70
20
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8849 |
PF-9601N
|
MAO | Metabolism; Neuroscience |
PF-9601N 是一种单胺氧化酶 B (MAO-B) 抑制剂,在多种体内外模型中表现出抗帕金森病 (PD) 的神经保护作用。它可用于研究兴奋性毒性介导的神经退行性疾病。 | |||
T1308 |
Orphenadrine hydrochloride
Mebedrol,Mephenamin,盐酸邻甲苯海拉明 |
Sodium Channel; NMDAR; Norepinephrine; iGluR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
Orphenadrine hydrochloride (Mephenamin) 是一种非竞争性的NMDA 受体拮抗剂, Ki=6.0 ± 0.7 μM。 | |||
T6618 |
Orphenadrine Citrate
Flexon,Flexoject,Banflex,枸酸芬那君,奥芬那君 |
AChR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Orphenadrine Citrate (Flexon) 是NMDA 受体拮抗剂,Ki 为6.0μM,还是HERG 钾离子通道阻断剂。它是一种骨骼肌松弛剂,它作用于中枢神经系统以产生肌肉松弛作用。 | |||
T2343 |
AS601245
|
JNK | MAPK |
AS601245 是 c-Jun NH2-末端激酶 (JNK) 的抑制剂,具有神经保护特性。 | |||
T21470L |
Davunetide acetate
Davunetide acetate(211439-12-2 Free base) |
Beta Amyloid; Microtubule Associated | Cytoskeletal Signaling; Neuroscience |
Davunetide acetate 源自哺乳动物 CNS 中存在的活性依赖性神经保护蛋白。 Davunetide acetate 是一种微管稳定肽,可抑制 Aβ 聚集和 Aβ 诱导的神经毒性。 Davunetide acetate 具有神经保护、神经营养和认知保护特性。 | |||
T21268L |
Semax acetate(80714-61-0 free base)
|
Others | Others |
Semax acetate(80714-61-0 free base) 是一种合成的促肾上腺皮质激素 (ACTH) 肽类似物,具有神经保护、镇痛和抗焦虑特性。 | |||
T67908 |
ThioLox
|
Lipoxygenase | Metabolism |
ThioLox 是一种竞争性 15-脂氧合酶-1 (15-LOX-1) 抑制剂(IC50值为12 μM)。ThioLox 显示抗炎和神经保护特性。具有抗炎和神经保护作用,对谷氨酸毒性有很强的保护作用。 | |||
TP1188L |
Cortistatin 14, human, rat acetate
|
Somatostatin | GPCR/G Protein |
Cortistatin 14, human, rat acetate 是一种与 somatostatin-14 结构相似的神经肽,具有抗惊厥、神经保护作用和显着的抗炎特性。 Cortistatin 14, human, rat acetate 通过与生长抑素受体结合并发挥其功能。 | |||
TP1570L |
Cortistatin-14 acetate
Cortistatin-14 acetate(186901-48-4 Free base) |
Somatostatin | GPCR/G Protein |
Cortistatin-14 acetate 是一种与生长抑素-14结构相似的神经肽,通过生长抑素受体 (sst1-sst5) 结合并发挥作用。Cortistatin-14 acetate 具有抗惊厥、神经保护作用和显著的抗炎作用。 | |||
T50003 |
Debrisoquin hydriodide
1,2,3,4-tetrahydroisoquinoline-2-carboximidamide hydroiodide |
Others | Others |
Debrisoquin hydriodide (1,2,3,4-tetrahydroisoquinoline-2-carboximidamide hydroiodide) 具有抗氧化、抗炎和神经保护特性,也被发现可以调节某些神经递质的活性,包括多巴胺和血清素,使其成为治疗帕金森病和抑郁症等神经疾病的有前途的候选药物。 | |||
T22513 |
4-PPBP maleate
|
Sigma receptor; NMDAR | GPCR/G Protein; Neuroscience |
4-PPBP maleate 是一种有效的 σ1 受体(配体)激动剂。4-PPBP maleate 在Xenopus oocytes 表达的情况下可被认为是一种具有选择性、非竞争性的 NR1a/2B NMDA 受体 拮抗剂。4-PPBP maleate 具有神经保护特性。 | |||
T77332 |
TV 3279
|
BCL; PKC | Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling |
TV 3279是一种新型ChE-MAI 抑制剂 ,神经保护特性取决于它们诱导抗凋亡蛋白PKC、Bcl-2、Bcl-x 和SOD 的能力,并阻止促凋亡酶甘油醛磷酸脱氢酶在PC-12和神经母细胞瘤细胞中的核易位。 | |||
T7826 |
6-Chloropurine riboside
|
Others | Others |
6-Chloropurine riboside (6-CPR)是一种嘌呤核苷类似物,已被发现具有广泛的生物活性。它可以抑制肿瘤细胞的生长并诱导其凋亡,还被证明具有抗炎、抗病毒和抗真菌的特性,也被发现具有神经保护作用,并已用于治疗神经疾病。 | |||
T21687 |
Conoidin A
|
Parasite | Microbiology/Virology |
