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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T69709 | GST-HG131 | ||
GST-HG131 是一种特异性的乙肝病毒 (HBV) 表面抗原抑制剂,属于二氢苯并吡哆醛 (DBP) 类化合物。GST-HG131 抑制 HBsAg 和 HBeAg 的特异性和效力很强 (EC50=28.2 nM, 16.0 nM)。GST-HG131 还具有良好的动物安全性。 | |||
T8461 |
SKI V
|
Apoptosis; PI3K; S1P Receptor | Apoptosis; GPCR/G Protein; PI3K/Akt/mTOR signaling |
SKI V 是一种非竞争性非脂质鞘氨醇激酶抑制剂,对 GST-hSK 的IC50为 2 μM。 它减少有丝分裂的第二信使鞘氨醇-1-磷酸的形成,可诱导细胞凋亡并具有抗肿瘤活性。它还抑制PI3K,对 hPI3k 的IC50为 6 μM。 | |||
T1052 |
Proglumide
二丙谷酰胺 |
cholecystokinin | GPCR/G Protein |
Proglumide (Binoside) 是一种非肽的、口服具有活性的胆囊收缩素(CCK)-A/B 受体拮抗剂。它能够选择性阻断 CCK 在中枢神经系统中的作用。它能够抑制胃分泌,具有保护胃十二指肠粘膜的能力,并表现出抗癫痫和抗氧化活性。 | |||
T78800 |
GST-IN-1
|
||
GST-IN-1 (compound 16) 为一种谷胱甘肽 S-转移酶 (GST) 抑制剂,其半抑制浓度 (IC50s) 分别针对sjGST为1.55 μM,针对hGSTM2为2.02 μM。 | |||
T69708 | Azilsartan mopivabil | ||
Azilsartan mopivabil 是血管紧张素 II 受体 (angiotensin II receptor) 的强效拮抗剂。 | |||
T26629 |
Angstrom6
A-6,A 6 peptide,A6,A 6,A6 peptide,A-6 peptide |
PAI-1 | Metabolism |
Angstrom6 (A-6 peptide) 是一种从单链尿激酶纤溶酶原激活剂(scuPA)中提取的 8 肽,它能干扰 uPA/uPAR 级联反应并抑制下游效应。Angstrom6 具有抗肿瘤活性,能通过与 CD44 结合并调节 CD44 介导的细胞信号传导,抑制肿瘤细胞的迁移、侵袭和转移。 | |||
T11505 |
GSTO1-IN-1
|
Glutathione Peroxidase; GST | Metabolism; oxidation-reduction |
GSTO1-IN-1 是谷胱甘肽 S-转移酶 omega 1 抑制剂,IC50=31 nM。 | |||
T12519 |
Sodium metatungstate
POM-1,聚钨酸钠,Sodium polyoxotungstate |
Phosphatase | Metabolism |
Sodium metatungstate (Sodium polyoxotungstate) 是一种外核苷三磷酸二磷酸水解酶抑制剂,能够抑制 ATP 的分解,并阻断中枢突触传递,这是独立于抑制 NTPDase 而发挥作用的。 | |||
T71081 | Nagstatin | ||
Nagstatin is an inhibitor of N-acetyl-beta-D-glucosaminidase and is produced by Streptomyces amakusaensis MG846-fF3. | |||
T64775 | Sodium tungstate(VI) | ||
Sodium tungstate(VI) 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 T64775。 | |||
T15379 |
GGsTop
Nahlsgen |
Others | Others |
GGsTop is a non-toxic and irreversible inhibitor of γ glutamyl transpeptidase (GGT) (Ki: 170 μM for Human GGT). GGsTop protects hepatic ischemia-reperfusion injury in the rat model. GGsTop shows Kons of 150±10 and 51±3 /(M·s) against E.coli GGT and human GGT, respectively. | |||
T11504 | GSTO-IN-2 | Others | Others |
GSTO-IN-2 is a glutathione S-transferase inhibitor (IC50s: 1.4, 16.3, and 3.6 μM for GSTP1-1, GSTM1, and GSTA2). | |||
T64830 | Tetrapotassium decatungstate | ||
Tetrapotassium decatungstate 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 T64830。 | |||
T64579 | Tetrabutylammonium decatungstate | ||
Tetrabutylammonium decatungstate 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 T64579。 | |||
T64838 | Tetrabutylphonium decatungstate | ||
Tetrabutylphonium decatungstate 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 T64838。 | |||
TQ0003L1 |
740 Y-P acetate
PDGFR 740Y-P Acetate,740YPDGFR acetate,740 Y-P acetate(1236188-16-1 Free base) |
PI3K | PI3K/Akt/mTOR signaling |
740 Y-P acetate (740YPDGFR acetate) 是一个有效的且具有细胞渗透性的 PI3K 激活剂。740 Y-P acetate 倾向和含有 p85 的 N- 和 C- 末端 SH2 结构域的 GST 融合蛋白结合,但不能单独结合 GST。 | |||
T5862 |
Ezatiostat TFA
TER199(free base),Ezatiostat TFA (free base),Ezatiostat,TLK199 |
GST | oxidation-reduction |
Ezatiostat TFA (TLK199) 是一种具有造血刺激活性的谷胱甘肽 S-转移酶 (GST) P1-1 的脂质体小分子谷胱甘肽类似物抑制剂。 | |||
TQ0003 |
740 Y-P
740YPDGFR,PDGFR 740Y-P |
PI3K; Autophagy | Autophagy; PI3K/Akt/mTOR signaling |
740 Y-P (740YPDGFR) 是一个细胞渗透性PI3K 激活剂。它能结合含有 p85 的 N- 和 C- 末端 SH2 结构域的 GST 融合蛋白。 | |||
T0153 |
Oltipraz
吡噻硫酮,NSC 347901,RP 35972 |
