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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T71832 | CTX-0124143 | Histone Acetyltransferase | Chromatin/Epigenetic |
CTX-0124143 是一种组蛋白乙酰转移酶抑制剂,对 KAT6A 的 IC50 值为 1.0μM。CTX-0124143 可用于研究细胞衰老。 | |||
T2042 |
CTX-0294885
|
Others | Others |
CTx0294885 是新型的二苯胺嘧啶化合物,在体外对广泛激酶有抑制作用,可用作琼脂糖凝胶激酶检测试剂。 | |||
TP1289 |
Cardiotoxin Analog (CTX) IV (6-12) TFA
Cardiotoxin Analog (CTX) IV (6-12) (TFA)(115722-23-1,FREE) |
Others | Others |
Cardiotoxin Analog (CTX) IV (6-12) TFA(115722-23-1 free base) 是 Cardiotoxin Analog (CTX) IV 的部分肽。从台湾眼镜蛇毒液中分离出的心脏毒素类似物 IV。 CTX IV 是一种独特的蛇毒心脏毒素。 | |||
T3715 |
Acebilustat
阿西鲁司特,CTX-4430 |
Aminopeptidase; LTR | Immunology/Inflammation; Metabolism |
Acebilustat (CTX-4430) 是一种具有口服活性的白三烯 A4 水解酶抑制剂,可用于炎症研究。 | |||
T9167 |
PF-9363
CTX-3648 |
Histone Acetyltransferase | Chromatin/Epigenetic |
PF-9363 (CTX-3648) 是一种有效且高选择性的 KAT6A/KAT6B 抑制剂,可用于癌症研究。 | |||
TP1455 |
Cardiotoxin Analog (CTX) IV (6-12)
Cardiotoxin Analog (CTX) IV 6-12 |
||
Cardiotoxin Analog (CTX) IV (6-12) is a part peptide of Cardiotoxin Analog (CTX) IV. Cardiotoxin analogues IV isolated from the venom of Taiwan Cobra. | |||
T19251 |
CTX-0294885 hydrochloride (1439934-41-4 free base)
CTX-0294885 hydrochloride |
Others | Others |
CTX-0294885 hydrochloride is an agarose-supported kinase capture reagent. | |||
T23707 |
alpha-Conotoxin imi
alpha-Ctx-imi |
||
alpha-Conotoxin imi is a nicotinic acetylcholine receptor ligand. | |||
T62049 |
CTX-712
|
||
CTX-712 是 有效的cdc2 样激酶 (CLK) 抑制剂。CTX-712 可以抑制癌症存活和癌细胞生长。 | |||
T76734 | CTX-471 | ||
CTX-471 是 CD137 的全人源单克隆抗体。CTX-471 对重组人、食蟹猴 CD137 和小鼠 CD137 具有结合亲和力,Kd 值分别为 50 nM、61 nM 和 748 nM。CTX-471 可用于免疫调节和癌症的研究。 | |||
T82664 |
CTX-2026
|
||
CTX-2026是一种与CD277结合的纯人源抗体,在卵巢肿瘤模型中表现出抗肿瘤活性,适用于癌症研究。 | |||
T72214 | CTX-0294885 hydrochloride | ||
CTX-0294885 hydrochloride 是一种广谱激酶抑制剂,可以从 MDA-MB-231 细胞中捕获 235 种激酶,且可捕获AKT 家族中的所有成员。CTX-0294885 hydrochloride 是一种强大的激酶组信号网络分析试剂,可用于炎症、糖尿病和癌症等疾病的研究。 | |||
T15016 |
CTX1
|
p53 | Apoptosis |
CTX1 is a small molecule activator of p53. | |||
T4584 |
BMS-813160
BMS 813160 |
CCR | Immunology/Inflammation; Microbiology/Virology |
BMS-813160 是CCR2/CCR5双重拮抗剂。有用于心血管的研究潜力。 | |||
T60050 |
ANT3310
|
Antibacterial | Microbiology/Virology |
ANT3310 是一种广谱共价丝氨酸 β-内酰胺酶抑制剂,对 AmpC、CTX-M-15、TEM-1、OXA-48、OXA-23 和 KPC-2 的 IC50 范围为 1 nM 至 175 nM。 ANT3310 可用于细菌感染研究。 | |||
T38941 |
FPI-1523 sodium
|
Endogenous Metabolite; Antibacterial | Metabolism; Microbiology/Virology |
FPI-1523 sodium 是阿维巴坦的衍生物,是一种强效的 β-内酰胺酶抑制剂,对 CTX-M-15 和 OXA-48 的 K d s 分别为 4 nM 和 34 nM。FPI-1523 sodium 对 PBP2 有抑制作用,其 IC 50 为 3.2 μM。FPI-1523 sodium具有相当高的抗菌活性。 | |||
T10422 |
Avibactam free acid
NXL-104 free acid |
Antibacterial | Microbiology/Virology |
