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Cat No. | Product Name | Synonyms | Targets |
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T3161L | BACE-IN-1 acetate | BACE-IN-1 acetate (350228-37-4,Free base) | BACE |
BACE-IN-1 acetate (BACE-IN-1 acetate (350228-37-4,Free base)) has been used as β-site amyloid precursor protein (APP) cleaving enzyme-1 (BACE1) inhibitor in BACE1 inhibitor assay. β-Site amyloid precursor protein (APP) c... | |||
T10449 | BACE-1 inhibitor 1 | Others | |
BACE-1 inhibitor 1 (Compound 8a) is an effective BACE-1 inhibitor (IC50: 56 nM). | |||
T62181 | BACE-IN-1 | ||
BACE-IN-1 is an imidazo[1,2-a]pyridine derivative that inhibits the β-site amyloid precursor protein cleavage enzyme (BACE) sentence.BACE-IN-1 has the potential to investigate diseases involving BACE, such as Alzheimer's... | |||
T62995 | BACE-1 inhibitor 2 | ||
BACE-1 Inhibitor 2 is a potent, CNS-permeable inhibitor of BACE-1, exhibiting an IC50 value of 1.5 nM in enzymatic assays [1]. | |||
T60691 | AChE/BChE/BACE-1-IN-2 | ||
AChE/BChE/BACE-1-IN-2 (Compound 4o) exhibits remarkable antioxidant potential and considerable binding capability towards PAS-AChE. AChE/BChE/BACE-1-IN-2 is an orally active AChE, BACE-1 and BChE inhibitor with IC 50 val... | |||
T61206 | AChE/BChE/BACE-1-IN-1 | ||
AChE/BChE/BACE-1-IN-1 (Compound 4k) is an orally active inhibitor that targets acetylcholinesterase (AChE), butyrylcholinesterase (BChE), and β-site amyloid precursor protein cleaving enzyme 1 (BACE-1). It displays IC50 ... | |||
T11175 | Elenbecestat | E2609 | Beta-Secretase , BACE |
Elenbecestat (E2609) is an effective oral bioutilization and CNS penetrating ACE-1 inhibitor for the treatment of Alzheimer's disease. | |||
T12188 | NB-360 | BACE | |
NB-360 is a potent and brain-penetrable inhibitor of BACE1 and BACE2 with IC50s of 5, 5, and 6 nM for mouse and human BACE1 and BACE2. NB-360 exhibits excellent selectivity over the related aspartyl proteases pepsin, cat... | |||
T2639 | LY2811376 | Beta Amyloid , Beta-Secretase , BACE | |
LY2811376, an orally available non-peptidic β-secretase(BACE1) inhibitor (IC50: 239-249 nM), can decrease Aβ secretion (EC50: 300 nM). It has 10-fold selectivity towards BACE1 over BACE2, and more than 50-fold inhibition... | |||
T13253 | Umibecestat | CNP520 | BACE |
Umibecestat is an inhibitor of beta-site amyloid precursor protein cleaving enzyme-1 (BACE-1), with IC50s of 11 nM and 10 nM for human BACE-1 and mouse BACE-1, respectively. Umibecestat can be used for the research of al... | |||
T6058 | LY2886721 | Beta-Secretase , BACE | |
LY2886721, a BACE inhibitor, is used for the therapy of Alzheimer's Disease. | |||
T6772 | AZD3839 free base | AZD3839 | Beta-Secretase , BACE |
AZD3839 free base is a potent and selective BACE1 inhibitor with Ki of 26.1 nM, about 14-fold selectivity over BACE2. Phase 1. | |||
T4398 | LX2343 | Beta Amyloid , Beta-Secretase , BACE , PI3K , Autophagy | |
LX2343 is a BACE1 enzyme inhibitor with an IC50 value of 11.43±0.36 μM. LX2343 acts as a non-ATP competitive PI3K inhibitor with an IC50 of 15.99±3.23 μM. LX2343 stimulates autophagy in its promotion of Aβ clearance. | |||
T7011 | Verubecestat | MK-8931 | Beta-Secretase , BACE |
Verubecestat (MK-8931) (MK-8931) is an effective and specific β-secretase inhibitor and β-site APP-cleaving enzyme 1 inhibitor or BACE1 protein inhibitor. | |||
T10451 | BACE1-IN-2 | BACE | |
BACE1-IN-2 is a BACE1 inhibitor (IC50: 22 nM). | |||
T10453 | BACE1-IN-5 | Beta Amyloid , BACE | |
BACE1-IN-5 (Compound 15), a potent β-site amyloid precursor protein cleaving enzyme 1 (BACE1) inhibitor, demonstrates significant efficacy with an IC50 of 9.1 nM for BACE1 inhibition and an impressive IC50 of 0.82 nM aga... | |||
