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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T61093 |
MicroRNA-21-IN-2
|
Others | Others |
microRNA-21-IN-2,一种潜在的miR-21抑制剂,其AC50值为3.29 μM,主要用于癌症研究。 | |||
T63879 |
microRNA-21-IN-1
|
Others | Others |
microRNA-21-IN-1(compound 7A)是一种高效microRNA抑制剂,对Hela和HCT-116细胞显示出抗增殖活性,IC50值分别为5.5 μM和2.8 μM,并能促进Hela细胞凋亡(apoptosis)。该化合物通过上调microRNA-21下游功能靶点(PTEN、EGR1、SLIT2)的表达,有助于抗癌研究。 | |||
T10831L |
Cl-amidine hydrochloride
|
Apoptosis; PAD | Apoptosis; Chromatin/Epigenetic |
Cl-amidine hydrochloride 是一种口服有效的PAD 抑制剂,可阻断组蛋白 3 瓜氨酸化和中性粒细胞胞外陷阱的形成,并提高败血症小鼠的存活率。它可诱导癌细胞凋亡,还可诱导 miR-16 引起细胞周期阻滞。 | |||
T11850 |
LIN28 inhibitor LI71
|
Others | Others |
LIN28 inhibitor LI71 是一种有效的细胞渗透性 LIN28 抑制剂,可消除 LIN28 介导的寡尿苷酸化,IC50 为 7 uM。它能直接绑定 CSD,抑制 LIN28 对 let-7 的作用活性。 | |||
T16538 |
PIN1 inhibitor API-1
|
Others | Others |
PIN1 inhibitor API-1 是特殊的 Pin1抑制剂,可直接特异性地与 Pin1 肽基脯氨酰异构酶结构域结合,并抑制 Pin1 顺反异构活性。它保留 pXPO5 的活性构象,恢复 pXPO5 将前 miRNA 从细胞核转运到细胞质的能力,从而上调抗癌 miRNA 的生物发生,抑制体内外肝癌的发生。 | |||
T11851 |
Lin28-let-7a antagonist 1
|
Others | Others |
Lin28-let-7a antagonist 1 对 Lin28A-let-7a-1 相互作用的 IC50 为 4.03 μM,对 Lin28-let-7a 相互作用有明显的拮抗作用。 | |||
T8333 |
Aurintricarboxylic acid
ATA,NSC-4056,NSC4056,金精三羧酸,NSC 4056 |
Apoptosis; P2X Receptor; Influenza Virus; Topoisomerase | Apoptosis; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Aurintricarboxylic acid (NSC-4056) 是高效的αβ-亚甲基-ATP 敏感选择性P2X1Rs 和P2X3Rs 变构拮抗剂。 它是核糖核酸酶和拓扑异构酶 II 的有效抑制剂,可阻止核酸与酶结合。 | |||
T0717L |
Enoxacin
依诺沙星,NSC 629661,AT 2266,Pd107779,CI 919 |
DNA/RNA Synthesis; Topoisomerase; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Enoxacin (NSC-629661) 是一种可干扰DNA 复制的氟喹诺酮,抑制细菌 DNA 促旋酶 (IC50=126 µg/ml) 和拓扑异构酶 IV (IC50=26.5 µg/ml)。它是特异性癌症生长抑制剂,可有效抑制革兰氏阳性和阴性细菌。 | |||
T2514 |
Linifanib
利尼伐尼,ABT-869,RG3635,AL-39324 |
Apoptosis; c-Fms; VEGFR; FLT; CSF-1R; PDGFR; c-Kit; Autophagy | Angiogenesis; Apoptosis; Autophagy; Tyrosine Kinase/Adaptors |
Linifanib (AL-39324) 是一种高效口服的VEGFR 和PDGFR 家族多靶点抑制剂,具有显著的抗肿瘤活性。它对无关 RTKs、可溶性酪氨酸激酶或丝氨酸/苏氨酸激酶的活性要低得多。它是特异性 miR-10b 抑制剂,阻断miR-10b 的生物合成。 | |||
T0717 |
Enoxacin hydrate
CI-919 hydrate,Enoxacin Sesquihydrate,依诺沙星半水合物,AT-2266 hydrate,依诺沙星倍半水合物 |
DNA gyrase; DNA/RNA Synthesis; Topoisomerase; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Enoxacin hydrate (AT-2266 hydrate) 是氟喹诺酮,可干扰DNA 复制,抑制细菌 DNA 促旋酶 (IC50=126 µg/ml) 和拓扑异构酶 IV (IC50=26.5 µg/ml)。它是特异性癌症生长抑制剂,抑制革兰氏阳性和阴性细菌。 | |||
T23777 |
BCI-137
BCI137 |
Others | Others |
BCI-137 是 Argonaute 2 配体。它通过靶向 MicroRNA 结合域来发挥作用。 | |||
T38680 |
RJW100
|
Others | Others |
RJW100是一种化合物,作为肝受体同源体1(LRH-1, NR5A2)和类固醇生成因子-1(SF-1, NR5A1)的强效激动剂,分别展现出6.6和7.5的pEC50值。此外,RJW100能强力激活miR-200c(miRNA-200c, microRNA-200c)启动子。 | |||
T8902 |
DOTMA
