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20

Compounds

Cat No. Product Name Synonyms Targets
TN7041 (-)-Epipodophyllotoxin Apoptosis
(-)-Epipodophyllotoxin (2) is an antiproliferative agent against cancer cells with GI50s of 0.36 and 0.24 μM in HeLa cells and MCF-7 cells, respectively. (-)-Epipodophyllotoxin can inhibit mitotic spindle assembly in vit...
T2773 Vindoline Microtubule Associated
Vindoline is an indole alkaloid that exhibits antimitotic activity by inhibiting microtubule assembly.
T16674 Pseudouridine Endogenous Metabolite
Pseudouridine is the most abundant modified nucleoside in non-coding RNAs. It enhances the function of transfer RNA and ribosomal RNA by stabilizing RNA structure.
T16366 NVR 3-778 HBV
NVR 3-778 is a first-in-Class and oral bioavailable HBV CAM belonging to the SBA class It has anti-HBV activity.
T1008 Cephalexin Cefalexin,Cephacillin Antibacterial , Antibiotic
Cephalexin (Cephacillin) is a cephalosporin antibiotic.
T17011 TCH-165 Proteasome
TCH-165 is a small molecule modulator of proteasome assembly, resulting in an increase in 20S levels. The increase in the level of free 20S corresponds to enhanced proteolysis of IDPs.
T0204 Protriptyline hydrochloride Protriptyline HCl 5-HT Receptor , AChE
Protriptyline Hydrochloride is the hydrochloride salt form of protriptyline, a tricyclic secondary amine with an antidepressant property. Protriptyline hydrochloride (Protriptyline HCl) blocks the re-uptake of norepineph...
T6439 Cetylpyridinium Chloride Cetamium,Pristacin,Hexadecylpyridinium Chloride Others , HBV , Antibacterial
Cetylpyridinium Chloride (Hexadecylpyridinium Chloride) is a cationic quaternary ammonium compound used as oropharyngeal antiseptic.
T4475 JNJ-632 HBV
JNJ-632 is a hepatitis B virus (HBV) capsid assembly modulator.
T2937 4'-Demethylepipodophyllotoxin 4'-DMEP,4-Demethylepipodophyllotoxin,DMEP,4'-O-demethylepipodophyllotoxin Microtubule Associated
4'-Demethylepipodophyllotoxin (DMEP) is a potent inhibitor of microtubule assembly.
T36850 Curvulin Microtubule Associated
Curvulin is the active metabolite isolated from Paraphoma sp. VIZR 1.46. Curvularin inhibits iNOS expression and microtubule assembly.
T16788 Rosabulin STA 5312 Others , Microtubule Associated
v Rosabulin (STA 5312) is an orally active microtubule inhibitor with potency. Rosabulin inhibits microtubule assembly and has broad-spectrum antitumor activity.
T16016 Maytansinol Ansamitocin P-0 Apoptosis , Microtubule Associated
Maytansinol (Ansamitocin P-0) inhibits microtubule assembly and causes microtubule disassembly in vitro.
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) is a self-assembly of N- and C-protected tetrapeptide.
T6071 Parbendazole SKF 29044 Microtubule Associated , Parasite
Parbendazole (SKF 29044) is a potent inhibitor of microtubule assembly(EC50 : 8.79 nM).Parbendazole is a carbamate ester-amine. It finds applications in control or treatment of nematode infestations.
TQ0017 AB-423 HBV
AB-423 is an inhibitor of HBV capsid assembly, and potently inhibits HBV replication (EC50/EC90: 0.08-0.27 μM/0.33-1.32 μM in cells).
T21351 Maytansine NSC-153858,NSC153858,Maitansina,NSC 153858,Maitansine Microtubule Associated , Antibiotic
Maytansine (NSC-153858), an ansamycin antibiotic originally isolated from the Ethiopian shrub Maytenus serrata, inhibits the assembly of microtubules by binding to tubulin at the rhizoxin binding site.
T78557 HOIPIN-1 JTP0819958 NF-κB
HOIPIN-1 (JTP0819958) is a selective and potent inhibitor of linear ubiquitin chain assembly complex (LUBAC) (IC50 >2.8 μM).HOIPIN-1 inhibits LUBAC-mediated NF-kB activation.
T28506 Rbin-2 Phosphatase
Rbin-2 is a cell-permeable, potent, selective and reversible inhibitor of Midasin (Mdn1).Rbin-2 directly targets the AAA+ ATPase Midasin and inhibits eukaryotic ribosome production, making it a potent probe for the study...
T8951 JTP 0819958 - HOIPIN-1 IκB/IKK
JTP-0819958 is a selective linear ubiquitin chain assembly complex (LUBAC) inhibitor with an IC50 of 2.8 μM[1]. JTP-0819958 suppress LUBAC-mediated NF-kB activation in vitro[2].
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