Conoidin A 是刚地弓形虫过氧化物酶 II 的细胞通透性抑制剂,有杀线虫特性。它共价结合 TgPrxII 的过氧化物催化位点 Cys47,不可逆地抑制其过氧化物活性,IC50为 23 µM。它也抑制哺乳动物 PrxI 和 PrxII 的氧化。它具有抗氧化、神经保护作用,可研究缺血性心脏病。 | |||
T23265 |
RS 67333 hydrochloride
RS 67333 (hydrochloride),RS 67333 HCl,盐酸RS67333 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
RS 67333 hydrochloride (RO5203648) 是一种有效的、选择性的5-HT4 受体 (5-HT4R) 部分激动剂,在豚鼠纹状体中的 pKi 为 8.7。RS 67333 hydrochloride 对其他几种受体的亲和力较低,包括 5-HT1A、5-HT1D、5-HT2A、5-HT2C、多巴胺 D1、D2 和毒蕈碱 M1-M3 受体。RS 67333 hydrochloride 具有神经保护作用,可用于阿尔茨海默病研究。 | |||
T35056 |
Vindeburnol
RU 24722,RU24722,RU-24722 |
||
Vindeburnol is a cerebral vasodilator vincamine analog that bears neuroprotective properties. | |||
T31469 |
Dihydroergostin
DE145,DE-145,DE 145 |
||
Dihydroergostin is a ergot alkaloid that exhibits potential neuroprotective properties. | |||
T21268 |
Semax
|
||
Semax is a synthetic peptide analog of adrenocorticotropic hormone (ACTH) that has neuroprotective, analgesic, and anxiolytic properties. | |||
T14504 | BAY 38-7271 | Cannabinoid Receptor | GPCR/G Protein |
BAY 38-7271 has strong neuroprotective properties.[1] BAY 38-7271 is selective and highly potent and cannabinoid CB1/CB2 receptor agonist. With Kis of 1.85 nM and 5.96 nM for recombinant human CB1 receptor and CB2 receptor, respectively. | |||
T39120 |
Fluoroethylnormemantine
|
||
Fluoroethylnormemantine, a derivative of Memantine, acts as an N-methyl-D-aspartate (NMDA) receptor antagonist. It can function as a positron emission tomography (PET) tracer, known as [18F]-fluoroethylnormemantine. This compound displays anti-amnesic, neuroprotective, antidepressant-like, and fear-attenuating properties. | |||
T81409 |
Pregnanolone sulfate (pyridinium)
|
iGluR | Membrane transporter/Ion channel; Neuroscience |
Pregnanolone sulfate pyridinium是一种内源性神经类固醇,通过抑制NMDA受体发挥神经保护功能。 | |||
T61131 | MAO-B-IN-11 | ||
MAO-B-IN-11, also known as Compound 8c, is a highly potent inhibitor of monoamine oxidase B (MAO-B), with an IC50 value of 1.3 μM. Additionally, MAO-B-IN-11 exhibits neuroprotective properties [1]. | |||
T38601 |
GYKI-47261 dihydrochloride
|
||
GYKI-47261 dihydrochloride is a selective AMPA receptor antagonist, administered orally, and exhibits competitive activity with an IC 50 of 2.5 μM. It displays a wide range of anticonvulsive effects and demonstrates neuroprotective properties. Additionally, GYKI-47261 dihydrochloride is a potent inducer of CYP2E1. | |||
T69595 | Ispronicline hemigalactarate | ||
Ispronicline, also known as AZD3480; TC 1734; TC-0173, and RJR 1734, is a alpha4beta2 nicotinic acetylcholine receptor-selective agonist with cognition-enhancing and neuroprotective properties. Ispronicline is potentially useful for the treatment of attention-deficit/hyperactivity disorder in adults. | |||