Trimethyl[2,3-(dioleyloxy)propyl]ammonium Chloride,N-(1-(2,3-dioleyloxy)propyl)-N,N,N-trimethylammonium |
Others | Others |
DOTMA (N-(1-(2,3-dioleyloxy)propyl)-N,N,N-trimethylammonium) 作为 tetra-methylated DOTA 类似物,是一种阳离子脂类,被用作基因治疗的非病毒载体。它已被用作脂质体的成分,可用于封装 siRNA、microRNA 和寡核苷酸,并用于体外基因转染。在体外和体内均表现出良好的基因转染效果。DOTMA 诱导脂质体上的正电荷,从而促进脂质体与细胞膜的有效相互作用。 | |||
T16882 |
SID 3712249
MiR-544 Inhibitor 1 |
Others | Others |
SID 3712249 is an inhibitor of the biogenesis of microRNA-544 (miR-544). | |||
T28045 |
miR-21 Inhibitor-1
|
Others | Others |
miR-21 Inhibitor-1 is a microRNA-21 (miR-21) inhibitor. | |||
T13085 |
Targaprimir-96
|
Others | Others |
Targaprimir-96 is a potent microRNA-96 (miR-96) processing inhibitor. | |||
T16077 |
MIR96-IN-1
|
MALT | Immunology/Inflammation |
MIR96-IN-1 selectively inhibits biogenesis of microRNA-96, upregulating a protein target (FOXO1) and inducing apoptosis in cancer cells. | |||
T13085L |
Targaprimir-96 TFA (1655508-14-7 free base)
Targaprimir-96 TFA |
Others | Others |
Targaprimir-96 TFA is a potent microRNA-96 (miR-96) processing inhibitor. | |||
T39712 |
RGLS4326
RG4326,RGLS4326 |
Others | Others |
RGLS4326 (RG4326) is a short oligonucleotide inhibitor of microRNA-17 (miR-17), with a pioneering role in its class. This compound, with a research focus on autosomal dominant polycystic kidney disease (ADPKD), effectively suppresses the activity of miR-17 in HeLa cells, displaying an EC50 value of 28.3 nM. | |||
T73824 |
Thymidine 3',5'-diphosphate tetrasodium
|
Others | Others |
Thymidine 3',5'-diphosphate (Deoxythymidine 3′,5′-diphosphate) tetrasodium,为一种选择性抑制剂,主要针对葡萄球菌核酸酶及含1的都铎结构域(SND1,MicroRNA调控复合体RISC亚基)和[3,5-2H2]酪氨酸核酸酶([3,5-2H2] tyrosyl nuclease)。此化合物还展示了抗肿瘤活性,并可在生化反应中作为催化剂使用。 | |||
T74059 |
Targaprimir-96 TFA
|
Others | Others |
Targaprimir-96 TFA 是一种针对microRNA-96 (miR-96)加工的有效抑制剂,专门调节癌细胞内miR-96生成,引发凋亡(apoptosis)。此化合物与primary miR-96 (pri-miR-96)高亲和力结合,特异性作用于乳腺癌细胞的pri-miR-96,而对健康乳腺细胞无影响。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5S0246 |
Pseudoprotodioscin
山药 |
Others; Fatty Acid Synthase | Metabolism; Others |
Pseudoprotodioscin 是一种呋喃葡糖苷,抑制SREBP1/2和microRNA 33a/b 水平,降低胆固醇和甘油三酯合成相关的基因表达。 | |||
T1123 |
Camptothecin
NSC-100880,Campathecin,喜树碱,(S)-(+)-Camptothecin,CPT |
Apoptosis; Influenza Virus; Topoisomerase; Antibiotic; Antifungal; ADC Cytotoxin | Antibody-drug Conjugate/ADC Related; Apoptosis; DNA Damage/DNA Repair; Microbiology/Virology |
Camptothecin (CPT) 属于生物碱类天然产物,是一种 DNA 拓扑异构酶 I (Topo I) 的抑制剂 (IC50=679 nM),具有特异性。Camptothecin 具有抗肿瘤活性,可以诱导细胞凋亡。 | |||
TN1068 |
Tricin
|
Others; CDK | Cell Cycle/Checkpoint; Others |
Tricin 是米糠中大量存在的一种天然类黄酮。它通过抑制 CDK9 来抑制HCMV 的复制。它通过上调 FAK 靶向 microRNA-7 的表达来抑制 C6 胶质瘤细胞的增殖和侵袭。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPJ-01155 |
PDCD4 Protein, Human, Recombinant (His)