T10450 | BACE1-IN-1 | BACE | |
BACE1-IN-1 is a high brain penetrant BACE1 inhibitor (IC50s: 32 and 47 nM for human BACE1 and BACE2). | |||
T10452 | BACE1-IN-4 | BACE | |
BACE1-IN-4 is a potent and highly selective BACE1 inhibitor (IC50: 3.8 nM; Ki: 1.9 nM), more selective at BACE1 over BACE2. | |||
T3285 | Eslicarbazepine Acetate | Zebinix,Aptiom,BIA 2-093,Exalief,Stedesa | Beta-Secretase , Sodium Channel |
Eslicarbazepine Acetate (Zebinix) is an anticonvulsant medication approved for use in Europe, the United States and Canada as an adjunctive therapy for partial-onset seizures that are not adequately controlled with conve... | |||
T3161 | β-Secretase inhibitor-STA | Beta-Secretase | |
BACE-IN-1 is amyloid precursor protein beta-secretase inhibitor | |||
T39484 | BACE1-IN-6 | BACE1-IN-6 | |
BACE1-IN-6 is a BACE1 inhibitor with an IC 50 value of 1.5 nM. | |||
T62719 | AChE/BACE1/GSK3β-IN-1 | ||
AChE/BACE1/GSK3β-IN-1 is an orally active, blood-brain barrier-transparent, moderately bioavailable triple inhibitor of AChE/BACE1/GSK3β. AChE/BACE1/GSK3β-IN-1 can be used to study Alzheimer's disease (AD). | |||
T79022 | BACE1-IN-13 | Beta-Secretase | |
BACE1-IN-13 (Compound 36), an orally active inhibitor of BACE1, exhibits high potency with an IC50 of 2.9 nM and demonstrates greater efficacy in hAβ42 cells (IC50 = 1.3 nM). It is considered safe for the cardiovascular ... | |||
T63867 | BACE1-IN-12 | ||
BACE1-IN-12 is a potent BACE1 inhibitor (IC50: 8.9 μM) that can cross the blood-brain barrier. BACE1-IN-12 selectively inhibits BuChE (butylcholinesterase) activity (IC50: 3.2 μM). BACE1-IN-12 has potential for anti-Alzh... | |||
T73098 | BACE2-IN-1 | ||
BACE2-IN-1, a potent BACE2 inhibitor characterized by its exceptional selectivity and a Ki value of 1.6 nM, is utilized in the investigation of Type 2 Diabetes. | |||
T61956 | BACE1/2-IN-1 | ||
BACE1/2-IN-1 (compound 34) is an effective BACE1 and BACE2 inhibitor with IC50 of 0.01 and 0.0053 μM, respectively. BACE1/2-IN-1 has lower Pgp efflux ratio and improved passive permeability. The metabolic stability of BA... | |||
T77906 | Briobacept | BR 3FC | |
Briobacept (BR 3FC), a selective human monoclonal antibody, targets BLyS (BAFF) to induce B-cell apoptosis and is a recombinant glycoprotein comprising two BLyS receptor (BR3) molecules fused to the Fc domain of human Ig... | |||
T124932 | Fabacein | ||
Fabacein is a useful organic compound for research related to life sciences and the catalog number is T124932. | |||
T64074 | BACE1-IN-8 | ||
BACE1-IN-8 is a potent inhibitor of BACE1 (β-site APP lyase 1) (IC50: 3.9 μM). | |||
T80129 | Baceridin | Proteasome | |
Baceridin, a cyclic hexapeptide and proteasome inhibitor, can be isolated from the culture medium of Epiphytic Bacillus. It has the ability to impede cell cycle progression and induce apoptosis in tumor cells via a p53-i... | |||
T73076 | BACE1-IN-10 | Beta-Secretase | |
BACE1-IN-10 is a potent inhibitor of BACE1, demonstrating sub-micromolar activity against recombinant BACE1 (rBACE1) [1]. | |||
T83616 | SEW06622 | BACE , AChE | |
SEW06622 is a potent inhibitor of acetylcholinesterase (AChE) and beta-secretase-1 (BACE-1) and is a potential candidate for the treatment of Alzheimer's disease. | |||
T13434 | β-Secretase Inhibitor IV | Others | |
β-Secretase Inhibitor IV is a potent, cell-active inhibitor of BACE-1(IC50s of 15.6 and 16.3nM under BACE-1 concentrations of 2 nM and 100 pM, respectively). | |||
T71383 | NB-533 | ||
NB-533 is a macrocyclic peptidic BACE-1 inhibitor. | |||
T68278 | NB-216 | ||
