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Cat. No. | Product Name | Target | Signaling Pathways |
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TP1724L |
PUMA BH3 acetate
PUMA BH3 acetate(PUMA BH3 Free base) |
BCL | Apoptosis |
PUMA BH3 acetate (PUMA BH3 Free base) 是一种 p53 凋亡阳性调节因子 (PUMA) BH3 结构域多肽,可作为 Bak 的直接激活剂,Kd 为 26 nM。 | |||
TP1724 |
PUMA BH3
|
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PUMA BH3 is a p53 upregulated modulator of apoptosis (PUMA) BH3 domain peptide, acts as a direct activator of Bak, with a Kd of 26 nM.This is a PUMA BH3 domain peptide. PUMA proteins bind Bcl-2, localize to the mitochondria, and induce cytochrome C releas | |||
TP1712 |
PUMA BH3 (TFA)
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PUMA BH3 (TFA) is a p53 upregulated modulator of apoptosis (PUMA) BH3 domain peptide, acts as a direct activator of Bak, with a Kd of 26 nM. | |||
T75980 |
PUMA BH3 TFA
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PUMA BH3 (TFA) 是一种 p53 正向凋亡调控因子 (PUMA) BH3 结构域多肽,作为Bak 的直接激活剂,Kd 值为 26 nM。 | |||
T83751 |
PUMA BH3 (human) TFA
|
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PUMA BH3是一个由p53上调凋亡调节器(PUMA)的BH3域组成的肽,并激活促凋亡蛋白Bak。PUMA BH3与Bak结合(在HEPES和CHAPS缓冲液中的Kds分别为290和26 nM),诱导Bak同源寡聚化和Bak介导的膜透性增加。 | |||
TQ0108 |
MK-6892
|
GPR | Endocrinology/Hormones; GPCR/G Protein |
MK-6892 是烟酸受体GPR109A 选择性激动剂。它作用于人 GPR109A 的Ki=4 nM,EC50=16 nM。 | |||
T36083 |
DS-7423
|
PI3K; mTOR | PI3K/Akt/mTOR signaling |
DS-7423 是PI3K 和mTOR 的有效抑制剂,抑制PI3Kα 和 mTOR 的IC50分别为15.6 nM 和 34.9 nM。DS-7423表现出抗癌活性。 | |||
T15432 |
GSK256073
|
GPR; Others | Endocrinology/Hormones; GPCR/G Protein; Others |
GSK256073 是一种口服有活性的GPR109A 选择性激动剂,也是一种持久的人HCA2激动剂(pEC50:7.5) 。它能够减少脂降解,而显著改善葡萄糖稳态,对 2 型糖尿病和血脂异常具有潜在的研究价值。 | |||
T19700 |
IBC 293
IBC293,1-异丙基-1H-1,2,3-苯并噻唑-5-羧酸,IBC-293 |
GPR | Endocrinology/Hormones; GPCR/G Protein |
IBC 293 对 GPR109B 的选择性高于烟酸受体 GPR109A。 IBC 293 是 GPR109B 的高选择性激动剂,GPR109B 是一种在脂肪细胞中表达的人类孤儿 G 蛋白偶联受体。 | |||
T0794 |
Mepenzolate Bromide
Colibantil,Cantil,溴美喷酯,Cantilaque |
AChR | Neuroscience |
Mepenzolate Bromide (Colibantil) 是一种可口服的毒蕈碱受体拮抗剂,对hM2R 和hM3R 的Ki 分别为 0.68 和 2.6 nM。它是GPR109A 抑制剂,可用于抑制与肠易激综合征相关的胃肠道过度运动。 | |||
T16682 |
Pumaprazole
BY-841,普马拉唑 |
Proton pump | Membrane transporter/Ion channel |
Pumaprazole (BY-841) 是一种有效的、可逆的质子泵拮抗剂。 | |||
T71691 |
Pumafentrine
BY 343 |
PDE | Metabolism |
Pumafentrine(BY 343) 是 PDE3/PDE4双重抑制剂,可降低小鼠实验性结肠炎的临床评分和 TNF 表达。 | |||
T69218 |
PUMAi HCl
|
Others | Others |
PUMAi is an inhibitor of p53 up-regulated modulator of apoptosis (PUMA), a BH3-only Bcl-2 family member, mitigating acetaminophen (APAP)-induced hepatocyte necrosis and liver injury. | |||
T16030 |
Mcl1-IN-8
|
Others | Others |
Mcl1-IN-8 is an Mcl-1-PUMA interface inhibitor (Ki: 0.3 μM). In cancer cells, Mcl1-IN-8 shows dual activity on reducing PUMA-dependent apoptosis while deactivating Mcl-1-mediated anti-apoptosis. | |||
T73000 |
SIRT2-IN-11
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Others | Others |
SIRT2-IN-11 (AEM1) 是选择性的SIRT2抑制剂,IC50值为 18.5 μM。SIRT2-IN-11 以 p53 依赖的诱导细胞凋亡,激活CDKN1A,PUMA 和NOXA 的表达,并且促进 p53 的乙酰化。SIRT2-IN-11 可用于 p53 相关的癌症研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T12095 |
Monomethyl fumarate
|
GPR; Drug Metabolite | Endocrinology/Hormones; GPCR/G Protein; Metabolism |
Monomethyl fumarate 是 Dimethyl fumarate 的活性代谢产物。Monomethyl fumarate 是一种 GPR109A 激动剂。Monomethyl fumarate 是一种 GPR109A 激动剂具有用于多种神经保护途径和其他视网膜疾病模型的潜力。 | |||
T5668 |
Triacetylresveratrol
乙酰化白藜芦醇,三乙酰基白藜芦醇,Acetyl-trans-resveratrol |
BCL; NF-κB; STAT | Apoptosis; JAK/STAT signaling; NF-κB; Stem Cells |
Triacetylresveratrol (Acetyl-trans-resveratrol) 是 Resveratrol 的乙酰化类似物,可降低 STAT3和 NF-κB 磷酸化,具有抗癌作用。 | |||
TMA1743 |
Ergosterol peroxide
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ERK; VEGFR; p38 MAPK; Wnt/beta-catenin; Akt; JAK; CDK; JNK; STAT; Antifection | Angiogenesis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; JAK/STAT signaling; MAPK; Microbiology/Virology; PI3K/Akt/mTOR signaling; Stem Cells; Tyrosine Kinase/Adaptors |
Ergosterol peroxide is an inhibitor of osteoclast differentiation, which has antiviral, trypanocidal, antitumor, and antiangiogenic actions, it can stimulate Foxo3a activity by inhibiting pAKT and c-Myc and activating pro-apoptotic protein Puma and Bax to |
Cat. No. | Product Name | Species | Expression System |
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TMPH-01552 |
IRF1 Protein, Human, Recombinant (GST & His)
IRF1,Interferon regulatory factor 1 |
Human | Baculovirus Insect Cells |
Transcriptional regulator which displays a remarkable functional diversity in the regulation of cellular responses. Regulates transcription of IFN and IFN-inducible genes, host response to viral and bacterial infections, regulation of many genes expressed during hematopoiesis, inflammation, immune responses and cell proliferation and differentiation, regulation of the cell cycle and induction of growth arrest and programmed cell death following DNA damage. Stimulates both innate and acquired imm... |