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Cat No. | Product Name | Synonyms | Targets |
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T40335 | AChE-IN-3 | NO Synthase , AChE | |
AChE-IN-3 had inhibitory effect on AChE and stronger inhibitory effect on NO, with EC50 of 0.57 μM. | |||
Fr12799 | AChE-IN-23 | ||
AChE-IN-23 (compound 3h) is an inhibitor of acetylcholinesterase (AChE) with an IC 50 value of 48.3 μM [1]. | |||
T77758 | AChE/BuChE-IN-4 | AChE | |
AChE/BuChE-IN-4 is a multi-target AChE/BuChE inhibitor with oral activity and blood-brain barrier permeability, with IC50 values of 2.08 and 7.41 μM for AChE and BuChE, respectively. | |||
T9989 | AChE-IN-27 | Others | |
AChE-IN-27 is a small molecule used for high-throughput assays. | |||
T62360 | AChE-IN-26 | AChE | |
AChE-IN-26 (compound 4a) is an AChE (acetylcholinesterase) inhibitor (IC50: 0.42 μM). | |||
T77352 | ACHE Inhibitor 12 | ||
ACHE Inhibitor 12 inhibited acetylcholinesterase with an IC50 value of 0.38 µM. | |||
T61969 | AChE/BChE-IN-10 | AChR , AChE | |
AChE/BChE-IN-10 is a potent dual inhibitor of AChE and BChE with IC50 values of 0.176, and 0.47 μM, respectively. AChE/BChE-IN-10 exhibits good blood brain barrier permeability. AChE/BChE-IN-10 can inhibit Aβ-aggregation... | |||
T80671 | ACHE-IN-38 | 5,6-Dimethoxy-2-(piperidin-4-yl)methylene-indan-1-one | Antifungal |
ACHE-IN-38 is a potent Acetylcholinesterase inhibitor that can be used for the synthesis of compounds with anti-inflammatory, anti-tumor, and antibacterial activities. | |||
T60891 | AChE/BChE/MAO-B-IN-1 | MAO , AChE | |
AChE/BChE/MAO-B-IN-1 is a reversible, non-time-dependent inhibitor of AChE, BChE and MAO-B that crosses the blood-brain barrier and exhibits inhibitory effects on hAChE, hBChE and hMAO-B with IC50s of 7.31, 0.56 and 26.1... | |||
T79553 | AChE-IN-34 | ||
AChE-IN-34 (compound 5l) is a potent, selective AChE inhibitor exhibiting an IC50 of 3.98 µM and negligible BChE inhibition. It demonstrates mixed-mode inhibition of AChE with a Ki of 0.044 µM using acetylthiocholine sub... | |||
T62728 | AChE-IN-24 | ||
AChE-IN-24 is a potent inhibitor of AChE that crosses the blood-brain barrier. hAChE is strongly inhibited by AChE-IN-24 (IC50: 0.053 μM). aChE-IN-24 can be used to study Alzheimer's disease (AD). | |||
T61049 | AChE-IN-11 | ||
AChE-IN-11 (compound 5C) can be used in the Alzheimer's disease research with neuroprotective effects and good antioxidant activity (ORAC = 2.5 eq). AChE-IN-11 is a good multifunctional agent with IC 50 values of 7.9 μM... | |||
T63628 | AChE-IN-19 | ||
AChE-IN-19 is a potent inhibitor of AChE (IC50: 0.56 μM) and also exhibits inhibition of Aβ aggregation. aChE-IN-19 exhibits neuroprotective effects and is virtually non-toxic to SH-SY5Y cells. aChE-IN-19 can be used to ... | |||
T61845 | AChE-IN-21 | ||
AChE-IN-21 (Compound I-8) is a highly potent and selective orally active inhibitor of acetylcholinesterase (AChE). It exhibits an impressive inhibitory concentration (IC50) of 2.66 nM. Additionally, AChE-IN-21 demonstrat... | |||
T83186 | AChE-IN-42 | ||
Compound AChE-IN-42, also known as Compound 28, is an acetylcholinesterase (AChE) inhibitor with an inhibition constant (K i) of 0.44 μM [1]. | |||
T83185 | AChE-IN-43 | ||
AChE-IN-43 is a potent, selective AChE inhibitor with a K i of 0.41 μM, applicable in the study of neurological diseases [1]. | |||
T74382 | AChE-IN-4 | ||
AChE-IN-4 is an acetylcholine esterase inhibitor (AChEI) with an IC50 value of 24.1 μM. | |||
