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- Catálogos PDF
Chemical Hay 28543 productos.
Curcumin analog C1
Curcumin analogue C1 is an effective oral activator of transcription factor EB (TFEB), which can be used in the study of neurodegenerative diseases.
Nelonicline
Nelonicline (ABT-126) is a nicotinic acetylcholine receptor agonist.
Nelonicline
Nelonicline (ABT-126) is a nicotinic acetylcholine receptor agonist.
Atamparib (RBN-2397)
Atamparib (RBN-2397) is a potent, orally active NAD+ competitive PARP7 inhibitor with an IC50 value of less than 3 nM. Atamparib (RBN-2397) can directly inhibit cell proliferation and restore type I interferon signaling by inhibiting PARP7 in tumor cells to stimulate innate or adaptive antitumor immune responses.
Atamparib (RBN-2397)
Atamparib (RBN-2397) is a potent, orally active NAD+ competitive PARP7 inhibitor with an IC50 value of less than 3 nM. Atamparib (RBN-2397) can directly inhibit cell proliferation and restore type I interferon signaling by inhibiting PARP7 in tumor cells to stimulate innate or adaptive antitumor immune responses.
JBSNF-000088 (6-Methoxynicotinamide)
Jbsnf-000088 (6-methoxynicotinamide) is a niacinamide (NA) analogue, which is a potent NNMT inhibitor. Jbsnf-000088 (6-methoxynicotinamide) is a niacinamide n-methyl transferase (NNMT) inhibitor. The IC50 of monkey NNMT and mouse NNMT were 1.8 µM, 2.8 µM and 5.0 µM, respectively. In animal models of metabolic diseases, JBSNF-000088 inhibits NNMT activity,...
3-Bromopyruvate (3-Bromopyruvic acid)
3-Bromopyruvate (3-Bromopyruvic acid) is a hexokinase II inhibitor, which is an effective antitumor agent on the hepatoma cells.
TFAP
TFAP is a selective cyclooxygenase-1 (COX-1) inhibitor with IC50 of 0.8 μM.
TFAP
TFAP is a selective cyclooxygenase-1 (COX-1) inhibitor with IC50 of 0.8 μM.
CU-CPT-8m
CU-CPT8m is an antagonist of toll-like receptor 8 (TLR8) with Kd of 220 nM and IC50 of 67 nM in assay.
DIDS sodium salt
DIDS sodium salt (MDL101114ZA) is a dual ABCA1 and VDAC1 inhibitor. DIDS sodium salt is also an anion transport inhibitor, which inhibits the ClC-Ka chloride channel and the bacterial ClC-ec1Cl-/H+ exchanger with IC50s of 100 μM and ~300 μM, respectively.
NGI-1
NGI-1 (ML414) is an inhibitor of Asparagine (N)-linked glycoslysation, which inhibits the oligosaccharyltransferase, preventing the attachment to the protein.