118
11
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T17011 |
TCH-165
|
Proteasome | Proteases/Proteasome; Ubiquitination |
TCH-165 是一种蛋白酶体组装的小分子调节剂,可增加游离 20S 水平,进而增强 IDP 蛋白水解。 | |||
T16366 |
NVR 3-778
|
HBV | Microbiology/Virology |
NVR 3-778 是一种 SBA 类的口服有效HBV CAM 衣壳组装调制剂,具有抗 HBV 活性。 | |||
T1008 |
Cephalexin
头孢氨苄,Cefalexin,Cephacillin |
Antibacterial; Antibiotic | Microbiology/Virology |
Cephalexin (Cephacillin) 是一种强口服活性的头孢菌素抗生素。它通过破坏细菌细胞壁的生长来杀死革兰氏阳性和一些革兰氏阴性细菌。它可研究肺炎、链球菌性咽喉炎、细菌性心内膜炎等。 | |||
T6439 |
Cetylpyridinium Chloride
西吡氯铵,Cetamium,Pristacin,Hexadecylpyridinium Chloride |
Others; HBV; Antibacterial | Microbiology/Virology; Others |
Cetylpyridinium Chloride (Hexadecylpyridinium Chloride) 是阳离子季铵,是一种广谱抗菌剂。它有效抑制 HBV 衣壳装配,IC50为 2.5 μM。它被用于杀虫剂和各种漱口水以及其他个人护理产品中。 | |||
T0204 |
Protriptyline hydrochloride
盐酸普罗替林,Protriptyline HCl |
5-HT Receptor; AChE | GPCR/G Protein; Neuroscience |
Protriptyline hydrochloride (Protriptyline HCl) 是一种含有一个仲胺的三环结构抗抑郁试剂,可以用于抑郁和 ADHD 的相关研究。它使动物精力充沛起激励作用,并且有时用于嗜睡症的相关研究。 | |||
T4475 |
JNJ-632
|
HBV | Microbiology/Virology |
JNJ-632 是一种乙型肝炎病毒衣壳组装调节剂。 | |||
TP1159L |
Boc-Gly-Gly-Phe-Gly-OH acetate
Boc-Gly-Gly-Phe-Gly-OH acetate(187794-49-6 free base),GGFG acetate |
||
Boc-Gly-Gly-Phe-Gly-OH acetate (GGFG acetate)(187794-49-6 free base) 是 N 和 C 保护的四肽的自组装体。 | |||
T16788 |
Rosabulin
STA 5312 |
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
Rosabulin (STA 5312) 是一种具有口服活性的微管抑制剂,具有有效性。 Rosabulin 可抑制微管组装,具有广谱抗肿瘤活性。 | |||
TQ0017 |
AB-423
|
HBV | Microbiology/Virology |
AB-423 是一种 HBV 衣壳组装抑制剂,抑制 HBV 复制。在细胞中,EC50/EC90值分别为 0.08-0.27 μM/0.33-1.32 μM。 | |||
T6071 |
Parbendazole
SKF 29044,帕苯咪唑 |
Microtubule Associated; Parasite | Cytoskeletal Signaling; Microbiology/Virology |
Parbendazole (SKF 29044) 是一种有效的 microtubule 重组抑制剂,能够破坏微管蛋白,EC50值为 530 nM,也是广谱驱虫剂。 | |||
T3628 |
Madrasin
DDD00107587 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Madrasin (DDD00107587) 是剪接抑制剂,在体外能够阻止剪接中间体和产物的形成,并干扰剪接体组装途径中的一个或多个早期步骤。它能在体外抑制 pre-mRNA 的剪接,并修饰细胞中内源性 pre-mRNA 的剪接。 | |||
T8951 |
JTP 0819958 - HOIPIN-1
|
IκB/IKK | NF-κB |
JTP 0819958 - HOIPIN-1 是一种选择性线性泛素链组装复合物 (LUBAC) 抑制剂,IC50 为 2.8 μM。 JTP-0819958 在体外抑制 LUBAC 介导的 NF-kB 活化[2]。 | |||
T28506 |
Rbin-2
|
Phosphatase | Metabolism |
Rbin-2 是一种具有细胞渗透性、强效性、选择性和可逆性的 Midasin(Mdn1) 抑制剂。Rbin-2 直接靶向 AAA+ ATPase Midasin,抑制真核生物核糖体的生成,是研究真核生物核糖体组装过程的强效探针。 | |||
