130
8
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1761L |
Handle region peptide, rat acetate
Handle region peptide, rat acetate(749227-53-0 free base) |
Others | Others |
Handle region peptide, rat acetate(749227-53-0 free base) 是一种肾素原受体拮抗剂,可抑制糖尿病肾病的进展并具有抗炎作用。 | |||
T21434 |
Sulfacetamide
NSC 63871,磺胺醋酰,NSC-63871,Sebizon,Region,NSC63871,Sulphacetamide,Acetosulfamine |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Sulfacetamide (NSC-63871) 是一种抗生素,通过限制细菌生存所需的叶酸的存在来治疗睑缘炎或结膜炎,有潜力用于眼部感染的研究。 | |||
TP1761 |
Handle region peptide, rat
|
||
Handle region peptide, rat, functions as a prorenin receptor antagonist, effectively inhibiting the development of diabetic nephropathy while also exhibiting anti-inflammatory properties specifically within the eye. | |||
T22865 |
immunoglobulin light chain variable region fragment [Homo sapiens]
|
Others | Others |
Immunoglobulin light chain variable region fragment [Homo sapiens] is a fragment (Phe-Thr-Leu-Lys-Ile-Ser-Arg) on the variable region of the human immunoglobulin light chain. | |||
TP2259 |
immunoglobulin light chain variable region fragment [Homo sapiens]/[Mus musculus]
|
Others | Others |
Immunoglobulin light chain variable region fragment [Homo sapiens]/[Mus musculus] is a fragment on the variable region of the human and mouse immunoglobulin light chain. Immunoglobulins (Ig) are the antigen recognition molecules of B cells. An Ig molecule | |||
T22856 |
IgG light chain variable region [Homo sapiens]/IgM/kappa antibody [Mus musculus]
|
Others | Others |
IgG has four forms, provides the majority of antibody-based immunity against invading pathogens. The only antibody capable of crossing the placenta to give passive immunity to the fetus. Eliminates pathogens in the early stages of B cell-mediated (humoral | |||
T83511 |
[Ala127] Hepatitis B Virus Pre-S Region (120-131)
|
||
[Ala127] Hepatitis B Virus Pre-S Region (120-131) 是一种肽,序列为MQWNSTAFHQT。该肽适用于活性增强的研究。 | |||
T76528 |
Hepatitis b virus pre-s region (120-145)
|
||
Hepatitis b virus pre-s region (120-145) 是一种 preS2 肽,可抑制单链 Fv 片段 (scFv) 或IgG 与 r-HBsAg 的结合。 | |||
T3071 |
Olverembatinib
GZD 824 |
Bcr-Abl | Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
Olverembatinib (GZD 824) 是一种高效的、口服具有活性的pan-Bcr-Abl 抑制剂,具有抗肿瘤活性。它能广泛而有效地抑制突变型 Bcr-Abl。它对天然的 Bcr-Abl 和 Bcr-AblT315I 作用的IC50值分别为 0.34 nM 和 0.68 nM。 | |||
T2429 |
Olverembatinib dimesylate
GZD824 Dimesylate,HQP1351 |
Bcr-Abl | Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
Olverembatinib dimesylate (GZD824 Dimesylate) 是一种高效的、口服具有活性的pan-Bcr-Abl 抑制剂,具有抗肿瘤活性。它能广泛而有效地抑制突变型 Bcr-Abl。它对天然的 Bcr-Abl 和 Bcr-AblT315I 作用的IC50值分别为 0.34 nM 和 0.68 nM。 | |||
