It has no effect on D6D or D9D activity. D5D-IN-326 reduces insulin resistance and decreases body weight in die | |||
T35675 |
SW203668 (trifluoroacetate salt)
|
||
SW203668 is an irreversible inhibitor of stearoyl-CoA desaturase (IC50 = 54 nM). It is selectively cytotoxic to H2122, H460, HCC44, and HCC95 cell lines that express cytochrome P450 (CYP) isoform CYP4F11 over eight other cancer cell lines that lack CYP4F11 in vitro (IC50s = 22-116 and >10,000 nM, respectively) and ectopic expression of CYP4F11 in SW203668-insensitive H1155 cells results in sensitization to SW203668. In vivo, SW203668 reduces tumor growth rate without reducing sebocyte production... | |||
T38278 |
9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic Acid
|
||
9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic acid is an ω-3 very long-chain polyunsaturated fatty acid. It has been used to study the desaturation and elongation of ω-3 polyunsaturated fatty acids. It is elongated to form C26:5 or acted on by δ6 desaturase to form C24:6. 9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic acid is found at low levels in mouse brain and spleen and levels decrease in the brain and spleen of old and exceptionally old mice. | |||
T35810 |
C24 dihydro Ceramide (d18:0/24:0)
Cer(d18:0/24:0) |
||
C24 dihydro Ceramide is a sphingolipid that has been found in the stratum corneum of human skin.[1] It is found in higher concentrations in female sebum compared to male sebum.[2] C24 dihydro Ceramide levels positively correlate with cytotoxicity in CCRF-CEM, MOLT-4, COG-LL-317h, and COG-LL-332h T cell acute lymphoblastic leukemia (ALL) cell lines.[4] Levels of C24 dihydro ceramide are increased by 149.49-fold in dihydroceramide desaturase 1 (DEGS1) knockdown UM-SCC-22A human head and neck squam... | |||
T36099 |
Jacaric Acid
|
||
Jacaric acid is a conjugated polyunsaturated fatty acid first isolated from seeds of Jacaranda plants. Structurally, it is an 18-carbon ω-6 triene isomer of γ-linolenic acid . Jacaric acid induces cell cycle arrest and apoptosis in a variety of cancer cell lines (GI50 = 1-5 μM). It increases the production of reactive oxygen species, and cytotoxicity is abolished by the antioxidant α-tocopherol, suggesting that apoptosis results from oxidative stress. Jacaric acid is metabolized in vivo to conju... | |||
T38844 |
MK-8245 Trifluoroacetate
|
||
MK-8245 trifluoroacetate is a liver-targeting inhibitor of stearoyl-CoA desaturase (SCD) with IC50 of 1 nM for human SCD1 and 3 nM for both rat SCD1 and mouse SCD1, with anti-diabetic and anti-dyslipidemic efficacy. IC50 value: 1 nM (hSCD1) Target: SCD1 in vitro: MK-8245, a phenoxy piperidine isoxazole derivative, has been identified as a potent and liver-specific SCD inhibitor. It contains a tetrazole acetic acid moiety, which is the key molecule for OATPs recognition and liver-targeting. MK... | |||
T36887 |
8(E),10(E),12(Z)-Octadecatrienoic Acid
|
||
8(E),10(E),12(Z)-Octadecatrienoic acid is a conjugated polyunsaturated fatty acid (PUFA) that has been found inC. officinalisseed oil and has anticancer activity.1,2,3It inhibits the growth of Caco-2 cells when used at concentrations ranging from 10 to 50 μM.28(E),10(E),12(Z)-Octadecatrienoic acid (10 μM) induces formation of thiobarbituric acid reactive substances (TBARS) and apoptosis in DLD-1 colorectal adenocarcinoma cells.3It also inhibits prostaglandin biosynthesis in sheep vesicular gland... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3341 |
Elemicin
Elemicine,3,4,5-trimethoxyallylbenzene,榄香素 |
Influenza Virus; 5-HT Receptor; Stearoyl-CoA Desaturase (SCD) | GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience |
Elemicin (Elemicine) 是广泛分布于许多草药和香料中的一种烯基苯。它是芳香族食品中的主要成分之一,具有抗微生物,抗氧化剂和抗病毒活性,有遗传毒性和致癌性。它通过代谢激活抑制硬脂酰辅酶 A 去饱和酶 1。 | |||
T2919 |
Sesamin
Fagarol,Fsesamin,芝麻素 |
Others | Others |
Sesamin (Fsesamin) 是多不饱和脂肪酸生物合成中的选择性delta 5 去饱和酶抑制剂,是在芝麻油中存在丰富的木脂素。它对脑缺血具有有效的神经保护作用。 | |||
T4868 |
gamma-Linolenic acid
gamolenic acid,γ-Linolenic acid,γ-亚麻酸 |
Endogenous Metabolite | Metabolism |
gamma-Linolenic acid (gamolenic acid) 是一种 omega-6 (n-6),18 碳 (18C-) 多不饱和脂肪酸 (PUFA),可以从人乳和植物种子油中提取。 | |||
T41253 |
Sterculic acid
|
||
Sterculic acid 是一种硬脂酰辅酶 A 去饱和酶 1 (SCD1) 抑制剂。Sterculic acid 剂量依赖性抑制 delta-9 去饱和酶 (Δ9D) 活性,IC50值为 0.9 μM。 |