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Cat. No. | Product Name | ||
---|---|---|---|
L9700 | 内质网应激化合物库 | 193 compounds | |
193 个内质网应激相关的化合物集合,可用于高通量和高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1457 |
Deferasirox
ICL 670,CGP-72670,地拉罗司 |
Others; Ferroptosis; Antibacterial | Apoptosis; Microbiology/Virology; Others |
Deferasirox (CGP-72670) 是一种口服铁螯合剂,用于治疗慢性铁过载。 | |||
T19692 |
Deferitrin
GT 56252,GT 56 252,地夫立群,GT-56252,GT-56-252 |
Others | Others |
Deferitrin (GT-56-252) 是一种具有口服活性的三叉戟铁螯合剂,是去铁硫素 (DFT) 类似物。它有用于严重的 β 地中海贫血的潜力。它用于输血引起的慢性铁超负荷。 | |||
T8891 |
Homo-VK-II-36
Homo-V-II-36 |
Others | Others |
Homo-VK-II-36 (Homo-V-II-36) 是一种卡维地洛类似物,其作用是通过 RyR2 通道抑制储存超载诱导的钙释放。 | |||
T32046 |
HBED
CHELII,CHEL II,CHEL-II |
Others | Others |
HBED (CHELII) 是一种铁螯合剂,可用于治疗慢性铁过载和急性铁中毒的研究。 | |||
T10874 |
CP-060
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
CP-060 是一种 Ca2+ 拮抗剂,能够抑制 Ca2+ 过载,具有抗氧化、保护心脏的作用。 | |||
T13639 |
Deferasirox (Fe3+ chelate)
|
Apoptosis | Apoptosis |
Deferasirox (Fe3+ chelate) 是一种可口服的铁螯合剂,具有潜在的抗癌活性,抑制 MCL-1 的抗凋亡活性,可用于研究铁超负荷。 | |||
T85022 |
CN128
R-CN128 |
Others | Others |
CN128, an orally bioavailable iron chelator, features a side chain hydroxy group serving as an alternate sacrificial glucuronidation site to mitigate metabolic inactivation at the 3-hydroxy group. When administered at doses of 150 and 450 µmol/kg, CN128 enhances iron mobilization by 24.8% in a 59Fe-ferritin-loaded rat model of iron overload. | |||
T31363 |
Deferitazole magnesium
FBS0701,FBS-0701,SSP-004184,SHP-602,SHP602,Deferitazole free base |
Others | Others |
Deferitazole magnesium is a potential chelator for iron overload treatment. | |||
T68284 |
NP-04634
|
Others | Others |
NP-04634 is a calcium antagonist and protective agent against calcium overload and mitochondrial disruption. | |||
T40694 |
4-(3-Methyl-5-oxo-2-pyrazolin-1-yl)benzoic acid
|
Others | Others |
4-(3-Methyl-5-oxo-2-pyrazolin-1-yl)benzoic acid exhibits hypoglycemic activity and operates through a mechanism dependent on the response to oral glucose overload. | |||
T64249 |
CYP11B1-IN-2
|
Others | Others |
CYP11B1-IN-2 (compound 7aa) 是一种选择性的、口服具有活力的 CYP11B1 抑制剂,能够作用于 human CYP11B1 (IC50: 9 nM) 和 rat CYP11B1 (IC50: 25 nM)。CYP11B1-IN-2 能够用于研究皮质醇过量所致疾病。 | |||
T84718 |
Folic acid disodium
Vitamin B9 disodium,Vitamin M disodium |
Others | Others |
Folic acid disodium,Folic acid的口服活性钠盐形式,具有固有溶出速率(IDR)为4.96·105g/s。它作为单碳转移反应中的辅助因子,有助于防治神经管缺陷、缺血和癌症。Folic acid disodium的过量可能会损害胚胎大脑发展并促进癌前细胞变化的增长;而其缺乏则可能导致巨幼细胞性贫血。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TWP2911 |
Thymidine
beta-胸苷,5-Methyldeoxyuridine,Deoxyribothymidine,DThyd,NSC 21548,Thymidin |
Others; DNA/RNA Synthesis; Endogenous Metabolite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Others |
Thymidine (DThyd) 是一种细胞同步剂,是脱氧核糖核酸的特殊前体。它可在 DNA 复制前在 G1/S 边界阻滞细胞,是DNA 合成抑制因子。 | |||
T20819 |
Ammonium iron(III) citrate
