70
8
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1237 |
Azathioprine
硫唑嘌呤,BW 57-322 |
Apoptosis; GPR; Rho | Apoptosis; Cell Cycle/Checkpoint; Endocrinology/Hormones; GPCR/G Protein |
Azathioprine (BW 57-322) 是一种免疫抑制剂。 | |||
T15017 |
CU-T12-9
|
TLR | Immunology/Inflammation |
CU-T12-9 是特异性 TLR1/2激动剂,可激活先天免疫系统和适应性免疫系统。它选择性激活 TLR1/2 异二聚体,可通过促进 TLR1 和 TLR2 二聚而激活 NF-κB 信号,引起下游 TNF-α、IL-10 和 iNOS 增加。 | |||
T7222 |
GS-441524
GS 441524 triphosphate |
Others; SARS-CoV; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
GS-441524 是 Remdesivir 的主要活性代谢物,活性更优于 Remdesivir ,治疗患有自然发生的猫传染性腹膜炎的猫。 | |||
T40019 |
Thalidomide-5-NH2-CH2-COOH
|
Others | Others |
Thalidomide-5-NH2-CH2-COOH (compound 114) 是原肌球蛋白受体激酶的选择性抑制剂。它是 E3 连接酶的配体,具有研究一种或多种疾病的潜力。 | |||
T4990 |
Cefcapene pivoxil hydrochloride hydrate
Cefcapene Pivoxil Hydrochloride,盐酸头孢卡品酯 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefcapene pivoxil hydrochloride hydrate 是一种头孢菌素的前药,具有口服活性和广谱抗菌活性。它可研究掌跖脓疱病等感染性疾病。 | |||
T9567 |
Samatasvir
ATOLIHZIXHZSBA-BTSKBWHGSA-N,IDX719 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Samatasvir (ATOLIHZIXHZSBA-BTSKBWHGSA-N) 是 NS5A HCV 复制抑制剂。它能够有效的选择复制子及感染性 HCV,在基因型 1至5 复制子中,EC50= 2~24 pM。 | |||
T26804 |
Biclotymol
|
Others | Others |
Biclotymol 可用于感染性口咽疾病研究。 | |||
T16465 |
Penicillin G benzathine
Benzathine benzylpenicillin,Benzathine penicilline G |
Antibacterial | Microbiology/Virology |
Penicillin G benzathine 具有抗细菌感染活性,可用于研究早期梅毒。 | |||
T8686 |
VUN65671
|
Others | Others |
Compound 35 是埃博拉 (Mayinga) 和马尔堡 (安哥拉) 传染性病毒的优良抑制剂。 | |||
T72910 |
APOBEC3G-IN-1
|
Others | Others |
APOBEC3G-IN-1 (MN136.0185) 是一种靶向 APOBEC3G 抑制剂,具有抗 HIV 活性,可用于研究传染病和癌症。 | |||
T11815 |
Lanopepden
GSK 1322322,GSK-1322322B,GSK-1322322J |
Antibiotic | Microbiology/Virology |
Lanopepden (GSK 1322322) 是一种有效的肽去甲酰酶抑制剂,抑制金黄色葡萄球菌,抑制 ATCC 29213 和 ATCC 25923 菌株,可用于研究肺炎、皮肤病和传染病。 | |||
T14044 |
4E2RCat
|
PERK | Apoptosis |
4E2RCat 是一种 eIF4E-eIF4G 相互作用的抑制剂,IC50为13.5 μM。 | |||
T78748 |
MtUng-IN-1
|
Antibacterial | Microbiology/Virology |
MtUng-IN-1(Compound 18a)可抑制分枝杆菌尿嘧啶DNA糖基化酶(MtUng),IC50值为300 μM。MtUng-IN-1适用于癌症和传染病研究领域。 | |||
T6229 |
Daclatasvir
Daklinza,达卡他韦,EBP 883,达拉他韦,BMS-790052 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Daclatasvir (EBP 883) 是一种高度选择性的 HCV NS5A 抑制剂,EC50 为 9-50 pM,适用于细胞培养中的多种 HCV 复制子基因型和 JFH-1 基因型 2a 感染性病毒。 | |||
T76687 |
Ibalizumab
TNX-355,TMB-355 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Ibalizumab(TMB-355) 是一种人源化 IgG4 单克隆抗体,可作为 CD4 受体抑制, 通过与 CD4 受体结合来阻止 HIV-1进入细胞。Ibalizumab 具有抗HIV-1感染活性,可用于维持机体正常免疫功能。 | |||
