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Cat. No. | Product Name | Target | Signaling Pathways |
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T8526 |
Metformin
甲福明,二甲双胍,1,1-Dimethylbiguanide |
Mitophagy; AMPK; Autophagy | Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Metformin (1,1-Dimethylbiguanide) 是一种 AMPK 激活剂,具有血脑屏障渗透性。Metformin 可通过提高胰岛素敏感性和减少肠道对葡萄糖的吸收来改善血糖控制,常用于 2 型糖尿病的研究。 | |||
T0740 |
Metformin hydrochloride
Metformin HCl,盐酸二甲双胍,1, 1-Dimethylbiguanide hydrochloride,1,1-Dimethylbiguanide hydrochloride |
Mitophagy; AMPK; Autophagy | Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Metformin hydrochloride (1,1-Dimethylbiguanide hydrochloride) 是一种抗糖尿病药物,抑制结肠、前列腺等多种 Y 细胞的增殖,具有作为抗 Y 药物的潜在功能。它可以透过血脑屏障,诱导自噬。 | |||
T32758 |
Linagliptin mixture with metformin
Jentadueto Xr,Linagliptin / metformin,Jentadueto |
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Linagliptin mixture with metformin is used for the treatment of type 2 diabetes. | |||
T73712 |
Metformin-d6 hydrochloride
1,1-Dimethylbiguanide-d6 hydrochloride |
AMPK; Autophagy | Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Metformin-d6 hydrochloride (Metformin-d6 hydrochloride) 是 Metformin 的一种氘代化物,可用于研究 Metformin 在体内的代谢,常作为Metformin的内标。 | |||
T70806 |
Metformin icosapent
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Metformin icosapent is an AMP-activated protein kinase (AMPK) activator that improves glycemic control by improving insulin sensitivity and decreasing intestinal absorption of glucose. | |||
T71222 |
Metformin glycinate
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Metformin glycinate is an AMP-activated protein kinase (AMPK) activator that improves glycemic control by improving insulin sensitivity and decreasing intestinal absorption of glucose. | |||
T69405 | Metformin embonate | ||
Metformin embonate is an AMP-activated protein kinase (AMPK) activator that improves glycemic control by improving insulin sensitivity and decreasing intestinal absorption of glucose. | |||
T69049 |
Metformin orotate
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Metformin orotate is an AMP-activated protein kinase (AMPK) activator that improves glycemic control by improving insulin sensitivity and decreasing intestinal absorption of glucose. | |||
T20028 |
Janumet
Efficib,Janumet XR,Metformin / sitagliptin,Metformin hydrochloride mixture with sitagliptin phosphate |
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Metformin hydrochloride mixture with sitagliptin phosphate is an AMP-activated protein kinase stimulant. It is also a CD26 antigen inhibitor, Gluconeogenesis inhibitor, and Glucose modulator. | |||
T70804 |
Itasetron hydrochloride monohydrate
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Itasetron hydrochloride monohydrate is a potent 5HT-3 receptor antagonist. | |||
T8929 |
BC1618
2-Propanol, 1-[bis(phenylmethyl)amino]-3-[4-(trifluoromethyl)phenoxy]- |
Mitophagy; Others; E1/E2/E3 Enzyme; AMPK | Autophagy; Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling; Ubiquitination |
BC1618 (2-Propanol, 1-[bis(phenylmethyl)amino]-3-[4-(trifluoromethyl)phenoxy]-) 是一种具有口服活性的 Fbxo48 抑制剂,可刺激 Ampk 依赖性信号传导。它促进线粒体分裂,促进自噬并提高肝脏胰岛素敏感性。 | |||
T83971L |
LCC-12 FA
|
Antiviral; Antibacterial | Immunology/Inflammation; Microbiology/Virology |
LCC-12 FA 是一种由二甲双胍组成的二聚体,通过靶向线粒体铜 (ii) 从而诱导 NAD(H) 池减少。LCC-12 FA 可减少细菌和病毒感染小鼠模型中的炎症,可用于研究代谢疾病。 | |||
T8532 |
IM156
|
OXPHOS | Apoptosis |
IM156 (HL156A; HL271 acetate) 是衍生自二甲双胍的化合物,是一种强效的,具有口服活性的AMPK 激活剂。IM156 在动物模型中可缓解与年龄相关的认知下降。IM156 是一种有效的氧化磷酸化 (OXPHOS) 抑制剂,可用于实体肿瘤的研究。 | |||
T0242 |
Sitagliptin
西他列汀,MK0431,西格列汀 |
Proteasome; DPP-4; Autophagy | Autophagy; Proteases/Proteasome; Ubiquitination |
Sitagliptin (MK0431) 是一种有效的 DPP4抑制剂,在 Caco-2 细胞中,IC50值为 19 nM。它是一种新型口服降糖药,可单独使用或与二甲双胍或噻唑烷二酮联合用于治疗 2 型糖尿病。 | |||
T11570 |
HL271
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AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
HL271, a derivative of metformin, is a potent AMPK activator that increases AMPK phosphorylation. HL271 attenuates aging-associated cognitive impairment. | |||
T83866 | LCC-12 formate | ||
LCC-12是一种铜(II)螯合剂,为二甲双胍的衍生物。作为单体,它能结合铜(II)并在20 µM的浓度下减少氢过氧化物依赖的NADH向NAD+的氧化。在10 µM的浓度下,LCC-12降低一次性人类细胞因子激活的单核衍生的巨噬细胞(MDMs)中IL-1β、IL-2、IL-6、IL-8和TNF-α的细胞因子水平,以及JAK2、STAT2和IL-1受体相关激酶4(IRAK4)的水平。此外,同样浓度的LCC-12减少了细胞因子激活的MDMs中CD80+和CD86+的数量。每日0.3 mg/kg的剂量可提高LPS或盲肠结扎穿孔模型小鼠的存活率。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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TN2252 |
Syrosingopine
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Dopamine Receptor | GPCR/G Protein; Neuroscience |
Syrosingopine 是 MCT1和 MCT4双重抑制剂,对 MCT4 的效力高 60 倍,可防止乳酸和 H+ 流出。它是可口服抗高血压药物,联合二甲双胍具有研究癌症疾病的潜力。 | |||
T35532 |
Galegine hydrochloride
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Galegine hydrochloride, a guanidine derivative derived from G. officinalis, plays a role in inducing weight loss in mice and has contributed to the development of biguanides, including metformin and phenformin. This compound stimulates AMPK activation in 3T3-L1 adipocytes, L6 myotubes, H4IIE rat hepatoma, and HEK293 human kidney cell lines. Additionally, galegine hydrochloride exhibits antibacterial properties, particularly demonstrating a minimum inhibitory concentration of 4 mg/L against Staph... |