T0682 |
Lamivudine
GR109714X,BCH-189,拉米夫定 |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Lamivudine (BCH-189) 是一种核苷逆转录酶抑制剂,可抑制HIV 逆转录酶1和2 以及乙型肝炎病毒的逆转录酶。 | |||
TP1540 |
Jagged-1 (188-204)
Jagged-1 188-204 |
Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
Jagged-1 (188-204) 是 JAG-1 蛋白的一个片段。其中 JAG-1 能够诱导单核细胞衍生的人树突状细胞成熟,是一种在培养的和原发性多发性骨髓瘤细胞中高度表达的 Notch 配体。 | |||
T1706 |
4-Hydroxy-3-nitrophenylacetic acid
|
Others | Others |
4-Hydroxy-3-nitrophenylacetic acid 是一种小分子药物,在 Ig 重链 V-I 区和 Ig γ-2 链 C 区具有活性。 | |||
T7541 |
PTP inhibitor 1
PTP Inhibitor II,alpha-溴-4-甲氧基苯乙酮 |
Phosphatase | Metabolism |
PTP inhibitor 1 是蛋白酪氨酸磷酸酶 (PTP) 抑制剂,具有抗血管生成作用。 | |||
T6152 |
PD318088
|
MEK | MAPK |
PD318088 是非 ATP 竞争性的MEK1/2变构抑制剂,是 PD184352 的结构类似物。它在MEK1 活性位点与 ATP 结合位点相邻的区域与 ATP 同时结合,可用于癌症研究。 | |||
T8864 |
Thymidylate Kinase Inhibitor, YMU1
|
Others | Others |
YMU1 是一种选择性抑制剂,特异性作用于人胸苷酸激酶 (IC50: 610 nM) 。 | |||
TP1459L |
Gly-Arg-Gly-Asp-Ser acetate(96426-21-0 free base)
|
Integrin | Cytoskeletal Signaling |
Gly-Arg-Gly-Asp-Ser acetate(96426-21-0 free base) 是一种源自纤连蛋白的细胞结合区域的细胞结合蛋白结构域。 | |||
TP1615L |
IKKγ NBD Inhibitory Peptide acetate
IKKγ NBD Inhibitory Peptide acetate(372146-18-4 free base) |
NF-κB | NF-κB |
IKKγ NBD Inhibitory Peptide acetate 是一种 NEMO 结合结构域肽(NBD 肽)乙酸盐,对应于 NEMO 氨基末端 α-螺旋区域。它显示可阻断 TNF-α 诱导的 NF-kB 活化。 | |||
T77484 |
Atibuclimab
|
TNF | Apoptosis |
Atibuclimab 是一种靶向 CD14 的嵌合单克隆抗体,由小鼠可变区和人类 IgG4 Fc 区构成。Atibuclimab 可用于治疗肌萎缩侧索硬化症。Atibuclimab 可减少 LPS 诱导的病症,并对 LPS 诱导的促炎细胞因子释放有抑制作用,可延迟抗炎细胞因子可溶性 TNF 受体 I 型的释放, | |||
T77100 |
Nirsevimab
MEDI8897 |
RSV | Microbiology/Virology |
Nirsevimab (MEDI8897) 是一种具有修饰 Fc 区的重组人呼吸道合胞病毒 (RSV) 单克隆抗体。Nirsevimab 高效靶向 RSV-B ,Kd 值为 1.5 nM。Nirsevimab 可用于预防 RSV 感染。 | |||
T13176 |
TNO155
Batoprotafib |
Phosphatase | Metabolism |
TNO155 是具有口服活性野生型SHP2的选择性变构抑制剂 (IC50= 0.011 µM)。它有研究 RTK 依赖性恶性肿瘤(尤其是晚期实体瘤)的潜力。 | |||
T8958 |
PU-H54
|
GPR | Endocrinology/Hormones; GPCR/G Protein |
PU-H54 是一种基于嘌呤的 Grp94 抑制剂。它是一种基于 Grp94 选择性间苯二酚的抑制剂,通过探测 Grp94 中 S2 亚袋的专有结合区而分离。 | |||
TP2308 |
TB500 acetate(885340-08-9 free base)
Frag17-23 Acetate,TB500 Acetate |
Others | Others |
TB500 acetate(885340-08-9 free base) (Frag17-23 Acetate) 是胸腺素 β4 活性区域的合成版本。它促进内皮细胞分化、真皮组织中的血管生成、角质形成细胞迁移、胶原沉积和减少炎症。 | |||
T73133 |
FGF22-IN-1
|
Others | Others |
FGF22-IN-1 是一种潜在的 CD4 N-末端免疫球蛋白可变区样结构域(CD4 D1)抑制剂。FGF22-IN-1 可抑制CD4 与主要组织相容性复合体 (MHC) II 类蛋白之间的相互作用,抑制免疫应答。 | |||
T63971 |
Canocapavir
ZM-H1505R |
HBV | Microbiology/Virology |
Canocapavir (ZM-H1505R)是一种新型可口服的 HBV 衣壳蛋白调节剂,具有抗病毒活性,可诱导 HBV 核心蛋白连接子区域的构象变化,可用于治疗乙型肝炎病毒。 | |||
T1786 |
Daclatasvir dihydrochloride
