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抑制剂 & 化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T21343	PTZ-343 PTZ-343 sodium,PTZ 343,吩噻嗪-10-基-丙基磺酸钠盐	Others	Others
	PTZ-343 是一种鲁米诺的强效发光增强剂 (enhancer)。它极大的增强了过氧化物酶催化的鲁米诺化学发光氧化反应 (>80%) 的光输出。
T1413	Pentetrazol Metrazole,Pentylenetetrazole,Pentylenetetrazol,戊四唑,PTZ,pentamethylenetetrazol,Cardiazol	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	Pentetrazol 是一种 GABA(A) 受体拮抗剂，具有中枢神经系统和呼吸兴奋剂的活性。
T34189	PTZ-256 phenothiazine derivative,PTZ256
	PTZ-256 is a phenothiazine derivative with chemical name: 3-(10H-phenothiazin-10-yl)propane-1-amine. PTZ-256 has molecule weight 256, therefore, we call it as PTZ-256.
T34270	Razupenem SMP601,SMP 601,PTZ601,PTZ 601,PTZ-601,SMP-601
	Razupenem ( SMP-601, PTZ601) is a broad-spectrum injectable antibiotic derived from the carbapenem subgroup of β-lactam antibiotics. It has been developed as an alternative drug against bacteria that have developed antibiotic resistance to commonly used a
T81348	PTZ-LD
	PTZ-LD是一种phenothiazine衍生的荧光探针，专门用于检测脂滴(LDs)。在LDs中，PTZ-LD展示出显著的高特异性发射(Ex/Em=488/570-620 nm)。此探针还可以应用于糖尿病性白内障(DC)的研究工作。
T9285	TPTZ	Others	Others
	TPTZ 专门用作分析试剂。
T22171	WWL123	MAGL	Metabolism
	WWL123 是一种有效的选择性 ABHD6 抑制剂，IC50 为 430 nM。WWL123 可穿过血脑屏障并抑制脑实质中的 ABHD6。WWL123 阻断 ABHD6 在 Pentylenetetrazole (PTZ)诱导的 R6/2 小鼠癫痫样发作和自发性癫痫发作中发挥抗癫痫作用。

化合物

PTZ-343

Cat.No: T21343

Synonym: PTZ-343 sodium,PTZ 343,吩噻嗪-10-基-丙基磺酸钠盐

Target: Others

Pentetrazol

Cat.No: T1413

Synonym: Metrazole,Pentylenetetrazole,Pentylenetetrazol,戊四唑,PTZ,pentamethylenetetrazol,Cardiazol

Target: GABA Receptor

PTZ-256

Cat.No: T34189

Synonym: phenothiazine derivative,PTZ256

Target:

Razupenem

Cat.No: T34270

Synonym: SMP601,SMP 601,PTZ601,PTZ 601,PTZ-601,SMP-601

Cat. No.	Product Name	Target	Signaling Pathways
TN4322	Isopulegol	ATPase; Potassium Channel; GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	Isopulegol presents depressant- and anxiolytic-like effects, it also has anticonvulsant and bioprotective effects against PTZ-induced convulsions are possibly related to positive modulation of benzodiazepine-sensitive GABAA receptors and to antioxidant properties.Isopulegol presents significant gastroprotective effects in both ethanol- and indomethacin-induced ulcer models, which appear to be mediated, at least in part, by endogenous prostaglandins, K(ATP) channel opening, and antioxidant proper...