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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
127 Results for "
Sec
" in MedChemExpress (MCE) Product Catalog:
Products (127)
127 Results for "Sec" in MCE Product Catalog:
1
1 Cited Publications
SEC induces activation of ANXA7 GTPase via the AMPK/mTORC1/STAT3 signaling pathway. SEC selectively promotes apoptosis in cancer cells, expressing a high level of ITGB4 by inducing ITGB4 nuclear translocation .
17
17 Publications Verification
Eeyarestatin I, a potent endoplasmic reticulum-associated protein degradation (ERAD) inhibitor, is a potent protein translocation inhibitor. Eeyarestatin I inhibits Sec61 translocon. Eeyarestatin I targets the p97-associated deubiquitinating process (PAD) and inhibits atx3-dependent deubiquitination. Eeyarestatin I interferes at a step prior to proteasomal degradation. Eeyarestatin I induces cell death via the proapoptotic protein NOXA and has anticancer effects .
1
1 Cited Publications
Synonyms: KL-2
Target:
Áreas de investigación:
SEC inhibitor KL-2 (KL-2), a peptidomimetic lead compound, is a potent, selective super elongation complex (SEC) inhibitor and disrupts the interaction between the SEC scaffolding protein AFF4 and P-TEFb, resulting in impaired release of Pol II from promoter-proximal pause sites and a reduced average rate of processive transcription elongation. SEC inhibitor KL-2 exhibits an dose-dependent inhibitory effect on AFF4-CCNT1 interaction with a Ki of 1.50 μM .
1
1 Cited Publications
Synonyms: KL-1
SEC inhibitor KL-1 (KL-1) is a peptide-like lead compound that is an effective selective SEC inhibitor. SEC inhibitor KL-1 promotes apoptosis and has anti-tumor activity. SEC inhibitor KL-1 doses dependently inhibits the AFF4-CCNT1 interaction, with a Ki value of 3.48 μM .
1
1 Cited Publications
Sec61-IN-1 (compound A317) is a potent sec61 inhibitor that effectively targets glioma cells and enhances T cell cytotoxic effects[1][2].
1
1 Cited Publications
Target:
Áreas de investigación:
Sec61-IN-2 is a Sec61 inhibitor. Sec61-IN-2 shows a significant inhibitory effect on PD-1 related reporter gene cell models (PD1tsGluc) (IC50 = 42 nM), while it has almost no inhibitory activity in TNFα, Her3, and IL-2 pathway models. Sec61-IN-2 can be used for cancer research .
1
1
1 Cited Publications
Referencia número: HY-P73634
Pureza: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: SNAP25; Sec9; Prev. SNAP; Synaptosomal-Associated Protein, 25kDa; SNAP-25; SUP; Synaptosomal-Associated Protein 25; Synaptosomal-Associated 25 KDa Protein; DJ1068F16.2; Synaptosome Associated Protein 25kDa; BA416N4.2; Super Protein; RIC-4; DEE117; RIC4; C
Species:
Human
Source:
E. coli
Referencia número: HY-176763
No. CAS: 2376747-46-3
KZR-261 is a Sec61 translocase inhibitor. KZR-261 binds directly to the Sec61 channel, thereby inhibiting the biosynthesis of certain Sec61 substrate proteins, including oncogenic factors. KZR-261 activates the endoplasmic reticulum stress response. KZR-261 exhibits broad in vitro anticancer activity. KZR-261 shows antitumor efficacy in mouse models of cancer. KZR-261 can be used for the research of multiple myeloma, colorectal cancer, small cell lung cancer, pancreatic cancer, prostate cancer, non-Hodgkin's lymphoma, and mantle cell lymphoma .
Synonyms: CADA
Target:
Áreas de investigación:
Cyclotriazadisulfonamide (CADA) is a specific CD4-targeted HIV entry inhibitors. Cyclotriazadisulfonamide (CADA) inhibits the co-translational translocation of human CD4 (huCD4) into the ER lumen in a signal peptide (SP)-dependent way. Cyclotriazadisulfonamide is also a Sec61 translocon inhibitor .
Referencia número: HY-W042156
No. CAS: 456-12-2
Target:
Referencia número: HY-N0398
No. CAS: 80681-44-3
Category:
Umbelliferae/Apiaceae Extract Plant Flavonoids Flavones Peucedanum japonicum Thunb. Extract
Target:
Referencia número: HY-D1255
No. CAS: 1574299-37-8
Target:
Áreas de investigación:
NPPM 6748-481 is a potent and selective yeast Sec14 inhibitor with a yeast Sec14 IC50 of 211 nM. NPPM 6748-481 disrupts membrane trafficking, impairing trans-Golgi network-endosomal transport and endocytic transport. NPPM 6748-481 impairs Snc1 v-SNARE recycling, secretory invertase trafficking, and vacuolar carboxypeptidase Y processing. NPPM 6748-481 can be used for research on yeast infection .
Target:
Áreas de investigación:
Bragsin1 is a potent, selective and noncompetitive inhibitor of the ArfGEF BRAG2, inhibits Arf GTPase activation, with an IC50 of 3 μM. Bragsin1 binds to PH domain of BRAG2, and is a noncompetitive interfacial inhibitor. Bragsin1 has no effect on the Sec7 domain of human ArfGEFs. Anti-cancer activity .
Target:
Áreas de investigación:
Sec61-IN-3 is a Sec61 inhibitor. Sec61-IN-3 shows a significant inhibitory effect on PD-1 related reporter gene cell models (PD1tsGluc) (IC50 = 42 nM), and also has certain inhibitory activity on Her3 (IC50 = 99 nM), IL2 (IC50 = 144 nM) related reporter pathways, but has a relatively weak inhibitory effect on the TNFα (IC50 = 580 nM) pathway. Sec61-IN-3 can be used for cancer research .
Referencia número: HY-RS12625
Target:
Áreas de investigación:
SEC63 Human Pre-designed siRNA Set A contains three designed siRNAs for SEC63 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
Referencia número: HY-W099984
No. CAS: 89-72-5
Target:
Áreas de investigación:
2-sec-Butylphenol is a ubiquitous pollutant found in aquatic environments and is highly lethal and accumulative to aquatic organisms .
Referencia número: HY-RS12615
Target:
Áreas de investigación:
SEC24A Human Pre-designed siRNA Set A contains three designed siRNAs for SEC24A gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
Referencia número: HY-RS12619
Target:
Áreas de investigación:
SEC31A Human Pre-designed siRNA Set A contains three designed siRNAs for SEC31A gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
