微信关注
Total item
Cart Subtotal
￥ 0.00 Neuronal Signaling
-
Lanabecestat
Catalog No. A12282 BACE1 inhibitorLanabecestat (AZD3293) is a potent, highly permeable, orally active and blood-brain barrier penetrating BACE1 inhibitor with a Ki of 0.4 nM. 了解更多 -
BACE1-IN-1
Catalog No. A12183 BACE1 inhibitorBACE1-IN-1 is a potent and highly brain penetrant BACE1 inhibitor with IC50s of 32 and 47 nM for human BACE1 and BACE2, respectively. 了解更多 -
β-Secretase Inhibitor IV
Catalog No. A21346 BACE-1 inhibitorβ-Secretase Inhibitor IV is a potent, cell-active BACE-1 inhibitor with IC50s of 15.6 and 16.3nM under BACE-1 concentrations of 2 nM and 100 pM, respectively. 了解更多 -
AZD3839 free base
Catalog No. A21606 BACE1 inhibitorAZD3839 (free base) is a potent and selective BACE1 inhibitor with IC50 of 23.6 uM, about 14-fold selectivity over BACE2, also a β-secretase enzyme inhibitor. 了解更多 -
AZD5423
Catalog No. A13249 -
Timosaponin b-II
Catalog No. A14591 -
Verubecestat (MK-8931)
Catalog No. A16113 β-secretase/BACE1 抑制剂Verubecestat (MK-8931)是一种有效的选择性β-分泌酶抑制剂，是BACE1蛋白抑制剂或Beta-site APP裂解酶1抑制剂。 了解更多 -
BACE1-IN-4
Catalog No. A18462 BACE1 inhibitorBACE1-IN-4 is a potent and highly selective BACE1 inhibitor, with an IC50 of 3.8 nM and a Ki of 1.9 nM, more selective at BACE1 over BACE2. Anti-Alzheimer??s disease. 了解更多 -
PF-06751979
Catalog No. A20066 BACE1 inhibitorPF-06751979 is a potent, brain penetrant, β-site amyloid precursor protein cleaving enzyme 1 (BACE1) inhibitor with an IC50 of 7.3 nM in BACE1 binding assay. 了解更多 -
Umibecestat (CNP520)
Catalog No. A18987 BACE-1 inhibitorUmibecestat (CNP520) is a beta-site amyloid precursor protein cleaving enzyme-1 (BACE-1) inhibitor with IC50s of 11 nM and 10 nM for human BACE-1 and mouse BACE-1, respectively. 了解更多 -
Ibuprofen (Advil)
Catalog No. A10461 COX-1 抑制剂Ibuprofen (Advil)是一种非甾体抗炎药(NSAID)，靶向COX-1，IC50为13 μM。 了解更多 -
Ibuprofen Lysine (NeoProfen)
Catalog No. A10462 -
Asaraldehyde (Asaronaldehyde)
Catalog No. A10090 -
Celecoxib
Catalog No. A10193 -
Pravadoline (WIN 48098)
Catalog No. A10749 COX 抑制剂Pravadoline (WIN 48098)是抗炎和前列腺素合成抑制剂，通过抑制环氧合酶（COX）发挥作用。 了解更多 -
Sulindac (Clinoril)
Catalog No. A10878 -
Flunixin meglumine
Catalog No. A11686 COX 抑制剂Flunixin Meglumin是一种有效的环氧化酶（COX）抑制剂，用作止痛剂，具有抗炎和解热作用。 了解更多 -
Acemetacin (Emflex)
Catalog No. A11692 -
Tolfenamic acid
Catalog No. A11693 COX-2 抑制剂Tolfenamic Acid是一种COX-2抑制剂，IC50为0.2μM。它是非甾体抗炎药（NSAID）的一类。它用于治疗偏头痛的症状。 了解更多 -
Nimesulide
Catalog No. A11694 -
Lornoxicam (Xefo)
