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Cat. No. | Product Name | Target | Signaling Pathways |
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T23686 |
AHR-activator-1023
Branching Morphogenesis Modulator 1023,Cpd 1023,Compound 1023,BMM 1023 |
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AHR-activator-1023 is the aryl hydrocarbon receptor activator. It is also a specific FGF2-induced branching morphogenesis modulator. | |||
T6351 |
MGCD-265 analog
MGCD-265,Glesatinib |
Apoptosis; VEGFR; c-Met/HGFR | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
MGCD-265 analog (Glesatinib) 是一种口服生物可利用的多靶点酪氨酸激酶抑制剂,具有抗肿瘤活性,对 c-Met 和 VEGFR2 的 IC50 分别为 29 nM 和 10 nM。 | |||
T8389 |
Trifluoperazine
三氟拉嗪,trifluoroperazine |
CaMK; Dopamine Receptor; Influenza Virus; Adrenergic Receptor; P-gp; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Trifluoperazine (trifluoroperazine) 是一种多巴胺 D2 受体抑制剂,可治疗精神分裂症。它是NUPR1抑制剂,具有抗癌活性。它是α1-adrenergic 受体拮抗剂,是流感病毒形态发生的可逆抑制剂。 | |||
T1222 |
Trifluoperazine dihydrochloride
Trifluoperazine 2HCl,盐酸三氟拉嗪,SKF5019,Urinox |
CaMK; Dopamine Receptor; Influenza Virus; Adrenergic Receptor; P-gp; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Trifluoperazine dihydrochloride (SKF5019) 是一种抗精神病药物,靶向中枢多巴胺受体。它是流感病毒形态发生的可逆抑制剂,是NUPR1抑制剂,具有抗癌活性。它是钙调蛋白抑制剂,还可抑制 P-糖蛋白,可研究精神分裂症。 | |||
T71508 | TCSA | ||
TCSA is an inhibitor of fungal morphogenesis, biofilm formation, and host cell invasion. | |||
T27089 |
CRT0066854
CRT0066854 HCl,CRT-0066854 HCl,CRT 0066854,CRT-0066854 |
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CRT-0066854 is a PKCι and PKCζ inhibitor. CRT0066854 was able to restore polarized morphogenesis in the dysplastic H-Ras spheroids. | |||
T27590 |
IHVR-11029
IHVR 11029 |
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IHVR-11029 is a potent inhibitor of ER α-glucosidase. IHVR-11029 is active against multiple hemorrhagic fever viruses and efficiently disrupts the morphogenesis of a broad spectrum of enveloped viruses. | |||
T78030 |
GRGESP
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GRGESP为胶原凝胶收缩抑制剂,能够抑制人成纤维细胞在胶原凝胶中的扩散,显著减少凝胶收缩,适用于结缔组织形态发生研究。 | |||
T38336 |
W140 (trifluoroacetate salt)
W140 (trifluoroacetate salt) |
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Sphingosine-1-phosphate (S1P) is a bioactive lipid that exhibits a broad spectrum of biological activities including cell proliferation, survival, migration, cytoskeletal organization, and morphogenesis. It exerts its activity by binding to five distinct G protein-coupled receptors, S1P1/EDG-1, S1P2/EDG-5, S1P3/EDG-3, S1P4/EDG-6, and S1P5/EDG-8. W140 is an inactive enantiomer of W146, a selective S1P1 antagonist (Ki = 77 nM), that binds to the S1P1 receptor with a Ki of 4.6 μM (2a = W146; 2b = W... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T72867 |
Fusarisetin A
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Fusarisetin A 是一种五环真菌代谢物,是一种腺泡形态发生抑制剂。 |