T63307 | AChE-IN-6 | ||
AChE-IN-6 is an optimal multifunctional ligand that significantly inhibits AChE activity with IC50 values of 0.20 μM and 37.02 nM for EeAChE and HuAChE, respectively, and has anti-Aβ activity (IC50= 1.92 μM for self-indu... | |||
T79583 | AChE-IN-36 | ||
AChE-IN-36 (compound A4) is an acetylcholinesterase inhibitor with an IC50 of 0.04 μM, influencing ROS levels and modulating the gene expression of NRF2 [1]. | |||
T62538 | AChE-IN-15 | ||
AChE-IN-15 (Compound 3d) is a reversible inhibitor of human acetylcholinesterase (huAChE) and human butyrylcholinesterase (huBChE) with IC50 values of 6.8 μM and 16.1 μM for huAChE and huBChE, respectively, with signific... | |||
T79584 | AChE-IN-37 | ||
AChE-IN-37 (compound A2) is an acetylcholinesterase inhibitor with an inhibitory concentration (IC50) of 0.23 µM. It alters reactive oxygen species (ROS) levels and modulates the gene expression of nuclear factor erythro... | |||
T83187 | AChE-IN-41 | ||
AChE-IN-41 (Compound 2), a Galantamine-Memantine hybrid, possesses cholinesterase inhibitory capabilities. This compound demonstrates enhanced plasma stability and similar microsomal stability in vitro but has a reduced ... | |||
T78905 | AChE-IN-29 | ||
AChE-IN-29, a 3-OH pyrrolidine derivative, acts as a cholinesterase (ChE) inhibitor with potent activity against human acetylcholinesterase (hAChE), electric eel acetylcholinesterase (eeAChE), and equine butyrylcholinest... | |||
T80011 | AChE-IN-46 | ||
AChE-IN-46 (compound 4), a β-cyclocostunolide, functions as an acetylcholinesterase (AChE) inhibitor [1]. | |||
T62590 | AChE-IN-25 | ||
AChE-IN-25 is a selective, potent, non-competitive inhibitor of acetylcholinesterase (AChE) with an IC50 value of 2.95 μM. AChE-IN-25 can be used to study Alzheimer's disease. | |||
T63938 | AChE-IN-20 | ||
AChE-IN-20 is a potent inhibitor of AChE (IC50: 397.32 nM, Ki: 335.76 nM). AChE-IN-20 inhibits hCA-I (IC50: 84.14 nM, Ki: 97,86 nM), hCA-II (IC50: 69.24 nM, Ki: 76.23 nM) and α GLY (IC50: 52.08 nM, Ki: 57.93 nM). | |||
T64162 | AChE-IN-5 | ||
AChE-IN-5 (compound 5) is an orally active, blood-brain barrier-transparent substance with significant in vitro biological activity against AChE/5-HT1A/SERT. IC50: 2.29 nM). | |||
T79251 | AChE-IN-30 | ||
AChE-IN-30 is an acetylcholinesterase (AChE) inhibitor exhibiting neuroprotective effects with an inhibitory concentration (IC 50) of 4.4 μM. It prevents hydrogen peroxide (H 2 O 2)-induced apoptosis by inhibiting the ac... | |||
T62441 | AChE-IN-14 | ||
AChE-IN-14 is a potent cholinesterase inhibitor, acting on electric eel acetylcholinesterase (eeAChE) (IC50: 0.46 μM), human recombinant acetylcholinesterase (hAChE) (IC50: 0.48 μM) and equine serum butyrylcholinesterase... | |||
T79554 | AChE-IN-35 | ||
AChE-IN-35 (compound 5g) serves as an acetylcholinesterase inhibitor, exhibiting an inhibitory concentration 50 (IC50) value of 5.88 μM [1]. | |||
T62743 | AChE-IN-10 | ||
AChE-IN-10 (Compound 24r) is a potent inhibitor of AChE with an IC50 value of 2.4 nM. AChE-IN-10 decreases amyloid aggregation in the presence of AChE. AChE-IN-10 exhibited a potent inhibitory effect on AChE, reducing ta... | |||
T83184 | AChE-IN-44 | ||
AChE-IN-44 (Compound Tap4), an AChE inhibitor, is convertible into its thiazole salt form known as Tat2 [1]. | |||
T62541 | AChE-IN-22 | ||