T78557 |
HOIPIN-1
JTP0819958 |
NF-κB | NF-κB |
HOIPIN-1 (JTP0819958) 是一种具有选择性和有效性的线性泛素链组装复合物 (LUBAC) 抑制剂(IC50 >2.8 μM)。HOIPIN-1 对LUBAC 介导的 NF-kB 激活有抑制作用。 | |||
T6267 |
Lomitapide
AEGR-733,洛美他派,BMS-201038 |
CETP | Metabolism |
Lomitapide (AEGR-733) 是一种高效的微粒体甘油三酯转移蛋白(MTP)抑制剂,体内试验的IC50值为8 nM。 | |||
T11409 |
GLP-26
|
HBV | Microbiology/Virology |
GLP-26 是一种HBV 衣壳组装调节剂,抑制 Hep AD38 系统中的 HBV DNA 复制,IC50值为3 nM。 在 1 μM 时,使 cccDNA 降低> 90%。它破坏前基因组 RNA 的衣壳化,导致核衣壳解体,并减少 cccDNA 库。 | |||
T25214 |
CCR-11
CCR11,CCR 11 |
Antibiotic | Microbiology/Virology |
CCR-11 是一种具有抗菌活性的绕丹宁衍生物。 CCR-11 可以抑制 B. subtilis细胞和 HeLa 细胞增殖。 CCR-11 通过抑制 FtsZ 的组装和 GTPase 活性来抑制细菌增殖和细菌胞质分裂。 CCR-11 具有潜在的抗肿瘤活性,可用于研究乳腺癌和小儿骨髓增生异常。 | |||
T3124 |
Carbendazim
Bavistin,Carbendazole,多菌灵,Mercarzole |
Antifungal | Microbiology/Virology |
Carbendazim (Mercarzole) 是一种具有抗肿瘤活性的苯并咪唑衍生物,可用于癌症研究。它是一种口服广谱苯并咪唑杀菌剂,可作为真菌疾病研究的杀虫剂。 | |||
T60487 |
DDO-7263
|
Nrf2 | Immunology/Inflammation |
DDO-7263 是一种 1,2,4-Oxadiazole 衍生物, 通过与 Rpn6 结合上调 Nrf2,从而阻断 26S 蛋白酶体的组装和随后Nrf2 的泛素化降解。DDO-7263 是一种有效的Nrf2激活剂,能够激活 Nrf2-ARE 信号通路并发挥抗炎活性。 | |||
T15713 |
Larotaxel
XRP9881 |
P-gp | Membrane transporter/Ion channel; Neuroscience |
Larotaxel (XRP9881) 是一种紫杉烷类似物,具有抗癌活性,通过促进微管蛋白装配和稳定微管发挥其细胞毒性作用,并通过细胞凋亡诱导细胞死亡。Larotaxel (XRP9881) 是一种可穿过血脑屏障的化合物,对 Docetaxel 的亲和力比 P-糖蛋白 1 高,可用于研究乳腺癌和膀胱癌。 | |||
T2162 |
Maribavir
BW1263W94,GW257406X,Benzimidavir,马立巴韦,1263W94 |
Others; HCV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
Maribavir (GW257406X) 是一种可口服的苯并咪唑核苷化合物,具有抗巨细胞病毒的活性。 | |||
T15576 |
Indibulin
2-(1-(4-氯苄基)-1H-吲哚-3-基)-2-氧代-N-(吡啶-4-基)乙酰胺,ZIO 301,D 24851 |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Indibulin (D 24851) 是一种口服有效的微管蛋白合成抑制剂,具有抗有丝分裂和抗肿瘤活性,且神经毒性小。它降低了肌间神经张力,产生异常的纺锤体,激活有丝分裂检查点蛋白 Mad2 和 BubR1,并诱导有丝分裂停滞和细胞凋亡。 | |||
T72083 |
Octadecyl Rhodamine B chloride
|
||
Octadecyl Rhodamine B chloride 也被叫做RBOE, 是一种极性敏感染料,常作为一种发色基团与其他化合物一起使用,可用于给细胞膜染色,在有机分子组装、膜结构及蛋白质结构域中的电子能量转移中都有应用。 | |||
T2511 |
Plinabulin
普那布林,NPI-2358 |
Microtubule Associated | Cytoskeletal Signaling |
Plinabulin (NPI-2358) 是一种抗微管蛋白解聚肿瘤细胞的血管破坏剂,选择性地靶向并结合到微管蛋白的秋水仙碱结合位点,从而中断微管动力学的平衡。它对人肿瘤细胞系具有抑制作用,对 HT-29 细胞系的IC50值为 9.8 nM。 | |||
T16500 |
PF-3450074
PF-74 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