T76251L |
Ac-FEID-CMK TFA
|
Pyroptosis | Apoptosis; Immunology/Inflammation |
Ac-FEID-CMK TFA 是一种选择性斑马鱼 GSDMEb 衍生肽抑制剂,可减少感染性休克的死亡率和肾损伤。Ac-FEID-CMK TFA 在体内可抑制焦亡,缓解败血性 AKI (急性肾损伤),抑制 caspy2 介导的非典型炎症小体通路发挥作用。 | |||
T60440 |
Antiviral agent 17
|
||
Antiviral agent 17 (Compound 4) 是一种抗感染剂,在人类复制子试验中显著保留其抗病毒作用,EC50值为0.015 μM。Antiviral agent 17 对小鼠诺如病毒(MNV)表现出良好的抗病毒活性。Antiviral agent 17 在研究传染性和恶性疾病方面具有潜力。 | |||
T38894 |
IHVR-17028
|
Influenza Virus; Glucosidase | Metabolism; Microbiology/Virology |
IC50 为 0.24 μMIHVR-17028 是一种有效的广谱的 ER α-葡萄糖苷酶 I (α-glucosidase?I) 抑制剂,IC50 为 0.24 μM,具有抗病毒活性。 IHVR-17028 对 BVDV、TCRV 和 DENV 具有抑制作用, EC50 分别为0.4 μM、0.26 μM 和0.3 μM。IHVR-17028 可用于研究传染病。 | |||
T0454L |
Florfenicol
SCH-25298,氟苯尼考,(-)-Florfenicol |
Antibacterial; Antibiotic | Microbiology/Virology |
Florfenicol (SCH-25298) 是一种常见得兽用抗生素,能用于研究牛呼吸疾病,在水产养殖业中可以用来控制鲶鱼肠道败血病,也可诱导鸡蛋早期胚胎死亡,LC50 值为 1.07 μg/g。 | |||
T28329 |
PD 134922
PD134922,PD-134922 |
||
PD 134922 is a HIV-1 protease inhibitors. Inactivation of the protease prevents infectious virion formation. | |||
T28330 |
PD 135390
PD135390,PD-135390 |
||
PD 135390 is a HIV-1 protease inhibitors identified by rational selection. Inactivation of the protease prevents infectious virion formation. | |||
T60875 |
Polvitolimod
|
||
Polvitolimod 是一种用于治疗传染病和癌症的 TLR7激动剂。 | |||
T63406 |
HCV-IN-35
|
||
HCV-IN-35 是 HCV 的有效抑制剂,表现出潜力进行感染性疾病的研究。 | |||
T61523 |
FWM-5
|
||
FWM-5 is a powerful inhibitor of NSP13 helicase, a key enzyme in the life cycle of the SARS-CoV-2 virus. With its potential in researching infectious diseases, FWM-5 emerges as a promising compound [1]. | |||
T69657 | GS-441524 HCl | ||
GS-441524 is a potent inhibitor of feline infectious peritonitis (FIP) virus with an EC50 of 0.78 μM.. GS-441524 strongly inhibits feline infectious peritonitis (FIP) virus in tissue culture and experimental cat infection studies. GS-441524 is a molecular precursor to a pharmacologically active nucleoside triphosphate molecule. These analogs act as an alternative substrate and RNA-chain terminator of viral RNA dependent RNA polymerase. GS-441524 was non-toxic in feline cells at concentrations ... | |||
T61591 |
SARS-CoV-2-IN-20
|
||
SARS-CoV-2-IN-20 (Compound 1a) is a highly effective inhibitor of SARS-CoV-2, displaying an impressive EC50 value of 6.5 μM. With its exceptional inhibitory properties, SARS-CoV-2-IN-20 holds great potential for advancing research on infectious diseases [1]. | |||
T5351 |
PU-WS13
PU WS13 |
Estrogen/progestogen Receptor | Endocrinology/Hormones |
