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Cat. No. | Product Name | ||
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L7810 | 高溶解性多官能团片段化合物库 | 1159 compounds | |
高溶解性多官能团片段库包含1159 种片段分子 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0946 |
Mepivacaine hydrochloride
Mepivacaine HCl,盐酸甲哌卡因 |
Sodium Channel | Membrane transporter/Ion channel |
Mepivacaine hydrochloride (Mepivacaine HCl) 是具有局部麻醉特性的酰胺衍生物。Mepivacaine hydrochloride 与神经元细胞膜上特定的电压门控钠离子通道结合,抑制钠离子内流和膜去极化。 | |||
T0364 |
Dibucaine
地布卡因,Cinchocaine |
CaMK; Sodium Channel; AChR | Membrane transporter/Ion channel; Neuroscience |
Dibucaine (Cinchocaine) 是钠通道抑制剂和有效的SChE 抑制剂。 | |||
T6953 |
Prilocaine
Citanest,丙胺卡因,Propitocaine,NSC 40027 |
ATPase; Sodium Channel | Membrane transporter/Ion channel |
Prilocaine (NSC-40027) 是一种氨基酰胺类局部麻醉剂,作用于神经元膜上的钠通道并限制癫痫发作的扩散。它是Na/K-ATPase 抑制剂,具有神经毒性作用。 | |||
T0386 |
Ropivacaine hydrochloride
盐酸罗哌卡因,Ropivacaine monohydrochloride |
Potassium Channel; Sodium Channel | Membrane transporter/Ion channel |
Ropivacaine hydrochloride (Ropivacaine monohydrochloride) 是钠通道阻断剂,通过可逆地抑制钠离子内流从而引起神经纤维脉冲传导阻滞。Ropivacaine hydrochloride 也是 K2P(双孔钾通道)TREK-1的抑制剂。在动物实验模型中,Ropivacaine hydrochloride 可用于神经性疼痛的缓解。 | |||
T0796 |
Prilocaine hydrochloride
Prilocaine HCl,Propitocaine hydrochloride,Xylonest,盐酸丙胺卡因 |
ATPase; Sodium Channel | Membrane transporter/Ion channel |
Prilocaine hydrochloride (Prilocaine HCl) 是一种氨基酰胺类局部麻醉剂,作用于神经元膜上的钠通道并限制癫痫发作的扩散。它是Na/K-ATPase 抑制剂,具有神经毒性作用。 | |||
T31773 |
Fenlean
FLZ |
Beta Amyloid; Src | Angiogenesis; Neuroscience; Tyrosine Kinase/Adaptors |
Fenlean (FLZ) 是酪氨酸激酶 Src 抑制剂,是来自Annona glabra的鳞甲酰胺的合成环状衍生物,具有细胞保护活性,在帕金森病慢性 MPTP/丙磺舒类小鼠模型中保护酪氨酸羟化酶功能。Fenlean 可以抑制线粒体中Aβ的产生,可用于研究年龄相关性黄斑变性和帕金森。 | |||
T67896 |
CB2R/FAAH modulator-1
|
Cannabinoid Receptor; FAAH | GPCR/G Protein; Metabolism; Neuroscience |
CB2R/FAAH modulator-1是一种大麻素2型受体(CB2R)激动剂,同时也是脂肪酸酰胺水解酶(FAAH)抑制剂(IC50=4 μM),可减少促炎和增加抗炎细胞因子的产生,常用于炎症研究。对 CB2R 和 CB1R 的Kis 分别为14.8 nM 和241.3 nM。 | |||
T0030 |
Bupivacaine hydrochloride
Vivacaine,Bupivacaine HCl,盐酸布比卡因 |
Sodium Channel | Membrane transporter/Ion channel |
Bupivacaine hydrochloride (Vivacaine) 是NMDA 受体抑制剂,可用于慢性疼痛的研究。它可阻断钠、L-钙和钾通道,还阻断SCN5A 通道,IC50为 69.5 μM。 | |||
T36380 |
GLP-1 (1-36) amide (human, rat) (trifluoroacetate salt)
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GLP-1 amide is a peptide hormone cleaved from proglucagon in the pancreas.1,2 Mice lacking the glucagon receptor (Gcgr-/-) have approximately nine-fold higher levels of total GLP-1 amide, including GLP-1 (1-36) amide and truncated GLP-1 (7-36) amide , in pancreatic tissue compared to wild-type mice.2References1. Schjoldager, B.T., Mortensen, P.E., Christiansen, J., et al. GLP-1 (glucagon-like peptide 1) and truncated GLP-1, fragments of human proglucagon, inhibit gastric acid secretion in humans... | |||
T37934 |
15-keto-17-phenyl trinor Prostaglandin F2α
15-keto-17-phenyl trinor Prostaglandin F2α |
Others | Others |
Bimatoprost is an F-series prostaglandin (PG) analog which has been approved for use as an ocular hypotensive drug. Oxidation of the C-15 hydroxyl group and amide hydrolysis of Bimatoprost produces 15-keto-17-phenyl trinor PGF2α. 15-keto-17-phenyl trinor PGF2α is a potential metabolite of bimatoprost when administered to animals. 15-keto PG analogs are potential minor impurities in commercial preparations of their corresponding bulk drug compounds. Although much less potent that the parent compo... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7846 |
Aegeline
|
Others; Antifungal | Microbiology/Virology; Others |
Aegeline 是从 Aegle marmelos 的叶子中分离出来的一种生物碱酰胺,有抗高血糖和抗血脂异常的活性。 | |||
T0012 |
Cinchonine
LA40221,(8R,9S)-Cinchonine,奎宁树,辛可宁 |
Apoptosis; P-gp; Parasite | Apoptosis; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Cinchonine (LA40221) 是金鸡纳树皮中的一种天然产物。它可激活内质网应激诱导的人肝癌细胞凋亡。它是一种酰胺类局部麻醉剂。 | |||
T5S0018 |
Betulonic acid
路路通酸,(+)-Betulonic acid,Betunolic acid,Liquidambaric acid |
Parasite; HSV | Microbiology/Virology |
Betulonic acid (Liquidambaric acid) 是一种在许多植物中存在的三萜类天然产物,具有抗肿瘤,抗炎,抗寄生虫和抗病毒的活性。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-01189 |
GFPT1 Protein, Human, Recombinant
GFAT1,CMSTA1,GFAT,glutamine--fructose-6-phosphate transamina... |
Human | E. coli |
Glutamine:fructose-6-phosphate amidotransferase 1 (GFAT), also known as GFPT1, is a member of the N-terminal nucleophile aminotransferases and the first rate-limiting enzyme for the entry of glucose into the hexosamine biosynthesis pathway (HBP) in mammals. GFAT transfers the amino group from the L-glutamine amide to the D-fructose 6-phosphate, producing glutamic acid and glucosamine 6-phosphate. GFAT exists as a homotetramer in cytoplasm, and is proposed to be most likely involved in re... |