AChE-IN-22 (compound 10q) is a selective inhibitor of acetylcholinesterase (AChE) that acts on both AChE (IC50: 0.88 μM) and BuChE (IC50: 10 μM). AChE-IN-22 binds to both the CAS (catalytic active site) and PAS (peripher... | |||
T63990 | AChE-IN-12 | ||
AChE-IN-12 is a potent inhibitor of acetylcholinesterase (AChE) that crosses the blood-brain barrier (BBB) and acts on rat AChE (IC50: 0.41 μM) and electric eel AChE (IC50: 1.88 μM). AChE-IN-12 significantly inhibited Cu... | |||
T78939 | AChE-IN-31 | ||
AChE-IN-31 (compound 1), a non-competitive acetylcholinesterase (AChE) inhibitor, exhibits potential for Alzheimer's disease research [1]. | |||
T79691 | AChE-IN-40 | ||
AChE-IN-40 (Compound 5C), with an inhibitory concentration 50 (IC50) of 120 nM, is an acetylcholinesterase (AChE) inhibitor suitable for Alzheimer's disease research [1]. | |||
T61648 | AChE-IN-8 | ||
AChE-IN-8 (Compound 19) is a highly potent inhibitor of acetylcholinesterase (AChE), exhibiting an IC50 value of 1.95 μM. This compound shows promise for further investigation in the research of Alzheimer's disease [1]. | |||
T83183 | AChE-IN-45 | ||
AChE-IN-45 (Compound 14) is an acetylcholinesterase (AChE) inhibitor exhibiting an IC50 value of 11.57±0.45 nM, and it demonstrates both antioxidant and neuroprotective activities [1]. | |||
T73245 | AChE-IN-9 | ||
AChE-IN-9, a Tacrine glycoconjugate connected to acetylated β-Glucose, acts as an AChE inhibitor, demonstrating an IC 50 value of 0.4 μM and exhibiting reduced hepatotoxicity in healthy cells. This compound finds use in ... | |||
T61936 | AChE-IN-7 | ||
AChE-IN-7 (Compound 16) is a selective and effective acetylcholinesterase inhibitor with IC50 of 0.045 μM and 19.68 μ M for eeAChE and eeBuChE, respectively. AChE-IN-7 has high permeability of blood-brain barrier. AChE-I... | |||
T78817 | AChE-IN-39 | ||
AChE-IN-39 (Compound 7c), with an IC50 value of 0.058 μM, is an acetylcholinesterase (AChE) inhibitor known for its DPPH scavenging activity and potential to ameliorate cognitive impairments in an aluminum chloride (AlCl... | |||
T60721 | AChE/BChE-IN-5 | ||
AChE/BChE-IN-5 (BMC-16) is an AChE and BChE dual inhibitor that can cross the BBB. The IC 50 values of AChE/BChE-IN-5 for human AChE (hAChE) and human BChE (hBChE) are 266 nM and 10.6 nM , respectively [1]. | |||
T72874 | SEH/AChE-IN-2 | ||
sEH/AChE-IN-2 and acetylcholinesterase ( AChE ). sEH/AChE-IN-2 provides cumulative effects against neuroinflammation and memory impairment. sEH/AChE-IN-2 has the potential for the research of Alzheimer's disease (AD) . | |||
T60529 | AChE/BChE-IN-3 | ||
AChE/BChE-IN-3 (BMC-1) is an AChE and BChE dual inhibitor with IC 50 values of 6.08 μM for electric eel AChE (elAChE) and 0.383 μM for equine serum BChE (eqBChE), respectively [1]. | |||
T72892 | AChE/MAO-IN-1 | ||
AChE/MAO-IN-1 is a potent inhibitor of human acetylcholinesterase (AChE), monoamine oxidase A (MAO-A), and monoamine oxidase B (MAO-B), demonstrating inhibitory concentrations (IC50) of 0.0248 μM, 0.0409 μM, and 0.1108 μ... | |||
T61620 | AChE/PDE4-IN-1 | ||
AChE/PDE4-IN-1 (compound 12c) is a highly effective and specific dual inhibitor of PDE4 and AChE, with IC50 values of 0.28 μM and 1.88 μM for AChE and PDE4D, respectively. This compound demonstrates notable potential in ... | |||
T79548 | AChE/BChE-IN-13 | ||
AChE/BChE-IN-13 (compound 5j) serves as a potent dual inhibitor of both acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), exhibiting half-maximal inhibitory concentrations (IC50) of 20.89 μM for AChE and 17.3... | |||
T72875 | SEH/AChE-IN-3 | ||
