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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6972 |
RS-1
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
RS-1 是一种 RAD51 的激活剂,同时可增强 CRISPR/Cas9 的活性。 | |||
T24741 |
RS1-PDK1 inhibitor
RS-1,RS1,RS 1 |
PDK | PI3K/Akt/mTOR signaling |
RS1-PDK1 inhibitor (RS 1) 是一种选择性的蛋白激酶PDK1抑制剂,可用来治疗和预防疾病或失调。 | |||
T7519 |
RS-127445 hydrochloride
4-(4-氟-1-萘基)-6-(1-甲基乙基)-2-嘧啶胺盐酸盐,RS 127445,MT 500 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
RS-127445 hydrochloride (MT 500) 是一种可口服的,高亲和力选择性5-HT2B 受体拮抗剂,pKi 为 9.5,比作用于其他受体和离子通道的选择性高 1000 倍。 | |||
T21468 |
CVT-2738
UNII-NYS3I6283H,CVT 2738,EC 610-916-8,CVT2738,RS-94287,N-(2,6-二甲基苯基)-1-哌嗪乙酰胺 |
Others | Others |
CVT-2738 (RS-94287) 是雷诺嗪的代谢物。 Ranolazine 是一种部分脂肪酸氧化 (pFOX) 抑制剂和抗心绞痛药物。 | |||
T6018 |
Zosuquidar trihydrochloride
唑喹达三盐酸盐,Zosuquidar (LY335979) 3HCl,RS 33295-198 trihydrochloride,RS 33295-198 (D06387) 3HCl,Zosuquidar 3HCl,LY-335979 trihydrochloride |
P-gp | Membrane transporter/Ion channel; Neuroscience |
Zosuquidar trihydrochloride (LY-335979 trihydrochloride) 是一种P-糖蛋白抑制剂,Ki 值为 59 nM。 | |||
T68051 |
Delequamine
RS 15385-197 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Delequamine (RS 15385-197) 是一种有效的选择性 α2-肾上腺素受体拮抗剂。 | |||
T11032 |
DHPG
(RS)-3,5-DHPG,DL-Α-(3,5-二羟基苯基)甘氨酸 |
GluR | Neuroscience |
DHPG ((RS)-3,5-DHPG) 是一种氨基酸,是选择性代谢型谷氨酸受体 mGluR 的激动剂,也是与磷脂酶 D 耦合的 mGluR 的有效拮抗剂。 | |||
T16799 |
RS-246204
|
Others | Others |
RS-246204 is an R-spondin-1 substitute compound. RS-246204 is able to initiate small intestinal organoids without the use of the R-spondin-1 protein. | |||
T24740 | RS-104966 | ||
RS-104966 is an inhibitor of collagenase that acts by inducing the conformational change in the side-chains of the S1 pocket of MMP-1. | |||
T60242 |
(RS)-AMPA monohydrate
|
||
(RS)-AMPA ((±)-AMPA) monohydrate 是谷氨酸的一种类似物,对兴奋性神经递质 L-谷氨酸 (L-glutamic acid) 有激动作用。(RS)-AMPA monohydrate 不会干扰海藻酸或 NMDA 受体的结合位点。 | |||
T13439 |
(RS)-Butyryltimolol
|
Cysteine Protease | Proteases/Proteasome |
(RS)-Butyryltimolol 是 Butyryltimolol 的消旋体。Butyryltimolol 是 Timolol 的有效前药。Timolol 用于青光眼研究,但是难以透过角膜,经化学结构修饰后得到 Butyryltimolol,透过眼角膜的能力增强。Butyryltimolol 进入眼球后,经酶水解再生成 Timolol 而起作用。Butyryltimolol 是一种 β-肾上腺素能 (β-adrenergic) 阻滞剂。 | |||
T70661 |
Azalanstat mesylate
|
||
Azalanstat mesylate is an anti-obesity drug acting as a lanosterol 14α-demethylase inhibitor. Azalanstat mesylate has been shown to inhibit cholesterol synthesis in HepG2 cells, human fibroblasts, hamster hepatocytes and hamster liver, by inhibiting the cytochrome P450 enzyme lanosterol 14 alpha-demethylase. When administered orally to hamsters fed regular chow, RS-21607 (50 mg/kg/day) lowered serum cholesterol in a dose-dependent manner (ED50 = 62 mg/kg) in a period of 1 week. It preferentially... | |||
T70660 |
Azalanstat HCl
|
||
Azalanstat HCl is an anti-obesity drug acting as a lanosterol 14α-demethylase inhibitor. Azalanstat HCl has been shown to inhibit cholesterol synthesis in HepG2 cells, human fibroblasts, hamster hepatocytes and hamster liver, by inhibiting the cytochrome P450 enzyme lanosterol 14 alpha-demethylase. When administered orally to hamsters fed regular chow, RS-21607 (50 mg/kg/day) lowered serum cholesterol in a dose-dependent manner (ED50 = 62 mg/kg) in a period of 1 week. It preferentially lowered l... | |||
T10462L |
Bavisant dihydrochloride hydrate
JNJ31001074AAC |
Others | Others |
Bavisant dihydrochloride hydrate (JNJ31001074AAC) is a highly selective, orally active antagonist of the human H3 receptor with a novel mechanism of action, involving wakefulness and cognition, with potential as a treatment for ADHD. in vivo: Mean change |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T82318 | Ginsenoside Rs1 | ||
Ginsenoside Rs1为人参根中提取的一种人参皂苷类化合物。 |