PF-3450074 (PF-74)是 HIV-1 衣壳蛋白的特异性抑制剂,可广谱抑制 HIV 分离株。它在 HIV-1 感染的早期阶段起作用,通过与 CPSF6 和 NUP153 的结合直接竞争来抑制病毒复制,并阻断病毒生命周期的脱膜,组装和逆转录步骤。 | |||
T3317 |
SZL P1-41
|
Apoptosis; Others; E1/E2/E3 Enzyme | Apoptosis; Others; Ubiquitination |
SZL P1-41 是 Skp2 抑制剂,可以阻止 Skp2-Skp1 复合物的组装。 它选择性地抑制 Skp2 SCF E3 连接酶活性,还在体内外抑制 Skp2 介导的 p27 和 Akt 泛素化。 它通过触发细胞衰老和抑制糖酵解来抑制 Y 细胞和 Y 干细胞的存活,有抗肿瘤作用。 | |||
T10446 |
BA-53038B
|
Others | Others |
BA-53038B is an HBV core protein allosteric modulator (CpAM), binding to the HAP pocket and modulating HBV capsid assembly in a distinct manner (EC50: 3.32 μM). | |||
T28288 |
Pacidamycin I
A-68567,A 68567,A68567 |
||
Pacidamycin I is an antimicrobial nucleoside antibiotics. Pacidamycin I inhibits translocase I, a key enzyme in peptidoglycan assembly. | |||
TP2360 |
A2-Binding peptide
|
||
A2-Binding peptide has involved in the assembly of MHC Class I molecules. | |||
T71584 |
Microtubule Inhibitor 185322
|
||
Microtubule inhibitor 185322 is an inhibitor of microtubule assembly, inducung mitotic arrest and apoptosis of MM cells. | |||
T28821 |
SMR000071098
SMR-000071098,SMR 000071098 |
||
SMR000071098 is an inhibitor of Fe-S cluster-dependent aconitase. SMR000071098 interacts with Suf proteins to inhibit iron-sulfur (Fe-S) cluster assembly. | |||
T71203 |
JBIR-22
|
||
JBIR-22 is a natural inhibitor for protein−protein interaction of the homodimer of proteasome assembly factor 3. | |||
T29198 |
Z060228
Z 060228,Z-060228 |
||
Z060228 is an potent anti-HBV inhibitor. The HBV DNA replication was effectively inhibited by Z060228 in the supernatants of the HepG2.2.15 cells. Z060228 exhibited effects on the self-assembly of Cp149. SEC data revealed that Z060228 altered the equilibr | |||
TP1643 |
Alpha 1(I) Collagen (614-639), human
|
||
This is a peptide inhibitor of collagen fibrillar matrix assembly. | |||
T26076 |
Rhizoxin
WF1360,WF 1360,WF-1360 |
||
Rhizoxin is an antitumor drug isolated from the fungus Rhizopus chinensis. It is a macrocyclic lactone compound that binds to tubulin and inhibits microtubule assembly. | |||
T26756 |
BCM-599
BCM 599 |
||
BCM-599 is a HBV capsid assembly inhibitor. BCM-599 showed IC50 of 0.88 μM and CC50 of 144 μM in HepG2.2.15 cells. | |||
T14800 |
Bromo-PEG3-phosphonic acid diethyl ester
|
Others | Others |
Bromo-PEG3-phosphonic acid diethyl ester is a polyethylene glycol (PEG) derivative commonly employed as a linker for the assembly of proteolysis targeting chimeras (PROTACs)[1]. | |||