HIF/HIF Prolyl-Hydroxylase; HIV Protease; Reverse Transcriptase; Nrf2; HIF | Angiogenesis; Chromatin/Epigenetic; Immunology/Inflammation; Metabolism; Microbiology/Virology; Proteases/Proteasome |
Oltipraz (RP 35972) 是一种 Nrf2的强效激活剂。它时间依赖性地抑制 HIF-1α激活,IC50为 10 μM,浓度 ≥ 10 μM 时完全消除 HIF-1α诱导。 | |||
T12189 |
NBDHEX
|
Apoptosis; Glutathione Peroxidase; Autophagy | Apoptosis; Autophagy; Metabolism |
NBDHEX 是一种谷胱甘肽 S-转移酶 P1-1 抑制剂,也是晚期自噬抑制剂。它诱导肿瘤细胞凋亡,通过抑制 GST 的催化活性,避免抑制剂被特异性泵从细胞中排出,以及破坏 GSTP1-1和关键信号传导因子之间的相互作用,从而起到抗癌的作用。 | |||
T75723 |
740 Y-P TFA
|
||
740 Y-P TFA (740YPDGFR;PDGFR740Y-P) 是一个有效的,具有细胞渗透性的PI3K 激活剂。740 Y-P TFA 很容易结合含有 p85 的 N- 和 C- 末端 SH2 结构域的 GST 融合蛋白,但不能单独结合 GST。 | |||
T81136 | S-Octylglutathione | ||
S-Octylglutathione 是一种针对谷胱甘肽硫转移酶 (GST) 的竞争性抑制剂。 | |||
T75929 |
Caffeic acid-pYEEIE TFA
|
||
Caffeic acid-pYEEIE TFA 是一种非磷酸肽抑制剂,对 GST-Lck-SH2 结构域具有强大的结合亲和力。 | |||
T33957 |
PF-Alkyne
PF Alkyne |
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PF-Alkyne is a fluorophosphonate-based probe which specifically and covalently reacts with the tyrosine-111 residue of the Schistosoma japonicum GST (sjGST) tag. PF-Alkyne rapidly and site-selectively immobilizes sjGST fusion proteins. | |||
T40349 |
DS45500853
|
||
DS45500853, an estrogen-related receptor α (ERRα) agonist, acts as an inhibitor of the binding interaction between receptor-interacting protein 140 (RIP140) corepressor peptide (10 nM) and GST-ERRα ligand-binding domain (LBD; 1.2 μM), exhibiting an IC50 of 0.80 μM. This compound holds potential for research pertaining to metabolic disorders, particularly type 2 diabetes mellitus (T2DM). | |||
T60759 |
DS20362725
|
||
DS20362725 是可用于代谢紊乱研究,如二型糖尿病的雌激素相关受体 α (ERRα) 激动剂。DS20362725 抑制受体相互作用蛋白 140 (RIP140) 辅助抑制肽 (10 nM) 和 GST-ERRα 配体结合结构域 (LBD; 1.2 μM) 之间的结合的 IC50值为 0.6 μM。 | |||
T83931 |
JQ1-FITC
|
||
JQ1-FITC是一种荧光BET溴结构域探针。它与BRD4(BD1)和BRD4(BD2)具有高亲和力绑定(KD,app值分别为6.5 nM和5.8 nM,使用GST标签的BRD4蛋白,通过CoraFluorTR-FRET实验测定;在荧光偏振实验中,对于BRD4(BD1)的值为58.7 nM)。激发和发射峰(λ)分别为495 nm和525 nm。 | |||
T35979 |
Benastatin C
|
||
Benastatin C is a polyketide synthase-derived benastatin that has been found inStreptomycesand has diverse biological activities.1,2It inhibits glutathione S-transferase (GST; IC50= 24 μg/ml for the rat liver enzyme).2Benastatin C also inhibits the esterase activity of isolated porcine pancreatic lipase (IC50= 10 μg/ml). It increases LPS- or concanavalin A-induced blastogenesis of isolated mouse spleen lymphocytes in a concentration-dependent manner. 1.Xu, Z., Schenk, A., and Hertweck, C.Molecul... | |||
T70798 |
Benastatin B
|
||
Benastatin B is a polyketide synthase-derived benastatin that has been found in Streptomyces and has diverse biological activities. It inhibits glutathione S-transferase (GST; Ki = 3.7 µM for the rat liver enzyme).2 Benastatin B also inhibits the transglycosylase activity of A. baumannii, C. difficile, E. coli, and S. aureus recombinant penicillin-binding proteins (PBPs; IC50s = 16, 53.3, 30.7, and 31.6 µM, respectively).3 It is active against several bacteria, including methicillin-resistant S.... | |||
T35978 | Benastatin A | ||
Benastatin A is a polyketide synthase-derived benastatin that has been found inStreptomycesand has diverse biological activities.1,2,3It inhibits glutathione S-transferase (GST; Ki= 5 μM for the rat liver enzyme).2Benastatin A is active against several bacteria, including methicillin-resistantS. aureus(MRSA; MIC = 3.12 μg/ml). It induces apoptosis and cell cycle arrest at the G1/G0phase in Colon 26 mouse colon cancer cells when used at concentrations of 20 and 16 μM, respectively.3 1.Xu, Z., Sch... | |||