Avibactam (NXL-104) free acid is a covalent and reversible inhibitor of non-β-lactam β-lactamase (IC50s: 8 nM and 5 nM for β-lactamase TEM-1 and CTX-M-15). | |||
T10713 | CCR4 antagonist 2 | Calcium Channel | Membrane transporter/Ion channel; Metabolism |
CCR4 antagonist 2 (Compound 31) is a novel potent, orally bioavailable small molecule antagonists of CC chemokine receptor 4 (CCR4) that inhibits Treg trafficking into the Tumor Microenvironment without suppressing the number of Treg in healthy tissues. CCR4 antagonist 2 (Compound 31) exhibits IC50 values of Ca2+flux and (chemotaxis) CTX are 40 nM and 70 nM, respectively. | |||
T60874 | Avibactam sodium dihydrate | ||
Avibactam sodium (NXL-104) dihydrate 抑制 CTX-M-15和 β-内酰胺酶 TEM-1,IC50值分别为 5 nM 和 8 nM。Avibactam sodium (NXL-104) dihydrate 是非 β-内酰胺 β-内酰胺酶的可逆共价抑制剂。 | |||
T38940 | FPI-1523 | ||
FPI-1523, a derivative of Avibactam, is a potent inhibitor of β-lactamase enzymes. It has Kd values of 4 nM and 34 nM for CTX-M-15 and OXA-48, respectively. Additionally, FPI-1523 inhibits PBP2 with an IC50 of 3.2 μM and demonstrates significant antimicrobial activity. | |||
T60711 | Avibactam sodium hydrate | ||
Avibactam sodium hydrate (NXL-104 hydrate) 是 β-内酰胺酶的共价可逆抑制剂,不含β-内酰胺核心 。Avibactam sodium hydrate 抑制 β-内酰胺酶CTX-M-15和TEM-1,IC50分别为5 nM 和 8 nM。 | |||
T73902 |
Desacetylcefotaxime
|
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Desacetylcefotaxime, Cefotaxime的一种体内代谢物,具有类似其母体化合物对多种需氧和厌氧细菌的体外抗菌活性。 | |||
T39662 | CCR4 antagonist 3 hydrochloride | ||
CCR4 antagonist 3 hydrochloride is an orally active, potent and selective CCR4 antagonist. CCR4 antagonist 3, featuring a novel piperidinyl-azetidine motif, has IC 50 s of 22 nM and 50 nM in the calcium flux and CTX assay. CCR4 antagonist 3 has antitumor activity. | |||
T39661 |
CCR4 antagonist 3
CCR4 antagonist 3 |
||
CCR4 antagonist 3 is an orally active, potent and selective CCR4 antagonist. CCR4 antagonist 3, featuring a novel piperidinyl-azetidine motif, has IC 50 s of 22 nM and 50 nM in the calcium flux and CTX assay. CCR4 antagonist 3 has antitumor activity. | |||
T61204 |
FPI-1465
|
||
FPI-1465 是丝氨酸-β-内酰胺酶和青霉素结合蛋白 (PBP) 的双重抑制剂。FPI-1465 抑制PBP2,IC50为 1.0 μg/mL。FPI-1465 作用于 β-内酰胺酶 CTX-M-15 和 OXA-48,Kd 分别为 0.011 和 5.3 μM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37177 |
Norcholic Acid
|
||
Norcholic acid is a bile acid and 23-carbon derivative of cholic acid .1Levels of norcholic acid are increased in the urine of patients with liver cirrhosis or cerebrotendinous xanthomatosis (CTX), an inborn error of metabolism characterized by a deficiency in the mitochondrial enzyme sterol 27-hydrolylase (CYP27A1) that leads to progressive neurological symptoms.2,3,4 |