T12816 | (S)-Trolox | Others | Others |
(S)-Trolox, an analogue of vitamin E, substitutes the phytyl chain with a carboxyl group. This compound serves as a model substance in structural studies and as a standard for assessing antioxidant activity. Moreover, (S)-Trolox exhibits potent and specific neuroprotective and antioxidant properties. | |||
T40245 |
Miroestrol
|
||
Miroestrol is a potent phytoestrogen compound with multifaceted biological effects. It induces a mammogenic effect and demonstrates neuroprotective properties, along with the ability to prevent bone loss in ovariectomized mice. Additionally, Miroestrol has been shown to reduce the risk of cancer [4]. | |||
T70064 |
PDE1-IN-1
|
||
PDE1-IN-1can enhance levels of the second messengers cAMP/cGMP leading to the expression of neuronal plasticity-related genes, neurotrophic factors, and neuroprotective molecules. These neuronal plasticity enhancement properties make PDE1 inhibitors good candidates as therapeutic agents in many neurological conditions. | |||
T61528 |
FGFR-IN-7
|
||
FGFR-IN-7 (compound 17) is an orally active, potent FGFR modulator with the ability to penetrate the blood-brain barrier. It exhibits neuroprotective properties, enhancing brain exposure and decreasing the likelihood of phospholidosis. FGFR-IN-7 proves valuable for research on neurodegenerative diseases [1]. | |||
T37096 | Sepimostat dimethanesulfonate | ||
Sepimostat dimethanesulfonate (FUT-187) exhibits neuroprotective activity via NR2B N-methyl-D-aspartate receptor antagonism at the Ifenprodil-binding site of the NR2B subunit. Sepimostat dimethanesulfonate inhibits the Ifenprodil binding with a Ki value of 27.7 μM[1]. Sepimostat (1 to 100 nmol/eye, intravitreal injection) exhibits significant neuroprotective effect[1]. ... | |||
T80634 |
MAO-B-IN-19
|
Monoamine Oxidase | Neuroscience |
MAO-B-IN-19, 作为选择性MAO-B抑制剂,表现出神经保护和抗炎特性,其IC50值为0.67 μM。 | |||
T13734 | ILS-920 | Others | Others |
ILS-920 is a Rapamycin analog characterized by diminished immunosuppressive effects but remarkable neuroprotective properties. It exhibits selective binding affinity towards the immunophilin FKBP52 as well as the β1-subunit of L-type voltage-gated calcium channels (VGCC). ILS-920 displays a notable 200-fold preference for FKBP52 over FKBP12. | |||
T61660 | FGFR-IN-3 | ||
FGFR-IN-3 (compound 6) is a highly potent and orally active modulator of FGFR (fibroblast growth factor receptor). It has the ability to penetrate the blood-brain barrier (BBB). Additionally, FGFR-IN-3 exhibits significant neuroprotective properties. Therefore, it holds potential for research on neurodegenerative diseases [1]. | |||
T39119 |
Fluoroethylnormemantine hydrochloride
|
||