sEH/AChE-IN-3 (15) serves as a dual inhibitor targeting both soluble epoxide hydrolase (sEH) and acetylcholinesterase (AChE), demonstrating potent activity and the ability to cross the blood-brain barrier (BBB). It exhib... | |||
T79966 | AChE/BChE-IN-14 | ||
AChE/BChE-IN-14 (compound 13), a benzylisoquinoline alkaloid extracted from Fissistigma polyanthum roots, demonstrates inhibitory effects on both acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), coupled with... | |||
T72763 | AChE/BuChE-IN-1 | ||
AChE/BuChE-IN-1, a selective butyrylcholinesterase (BuChE) inhibitor derived from chrysin, exhibits a potent efficacy with an IC50 of 0.48 μM against BuChE and a lesser inhibitory effect on acetylcholinesterase (AChE) wi... |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T75544 | AChE/BChE-IN-11 | ||
AChE/BChE-IN-11 (compound 1), a natural product derived from artichoke leaves, is a dual inhibitor of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) with IC50 values of 70 μM for AChE and 71 μM for BChE, re... | |||
TN1899 | Lycoramine | AChE | |
Lycoramine is a natural product isolated from Lycoris radiate. Lycoramine is a potent acetylcholinesterase (AChE) inhibitor | |||
TN1858 | Leptomerine | AChE | |
Leptomerine (IC50 = 2.5 mM) shows potent anticholinesterasic activity. | |||
Fr14127 | Coumaran | 2,3-Dihydrobenzofuran | Endogenous Metabolite , AChE |
Coumaran (2,3-Dihydrobenzofuran) is an acetylcholinesterase (AChE) inhibitor isolated from leaves of L. camara. Coumaran(2,3-Dihydrobenzofuran) can be used as a biopesticide. 2,3-dihydrobenzofuran is a member of the clas... | |||
TN3500 | Beta-Amyrone | β-Amyron | COX , AChR , PPAR , Antifection |
beta-Amyrone (β-Amyron) has antifungal activity against Chikungunya virus replication with an EC50 of 86 uM. beta-Amyrone has anti-inflammatory activity through inhibiting the expression of COX-2. beta-Amyrone exhibits a... | |||
T2S1200 | Sinapine | Antioxidant , P-gp , AChE | |
1. Sinapine, an alkaloid from seeds of the cruciferous species, can be used as an effective natural compound for chemo-resistance. 2. Sinapine has antioxidant and radio-protective activities. | |||
TN2298 | Vincosamide | AChE | |
Vincosamide is an alkaloid from Psychotria leiocarpa extract, inhibits the acetylcholinesterase (AChE) activity with anti-inflammatory activity. Vincosamide can effect relaxation of the supercoiled pBR322 plasmid DNA in ... | |||
T3392 | Sinapine thiocyanate | P-gp , AChE | |
Sinapine Thiocyanate, is a derivative of Sinapine (S486605), an alkaloidal amine found in black mustard seeds. It is the choline ester of Sinapic Acid (S486800). It is also a phenolic-chloine conjugates, acting as anti-o... | |||
T4852 | Trimyristin | Trimyristoylglycerol,Tritetradecanoin,Glyceryl trimyristate,1,2,3-Tritetradecanoylglycerol | Phosphatase , Endogenous Metabolite , AChE |
Trimyristin (Tritetradecanoin) is primarily located in the membrane (predicted from logP) and adiposome. glyceryl trimyristate exists in all eukaryotes, ranging from yeast to humans. In humans, glyceryl trimyristate is i... | |||
TN1653 | Fustin | ERK , Beta Amyloid , AChR | |
Fustin is the phytogenic flavanol component of the plant Rhus verniciflua Stokes. Fustin shows protective effects on 6-hydroxydopamine-induced neuronal cell death. | |||
TN4675 | Nortrachelogenin | (-)-Wikstromol,(-)-Nortrachelogenin | Apoptosis , Antifungal |