BMS-790052 dihydrochloride,盐酸达拉他韦 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Daclatasvir dihydrochloride (BMS-790052 dihydrochloride) 是有机阴离子转运多肽 1B(OATP1B) 和 OATP1B3抑制剂,IC50分别为 1.5 µM 和 3.27 µM。它也具有口服活性的 HCV NS5A 蛋白抑制剂,多种 HCV 复制子基因型的 EC50范围为 9-146 pM。 | |||
TP1143L |
Fibrinopeptide A, human acetate
Fibrinopeptide A, human acetate(25422-31-5 free base),Human fibrinopeptide A acetate |
Others | Others |
Fibrinopeptide A, human acetate (Human fibrinopeptide A acetate)(25422-31-5 free base) 是一种 16 个残基的短多肽,由凝血酶从纤维蛋白原上切割下来。纤维蛋白肽 A (FPA) 由纤维蛋白原蛋白的 N 末端 Aα 区域在被凝血酶切割后产生。 | |||
T38192 |
Unifiram
|
Others | Others |
Unifiram 是一种认知增强剂。 Unifiram 诱导大鼠海马 CA1 区场兴奋性突触后电位 (fEPSP) 幅度的持久增加 (EC50= 27 nM) 并增加大鼠大脑皮层中乙酰胆碱 (ACh) 的释放。 | |||
TP1002L |
γ-1-MSH, amide acetate (72629-65-3 free base)
γ-1-MSH, amide acetate |
Others | Others |
γ-1-MSH, amide acetate (72629-65-3 free base) 是 ACTH/β-内啡肽 (β-EP) 前体蛋白 N 末端区域的一种推定激素,RIA 使用抗 γ-3-MSH 抗血清对产生 ACTH 的小鼠进行了研究垂体肿瘤细胞,AtT-20/D16v。 | |||
TP1785L |
Peptide T acetate(106362-32-7 free base)
|
Others; HIV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
Peptide T acetate(106362-32-7 free base) 是一种来自 HIV-1 gp120 V2 区域的八肽。它是一种合成八肽,其可能的作用机制是 gp120 对 CD4 受体的竞争性抑制以及与血管肠肽受体的结合和抑制细胞因子作用。 | |||
T60619 |
CDK9-IN-15
|
CDK | Cell Cycle/Checkpoint |
CDK9-IN-15 是一种有效的小分子CDK9抑制剂,可通过降解、抑制 CDK9 来阻断正性转录延长因子 P-TEFb (positive transcription elongation factor b) 对 RNA Poly-II C末端区域的磷酸化,抑制转录,迅速降低细胞内 mRNA 水平,从而引起肿瘤细胞凋亡。 | |||
T7084 |
2-Bromo-4'-hydroxyacetophenone
SHP-1 Inhibitor II,PTP Inhibitor I,α-Bromo-4-hydroxyacetophenone,4-Hydroxyphenacyl bromide,2-溴-4'-羟基苯乙酮 |
Phosphatase | Metabolism |
2-Bromo-4'-hydroxyacetophenone(PTP Inhibitor I) 是一种PTP1B 的有效抑制剂,其Ki=42 μM。 | |||
T70540 |
Pinokalant
LOE-908 |
SARS-CoV; TRP/TRPV Channel | Membrane transporter/Ion channel; Microbiology/Virology |
Pinokalant (LOE-908) 是一种新型非选性阳离子通道抑制剂。Pinokalant 在体内实验中可显著减少皮质梗死体积,可改善缺血半影区的代谢和电生理状态,可减少大鼠大脑中动脉闭塞后急性期磁共振图像上的病变大小。Pinokalant是一种潜在的SARS-CoV-2蛋白酶抑制剂,可用于研究脑卒中。 | |||
T76883 |
Talacotuzumab
CSL 362,JNJ 56022473 |
Immunology/Inflammation related; Interleukin | Immunology/Inflammation |
Talacotuzumab (JNJ 56022473) 是一种含有修饰的 Fc 结构的IgG1 型完全人源化的 CD123 中和单克隆抗体。Talacotuzumab 对 CD123、CD32b/c、CD16-158F、CD16-158V 具有很高的亲和力, KD 分别为 0.43 nM、188 nM、46 nM、16.8 nM。Talacotuzumab 通过抑制 IL-3 与 CD123 结合进而抑制靶细胞中的 IL-3 信号传导。Talacotuzumab 诱导 Fc 区发生突变以增加对 CD16 (FcγRIIIa) 的亲和力,从而加强抗体依赖性细胞介导的细胞毒性 (ADCC)。Talacotuzumab 急性髓性白血病 (AML) 异种移植小鼠模型中抑制白血病细胞生长。 | |||
T22043 |
BCATc Inhibitor 2
|
Others | Others |
BCATc Inhibitor 2 是选择性分支链氨基转移酶抑制剂,可用于神经退行性疾病的研究。能够抑制 rBCATc (IC50:0.2 μM),hBCATc (IC50:0.8 μM)、 rBCATm (IC50:3.0 μM)。其中BCATc 也称为 BCAT1,存在于细胞质基质中的亚型。 | |||
