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Targets Recommended: Rho

11

抑制剂 & 化合物

1

天然产物

1

重组蛋白

2

同位素标记化合物

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Cat. No. Product Name Target Signaling Pathways
T14004 1A-116

Rho Cell Cycle/Checkpoint
1A-116 是 Rac1的抑制剂,对几种类型的癌症具有抗肿瘤和抗转移作用,如乳腺癌。
T9356 (E/Z)-GO289

Casein Kinase Metabolism; Stem Cells
(E/Z)-GO289 是一种选择性酪蛋白激酶 2 抑制剂,IC50值为 7 nM。它可显着延长昼夜节律周期,表现出与细胞时钟功能相关的癌细胞生长的细胞类型依赖性抑制。
T32401 KL044

KL 044,KL-044

Others Others
KL044 是一种隐花色素 1(CRY1) 激活剂,可延长昼夜节律并抑制 PER2 的活性。 KL044 通过抑制cAMP/PKA/CREB 通路来抑制黑色素生成。
T9608 KL201

Others Others
KL201 是一种昼夜节律调制器,是 CRY1选择性的 稳定剂, 对 CRY2 没有稳定作用。KL201 延长了细胞和组织中的昼夜节律周期。
T7219 Flecainide acetate

Flecainide (acetate),氟卡胺,R-818,醋酸洗必太

Sodium Channel Membrane transporter/Ion channel
Flecainide acetate (R-818) 是位于心脏的 Nav1.5钠离子通道的阻断剂,具有抗心律失常的作用。
T24083 Gallopamil, (-)-

(-)-Methoxyverapamil,(S)-Gallopamil,(-)-Gallopamil,(-)-D 600

Others Others
Gallopamil, (-)- is an L-type calcium channel blocker. It is used in the treatment of abnormal heart rhythms.
T24082 Gallopamil HCl, (-)-

L-Gallopamil hydrochloride,(S)-Gallopamil hydrochloride,(-)-Gallopamil hydrochloride

Others Others
Gallopamil HCl, (-)- is an L-type calcium channel blocker. It is used in the treatment of abnormal heart rhythms.
T27430 GR 196429

GR-196429,GR 196,429,GR-196,429,GR196429,GR196,429

Others Others
GR 196429, a melatonin receptor agonist, exhibits selectivity for the MT1 subtype. This compound not only promotes sleep and alters circadian rhythms but also stimulates melatonin release in mice.
T70812 PF-05236216 hydrochloride

Others Others
PF-05236216 hydrochloride is a brain penetrant, potent and selective inhibitor of casein kinase 1 delta/epsilon (CK1δ/ε) that modulates circadian rhythms in mice.
T80849 VU661

Others Others
VU661, 一种吩嗪甲酰胺类化合物,作为昼夜节律调节剂能促使昼夜节律周期延长,该小分子具备氧化还原活性。
T63375 FT709

Others Others
FT709 是选择性的USP9X 有效抑制剂 (IC50: 82 nM)。其中USP9X 与中心体功能、EGF 受体降解、有丝分裂期间的染色体排列、化学致敏和昼夜节律有关。

化合物

1A-116
Cat.No: T14004
Synonym:
Target: Rho
(E/Z)-GO289
Cat.No: T9356
Synonym:
Target: Casein Kinase
KL044
Cat.No: T32401
Synonym: KL 044,KL-044
Target: Others
KL201
Cat.No: T9608
Synonym:
Target: Others
Flecainide acetate
Cat.No: T7219
Synonym: Flecainide (acetate),氟卡胺,R-818,醋酸洗必太
Target: Sodium Channel
Gallopamil, (-)-
Cat.No: T24083
Synonym: (-)-Methoxyverapamil,(S)-Gallopamil,(-)-Gallopamil,(-)-D 600
Target: Others
Gallopamil HCl, (-)-
Cat.No: T24082
Synonym: L-Gallopamil hydrochloride,(S)-Gallopamil hydrochloride,(-)-Gallopamil hydrochloride
Target: Others
GR 196429
Cat.No: T27430
Synonym: GR-196429,GR 196,429,GR-196,429,GR196429,GR196,429
Target: Others
PF-05236216 hydrochloride
Cat.No: T70812
Synonym:
Target: Others
VU661
Cat.No: T80849
Synonym:
Target: Others
FT709
Cat.No: T63375
Synonym:
Target: Others
Cat. No. Product Name Target Signaling Pathways
T7938 Quinidine

奎尼丁,奎宁树

Parasite Microbiology/Virology
Quinidine 是一种抗心律失常剂,也是 K+通道的有效阻断剂,其 IC50值为 19.9 μM。它是一种选择性细胞色素 P450db 的有效抑制剂,也可研究疟疾。

天然产物

Quinidine
Cat.No: T7938
Synonym: 奎尼丁,奎宁树
Target: Parasite
Cat. No. Product Name Species Expression System
TMPY-00286 Neuropeptide Y Protein, Human, Recombinant (hFc)

PYY4,neuropeptide Y

Human HEK293 Cells
NPY (Neuropeptide Y) is a Protein Coding gene. This gene encodes a neuropeptide that is widely expressed in the central nervous system and influences many physiological processes, including cortical excitability, stress response, food intake, circadian rhythms, and cardiovascular function. NPY is a neuromodulator that is widely expressed throughout the central nervous system (CNS) and is consecrated with classic neurotransmitters including GABA and glutamate. NPY/Agouti-related protein (AgRP) ne...

重组蛋白

Neuropeptide Y Protein, Human, Recombinant (hFc)
Cat.No: TMPY-00286
Species: Human
Expression System: HEK293 Cells
Cat. No. Product Name Target Signaling Pathways
TMIH-0469 Quinidine-d3

Quinidine-d3 是 Quinidine 的氘代化合物。Quinidine 的 CAS 号为 56-54-2。Quinidine 是一种抗心律失常剂,也是 K+通道的有效阻断剂,其IC50值为 19.9 μM。它是一种选择性细胞色素 P450db 的有效抑制剂,也可研究疟疾。
TMID-0183 Flecainide-d4 Acetate

Flecainide-d4 Acetate 是 Flecainide Acetate 的氘代化合物。Flecainide Acetate 的 CAS 号为 54143-56-5。Flecainide acetate 是位于心脏的 Nav1.5钠离子通道的阻断剂,具有抗心律失常的作用。

同位素标记化合物

Quinidine-d3
Cat.No: TMIH-0469
Synonym:
Target:
Flecainide-d4 Acetate
Cat.No: TMID-0183
Synonym:
Target:
TargetMol Loading
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