Nortrachelogenin ((-)-Wikstromol), which can be extracted from Partrinia scabiosaefolia, has antifungal activity and induces membrane disruption and cysteinyl asparagin-dependent apoptosis. | |||
TC0014 | Trachelanthine | Others | |
Trachelanthine is a natural product from Eupatorium fortunei. | |||
TN4673 | (+)-Nortrachelogenin | Wikstromol | Apoptosis , HIV Protease , PI3K , Antifection |
(+)-Nortrachelogenin is a lignan isolated from Wikstroemia indica C.A. Meyer (Thymelaeaceae). (+)-Nortrachelogenin possesses antileukemic activity. | |||
T3855 | Tracheloside | Estrogen Receptor/ERR , Phosphorylase | |
Tracheloside significantly decreases the activity of alkaline phosphatase (IC50: 0.31 μg/ml), a level of inhibition comparable to that of tamoxifen (IC50: 0.43 μg/ml). | |||
TN4674 | Nortrachelogenin-8'-O-beta-glucoside | Others | |
Nortrachelogenin-8'-O-beta-glucoside is a lignan with a diarylhydroxybutyrolactone skeleton which isolated from the leaves and stems of Trachelospermum jasminoides (Lindl.) Lem. | |||
TN6508 | Trachelogenin | (-)-Trachelogenin | Virus Protease , c-Myc , HCV Protease , Wnt/beta-catenin |
Trachelogenin ((-)-Trachelogenin), isolated from Combretum fruticosum, is an HCV entry inhibitor with anti-proliferative effects. Its mechanism is related to affecting the phosphorylation of key proteins such as β-Cateni... | |||
TN7058 | Dihydrolapachenole | 6-methoxy-2,2-dimethyl-3,4-dihydro-2H-benzo[h]chromene | Others |
Dihydrolapachenole (6-methoxy-2,2-dimethyl-3,4-dihydro-2H-benzo[h]chromene) can be isolated from T. chrysantha. | |||
TN3974 | Epinortrachelogenin | Others | |
Epinortrachelogenin is a natural product of Cephalotaxus, Cephalotaxaceae. The catalog number is TN3974 and the CAS number is 125072-69-7. Epinortrachelogenin can be used as a reference standard. | |||
TN6543 | Trachelogenin 4'-O-beta-gentiobioside | ||
Trachelogenin 4'-O-beta-gentiobioside is a natural product for research related to life sciences. The catalog number is TN6543 and the CAS number is 106647-13-6. | |||
TN5158 | Trachelanthamine | Others | |
Trachelanthamine is a natural product from Eupatorium fortunei. | |||
TN5159 | Trachelosiaside | Others | |
Trachelosiaside shows moderate activity against lipoxygenase. | |||
T40810 | Rachelmycin | NSC298223,CC-1065 | |
Rachelmycin (CC-1065; NSC 298223) is a potent naturally antibiotic isolated from Streptomyces zelensis . Rachelmycin binds non-covalently and covalently (N-3 adenine adduct) in the minor groove of B-form DNA. Rachelmycin... | |||
TMA1065 | Nortracheloside | Others | |
Nortracheloside is a natural product of Trachelospermum, Apocynaceae. The catalog number is TMA1065 and the CAS number is 33464-78-7. Nortracheloside can be used as a reference standard. | |||
TN3513 | Bis-5,5-nortrachelogenin | Others | |
Bis-5,5-nortrachelogenin has anti-allergic activity, it inhibited NO production with IC50 value of 48.6 microM. | |||
T81650 | Nortrachelogenin 4'-O-β-gentiobioside | ||
Nortrachelogenin 4'-O-β-gentiobioside (compound 20) is a lignan extracted from the aerial components of Trachelospermum [1]. | |||
T83286 | 5-Methoxytracheloside | ||
5-Methoxytracheloside, a lignan lactone, is isolated from the stems and leaves of Trachelospermum jasminoides [1]. | |||
TN6509 | Nortrachelogenin-5'-C-beta-glucoside | ||
Nortrachelogenin-5'-C-beta-glucoside is a natural product of Trachelospermum, Apocynaceae. The catalog number is TN6509 and the CAS number is 858127-39-6. Nortrachelogenin-5'-C-beta-glucoside can be used as a reference s... | |||
