50
9
1
1
5
Cat. No. | Product Name | ||
---|---|---|---|
L1720 | 核苷类化合物库 | 334 compounds | |
334 种核苷类化合物,包括核苷酸、核苷酸类似物及衍生物等,适用于抗病毒、抗肿瘤、抗真菌、抗抑郁等药物的研发; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T20993 |
Memantine
|
Others | Others |
Memantine 是口服具有活性的、非竞争性的N-甲基-D-天冬氨酸受体拮抗剂,可用于研究中重度阿尔茨海默病。 | |||
T7061 |
Duloxetine
|
Serotonin Transporter | Neuroscience |
Duloxetine 是一种 5 羟色胺-去甲肾上腺素重吸收 (serotonin-norepinephrine reuptake) 抑制剂,Ki=4.6 nM,可作用于广泛性焦虑症的研究。 | |||
T21635 |
PD184161
|
MEK | MAPK |
PD 184161 是一种口服有效的,时间和浓度依赖的 MEK 抑制剂,IC50为10-100 nM。它诱导抑郁样行为,抑制细胞增殖并诱导细胞凋亡。 | |||
T15799 |
LY2940094
LY-2940094 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
LY2940094 (LY-2940094) 是一种口服有效的选择性 NOP 受体拮抗剂,可降低动物模型的自身给药酒精依赖,对 NOP 受体具有高亲和力,Ki 为 0.105 nM,和拮抗活力,Kb 为 0.166 nM。 | |||
T14782 |
Brilaroxazine
RP5063 |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Brilaroxazine (RP5063) 是一种有效的多模式多巴胺/5-HT 调节剂。 Brilaroxazine 是多巴胺 D2、D3 和 D4 受体、5-HT1A (Ki = 1.5 nM) 和 5-HT2A (Ki = 2.5 nM) 的部分激动剂,具有拮抗活性 5-HT2B 和 5-HT7 受体,Ki 分别为 0.19 nM 和 2.7 nM。 Brilaroxazine 可用于研究神经精神和神经系统疾病的认知障碍。 | |||
T16481 |
PF-04995274
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
PF-04995274 是强效,高亲和力,口服活性血清素 4 受体的部分激动剂。它是可脑渗透的,可用于与阿尔茨海默症相关的认知障碍的研究。 | |||
T7805 |
GW791343 dihydrochloride
GW791343 (HCl) |
P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
GW791343 dihydrochloride (GW791343 (HCl)) 是有种属特异性的 P2X7变构调节剂,对人 P2X7的 pIC50为6.9-7.2。 | |||
T1279 |
Vilazodone
维拉佐酮,SB659746A,EMD 68843 |
5-HT Receptor; Serotonin Transporter | GPCR/G Protein; Neuroscience |
Vilazodone (SB659746A) 是一种可口服的选择性 5 -羟色胺再摄取抑制剂 (SSRI) 和部分5-HT1A 受体激动剂。它有抗抑郁作用,可用于抑郁症和情绪性疾病的研究。 | |||
T1445 |
Agomelatine
Thymanax,S-20098,Valdoxan,阿戈美拉汀 |
Melatonin Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Agomelatine (Valdoxan) 是褪黑激素受体的强效激动剂和 5-羟色胺-2C (5-HT2C) 受体的拮抗剂,在猪和人 5-HT2C 克隆受体中pKi 分别为 6.4 和 6.2。 | |||
T5135 |
Flupentixol dihydrochloride
盐酸氟哌噻吨,Fupentixol Dihydrochloride,Flupenthixol dihydrochloride,(E/Z)-Flupentixol Dihydrochloride |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Flupentixol dihydrochloride 是噻克西酮类试剂,能够用于研究精神分裂症以及抗焦虑和抑郁障碍。 | |||
T1471 |
Duloxetine hydrochloride
Duloxetine HCl,盐酸度洛西汀,LY-248686 hydrochloride,(S)-Duloxetine hydrochloride,LY-248686 HCl |
Dopamine Receptor; 5-HT Receptor; Serotonin Transporter; Norepinephrine | GPCR/G Protein; Neuroscience |