NB-216 is a macrocyclic peptidic BACE-1 inhibitor. | |||
T83686 | Mca-SEVNLDAEFR-K(Dnp)-RR-NH2 acetate | ||
Mca-SEVNLDAEFR-K(Dnp)-RR-NH2 is a fluorogenic substrate designed for the quantification of β-secretase (BACE) activity. When cleaved by BACE, it liberates 7-methoxycoumarin-4-acetyl (Mca), a compound whose fluorescence, ... | |||
T27944 | LY3202626 | LY 3202626,LY-3202626 | |
LY3202626, an amyloid precursor protein secretase (BACE protein) inhibitor, is used for the treatment of Alzheimer's disease. | |||
T37661 | LY 2886721 Hydrochloride | ||
Potent and selective β-secretase (BACE) inhibitor (IC50 values are 10.2 and 20.3 nM for human BACE2 and BACE1, respectively). Displays >5,000-fold selectivity for BACE over other proteases including cathepsin D, pepsin a... | |||
T26705 | AZ-4217 | AZ4217,AZ 4217 | |
AZ-4217 is a high potency BACE inhibitor. It displays acute central efficacy in different in vivo models and reduced amyloid deposition in Tg2576 mice. AZ-4217 has IC50 160 pM in human SH-SY5Y cells with an excellent in ... | |||
T81836 | Mca-SEVNLDAEFK(Dnp)-NH2 | ||
Mca-SEVNLDAEFK(Dnp)-NH2 is a fluorogenic substrate featuring a 7-methoxycoumarin moiety whose fluorescence is quenched by the adjacent 2,4-dinitrophenyl group through resonance energy transfer. This compound serves as a ... | |||
T70800 | Elenbecestat free base | ||
Elenbecestat,also known as E2609 is a BACE1 inhibitor. By inhibiting BACE, a key enzyme in the production of Aβ peptides, E2609 decreases the formation of these peptides which can aggregate into toxic oligomers and proto... | |||
T79299 | HAChE-IN-3 | Monoamine Oxidase | |
hAChE-IN-3 (compound 5c) serves as a potent inhibitor for AChE, BuChE, MAO-B, and BACE-1, with respective IC50 values of 0.44, 0.08, 5.15, and 0.38 μM, demonstrating its ability to cross the blood-brain barrier. This com... | |||
T62180 | CB1/2 agonist 2 | ||
CB1/2 agonist 2 (compound 23) is a potent non-selective cannabinoid ligand with Ki of 3.5 nM and 1.2 nM, respectively. CB1/2 agonist 2 is a full agonist of CB1 and a competitive inverse agonist of CB2. BACE-IN-1 is a com... |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T5S2361 | Epiberberine | ERK , Beta-Secretase , MEK , BACE , AMPK , AChR , AChE | |
1. Epiberberine may be caused drug interactions based on CYP2D6 enzyme. 2. Epiberberine has anti-adipogenic effect is mediated by downregulation of the Raf/MEK1/ERK1/2 and AMPKα/Akt pathways during 3T3-L1 adipocyte diffe... | |||
T3769 | Tenuifolin | Others , Beta-Secretase , AChE | |
Tenuifolin has no inherent toxicity to either the transfected or wild type cells at the effective concentrations, it inhibits amyloid-β secretion in vitro. | |||
T8179 | Aloeresin D | Beta-Secretase , BACE | |
Aloeresin D, a natural chromone glycoside, inhibits β-Secretase (BACE1) activity (IC50: 39 μM). | |||
TN2190 | Scoulerine | Apoptosis , Beta-Secretase , BACE , Parasite | |
Scoulerine is an inhibitor of ß-site amyloid precursor protein cleaving enzyme 1(BACE1). Scoulerine a potent antimitotic compound that inhibits proliferation, arrests cell cycle, and induces apoptosis in cancer cells. | |||
T2S1181 | Aloenin | Aloenin A,Aloearbonaside | Beta-Secretase , AChR |
1. Aloenin (Aloenin A) and aloe-emodin are active principles for inhibition of c-ADH and c-ALDH activities in vitro. | |||
TN2217 | Sophoflavescenol | Others , Beta-Secretase , BACE , PDE , AChR , AChE | |
Sophoflavescenol is a mixed inhibitor of PDE5 with a K(i) value of 0.005 microM. Sophoflavescenol has antioxidant, anti-inflammatory, and apoptotic effects , these effects might contribute to the antitumor activity witho... | |||
