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12
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1808 |
Bak BH3
|
||
This peptide, generated from the BH3 domain of Bak (Flu-BakBH3), has been shown to have high-affinity binding to a surface pocket of the Bcl-XL protein that is required for its death antagonist function. | |||
T80029 |
Bak BH3 (72-87), TAMRA-labeled
|
||
BakBH3 (72-87), TAMRA-labeled,是一种具有生物活性的肽类化合物。 | |||
T4215 |
TCS-PIM-1-4a
5-[[3-(三氟甲基)苯基]亚甲基]-2,4-噻唑烷二酮,SMI-4a |
Apoptosis; Pim | Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling |
TCS-PIM-1-4a (SMI-4a) 是一种泛-Pim 激酶抑制剂,可通过激活 AMPK 来阻断 mTORC1的活性。它可杀死多种髓样和淋巴样细胞系,IC50值为 0.8 μM 至 40 μM。 | |||
T23771 |
BAK2-66
BAK2 66 |
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BAK2-66 is a selective antagonist of the dopamine D3 receptor. | |||
T23861 |
CAY10526
CAY-10526,BTH,CAY 10526 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
CAY10526 (BTH) 是 mPGES-1 的选择性抑制剂,可抑制 NF-κB 信号通路。 | |||
T124107 |
Bakuchalcone
|
||
Bakuchalcone 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T124107。 | |||
T125549 |
12-Hydroxyisobakuchiol
|
||
12-Hydroxyisobakuchiol 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T125549。 | |||
T77034 |
Inbakicept
N-803 |
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Inbakicept (ALT-803) 是一种 IL-15超激动剂,由 IL-15突变体和 IL-15Rα-Fc 融合体组成。Inbakicept 可放大抗 CD20单抗介导的 NK 细胞反应和抗体依赖性细胞毒性 (ADCC)。INbakicept 也增加 NK 细胞的脱粒或 IFNγ 的产生。 | |||
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。 | |||
T14846 |
Bz 423
BZ48 |
Apoptosis; BCL | Apoptosis |
Bz 423 是一种有效的免疫调节剂,通过激活 Bax 和 Bak 来诱导线粒体外膜通透和细胞色素 c 释放来诱导细胞凋亡。Bz 423 在狼疮小鼠模型中显示出部分活性。 | |||
T2099 |
ABT-737
|
Mitophagy; BCL; Autophagy | Apoptosis; Autophagy |
ABT737 是 BH3 模拟物,是Bcl-2、Bcl-xL 和Bcl-w 抑制剂,EC50分别为 30.3 nM、78.7 nM 和 197.8 nM。它诱导自噬,有研究急性髓系白血病的潜力。它还诱导 BCL-2/BAX 复合物的破坏和 BAK 依赖性。 | |||
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。 | |||
T28117 |
MSN-50
MSN50,MSN 50 |
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MSN-50, an inhibitor of Bax and Bak oligomerization, inhibits liposome permeabilization, prevents genotoxic cell death and promotes neuroprotection. | |||
T16155 | MSN-125 | Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
MSN-125 effectively inhibits Bax/Bak-mediated apoptosis in HCT-116, BMK Cells, and primary cortical neurons protect primary neurons against glutamate excitotoxicity. MSN-125 is an effective Bax and Bak oligomerization inhibitor. MSN-125 prevents mitochond | |||
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。 | |||
T32344 |
JY-1-106
JY-1 106,JY-1106 |
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JY-1-106 is a BH3 α-helix mimetic, inducing apoptosis in a subset of cancer cells (lung cancer, colon cancer and mesothelioma) by disrupting Bcl-xL and Mcl-1 protein-protein interactions with Bak. | |||
T79242 |
Mcl-1 inhibitor 16
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Mcl-1 inhibitor16 (Compound 9)为基于铂的线粒体靶向性Mcl-1抑制剂。该化合物通过诱导Bax/Bak依赖的细胞凋亡(apoptosis),展现出对癌细胞的作用,可以单独使用或与ABT-199联合应用,表现出抗肿瘤活性。 | |||
T76073 |
BH3 hydrochloride
|
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BH3 hydrochloride是一种能够穿透血脑屏障的多肽,其机制是通过直接激活促凋亡蛋白Bax/Bak或中和抗凋亡Bcl-2家族蛋白(Bcl-2、Bcl-XL、Bcl-w、mcl1和A-1),从而诱导细胞凋亡。这一作用是通过与BH3结构域的结合实现的。 | |||
T26789 |
BH3I-2'
BH3I2',BH3I 2' |
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BH3I-2' is a cell-permeable BH3 mimetic. BH3I-2' induces apoptosis by specifically preventing BH3 domain-mediated interactions between pro-apoptotic and anti-apoptotic members of the Bcl-2 family, thereby blocking the interaction between Bcl-x and Bak BH3 by targeting the Bcl-x binding pocket. | |||