TN6786 | O-Desmethyl Galanthamine | Sanguinine | AChE |
O-Desmethyl Galanthamine (Sanguinine) is galanthamine-type alkaloid and it is an acetylcholinesterase (AChE) inhibitor, with an IC50 1.83 μM. | |||
T9862 | Pseudocoptisine chloride | Isocoptisine chloride | AChE |
Pseudocoptisine chloride (Isocoptisine chloride) is isolated from Corydalis Tuber with anti-inflammatory and anti-amnestic properties. Pseudocoptisine chloride inhibits acetylcholinesterase (AChE) activity (IC50 = 12.8 μ... | |||
TN1527 | (-)-Corynoxidine | Corynoxidine | Antibacterial , AChE , Antifection |
(-)-Corynoxidine is an AChE inhibitor derived from tubers of Stephania succifera. Corynoxidine exhibits antibacterial activities against Staphylococcus aureus and methicillin-resistant Staphylococcus aureus strains in di... | |||
T4S1725 | Galanthamine | Galantamine | Apoptosis , AChE |
Galanthamine (Galantamine) is an acetylcholinesterase (AChE)inhibitor(IC50 : 500 nM), can reduce brain damage induced by hypoxia-ischemia. | |||
T0086 | Galanthamine hydrobromide | Galantamine hydrobromide,Galanthamine HBr | AChR , AChE |
Galanthamine hydrobromide (Galantamine hydrobromide), a long-acting and centrally active AChE inhibitor (IC50:410 nM), is an allosteric potentiator at neuronal nicotinic ACh receptors. | |||
T2846 | Isoimperatorin | Antibacterial , AChE | |
Isoimperatorin is an anti-inflammatory agent, exhibits significant inhibitory effects on acetylcholinesterase (AChE). | |||
T13301 | Violanthin | AChE | |
Violanthin is a natural product isolated from the aerial parts of Piper bavinum and inhibits acetylcholinesterase (AChE) (IC50: 79.80 μM). It has potent antioxidant and antibacterial activities. | |||
TN6783 | Corysamine chloride | CORYSAMINE CHLORIDE(RG) | AChE |
Corysamine chloride (CORYSAMINE CHLORIDE(RG)) was identified to inhibit the activity of ACHE. | |||
TN1030 | N-p-trans-Coumaroyltyramine | AChE , Parasite | |
N-p-trans-Coumaroyltyramine is a natural product, is an acetylcholinesterase (AChE) inhibitor with an an IC50 of 122 μM. N-p-trans-Coumaroyltyramine exhibits anti-trypanosomal activity with an IC50 of 13.3 μM for T. bruc... | |||
T5S1025 | Picfeltarraenin IA | Picfeltarraenin A | AChE |
1. Picfeltarraenin IA (Picfeltarraenin A), IB, IV, X, XI are stronger AChE inhibitions than the known AChE inhibitor Tacrine. | |||
T11351 | Galanthamine N-Oxide | AChE | |
Galanthamine N-Oxide, an alkaloid extracted from Zephyranthes concolor bulbs, effectively inhibits acetylcholinesterase (AChE) from electric eel with an EC50 of 26.2 μM. It acts as a significant inhibitor of substrate ac... | |||
TN1799 | Isorubrofusarin-6-O-β-gentiobioside | Isorubrofusarin 10-gentiobioside | BACE , AChR |
Isorubrofusarin-6-O-β-gentiobioside is derived from from Cassia obtusifolia Linn seeds and shows promising inhibitory activity against AChE and BACE1. | |||
TN2443 | Chikusetsusaponin Ib | Chikusetsu saponin Ib | AChE |
Chikusetsusaponin Ib (Chikusetsu saponin Ib) is an inhibitor of AChE and can be used in studies about anti-Alzheimer's diseases. | |||
TN1589 | Dihydrowithaferin A | AChE | |
Dihydrowithaferin A is a withanolide isolated from Withania somnifera with activity against acetylcholinesterase (AChE). Dihydrowithaferin A in the diet may prevent or decrease the growth of tumors. | |||
T5721 | Dehydroevodiamine hydrochloride | AChE | |
Dehydroevodiamine (DHE), a natural compound isolated from Evodia rutaecarpa, can inhibit AChE. It has hypotensive and neuroprotective effects and modulates nitric oxide production. | |||