Catalog No. A11695 COX 抑制剂Lornoxicam (Xefo)是一种非甾体类COX-1/COX-2抑制剂。它是oxicam类的非甾体类抗炎药（NSAID），具有镇痛（缓解疼痛），抗炎和退烧（退烧）特性。 了解更多 -
Licofelone
Catalog No. A11697 COX/LOX 抑制剂Licofelone是一种COX/LOX双重抑制剂，被认为是治疗骨关节炎的药物。它可能会降低与其他仅抑制COX（环氧合酶）的非甾体类抗炎药有关的胃肠道毒性。利福非酮是第一种同时抑制两者的药物。 了解更多 -
Diclofenac sodium
Catalog No. A10304 COX 抑制剂Diclofenac Sodium是一种非选择性的COX抑制剂，完整细胞中的COX-1和-2的IC50分别为0.5μg/ml和0.5μg/ml，作用于绵羊COX-1和COX-2， IC50分别为60和220 nM，用作非甾体类抗炎药（NSAID）来减轻疼痛和减轻疼痛 肿胀发炎。 了解更多 -
Rofecoxib (Vioxx)
Catalog No. A11918 -
Indomethacin (Indocid, Indocin)
Catalog No. A10474 COX 抑制剂Indomethacin (Indocid, Indocin)是一种非选择性COX1和COX2抑制剂，IC50分别为0.1 μg/mL和5 μg/mL。吲哚美辛(吲哚满，吲哚满)是一种非甾体抗炎药，通常用于减轻发热、疼痛、僵硬和肿胀。 了解更多 -
Phenylbutazone (Butazolidin, Butatron)
Catalog No. A10720 COX 抑制剂Phenylbutazone (Butazolidin,Butatron)是一种具有研究意义的化合物，它是一种抗炎和抗增殖剂。 了解更多 -
Piroxicam (Feldene)
Catalog No. A10736 -
Fexofenadine HCl
Catalog No. A11859 COX 抑制剂/histamine H1 receptor 激动剂Fexofenadine Hydrochloride是一种抗组胺药，可抑制Cox-1，Cox-2，并且是组胺H1受体激动剂，IC50为246 nM。 了解更多 -
Iguratimod (T 614)
Catalog No. A11464 COX-2 抑制剂Iguratimod (T 614)是一种抗风湿剂，能够有效地抑制COX-2的活性，IC50值为20 μM (7.7 μg/mL)，而对 COX-1 无作用；Iguratimod同时为巨噬细胞移动抑制因子 (MIF) 抑制剂，IC50值为6.81 μM。 了解更多 -
Tepoxalin
Catalog No. A12879 -
Bromfenac sodium
Catalog No. A13244 -
Acetaminophen
Catalog No. A10030 COX 抑制剂Acetaminophen (paracetamol) 是选择性环氧合酶-2 (COX-2) 的抑制剂，IC50 值为 25.8 μM。Acetaminophen 是一种有效的肝 N-乙酰转移酶 2 (NAT2) 抑制剂。它是广泛使用的解热和止痛药。 了解更多 -
Naproxen sodium
Catalog No. A10623 COX 抑制剂Naproxen sodium是一种非选择性的环氧合酶（COX）抑制剂，具有抗炎，解热和镇痛作用。对秋水仙碱引起的认知障碍和氧化应激具有神经保护作用。 了解更多 -
FK 3311
Catalog No. A13332 -
Flufenamic acid
Catalog No. A13333 COX 抑制剂Flufenamic acid是一种非甾体类抗炎药（NSAID）。抑制钙激活的氯离子通道（CaCC）。也增加通过TRPC6通道的电流，并抑制通过TRPC3和TRPC7通道的电流。 了解更多 -
Valdecoxib
Catalog No. A13342 COX-2 抑制剂伐地考昔（Valdecoxib），也称为SC-65872，是一种非甾体类抗炎药（NSAID），用于治疗骨关节炎，类风湿性关节炎以及痛经和月经症状。 它是一种选择性的环氧合酶2（COX-2)抑制剂,IC50为5nM。 了解更多 -
Meclofenamate Sodium
Catalog No. A12520
FILTER BY:
购物选项
- 分类
-
- β-Amyloid (21)
- γ-Secretase (34)
- Beta-secretase (BACE) (14)
- COX (64)
- GABA Receptors (55)
- NMDA Receptors (40)
- CaMK (17)
- AChE (21)
- mAChR (50)
- nAChR (24)
- P2X Receptor (14)
- Purinergic (P2Y) Receptors (13)
- GlyT (5)
- 作用机制
-
- Inhibitor (抑制剂) (159)
- Agonist (激动剂) (41)
- Antagonist (拮抗剂) (86)
- Activator (激活剂) (4)
- Modulator (调节剂) (29)
- Blocker (阻断剂) (3)
- Inducer (诱导剂) (1)
- Potentiator (增强剂) (2)
- 靶点
-
- 5-lipoxygenase (1)
- COX (13)
- COX-1 (13)
- COX-2 (23)
- Histamine H1 receptor (1)
- HSP90 (1)
- LOX (1)
- Src (1)
ADOOQ 产品质量保证
We promise all products to perform as described.