T75166 | Influenza virus-IN-7 | ||
Influenza virus-IN-7 (Example 16) 是一种口服活性的帽依赖性核酸内切酶抑制剂,适用于流感病毒感染疾病的研究。 | |||
T73416 | BiCAPPA | ||
BiCAPPA 是一个二价抗朊病毒配体。BiCAPPA 可以减少痒病感染细胞中传染性构象形式的朊病毒蛋白 (PrPSc),EC50值为 0.32 μM。 | |||
TP1362 |
Angiogenin (108-122)
Angiogenin 108-122 |
||
Angiogenin (108-122) is an angiogenin peptide. Angiogenin (108-122) acts as a therapeutic agent for the prophylaxis and/or treatment of cancer, an infectious disease, a fibrotic disease, an inflammatory disease, a neurodegenerative disease, an autoimmune | |||
T70050 |
Boditrectinib
|
||
Boditrectinib 是一种有效的酪氨酸激酶抑制剂。Boditrectinib 是一种抗肿瘤药物。Boditrectinib 可用于癌症、炎症、神经退行性疾病和某些感染性疾病的研究。 | |||
TP1320 |
Angiogenin (108-122) TFA (112173-49-6 free base)
Angiogenin (108-122) TFA |
||
Angiogenin (108-122) TFA is an angiogenin peptide.Angiogenin (108-122) acts as a therapeutic agent for the prophylaxis and/or treatment of cancer, an infectious disease, a fibrotic disease, an inflammatory disease, a neurodegenerative disease, an autoimmu | |||
T62341 |
(R)-Larotrectinib
|
||
(R)-Larotrectinib 是一种 TRK 的有效抑制剂,作用于 TrkA (IC50: 28.5 nM)。(R)-Larotrectinib 能够用于研究癌症、炎症以及某些感染性疾病。 | |||
T61860 |
Enpp-1-IN-9
|
||
Enpp-1-IN-9, a powerful inhibitor of ectonucleotide pyrophosphatase-phosphodiesterase 1 (ENPP1), exhibits wide substrate specificity, capable of cleaving various bonds such as phosphodiester bonds of nucleotides and nucleotide sugars, as well as pyrophosphate bonds of nucleotides and nucleotide sugars. Its potential application lies in the fields of cancer and infectious disease research[1]. | |||
T76321 |
Brain Derived Basic Fibroblast Growth Factor (1-24)
|
||
Brain Derived BasicFibroblast Growth Factor(1-24) (FGF basic 1-24) 是一种合成肽,表现出抗细菌和抗HBV 的活性。Brain Derived BasicFibroblast Growth Factor(1-24) 可用于感染性疾病和免疫性疾病的研究。 | |||
T25365 |
EGA
|
Others | Others |
EGA 抑制致命毒素的中毒,并阻止多种其他酸依赖性细菌毒素和病毒进入哺乳动物细胞。EGA 是研究膜运输的有力工具,可用于治疗传染病。 | |||
T40211 |
eIF4E-IN-1
eIF4E-IN-1 |
||
eIF4E-IN-1 (WO2021003194A1, compound Y), is a highly effective inhibitor of eIF4E, a key protein involved in immunosuppression. By targeting immune checkpoint proteins such as PD-1, PD-L1, LAG3, TIM3, and IDO, eIF4E-IN-1 functions to disrupt immune suppression and promote immune release in specific diseases such as cancer and infectious diseases. | |||
T81943 |
Lemalesomab
IMMU-MN3 |
||
Lemalesomab (IMMU-MN3)为小鼠IgG1抗NCA-90单克隆抗体,具有Fab'片段结构。该化合物主要应用于炎症、感染性病变及其感染显像的研究领域。 | |||
T63888 |
Axl-IN-12
|
||
Axl-IN-12 是 AXL 的有效抑制剂。Axl-IN-12 能够用于研究增生性疾病、过敏性疾病、自身免疫性疾病、炎症性疾病、癌症、移植排斥、病毒性传染病或其他哺乳动物疾病。 | |||
T60673 |
