24
12
3
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 |
Others | Others |
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
|
Others | Others |
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
|
Others | Others |
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 |
||
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。 | |||
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。 | |||
T28117 |
MSN-50
MSN50,MSN 50 |
Others | Others |
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 | |||
T83751 |
PUMA BH3 (human) TFA
|
||
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。 | |||
TP1712 |
PUMA BH3 (TFA)
|
||
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. | |||
T32344 |
JY-1-106
JY-1 106,JY-1106 |
Others | Others |
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. | |||
T75980 |
PUMA BH3 TFA
|
||
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。 | |||
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。 | |||
T26789 |
BH3I-2'
BH3I2',BH3I 2' |
Others | Others |
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. | |||
T79242 |
Mcl-1 inhibitor 16
|
Others | Others |
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
|
||
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。 | |||
TP1724 |
PUMA BH3
|
||
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 | |||
T84388 |
HA-14-1
|
Others | Others |
HA-14-1, a small molecule, binds the surface pocket of Bcl-2 proteins (IC50= ~ 9 µM), including Bcl-xl and Bcl-W, and disrupts their interaction with the Bak peptide. This action induces apoptosis by activating Apaf-1 and caspase-9 and -3. Additionally, HA-14-1 effectively induces apoptosis in human acute myeloid leukemia (HL-60) cells, with a 50 µM concentration resulting in a 90% loss of cell viability. | |||
T29060 |
UNBS-1450
UNBS 1450,UBS1450,UBS-1450,UBS 1450 |
Others | Others |
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)
|
||
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
|
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. | |||
TN3484 | Bakkenolide Db | Others | Others |
Bakkenolide Db 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。 | |||
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. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01503 |
Humanin Protein, Human, Recombinant (hFc)
MT-RNR2,Humanin,Humanin mitochondrial |
Human | HEK293 Cells |
Plays a role as a neuroprotective factor. Protects against neuronal cell death induced by multiple different familial Alzheimer disease genes and amyloid-beta proteins in Alzheimer disease. Mediates its neuroprotective effect by interacting with a receptor complex composed of IL6ST/GP130, IL27RA/WSX1 and CNTFR. Also acts as a ligand for G-protein coupled receptors FPR2/FPRL1 and FPR3/FPRL2. Inhibits amyloid-beta protein 40 fibril formation. Also inhibits amyloid-beta protein 42 fibril formation.... | |||
TMPH-01502 |
Humanin Protein, Human, Recombinant (GST)
Humanin,Humanin mitochondrial,MT-RNR2 |
Human | E. coli |
Plays a role as a neuroprotective factor. Protects against neuronal cell death induced by multiple different familial Alzheimer disease genes and amyloid-beta proteins in Alzheimer disease. Mediates its neuroprotective effect by interacting with a receptor complex composed of IL6ST/GP130, IL27RA/WSX1 and CNTFR. Also acts as a ligand for G-protein coupled receptors FPR2/FPRL1 and FPR3/FPRL2. Inhibits amyloid-beta protein 40 fibril formation. Also inhibits amyloid-beta protein 42 fibril formation.... | |||
TMPH-01664 |
OMA1 Protein, Human, Recombinant (His & SUMO)
Overlapping with the m-AAA protease 1 homolog,OMA1,Metallopr... |
Human | E. coli |
Metalloprotease that is part of the quality control system in the inner membrane of mitochondria. Activated in response to various mitochondrial stress, leading to the proteolytic cleavage of target proteins, such as OPA1, UQCC3 and DELE1. Following stress conditions that induce loss of mitochondrial membrane potential, mediates cleavage of OPA1 at S1 position, leading to OPA1 inactivation and negative regulation of mitochondrial fusion. Also acts as a regulator of apoptosis: upon BAK and BAX ag... |