Fluoroethylnormemantine hydrochloride, a Memantine derivative, functions as an antagonist for the N-methyl-D-aspartate (NMDA) receptor. It can also serve as a positron emission tomography (PET) tracer, specifically as [18F]-Fluoroethylnormemantine hydrochloride. Notably, this compound displays a range of effects, including anti-amnesic, neuroprotective, antidepressant-like, and fear-attenuating properties. | |||
T74854 | GluN2B-NMDAR antagonist-1 | ||
GluN2B-NMDAR antagonist-1 是一种具有口服活性的GluN2B-NMDAR 拮抗剂。GluN2B-NMDAR antagonist-1 具有神经保护活性。 GluN2B-NMDAR antagonist-1 可用于缺血性损伤研究。 | |||
T61522 | Nrf2/HO-1 activator 2 | ||
Nrf2/HO-1 activator 2 (compound 13m), a difluoro-substituted derivative, is a highly potent activator of Nrf2/HO-1. It exhibits substantial neuroprotective and antioxidant properties by activating the Nrf2/HO-1 pathway through phosphorylation of ERK1/2, JNK, or Akt in PC12 cells. This compound finds utility in the investigation of Parkinson's disease (PD) [1]. | |||
T78592 |
Diapocynin
Dehydrodiacetovanillone |
||
Diapocynin (DeHydrodiacetovanillone),Apocynin的二聚体,是具有口服活性的NADPH氧化酶抑制剂。具备抗炎、神经保护及抗氧化效果。 | |||
T82292 |
Gluten Exorphin A5
|
||
Gluten Exorphin A5是一种小麦麸质的片段,它在周围神经系统和中枢神经系统中显示出具有神经保护的多样作用。 | |||
T73671 |
7β-Hydroxy-epi-androsterone
|
||
7β-Hydroxy-epi-androsterone (7β-Hydroxy-EpiA) 是一种与ERβ结合的内源性雄激素衍生物,具有抗炎和神经保护特性。该化合物来源于dehydroepiandrosterone。 | |||
T81635 | Nurr1 agonist 5 | ||
Nurr1 agonist 5 (compound 5o)为具神经保护性的Nurr1转录因子激动剂,其Kd值为0.5 μM,EC50值为3 μM。 | |||
T40701 |
Ezeprogind
AZP-2006 |
||
Ezeprogind (AZP-2006) is an orally active neurotrophic inducer that effectively addresses the underlying factors contributing to neurodegeneration, with a broad scope extending beyond the conventional targets like Abeta protein and tau protein. Exhibiting potent neuroprotective properties, Ezeprogind is a valuable tool for studying a range of neurological disorders, including progressive supranuclear palsy (PSP), tauopathies, Alzheimer's disease, Parkinson's disease, and others. | |||
T73507 |
NS1219
(R)-SPD502 |
||
NS1219 ((R)-SPD502) 是 NS 1209 的异构体。NS1209 是一种选择性AMPA 受体拮抗剂,具有神经保护活性。NS1209 可用于中风、神经性疼痛和癫痫的研究。 | |||
T77998 |
(Arg)9 acetate
Peptide R9 acetate,Nona-L-arginine acetate |
||
(Arg)9 (Nona-L-arginine) acetate 是一种细胞穿透肽(CPP),由9个L-精氨酸残基构成,显示出神经保护作用,其在谷氨酸模型中的IC50值为0.78 μM。 | |||
T39823 |
Apelin-12
|
||
Apelin-12 is a highly potent C-terminal fragment of a polypeptide that exhibits a strong affinity towards the orphan receptor APJ. It plays a role in maintaining body fluid balance and regulating feeding control in the central nervous system. Additionally, Apelin-12 functions as an inhibitor of HIV-1 entry through the APJ receptor and demonstrates neuroprotective properties. | |||
T39513 |