Programmed Cell Death Protein 4,Protein 197/15a,Neoplastic T... |
Human | E. coli |
Programmed Cell Death Protein 4 (PDCD4) is a member of the PDCD4 family. PDCD4 and EIF4A1 form a heterotrimer. One molecule of PDCD4 binds two molecules of EIF4A1. PDCD4 takes part in apoptosis via inhibiting translation initiation and cap-dependent translation.PDCD4 promotes colonic neoplastic transformation and tumor invasion. PDCD4 is an important target for microrna R-21 in breast cancer cells. Shortage of PDCD4 expression is associated with colorectal cancer. Overexpression of PDCD4 in carc... | |||
TMPY-04084 |
ANGPTL1 Protein, Canine, Recombinant (hFc)
angiopoietin-like 1 |
Canine | HEK293 Cells |
Angiopoietin-like protein 1 (ANGPTL1) has been reported to suppress migration and invasion in lung and breast cancer, acting as a novel tumor suppressor candidate. Downregulation of tumor suppressor signaling plays an important role in the pathogenesis of hepatocellular carcinoma (HCC).The downregulation of the angiopoietin-like protein ANGPTL1 is associated with vascular invasion, tumor thrombus, metastasis, and poor prognosis in HCC. Ectopic expression of ANGPTL1 in HCC cells effectively decre... | |||
TMPY-03397 |
TPPP3 Protein, Human, Recombinant (His)
CGI-38,TPPP3,p25gamma,tubulin polymerization-promoting prote... |
Human | E. coli |
TPPP3, a member of the Tubulin polymerization-promoting protein family, is an intrinsically unstructured protein that induces tubulin polymerization. TPPP3 is a marker in the developing musculoskeletal system. In tendons, Tppp3 is expressed in cells at the circumference of the developing tendons, likely the progenitors of connective tissues that surround tendons: the tendon sheath, epitenon, and paratenon. Tppp3 is also expressed in forming synovial joints. The onset of Tppp3 expression in joint... | |||
TMPH-01248 |
ADAR Protein, Human, Recombinant (His & SUMO)
ADAR1,IFI-4,136 kDa double-stranded RNA-binding protein,Inte... |
Human | E. coli |
Catalyzes the hydrolytic deamination of adenosine to inosine in double-stranded RNA (dsRNA) referred to as A-to-I RNA editing. This may affect gene expression and function in a number of ways that include mRNA translation by changing codons and hence the amino acid sequence of proteins; pre-mRNA splicing by altering splice site recognition sequences; RNA stability by changing sequences involved in nuclease recognition; genetic stability in the case of RNA virus genomes by changing sequences duri... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIJ-0162 |
Dexamethasone-d4
|
||
Dexamethasone-d4 是 Dexamethasone 的氘代化合物。Dexamethasone 的 CAS 号为 50-02-2。Dexamethasone是一种糖皮质激素受体激动剂和一种 IL 受体调节剂。在脂多糖诱导的巨噬细胞炎症反应中,它抑制含有炎性 microRNA-155 的外泌体的产生。 |