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Cat. No. | Product Name | Target | Signaling Pathways |
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T3495 |
Tasimelteon
他司美琼,VEC-162,BMS-214778 |
Melatonin Receptor; MT Receptor | GPCR/G Protein; Neuroscience |
Tasimelteon (BMS-214778) 是一种褪黑激素受体激动剂,用于治疗盲人的非 24 小时睡眠-觉醒障碍。 | |||
T26316 |
VEC-5
VEC5 |
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VEC-5 is a HIV-1 inhibitor. VEC5 have been evaluated for their inhibitory potential employing ligand receptor and protein-protein interactions studies. VEC-5 exhibited better interaction with Vif than RN18. | |||
T26317 |
VEC6
VEC-6,NSC11435,NSC 11435,NSC-11435,VEC 6 |
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VEC6 is a VEZF1–DNA interaction inhibitor that recapitulates RhoB loss in ischaemic retinopathy. | |||
T17220 |
Vecabrutinib
SNS-062 |
Tyrosine Kinases; BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
Vecabrutinib (SNS-062) (SNS-062) 是一种有效的,非共价的 BTK 和 ITK 抑制剂,Kd 值分别为 0.3 nM 和 2.2 nM。Vecabrutinib 对 ITK 的 IC50 值为 24 nM。 | |||
T5632 |
Suvecaltamide
MK-8998 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Suvecaltamide (MK-8998) 是一种选择性的 T 型钙通道抑制剂。 | |||
T10464L |
Atuveciclib Racemate
BAY-1143572 Racemate,阿维西利 |
CDK | Cell Cycle/Checkpoint |
Atuveciclib Racemate (BAY-1143572 Racemate) 是 Atuveciclib 的外消旋混合物。 Atuveciclib 是口服有效的 P-TEFb/CDK9高选择性抑制剂,CDK9/CycT1的 IC50为13 nM。 | |||
T1594 |
Vecuronium bromide
ORG NC 45,维库溴铵 |
AChR | Neuroscience |
Vecuronium bromide (ORG NC 45) 是一种合成的中效单季铵盐类固醇和非去极化神经肌肉阻滞剂,具有肌肉松弛活性。 | |||
T30789 |
Cefovecin Sodium
UK 287,074-02,UK-287,074-02,C13142,D01681,UK287,074-02 |
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Cefovecin Sodium(Convenia) is an antibiotic of the cephalosporin class, licensed for the treatment of skin infections in cats and dogs. | |||
T35042 |
Vecuronium
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Vecuronium is a biochemical. | |||
T10465 |
Atuveciclib S-Enantiomer
BAY-1143572 S-Enantiomer |
CDK | Cell Cycle/Checkpoint |
Atuveciclib S-Enantiomer (BAY-1143572 S-Enantiomer) 是 BAY-1143572的 S-对映异构体 ,是一种有效的选择性 CDK9抑制剂,抑制 CDK9/CycT1,IC50为 16 nM。 | |||
T10464 |
Atuveciclib
BAY-1143572 |
CDK | Cell Cycle/Checkpoint |
Atuveciclib (BAY-1143572) 是一种有效且高度选择性的口服 PTEFb/CDK9抑制剂。Atuveciclib (BAY-1143572) 抑制 CDK9/CycT1,IC50为 13 nM。 | |||
T79702 |
Nrf2 activator-9
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Nrf2 activator-9 (compound D-36) 是抑制oxLDL和HG诱导的HUVEC细胞凋亡的Nrf2激活剂,有助于预防动脉粥样硬化。该化合物可防止VEC损伤,展现出对心血管疾病的潜在治疗效果。 |
Cat. No. | Product Name | Species | Expression System |
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TMPY-01237 |
VE-Cadherin Protein, Mouse, Recombinant (His)
VECD,VE-Cad,Cd144,7B4,Vec,VEcad,c... |
Mouse | HEK293 Cells |
VE-Cadherin Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 63.5 kDa and the accession number is P55284. |