柠檬酸铁铵,柠檬酸铁 (III) 铵,Ferric ammonium citrate |
Others; Ferroptosis | Apoptosis; Others |
Ammonium iron(III) citrate (Ferric ammonium citrate) 是一种非运铁蛋白结合的铁的生理形式,会引起的细胞内铁超负荷从而导致细胞铁死亡,能增强蛋白质产生。 | |||
TN2082 |
Pinostrobin
|
Beta Amyloid; IL Receptor; Serine/threonin kinase; TNF | Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation; Metabolism; Neuroscience |
Pinostrobin 是一种 PCSK9抑制剂,可抑制 PCSK9 的催化活性。它是能够在多种植物中发现的黄酮类化合物,并具有抗氧化,抗炎,抗癌和神经保护作用。它是有前景的胆固醇调节和脂质管理剂。 | |||
TN5073 |
Strophanthidin
毒毛旋花子甙元,Strophanthidine,葡萄球菌素 |
ATPase; Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Strophanthidin (Strophanthidine) 是黄花夹竹桃中的一种类固醇,可增加舒张期和收缩期胞内 Ca2+浓度。它在 0.1 和 1 nmol/L 增加Na+/K+-ATPase 活性,1到100 μ mol/L 抑制Na+/K+-ATPase 活性,10 和 100 nmol/L 对Na+/K+-ATPase 活性无影响。 | |||
T3415 |
Secoisolariciresinol diglucoside
亚麻木酚素,LGM2605 |
ROS | Immunology/Inflammation |
Secoisolariciresinol diglucoside (LGM2605) 在铁过载诱导的氧化还原炎症损伤的体外模型中具有细胞保护作用。 Secoisolariciresinol Diglucoside(25 mg/kg b.w.) 通过抑制 ROS 水平介导的酶和非酶抗氧化剂水平升高来防止肝脏受到过氧化损伤,从而发挥抗高血糖作用。 | |||
TN1086 |
Dehydrotrametenolic acid
Dehydroeburicoic acid,去氢齿孔酸,松苓新酸 |
Apoptosis; TNF; NOS; Caspase; NO Synthase | Apoptosis; Immunology/Inflammation; Proteases/Proteasome |
Dehydrotrametenolic acid (Dehydroeburicoic acid) 是从茯苓的菌核中分离的一种甾醇,具有抗肿瘤活性、抗炎和抗糖尿病作用。它通过 caspase-3途径诱导细胞凋亡。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-04552 |
AKT1 Protein, Human, Recombinant (His)
RAC-ALPHA,v-akt murine thymoma viral oncogene homolog 1,RAC,... |
Human | Baculovirus Insect Cells |
v-akt murine thymoma viral oncogene homolog 1 (AKT1), or protein kinase B-alpha (PKB-ALPHA) is a serine-threonine protein kinase, belonging to the Protein Kinase Superfamily. AKT1 is a major mediator of the responses to insulin, insulin-like growth factor 1 (IGF1), and glucose. AKT1 also plays a key role in the regulation of both muscle cell hypertrophy and atrophy. AKT1 activity is required for physiologic cardiac growth in response to IGF1 stimulation or exercise training. In contrast, AKT1 ac... | |||
TMPK-01170 |
Hepcidin/HAMP Protein, Mouse, Recombinant (GST)
Hamp1,LEAP-1,PLTR,HFE2B,LEAP1,Hepc1,Hepc |
Mouse | E. coli |
Hepcidin, the main regulator of iron metabolism, is synthesized and released by hepatocytes in response to increased body iron concentration and inflammation. Deregulation of hepcidin expression is a common feature of genetic and acquired iron disorders: in Hereditary Hemochromatosis (HH) and iron-loading anemias low hepcidin causes iron overload, while in Iron Refractory Iron Deficiency Anemia (IRIDA) and anemia of inflammation (AI), high hepcidin levels induce iron-restricted erythropoiesis. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIJ-0342 |
Aniline-d5
|
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Aniline-d5 是 Aniline 的氘代化合物。Aniline 的 CAS 号为 62-53-3。Aniline 通过铁过载和通过血红素加氧酶 1 上调诱导氧化应激对脾脏产生毒性。它会导致 p-IKKα 和 p-IKKβ 显着增加,进而增加 NF-κB 和 AP-1 结合活性。 |