Antiviral agent 18
|
||
Antiviral agent 18 (Compound 5) 对鼠诺如病毒显示出良好的抗病毒活性。Antiviral agent 18 是一种抗感染剂,具有用于传染性和恶性疾病的研究潜力。 | |||
T63683 |
Axl-IN-11
|
||
Axl-IN-11 是 AXL 的有效抑制剂。Axl-IN-11 能够用于研究增生性疾病、过敏性疾病、自身免疫性疾病、炎症性疾病、癌症、移植排斥、病毒性传染病或其他哺乳动物疾病。 | |||
T63537 |
SARS-CoV-2 3CLpro-IN-1
|
||
SARS-CoV-2 3CLpro-IN-1 (Compound 14c) is a highly potent inhibitor specifically designed to target and inhibit the activity of SARS-CoV-2 3CL pro, which is a cysteine-protease found in the main coronaviruses. This particular enzyme has been recognized as a highly promising target for the development of effective antiviral drugs. Therefore, SARS-CoV-2 3CLpro-IN-1 holds significant potential for advancing research and development in the field of infectious diseases [1]. | |||
T69925 |
NVR3-778 hydrate
|
||
NVR 3-778 is the first capsid assembly modulator (CAM) that has demonstrated antiviral activity in hepatitis B virus (HBV)-infected patients. NVR 3-778 inhibited the generation of infectious HBV DNA-containing virus particles with a mean antiviral 50% effective concentration (EC50) of 0.40 µM in HepG2.2.15 cells. The antiviral profile of NVR 3-778 indicates pan-genotypic antiviral activity and a lack of cross-resistance with nucleos(t)ide inhibitors of HBV replication. | |||
T81388 |
Propiolactone
Betaprone,β-propiolactone,2-Oxetanone |
SARS-CoV | Microbiology/Virology |
Propiolactone (β-propiolactone; 2-Oxetanone) 作为一种病毒化学灭活剂,能够使病毒失去传染性。以1:1000 (v:v) 的比例与SARS-CoV共孵育,Propiolactone可用于制备流感病毒疫苗中的抑菌剂(Flu-BPL)。 | |||
T11819 |
Lascufloxacin
拉库沙星,KRP-AM1977X |
Others | Others |
Lascufloxacin () 是一种有效的、具有口服活性的氟喹诺酮类抗菌剂。Lascufloxacin 有效抑制由多种病原体 (包括对喹诺酮类耐药的菌株) 引起的感染。Lascufloxacin 可用于多种传染病的研究,包括下呼吸道感染。 | |||
T70642 |
Lanopepden camsylate
|
||
Lanopepden, also known as GSK-1322322 or GSK-322, is a potent and selective peptide deformylase inhibitor with good in vitro activity against bacteria associated with community-acquired pneumonia and skin infections. GSK1322322 had bactericidal activity against S. pneumoniae, H. influenzae, S. pyogenes, and S. aureus, demonstrating a ≥ 3-log(10) decrease in the number of CFU/ml at 4× MIC within 24 h in 29 of the 33 strains tested. GSK1322322 represents a valuable alternative therapy for the trea... | |||
T63607 | PD-1/PD-L1-IN-22 | ||
PD-1/PD-L1-IN-22 是 PD-1/PD-L1 蛋白-蛋白相互作用的小分子抑制剂,能够阻断 PD-1/PD-L1相互作用 (IC50: 0.732 μM)。PD-1/PD-L1-IN-22 能够用于研究癌症、传染病和自身免疫性疾病。 | |||
T75313 | Methdilazine | ||
Methdilazine hydrochloride,一种口服活性抗生素(组胺拮抗剂),在体外和体内均能有效抑制多种分枝杆菌的活性。其最小抑菌浓度(MIC)值介于5-15 μg/mL之间,适用于传染病相关研究。 | |||
T76526 |