Ladostigil hemitartrate
TV-3326 hemitartrate,Ladostigil hemitartrate |
||
Ladostigil hemitartrate (TV-3326) is a compound that acts as a dual inhibitor of cholinesterase and brain-selective monoamine oxidase (MAO). It has IC50 values of 37.1 μM for MAO-B and 31.8 μM for AChE. In addition, Ladostigil hemitartrate possesses neuroprotective, antioxidant, and anti-inflammatory properties. It is commonly used in research relating to depression and Alzheimer's disease. | |||
T76034 |
Cortistatin-14 TFA
|
||
Cortistatin-14 (TFA) 是一种神经肽,其结构与生长抑素-14相似,通过与生长抑素受体(sst1-sst5)结合来发挥效果。它具备抗惊厥、神经保护和显著抗炎作用。 | |||
T73214 |
RX 801077
2 BFI free base |
||
RX 801077 (2 BFI free base) 为选择性咪唑啉 I2 受体 (I2R) 激动剂,其Ki值为70.1 nM,展现抗炎及神经保护效果,具备用于创伤性脑损伤 (TBI) 研究的潜力。 | |||
T78907 | MAO-B-IN-22 | Monoamine Oxidase | Neuroscience |
MAO-B-IN-22(化合物6h)是高效的MAO-B抑制剂,IC50为0.014 μM。该化合物表现出高度的抗氧化活性、优秀的金属螯合特性、合适的BBB通透性以及显著的神经保护效果。 | |||
TP2019 |
[D-Ala2]-GIP (human)
|
||
Highly potent GIP receptor agonist (EC50 = 630 ± 119 pM). Displays equivalent cAMP stimulating properties and improved resistance to enzymatic degradation compared to native GIP in cells expressing wild type GIP receptor. Improves glucose tolerance, insul | |||
T78023 |
MR 409
|
||
MR 409是一种选择性的生长激素释放激素(GHRH)激动剂,能够显著增强脑缺血小鼠内源性神经发生,具有神经保护作用,并可抑制肺癌的体内生长。 | |||
T78067 |
Stobadine
(-)-Stobadine |
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
Stobadine是一种抗氧化剂,能抑制自由基导致的内质网膜流动性变化,可作为基于抗氧化和清除自由基机制的心脏和神经保护剂研发的侯选药物[sup][1]。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T65135 |
Kynurenic acid
Fibrostop 2,Quinurenic acid |
GPR; GluR; NMDAR | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Kynurenic acid (Quinurenic acid) 是一种内源性色氨酸活性代谢物,是一种 NMDA, glutamate, α7 nicotinic acetylcholine receptor 三重拮抗剂,也是 GPR35/CXCR8 激动剂,具有神经保护和抗惊厥特性,可用于研究神经分裂和与代谢相关的疾病。 | |||
T5S2076 |
Senkyunolide I
|
Others; Caspase | Apoptosis; Others; Proteases/Proteasome |
Senkyunolide I 是从川芎中分离得到的一种天然产物,具有神经保护作用,与其抗氧化和抗凋亡特性有关。 | |||
T2737 |
Neohesperidin
Hesperetin 7-O-neohesperidoside,NSC 31048,新橙皮苷 |
Antioxidant | oxidation-reduction |
Neohesperidin (NSC-31048) 是一种类黄酮化合物,存在于葫芦科植物中,具有抗氧化和抗炎活性。 | |||
Fr12596 |
3-Acetylcoumarin
|
Others | Others |
3-Acetylcoumarin 作为室温下铜催化 CN 偶联反应的实用配体。它具有神经保护和杀螨特性。 | |||
T2827 |
Asiatic acid
Asiantic acid,Dammarolic acid,积雪草酸 |
Apoptosis; p38 MAPK; Parasite | Apoptosis; MAPK; Microbiology/Virology |
Asiatic acid (Dammarolic acid) 是在Centella asiatica 中发现的一种五环三萜,有抗炎活性,可诱导黑色素瘤细胞的凋亡,有可能治疗皮肤癌。 | |||
T6S1101 |
Astragalin
Kaempferol 3-D-glucoside,Kaempferol 3-O-glucoside,kaempferol-3-glucoside,3-Glucosylkaempferol,Astragaline,紫云英苷,Kaempferol 3-β-D-glucopyranoside |
Apoptosis; NF-κB | Apoptosis; NF-κB |
Astragalin (Kaempferol 3-O-glucoside) 是一种具有生物活性的天然黄酮类化合物。 它具有多种药理特性,包括抗氧化、抗炎、抗癌、神经保护和心脏保护特性。 | |||
