Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12575 |
Unesbulin
PTC596 |
Apoptosis; BMI-1 | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Unesbulin (PTC596) 是一种口服有效和选择性的 B 细胞特异性莫洛尼氏鼠白血病病毒整合位点 1 抑制剂。它在急性髓细胞白血病细胞中可下调 MCL-1 并诱导不依赖 p53 的线粒体凋亡,具有抗白血病作用。 | |||
T60742 |
HIV-1 integrase inhibitor 8
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
HIV-1 integrase inhibitor 8 是一种 HIV-1 整合酶抑制剂,整合是HIV 复制的必要步骤。 | |||
T35617 |
Mitoguazone
MGBG,Methyl-GAG |
Apoptosis; HIV Protease | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
Mitoguazone (Methyl-GAG) 是一种可透过血脑屏障的选择性的 S-腺苷-蛋氨酸脱羧酶 (S-adenosyl-methionine decarboxylase) 抑制剂,可破坏多胺的生物合成。Mitoguazone 是一种具有抗肿瘤活性的合成多羰基衍生物,可抑制 HIV DNA 整合到单核细胞和巨噬细胞中的细胞 DNA 中,诱导细胞凋亡 (apoptosis)。Mitoguazone 具可用于预防急性白血病,霍奇金淋巴瘤和非霍奇金淋巴瘤。 | |||
T71786 | CID-1304264 | ||
CID-1304264 is an HIV-1 Rev pre-integration inhibitor. | |||
T68364 |
GS-9160
|
||
GS-9160 is a novel and potent inhibitor of human immunodeficiency virus type 1 (HIV-1) integrase (IN) that specifically targets the process of strand transfer. It is an authentic inhibitor of HIV-1 integration, since treatment of infected cells results in an elevation of two-long terminal repeat circles and a decrease of integration junctions. | |||
T82894 |
BETA-1
|
||
BETA-1作为首个分子内电荷转移聚集诱导发射集成分子(TICT-AIE integration molecule),在脂滴(LD)内呈现青色荧光,在线粒体中显现红色荧光。该分子适用于脂滴与线粒体的体内外同步双色成像。 | |||
T64096 |
Integrase-LEDGF/p75 allosteric inhibitor 1
|
||
Integrase-LEDGF/p75 allosteric inhibitor 1 是一种口服具有活力的 integrase-LEDGF/p75 (IN-LEDGF/p75) 变构抑制剂。Integrase-LEDGF/p75 allosteric inhibitor 1 能够抑制 HIV-1 DNA 整合,表现出抗病毒作用,能够作用于 HIV-1重组分子克隆 NL432 (EC50: 3.9 nM)。 | |||
T38896 |
VPM peptide
|
||
VPM peptide functions as a protease-cleavable dithiol cross-linker. It is capable of integration into the PEG-diacrylate (PEG-DA) macromer backbone, resulting in the formation of PEG hydrogel. | |||
T26968 |
CCT036477
CCT 036477,CCT-036477 |
||
CCT036477 is a selective inhibitor of wingless-type MMTV integration site family dependent transcription. CCT036477reduces the transcriptional activity of the T-cell factor and lymphoid enhancer factor transcription factor family at the ß-catenin level. | |||
T69782 | GS-9822 | ||
GS-9822 is a novel LEDGIN, an inhibitor that targets the binding pocket of LEDGF/p75 which is a cellular cofactor that substantially contributes to HIV integration site selection, displaying a block-and-lock phenotype in cell culture. | |||
T18473 |
N3-PEG3-vc-PAB-MMAE
|
Others | Others |
N3-PEG3-vc-PAB-MMAE, a drug-linker conjugate designed for Antibody-Drug Conjugates (ADC), features the integration of monomethyl auristatin E (MMAE), a tubulin inhibitor, via a 3-unit polyethylene glycol (PEG) linker. This compound demonstrates significant antitumor activity. | |||
T78059 |
Glucagon (Human)
Hyperglycemic-glycogenolytic factor,Glukagon |
Others | Others |
Glucagon 对蛋白质和氨基酸的代谢产生显著的调节作用。它抑制了氨基酸与肝脏、肌肉以及胰腺蛋白的结合,增加氮的排出,并促进肝脏内尿素的合成。同时,Glucagon 增加了肝脏中转氨酶和尿素循环酶的浓度,提高了肝脏对氨基酸的摄取,并加强了氨基酸与肝糖原之间的结合,从而降低了血液中的氨基酸浓度。 | |||
T83958 | CELT-327 | ||
CELT-327是一种高效且选择性的荧光hA2B/A3腺苷受体拮抗剂,其Kivalues在A2B和A3受体上分别为35.6 nM和45.7 nM。在表达A2B腺苷受体的HCT116细胞中,CELT-327表现出剂量依赖性的膜荧光标记,荧光信号快速扩散并在细胞单层中均匀分布。在活的HCT116紧凑球体中,CELT-327展现出整个球体直径上的均匀染色,可达到球体深层区域。CELT-327可作为荧光腺苷受体探针用于荧光结合分析、活细胞成像、流式细胞术和荧光偏振分析。它是GPCR放射标记配体的合适替代品。激发和发射最大值(λ)分别为589 nm和616 nm。这些波长与作为TR-FRET分析中接受体染料使用兼容,与CoraFluor1 TR-FRET供体一同使用。 |