T19730 |
12-Crown-4
12 C 4,12-Crown-4 ether,12C4,12-C-4 |
||
12-Crown-4 disrupts Aβ40 fibrils. 12-Crown-4 can enter into the hydrophobic core region and form competitive, hydrophobic interactions with key hydrophobic residues. | |||
T24106 |
GSK2163632A
GSK-2163632-A,GSK 2163632 A |
||
GSK2163632A is an insulin-like growth factor 1 receptor inhibitor that acts by binding to a novel region of the GRK active site cleft. | |||
T23925 |
CYD-2-11
CYD 2 11,CYD211 |
||
CYD-2-11 is an effective and selective Bax agonist. It acts by targeting the structural pocket proximal to S184 in the C-terminal region of Bax. | |||
T15659 |
KHK-IN-1 hydrochloride
|
Others | Others |
KHK-IN-1 hydrochloride is a potent inhibitor of ketohexokinase (KHK) (IC50: 12 nM). In the ATP-binding region of KHK, KHK-IN-1 hydrochloride interacts with Asp-27B. | |||
T19039 |
NIR-Thiol dinitrobenzenesulfonate
|
Others | Others |
NIR-Thiol dinitrobenzenesulfonate has both absorption and emission in the NIR region. It is capable of imaging endogenously produced thiol in living cells and mice. | |||
T31945 |
Glutamyl ribose 5-phosphate
Glu-R-S-P |
||
Glutamyl ribose 5-phosphate is obtained by the linkage region in ADP ribosylation of proteins. | |||
T31644 |
Enviroxime
LY-122772,LY 122772,LY122772,LY122771-72,NSC 346230 |
||
Enviroxime(LY 122772, NSC 346230) is an anti-infective and anti-disease agent. Enviroxime targets the 3A coding region of rhinovirus and poliovirus. | |||
T71348 |
UC-773587
|
||
UC-773587 is a novel inhibitor of Ras signaling, binding to the Ras switch II interaction region of SOS1. | |||
T35014 |
Valdice
|
||
Valdice is a village and municipality in Jičín District in the Hradec Králové Region of the Czech Republic. | |||
T76286 |
REDV
|
||
REDV 是纤连蛋白交替剪接的 III 型连接段 (IIICS) 区域的 CS5 位点内的活性序列。REDV 可以通过结合整合素α4β1介导与血浆纤连 IIICS 区域的粘附。REDV 可用于细胞粘附的研究。 | |||
T24756 |
SAMT-247
SAMT 247 |
||
SAMT-247 is an HIV inhibitor that acts by modifying the nucleocapsid NCp7 region of Gag in infected cells and blocking Gag processing and reducing infectivity. | |||
T31754 |
FD-1080
Heptamethine cyanine dye FD 1080,FD1080,Heptamethine cyanine dye FD1080,Heptamethine cyanine dye FD-1080 |
||
FD-1080 is a fluorophore with both excitation and emission in the NIR-II region for in vivo imaging. | |||
T27326 |
FK960
FK 59960,FK-960,FK-59960,FK59960 |
||
FK962 is an enhancer of somatostatin release, which exerts cognitive-enhancing actions in rats. FK960 increases synaptic density in the hippocampal CA3 region of aged rats. | |||
T28942 |
Telomestatin
SOT 095,GM95,(R)-Telomestatin,GM 95,GM-95 |