T69978 |
Brostallicin HCl
|
||
Brostallicin is a synthetic, alpha-bromoacrylic, second-generation minor groove binder (MGB), related to distamycin A, with potential antineoplastic activity. Brostallicin binds to DNA minor groove DNA, after having formed a highly reactive glutathione (GSH)-brostallicin complex in the presence of the enzyme glutathione S-transferase (GST), which is overexpressed in cancer cells; DNA replication and cell division are inhibited, resulting in tumor cell death. Compared to typical MGBs, this agent ... | |||
T19580 |
Thrombin (MW 37kDa)
凝血酶,Thrombin |
Thrombin | Proteases/Proteasome |
Thrombin (MW 37kDa) 是一种 Na+激活的胰蛋白酶样别构丝氨酸蛋白酶。它能够利用凝血酶识别序列对融合蛋白进行位点特异性切割,并可用于消化 GST 标记的蛋白。 | |||
T68581 |
AP23464
|
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AP23464 is a potent adenosine 5'-triphosphate (ATP)-based inhibitor of Src and Abl kinases, displays antiproliferative activity against a human CML cell line and Bcr-Abl-transduced Ba/F3 cells (IC(50) = 14 nM. AP23464 ablates Bcr-Abl tyrosine phosphorylation, blocks cell cycle progression, and promotes apoptosis of Bcr-Abl-expressing cells. Biochemical assays with purified glutathione S transferase (GST)-Abl kinase domain confirmed that AP23464 directly inhibits Abl activity. Importantly, the lo... | |||
T36057 |
Diallyl Tetrasulfide
ICD-1585 |
||
Diallyl tetrasulfide is an organosulfur compound that has been found in A. sativum and has diverse biological activities, including antimicrobial, antioxidant, and anticancer properties.[1],[2],[3],[4] It is active against the bacteria S. aureus and methicillin-resistant S. aureus (MRSA; MICs = 0.5 and 2 mg/L, respectively), as well as the fungi C. albicans, C. krusei, C. glabrata, A. niger, A. flavus, and A. fumigatus (MICs = 0.5, 4, 2, 1, 2, and 4 mg/L, respectively).[1] It reduces cadmium-ind... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T39668 |
Methyl propyl disulfide
|
Others | Others |
Methyl propyl disulfide 是在大蒜和洋葱中产生的挥发性含硫化合物,具有抗癌活性。 | |||
T7995 |
α-Angelica lactone
α-当归内酯,当归内酯,Alpha-Angelica Lactone |
Others; GST | Others; oxidation-reduction |
α-Angelica lactone 是一种乙烯基亲核试剂,也是一种天然存在的抗癌剂。它可以得到手性的 δ-氨基 γ,γ-二取代丁烯醇内酯羰基衍生物,并在 γ-碳上表现出亲电子俘获。它通过选择性增强谷胱甘肽-S-硫转移酶 (GST) 和 UDP-葡糖苷转移酶 (UGT) 解毒酶发挥强大的化学保护作用。 | |||
TN5562 |
10-Hydroxyligstroside
10-Hydroxyligustroside |
||
10-Hydroxyligstroside 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 TN5562,CAS号为 35897-94-0。 | |||
T3S0012 |
coniferyl ferulate
|
P-gp; GST | Membrane transporter/Ion channel; Neuroscience; oxidation-reduction |
Coniferyl ferulate 是从川芎中提取的一种天然产物,是强效的谷胱甘肽 S-转移酶抑制剂,强抑制人胎盘型谷胱甘肽 S-转移酶,IC50为 0.3 μM。它还可逆转多药耐药性并下调 P-糖蛋白。 | |||
TN1376 |
α-Solanine
alpha-Solanine,A-茄碱 |
MMP; Akt; PI3K | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Alpha-Solanine alters antioxidative enzyme activities and MDA and PCO concentrations and GST activity in fat body and midgut. | |||
TN2849 |
3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid
|
Antifection | Microbiology/Virology |
2-O-beta-d-Glucosyloxy-4-methoxybenzenepropanoic acid[3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid] exhibits glutathione S-transferase (GST) inhibitory and antifungal activities. |