T8306 | Epiberberine chloride | Epiberberine (chloride) | Reactive Oxygen Species , Beta-Secretase , BACE , AChR , AChE |
Epiberberine chloride (Epiberberine (chloride)) is an alkaloid isolated from Coptis chinensis, acts as a potent AChE and BChE inhibitor, and a non-competitive BACE1 inhibitor (IC50s: 1.07, 6.03 and 8.55 μM). | |||
TN7076 | Herbacetin-3,8-diglucopyranoside | Linocinamarin | Others |
herbacetin-3,8-diglucopyranoside (Linocinamarin) is a natural product. | |||
T5S1331 | Herbacetin | c-Met/HGFR , Akt | |
1. Herbacetin induces apoptosis in HepG2 cells, by ROS and PI3K/Akt pathway. 2. Herbacetin suppresses the HGF-induced motility of human breast cancer MDA-MB-231 cells by inhibiting c-Met and Akt phosphorylation. | |||
T82214 | Herbacetin-3-sophoroside-8--glucoside | ||
Herbacetin-3-sophoroside-8-glucoside is a naturally occurring compound that can be extracted from Equisetum hyemale [1]. | |||
TN3410 | Anatabine | Beta Amyloid , IL Receptor , TNF , NF-κB , BACE , COX , STAT | |
Anatabine shows anti-inflammatory activity in vitro and in vivo, which is mediated in part via an inhibition of STAT3 phosphorylation.Anatabine has anti-Alzheimer's disease effects, it inhibits BACE-1 transcription and r... | |||
TN1332 | 7-O-Methylaloeresin A | BACE | |
7-O-Methylaloeresin A shows significant antioxidant activity, it also has moderate inhibitory active on BACE. | |||
TN1434 | Bavachromene | BACE | |
Bavachromene exhibits a significant inhibitory effect on baculovirus-expressed BACE-1 in vitro. | |||
T79960 | Aloveroside A | ||
Aloveroside A, a triglucosylnaphthalene derivative extracted from Aloe vera using ethanol, exhibits modest inhibitory activity against bACE, demonstrating approximately 18.68% inhibition at a concentration of 100 μg/mL [... |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-00752 | BACE1 Protein, Human, Recombinant (His) | Human | HEK293 |
Beta-site APP-cleaving enzyme 1 (BACE1) is an aspartic-acid protease important in the formation of myelin sheaths in peripheral nerve cells. In the brain, This protein is expressed highly in the substantia nigra, locus c... | |||
TMPY-00651 | BACE1 Protein, Human, Recombinant (hFc) | Human | HEK293 |
Beta-site APP-cleaving enzyme 1 (BACE1) is an aspartic-acid protease important in the formation of myelin sheaths in peripheral nerve cells. In the brain, This protein is expressed highly in the substantia nigra, locus c... | |||
TMPY-00652 | BACE1 Protein, Human, Recombinant | Human | HEK293 |
Beta-site APP-cleaving enzyme 1 (BACE1) is an aspartic-acid protease important in the formation of myelin sheaths in peripheral nerve cells. In the brain, This protein is expressed highly in the substantia nigra, locus c... | |||
TMPY-00678 | BACE1 Protein, Mouse, Recombinant (His) | Mouse | HEK293 |
Beta-site APP-cleaving enzyme 1 (BACE1) is an aspartic-acid protease important in the formation of myelin sheaths in peripheral nerve cells. In the brain, This protein is expressed highly in the substantia nigra, locus c... | |||
TMPY-03065 | BACE2 Protein, Mouse, Recombinant (His) | Mouse | HEK293 |
BACE2, also known as beta secretase 2, belongs to the peptidase A1 family. It is a protease known to be an important enzyme involved in the cellular pathways. BACE2 has been shown to interact with GGA1 and GGA2. It is th... | |||
TMPJ-00782 | Amyloid Precursor Protein, Human, Recombinant (hFc) | Human | Human Cells |
Amyloid precursor protein (APP) is a type I membrane protein with several isoforms due to alternative splicing, performs physiological functions on the surface of neurons relevant to neurite growth, neuronal adhesion and... |