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 | |||
T29060 |
UNBS-1450
UNBS 1450,UBS1450,UBS-1450,UBS 1450 |
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UNBS-1450 is a sodium channel antagonist. UNBS-1450 is a hemi-synthetic cardenolide derived from 2″-oxovorusharin, it is effective against various cancer cell types with an excellent differential toxicity. At low nanomolar concentrations, UNBS-1450 induce | |||
T80224 |
Bid BH3 (80-99)
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Bid BH3 (80-99) 是一种具有促凋亡功能的生物活性肽,属于BCL-2蛋白家族中的"BH3仅限"(BOPS)亚群。作为第一个能够结合并激活Bcl-2、Bax和Bak的BOP,Bid扮演引发细胞凋亡的关键角色。它通过从细胞质迁移到线粒体膜来失活Bcl-2或激活Bax。特别地,在N末端位置的谷氨酰胺(Q)或谷氨酸(E),会自然转化为pGlu形式,其疏水性γ-内酰胺环被认为有助于增强肽针对胃肠道蛋白酶的稳定性。焦谷氨酰肽通常被划分为这类生物活性肽的一个常见子集,并且在HPLC分析中,作为评估肽纯度的重要指标被考虑在内。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3400 |
Bakuchiol
|
p38 MAPK; DNA/RNA Synthesis; Autophagy | Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; MAPK |
Bakuchiol 是一种从补骨脂种子中提取的植物雌激素,具有抗肿瘤和抗蠕虫特性,以及细胞毒活性和抗菌活性。 | |||
TWS1977 |
Kamebakaurin
尾叶香茶菜丙素,Kamebakaurine |
NF-κB | NF-κB |
Kamebakaurin (Kamebakaurine) 是一种提取自Isodon japonicus 中的天然产物,是一种NF-κB 的抑制剂,能够抑制 p50 的 DNA 结合活性。 | |||
TN3483 |
Bakkenolide D
|
IL Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Bakkenolide D has anti-allergic effect, it and bakkenolide D demonstrates inhibitory effect on the trachea contraction induced by histamine in vitro, they have obvious anti-histamine activities. | |||
T2S0606 |
Bakkenolide A
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IL Receptor; IκB/IKK; GSK-3; TNF; Akt; Caspase; PI3K; HDAC | Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Immunology/Inflammation; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells |
Bakkenolide A has antifeedant and growth inhibitory effects on neonate variegated cutworms, it inhibits leukemia by regulation of HDAC3 and PI3K/Akt-related signaling pathways. | |||
TN3485 |
Bakkenolide III
|
Others | Others |
Bakkenolide III may have cytotoxicity. | |||
TN2562 | 1-Oxobakkenolide S | Others | Others |
1-Oxobakkenolide S 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN2562,CAS号为 18456-02-5。 | |||
TN3484 | Bakkenolide Db | Others | Others |
Bakkenolide Db may have cytotoxicity. | |||
TN3486 |
Bakkenolide IIIa
|
ERK; BCL; IκB/IKK; NF-κB; Akt | Apoptosis; Cytoskeletal Signaling; MAPK; NF-κB; PI3K/Akt/mTOR signaling |
Bakkenolide IIIa has antioxidant, and neuroprotective effects, it protects against cerebral damage by inhibiting AKT and ERK1/2 activation and inactivated NF-κB signaling. | |||
TN2945 | 3-Hydroxybakuchiol | ATPase; Caspase | Apoptosis; Membrane transporter/Ion channel; Proteases/Proteasome |
3-Hydroxybakuchiol exerts cytotoxic and anti-proliferative effects on the TA3/Ha mouse mammary adenocarcinoma cell line and induces a decrease in the mitochondrial transmembrane potential, the activation of caspase-3, the opening of the mitochondrial perm | |||
TN3482 |
Bakkenolide B
|
NOS; COX | Immunology/Inflammation; Neuroscience |
Bakkenolide B has suppressive properties for allergic and inflammatory responses and may be utilized as a potent agent for the treatment of asthma. | |||
T6S0052 |
Chelerythrine
Toddalin,Broussonpapyrine,白屈菜红碱,Cheleritrine |
Apoptosis; BCL; PKC; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling |
Chelerythrine (Broussonpapyrine) 是一种天然生物碱,为有效、选择性的 Ca2+/磷脂依赖性PKC 拮抗剂,IC50值为 0.7 μM。它具有抗肿瘤、抗糖尿病、抗炎的活性。它抑制BclXL-Bak BH3肽结合,IC50为 1.5 μM,并从 BclXL 取代了 Bax。它诱导细胞凋亡和自噬。 | |||
TN3244 | 7-O-Methyleucomol | Others | Others |
7-O-Methyleucomol is a natural product from Eucomis bicolor Bak. |