T2883 |
Syringic acid
3,5-dimethyl ether Gallic Acid,SYRA,3,5-dimethoxy-4-hydroxy Benzoic Acid,丁香酸,NSC 2129 |
Others; Endogenous Metabolite; Antibacterial | Metabolism; Microbiology/Virology; Others |
Syringic acid (3,5-dimethoxy-4-hydroxy Benzoic Acid) 能抑制低密度脂蛋白的氧化。 | |||
T0437 |
Inosine
INO 495,NSC 20262,肌苷 |
ROS; Endogenous Metabolite; Adenosine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Inosine (NSC-20262) 是由腺苷分解代谢产生的一种内源性嘌呤核苷,是腺苷受体A1R 和A2AR 的激动剂,具有抗炎免疫调节,抗伤害和神经保护作用。 | |||
TN1772 |
Isoastilbin
|
Anti-infection; Tyrosinase; Antibacterial | Microbiology/Virology; Proteases/Proteasome |
Isoastilbin 是Rhizoma Smilacis glabrae 和Astragalus membranaceus 中的二氢黄酮醇糖苷。它抑制酪氨酸酶活性,还抑制葡萄糖基转移酶,IC50值为 54.3 μg/mL。它具有神经保护、抗氧化、抗微生物和抗凋亡活性,可研究阿尔茨海默氏病。 | |||
T11685 |
Isolongifolene
异长叶烯,(-)-Isolongifolene |
Apoptosis; Others | Apoptosis; Others |
Isolongifolene ((-)-Isolongifolene) 是一种从调料九里香中分离的三环倍半萜烯,具有抗氧化,抗炎,抗癌和神经保护的特性。它通过调节 PI3K/AKT/GSK-3β 信号通路来减轻鱼藤酮诱导的氧化应激,线粒体功能障碍和细胞凋亡。 | |||
TN1420 |
Bacopaside I
|
Others | Others |
Bacopaside I 是一种皂苷,分离自 Bacopa monniera 中,具有抗氧化活性和清除自由基的功能,有抗抑郁作用。 | |||
T3893 |
Forsythoside B
连翘酯苷 B,连翘脂苷B |
TNF; NF-κB | Apoptosis; NF-κB |
Forsythoside B 是传统中药植物独一味叶子中分离的一种苯乙醇苷。它可抑制 TNF-alpha,IL-6,IκB, 调节 NF-κB。它抑制炎症反应,具有抗氧化和神经保护作用。 | |||
T2S1008 |
Oxysophoridine
Sophoridine N-oxide,氧化槐定碱 |
Apoptosis; Antioxidant | Apoptosis; oxidation-reduction |
Oxysophoridine (Sophoridine N-oxide) 是从苦豆子中提取的一种生物碱,具有抗发炎,抗氧化应激和抗凋亡的作用。 | |||
TN2095 |
Pomiferin
|
NOS; NF-κB; PDE | Immunology/Inflammation; Metabolism; NF-κB |
Pomiferin is a natural product inhibitor of carbonic anhydrase I and II isoenzymes. It has anticancer, antibacterial and antidiabetic properties. Pomiferin has anti-inflammatory and neuroprotective activities. | |||
T79948 |
Kadsurenin B
|
||
Kadsurenin B为PAF(platelet-activating factor)拮抗剂,展现出神经保护作用。该化合物在药理学领域显示出广泛的研究潜力,包括抗菌、抗炎、神经保护、抗氧化、抗血小板聚集、细胞毒性和抗寄生虫等效能。 | |||
T77201 |
Rutin trihydrate
|
||
Rutin (Rutoside) trihydrate 是多功能天然黄酮苷,展现出抗氧化、抗炎、抗糖尿病及抗癌效果。此外,该化合物还具有心脏保护和神经保护活性。 | |||
T75571 | Withaphysalin D | ||
Withaphysalin D 是一种选择性抑制含GluN2B的N-甲基-D-天冬氨酸受体(NMDAR)的化合物。该物质可从睡莲中提取,对神经保护有益,能穿过血脑屏障。 | |||
T75890 |
Conantokin G TFA
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Conantokin G TFA 是一种 17 个氨基酸的肽,是一种有效,选择性和竞争性的 N-甲基-D-天冬氨酸 (NMDA) 受体拮抗剂。Conantokin G TFA 抑制鼠皮质神经元中NMDA 诱发的电流,IC50为 480 nM,具有神经保护作用。 | |||
T81117 | Spilanthol | ||
Spilanthol为一具有多种生物活性的化合物,包括镇痛、神经保护、抗氧化、抗诱变、抗癌、抗炎、抗菌以及杀虫作用。该化合物能够通过诱导cAMP抑制尿浓缩的负调节机制,且可作为利尿剂研究的候选物。 | |||
T75436 | Jatrorrhizine hydroxide | ||
Jatrorrhizine hydroxide, 一种从黄连中提取的生物碱,展现了神经保护、抗菌、抗疟原虫及抗氧化的活性。作为一种高效的乙酰胆碱酯酶(AChE)抑制剂(IC50=872 nM),其对BuChE的选择性高达115倍。此外,Jatrorrhizine hydroxide还能通过抑制uptake-2 transporter活性来减少血清素(5-HT)和去甲肾上腺素(NE)的摄取,表现出口服活性。 |