T28860 |
ST-148
ST148 |
||
ST-148 is a potent inhibitor for Dengue virus capsid. ST-148-enhanced capsid protein self-interaction perturbs assembly and disassembly of DV nucleocapsids, probably by inducing structural rigidity. | |||
T62467 | HBV-IN-18 | ||
HBV-IN-18 (Compound 3) 是一种 HBV 衣壳组装调节剂 (CpAM) (EC50: 2790 nM)。 | |||
TP2117 |
SAHM1
|
||
Notch pathway inhibitor - stabilized hydrocarbon-stapled alpha helical peptide. Targets the protein-protein interface and prevents Notch complex assembly. | |||
T80243 |
gp91 ds-tat
|
||
gp91 ds-tat 是一种生物活性肽,作为(NADPH氧化酶组装肽抑制剂)。 | |||
T62466 |
HBV-IN-17
|
||
HBV-IN-17 (compound 8) 是一种有效的 HBV 衣壳组装调节剂 (EC50: 511 nM)。 | |||
T21321 |
MK-0731
|
||
MK-0731, a synthetic small molecule with potential antineoplastic activity, selectively inhibits kinesin spindle protein (KSP), leading to the inhibition of mitotic spindle assembly, induction of cell cycle arrest during the mitotic phase and apoptosis in | |||
TP1159 |
Boc-Gly-Gly-Phe-Gly-OH
GGFG |
||
Boc-Gly-Gly-Phe-Gly-OH is a self-assembly of N- and C-protected tetrapeptide. | |||
T79270 |
TMV-IN-6
|
||
TMV-IN-6(Compound 4g)是抗病毒和杀真菌剂,其作用机制为结合烟草花叶病毒(TMV)CP,从而抑制病毒组装,并干扰TMVCP与RNA的组装过程。 | |||
T38710 |
JH295
|
||
JH295 is a highly potent and selective inhibitor of NIMA-related kinase 2 (Nek2), exhibiting irreversible inhibition activity with an IC 50 value of 770 nM. This compound effectively inhibits cellular Nek2 using the alkylation of Cys22. Importantly, JH295 does not exhibit any inhibitory effects toward Cdk1, Aurora B, or Plk1, which are kinases involved in mitotic processes. Furthermore, JH295 has no impact on bipolar spindle assembly or the spindle assembly checkpoint mechanism. | |||
T62505 | SHR5133 | ||
SHR5133 是一种高效的、口服具有活力的 HBV 衣壳组装调节剂,能够减少 HBV DNA (EC50: 26.6 nM)。 | |||
T60730 |
BA38017
|
||
BA38017 是HBV 核心蛋白有效的组装调节剂,可抑制HBV 的复制,EC50值为 0.20 μM。 | |||
T76054 |
SAHM1 TFA
|
||
SAHM1 TFA is a chemical compound that acts as a Notch pathway inhibitor by stabilizing a hydrocarbon-stapled alpha helical peptide. It specifically targets the protein-protein interface, effectively preventing the assembly of the Notch complex. | |||
T16997 |
Tasidotin hydrochloride
ILX651 |
Microtubule Associated | Cytoskeletal Signaling |