Ac-D-DGla-LI-Cha-C
|
||
Ac-D-DGla-LI-Cha-C 是一种有效的HCV 蛋白酶抑制剂肽。Ac-D-DGla-LI-Cha-C 可用于癌症、自身免疫性疾病、纤维化疾病、炎症性疾病、神经退行性疾病、感染性疾病、肺部疾病、心脏和血管疾病以及代谢性疾病的研究。 | |||
T62903 |
Enpp-1-IN-6
|
||
Enpp-1-IN-6 是抑一种有效的外核苷酸焦磷酸酶-磷酸二酯酶 1 (enpp-1) 抑制剂。其中 ENPP 1 具有广泛的特异性,能够切割多种底物(包括核苷酸和核苷酸糖的磷酸二酯键、核苷酸和核苷酸糖的焦磷酸键)。Enpp-1-IN-6 具有潜力用于癌症和传染病的研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8360 |
(-)-β-pinene
(-)-β-Pinene,左旋-beta-蒎烯,Nopinene,β-蒎烯 |
Antibacterial | Microbiology/Virology |
(-)-β-pinene (Nopinene) 是松节油的主要成分,具有抗菌活性,可抑制传染性支气管炎病毒,IC50为 1.32 mM。 | |||
TN1145 |
Isofebrifugine
|
Parasite | Microbiology/Virology |
Isofebrifugine 是一种来自虎耳草科植物常山的生物碱,具有抗疟抗感染活性。 | |||
T9218 |
Andrograpanin
19-HYDROXY-8(17),13-LABDADIEN-16,15-OLIDE,新穿心莲内酯苷元 |
p38 MAPK | MAPK |
Andrograpanin (19-HYDROXY-8(17),13-LABDADIEN-16,15-OLIDE) 是来自穿心莲的一种天然产物,具有抗炎和抗感染活性。 | |||
T3028 |
Tripterin
Celastrol,Tripterine,雷公藤红素 |
Apoptosis; Mitophagy; Proteasome; Autophagy | Apoptosis; Autophagy; Proteases/Proteasome; Ubiquitination |
Tripterin (Celastrol) 属于天然产物,是一种蛋白酶体抑制剂,抑制 20S 蛋白酶体的胰凝乳蛋白酶样活性 (IC50=2.5 μM)。Tripterin 具有抗炎、抗感染和免疫调节的作用。 | |||
TN1853 |
Lariciresinol
(+)-落叶松树脂醇 |
VEGFR; Antifection | Angiogenesis; Microbiology/Virology; Tyrosine Kinase/Adaptors |
Lariciresinol 是一种肠木脂素前体,它通过破坏真菌质膜具有杀真菌活性,并具有作为治疗人类真菌感染性疾病的新型抗真菌剂的治疗潜力。膳食 lariciresinol 可以减缓乳腺肿瘤的生长并降低人 MCF-7 乳腺癌异种移植物和致癌物诱导的大鼠乳腺肿瘤的血管密度。 | |||
T38141 |
Glycerophospholipids, cephalins
Phosphatidylethanolamines (egg) |
||
Glycerophospholipids, cephalins (Phosphatidylethanolamines (egg)) 是一种从鸡蛋中分离出来的磷脂酰乙醇胺的混合物,在 sn-1和 sn-2位置有各种脂肪酰基。Glycerophospholipids, cephalins 完全水解可得到1mol 的甘油、磷酸、乙醇胺和2mol 的脂肪酸。Phosphatidylethanolamines 在膜融合和细胞分裂过程中收缩环的拆卸中起作用,可调节膜的弯曲度。Phosphatidylethanolamines 能够在没有任何蛋白质或核酸的帮助下传播传染性朊病毒。Phosphatidylethanolamines 在细菌膜中的主要作用之一是分散由阴离子膜磷脂引起的负电荷。 | |||
TN3834 |
Derrone
|
Antifection | Microbiology/Virology |
Derrone may be interesting antimicrobial agents to be used against infectious diseases caused by many pathogens. It is also a novel Aurora kinase inhibitor, it can significantly inhibit the formation and growth of MCF7 tumor spheroids. | |||
TN3708 | Coronarin D | BCL; c-Myc; TNF; NF-κB; Caspase; COX; Antifection | Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation; Microbiology/Virology; Neuroscience; NF-κB; Proteases/Proteasome |
Coronarin D shows promising antifungal activity against C. albicans in vitro, the minimum inhibitory concentration (MIC) and the minimum fungicidal concentration (MFC) were 2 and 4 mg/mL, respectively; it is active against tested Gram-positive bacteria, i |