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Search Results for " amide-type "

9

抑制剂 & 化合物

3

天然产物

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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。
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)

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

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...

化合物

Mepivacaine hydrochloride
Cat.No: T0946
Synonym: Mepivacaine HCl,盐酸甲哌卡因
Target: Sodium Channel
Dibucaine
Cat.No: T0364
Synonym: 地布卡因,Cinchocaine
Target: CaMK, Sodium Channel, AChR
Prilocaine
Cat.No: T6953
Synonym: Citanest,丙胺卡因,Propitocaine,NSC 40027
Target: ATPase, Sodium Channel
Ropivacaine hydrochloride
Cat.No: T0386
Synonym: 盐酸罗哌卡因,Ropivacaine monohydrochloride
Target: Potassium Channel, Sodium Channel
Prilocaine hydrochloride
Cat.No: T0796
Synonym: Prilocaine HCl,Propitocaine hydrochloride,Xylonest,盐酸丙胺卡因
Target: ATPase, Sodium Channel
CB2R/FAAH modulator-1
Cat.No: T67896
Synonym:
Target: Cannabinoid Receptor, FAAH
Bupivacaine hydrochloride
Cat.No: T0030
Synonym: Vivacaine,Bupivacaine HCl,盐酸布比卡因
Target: Sodium Channel
GLP-1 (1-36) amide (human, rat) (trifluoroacetate salt)
Cat.No: T36380
Synonym:
Target:
15-keto-17-phenyl trinor Prostaglandin F2α
Cat.No: T37934
Synonym: 15-keto-17-phenyl trinor Prostaglandin F2α
Target:
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。

天然产物

Aegeline
Cat.No: T7846
Synonym:
Target: Others, Antifungal
Cinchonine
Cat.No: T0012
Synonym: LA40221,(8R,9S)-Cinchonine,奎宁树,辛可宁
Target: Apoptosis, P-gp, Parasite
Betulonic acid
Cat.No: T5S0018
Synonym: 路路通酸,(+)-Betulonic acid,Betunolic acid,Liquidambaric acid
Target: Parasite, HSV
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