Tasidotin hydrochloride is a peptide analog of the antimitotic depsipeptide dolastatin 15. Tasidotin hydrochloride is an inhibitor of microtubule assembly and microtubule dynamics. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2773 |
Vindoline
文朵灵,文多灵 |
Microtubule Associated | Cytoskeletal Signaling |
Vindoline 是从长春花叶片中提取的一种生物碱,通过抑制微管组装而表现出抗有丝分裂活性。 | |||
TN7041 |
(-)-Epipodophyllotoxin
|
Apoptosis | Apoptosis |
(-)-Epipodophyllotoxin 是一种从八角莲中分离的癌细胞抗增殖剂,在 HeLa 细胞和 MCF-7 细胞中的GI50值分别为 0.36 和 0.24 μM。它可在体外抑制有丝分裂纺锤体组装。 | |||
T16674 |
Pseudouridine
|
Endogenous Metabolite | Metabolism |
Pseudouridine 是非编码 RNA 中丰富的修饰核苷,通过稳定 RNA 结构增强核糖体 RNA 和的转移 RNA 功能。 | |||
T2937 |
4'-Demethylepipodophyllotoxin
4'-DMEP,4-Demethylepipodophyllotoxin,4'-脱甲基表鬼臼毒素,4'-去甲基表鬼臼毒素,DMEP,4'-O-demethylepipodophyllotoxin |
Microtubule Associated | Cytoskeletal Signaling |
4'-Demethylepipodophyllotoxin (DMEP) 是一种有效的微管组装抑制剂。 | |||
T16016 |
Maytansinol
美登醇,Ansamitocin P-0 |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Maytansinol (Ansamitocin P-0) 在体外抑制微管组装并导致微管分解。它与辐射联用,用于果蝇和人类癌细胞。 | |||
T36850 |
Curvulin
|
Microtubule Associated | Cytoskeletal Signaling |
Curvulin 是一种植物毒素,可以抑制微管组装,也可以抑制 iNOS 的表达。 | |||
T21351 |
Maytansine
NSC-153858,NSC153858,Maitansina,NSC 153858,Maitansine,美坦新 |
Microtubule Associated; Antibiotic | Cytoskeletal Signaling; Microbiology/Virology |
Maytansine (NSC-153858) 是从变叶美登木中分离的一种高效微管靶向天然产物,可诱导有丝分裂阻滞并在亚纳摩尔浓度杀死肿瘤细胞。 | |||
T4S0181 |
Hinokiflavone
日本扁柏黄酮,扁柏双黄酮 |
MMP; BCL; E1/E2/E3 Enzyme | Apoptosis; Proteases/Proteasome; Ubiquitination |
Hinokiflavone 是pre-mRNA 剪接活性的新型调节剂,通过抑制剪接体装配来阻止pre-mRNA 底物的剪接,特别是阻止 B complex 的形成。它是SUMO protease 蛋白酶抑制剂,能够抑制前哨蛋白特异性蛋白酶 1 的活性。 | |||
TN5107 |
Taxcultine
|
Others | Others |
Taxcultine can actively promote tubulin assembly. | |||
T10928 |
Cytochalasin A
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Cytochalasin A is a cell-permeable fungal toxin and is an oxidized derivative of cytochalasin B. Cytochalasin A is an inhibitor of HIV-1 protease (IC50 = 3 μM), inhibits actin polymerization and interferes with microtubule assembly by reacting with sulfhy | |||
T2S1797 |
Santalol
檀香醇;白檀油萜醇;檀香脑,檀香醇 |
Antioxidant; Antifungal | Microbiology/Virology; oxidation-reduction |
Santalol 是一种檀香醇的 α 和 β-异构体混合物。 其中α-santalol 分离自檀香油中,是一种有前途的抗癌药,能够预防口腔癌、前列腺癌、乳腺癌和皮肤癌。 |