||
Telomestatin is an inhibitor of the telomerase, it induces the formation of basket-type G-quadruplex (G4) structures from hybrid-type G-quadruplexes in the telomeric region. | |||
T83063 |
Anti-IgG-Fc (Human)
|
||
Anti-IgG-Fc (Human) 是抗体,特异性结合于人类IgG1。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6S2115 |
Ginkgolide J
BN 52024,7-beta-Hydroxyginkgolide A,银杏内酯 J,银杏内酯J |
PDE | Metabolism |
Ginkgolide J (BN 52024) 是一种银杏叶中非黄酮部分的主要成分(IC50:12-54 µM),具有神经保护和抗神经元凋亡功能。 | |||
T3891 |
Oroxylin A-7-O-glucuronide
Oroxylin A Glucoronide,千层纸素A-7-0-Β-D-葡萄糖醛酸苷,Oroxyloside,Oroxylin A 7-O-beta-D-glucuronide |
Others | Others |
Oroxylin A-7-O-glucuronide (Oroxylin A Glucoronide) 是一种类黄酮葡糖苷酸,提取自 Scutellaria baicalensis 干燥的根中,具有脯氨酰寡肽酶(POP)抑制作用。 | |||
T3S0209 |
Vincristine
|
ERK; p38 MAPK; NF-κB; Akt; JNK; mTOR | Cytoskeletal Signaling; MAPK; NF-κB; PI3K/Akt/mTOR signaling |
Vincristine 与微管蛋白结合并抑制微管的形成,从而抑制癌细胞的有丝分裂。 Vincristine 可用作微管去稳定剂,用于研究治疗血液系统癌症,如白血病和淋巴瘤以及儿童肉瘤的相关研究。 | |||
T20493 |
Palmitone
NSC-953,NSC953,NSC 953 |
||
In the CA3 hippocampal region, Palmitone against pentylenetetrazole-caused neuronal damage. | |||
T73070 |
STAT3-IN-14
|
||
STAT3-IN-14是一种STAT3抑制剂,具有STAT3磷酸化抑制活性,可直接与 STAT3的铰链区结合。 | |||
TN4890 |
Rabdosin B
|
Others | Others |
Rabdosin B shows cytotoxic activity against three human tumour HepG2, GLC-82 and HL-60 cell lines, it induces significant DNA damage to HepG2 cells in a time- and dose-dependent manner. Rabdosin B at higher concentrations inhibits root growth by affecting | |||
T36448 |
(E)-Ajoene
|
||
(E)-Ajoene is a disulfide that has been found inA. sativumand has diverse biological activities.1,2,3,4It is active against Gram-positive and Gram-negative bacteria (MICs = 10-250 and 150->500 μg/ml, respectively) and fungi (MICs = 15-50 μg/ml).1(E)-Ajoene inhibits proliferation of a variety of cancer cells, including MDA-MB-231 breast, HeLa cervical, and WHCO1 esophageal cancer cells (IC50s = 18.6, 61, and 39.2 μM, respectively).2It also inhibits human glutathione reductase andT. cruzitrypanoth... | |||
T36738 | 4′-Hydroxy-2′-methylacetophenone | ||
4′-Hydroxy-2′-methylacetophenone, an aroma compound of red wines, is isolated from cv. Bobal grape variety. 4′-Hydroxy-2′-methylacetophenone has ciliate toxicity. 4′-Hydroxy-2′-methylacetophenone inhibits the growth of T. pyriformis, with an IC50 of 0.65 mM[1][2]. [1]. GómezGarcía-Carpintero E, et, al. Aroma characterization of red wines from cv. Bobal grape variety grown in La Mancha region. Food Research International. 2011 Jan; 44(1): 61-70. [2]. Schüürmann G, et, al. Stepwise discrimination ... |