TN2130 | Manghaslin | Quercetin 3-O-rutinoside-(1->2)-O-rhamnoside | AChE , Glucosidase |
Manghaslin (Quercetin 3-O-rutinoside-(1->2)-O-rhamnoside) has considerable α-glucosidase inhibitory activity, illustrating the anti-diabetic potential of phenolic-rich litchi pulp extracts. Manghaslin also shows inhibito... | |||
T13681 | Epi-galantamine | AChE | |
Epi-galantamine, a diastereomer of galantamine, is an alkaloid extracted from the bulbs and flowers of the Caucasian snowdrop (Galanthus woronowii). It acts as an AChE inhibitor, featuring an EC50 of 45.7 μM. | |||
T3026 | (-)-Huperzine A | HupA,Huperzine A | Apoptosis , AChR , AChE , iGluR |
(-)-Huperzine A (HupA) , an active Lycopodium alkaloid extracted from the traditional Chinese herb, is a potent, selective and reversible acetylcholinesterase (AChE) inhibitor and has been widely used in China for the tr... | |||
TN1673 | Garcinone C | ATM/ATR , CDK , STAT , AChR , Antifection | |
Garcinone C is a xanthone derivative extracted from Garcinia oblongifolia Champ with anti-inflammatory, astringency, and granulation-promoting activities. Garcinone C is an AChE inhibitor and has potential cytotoxic effe... | |||
Fr16605 | Lupinine | AChR , AChE | |
Lupinine is an alkaloid capable of counteracting ethanol anesthesia. Lupinine is an AChE and BChE inhibitor and potential CD69 activator found in species of Loranthus, Calia, and Lupinus. It may also inhibit heparin. | |||
T11366 | Garcinol | Apoptosis , Endogenous Metabolite , Histone Acetyltransferase , AChR , AChE | |
Garcinol also inhibits histone acetyltransferases (HATs, IC50= 7 μM) and p300/CPB-associated factor (PCAF, IC50 = 5 μM). Garcinol has anti-inflammatory and anti-cancer activity. Garcinol, a polyisoprenylated benzophenone... | |||
TN6919 | Methyl tridecanoate | Beta Amyloid , AChE | |
Methyl tridecanoate is a natural product. | |||
T22464 | 1,2-Dimyristoyl-sn-glycerol | 1,2-DMG | Others , PKC |
1,2-Dimyristoyl-sn-glycerol (1,2-DMG) is able to increase AChE activity by 35-40% at concentrations of 25 micrograms/ml in the parasite S. mansoni.. | |||
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Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-03234 | Acetylcholinesterase Protein, Rat, Recombinant (His) | Rat | E. coli |
Terminates signal transduction at the neuromuscular junction by rapid hydrolysis of the acetylcholine released into the synaptic cleft. | |||
TMPY-06677 | Bla g 4 Protein, cockroaches, Recombinant | cockroaches | P. pastoris |
TMPY-01742 | Acetylcholinesterase Protein, Mouse, Recombinant (His) | Mouse | HEK293 |
Acetylcholinesterase, also known as ACHE, is an enzyme that degrades (through its hydrolytic activity) the neurotransmitter acetylcholine, producing choline and an acetate group. Acetylcholinesterase plays a crucial role... | |||
TMPJ-00695 | CuTA Protein, Human, Recombinant (His) | Human | E. coli |
Protein CutA (CUTA) posseses a signal peptide and is widely expressed in brain. CUTA mayforms part of a complex of membrane proteins attached to acetylcholinesterase (AChE). CUTA takes part in cellular tolerance to a bro... | |||
TMPH-01282 | ELAVL4 Protein, Human, Recombinant (His & Myc & SUMO) | Human | E. coli |
RNA-binding protein that is involved in the post-transcriptional regulation of mRNAs. Plays a role in the regulation of mRNA stability, alternative splicing and translation. Binds to AU-rich element (ARE) sequences in th... |