Duloxetine hydrochloride ((S)-Duloxetine hydrochloride) 是一种 5-羟色胺-去甲肾上腺素重吸收 (serotonin-norepinephrine reuptake) 抑制剂 (SNRI),Ki=4.6 nM,可用于广泛性焦虑症的研究。 | |||
T6526 |
GW791343 trihydrochloride
GW791343 3HCl |
P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
GW791343 trihydrochloride (GW791343 3HCl) 是 P2X7变构调节剂,有种属特异性,对人 P2X7的pIC50为6.9-7.2。 | |||
T1619 |
Trazodone hydrochloride
KB-831,盐酸曲唑酮,Trazodone HCl,AF-1161 |
5-HT Receptor; Adrenergic Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Trazodone hydrochloride (Trazodone HCl) 是5 羟色胺受体拮抗剂和重吸收抑制剂,用作抗抑郁药,可治疗失眠和焦虑。 | |||
T27599 |
Imiloxan
RS-21361,RS 21361,RS21361 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Imiloxan (RS-21361) 是一种 α2 肾上腺素能受体拮抗剂,可用于治疗重度抑郁症。 | |||
T6232 |
Vilazodone Hydrochloride
盐酸维拉佐酮,SB659746A,EMD 68843,Vilazodone HCl |
Others; 5-HT Receptor; Serotonin Transporter | GPCR/G Protein; Neuroscience; Others |
Vilazodone Hydrochloride (EMD 68843) 是 5-HT1A 受体和特异性 5-羟色胺再摄取抑制剂(SSRI) 的部分激动剂,用于治疗重度抑郁症。 | |||
T22442 |
Trazodone
曲唑酮,AF-1161 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Trazodone (AF-1161) 是一种 5-HT 2A/2C 受体拮抗剂,用作治疗主要焦虑症和抑郁症的抗抑郁药。 | |||
T68172 |
Zalospirone
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Zalospirone 是一种5-HT1A 受体激动剂,可用于研究焦虑症和重度抑郁症。 | |||
T10075 |
2-Methyl-5-HT
2-Methyl-5-hydroxytryptamine,2-甲基-5-羟基色氨酸盐酸 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
2-Methyl-5-HT (2-Methyl-5-hydroxytryptamine) 是5-HT3受体的选择性激动剂,显示出抗抑郁样作用。 | |||
T32737 |
Liafensine
BMS820836,BMS 820836,DB104,BMS-820836 |
Dopamine Receptor; 5-HT Receptor; Norepinephrine | GPCR/G Protein; Neuroscience |
Liafensine(BMS-820836) 是一种新型且具有选择性的三重单胺再摄取抑制剂,对血清素、去甲肾上腺素和多巴胺的再摄取具有抑制作用,可用于研究重度抑郁症和中枢神经系统疾病。 | |||
T22453 |
Venlafaxine
Wy 45030,文拉法辛 |
Serotonin Transporter | Neuroscience |
Venlafaxine (Wy 45030) 是一种口服有效的 5-羟色胺 (5-HT)/去甲肾上腺素 (NE) 重摄取的双重抑制剂,具有抗抑郁活性。 | |||
T78556 |
Antidepressant agent 5
|
Others | Others |
Antidepressant agent 5 是一种具有抗抑郁活性的 7-取代四氢异喹啉衍生物。Antidepressant agent 5 在研究抑郁症方面和木兰花碱作用效果类似,可用于预防和治疗抑郁症疾病。 | |||
T21013 |
Clomipramine
Chlorimipramine,Anafranil,Clomicalm,Anafranil (free base),Clomipramina,氯米帕明 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Clomipramine (Clomicalm) 是一种三环类抗抑郁药,能够有效阻断 5-HT 再摄取 (IC50:1.5 nM) ,可用于研究强迫症 (OCD) 及抑郁症。 | |||
T1189 |
Milnacipran hydrochloride
盐酸米那普仑,Milnacipran HCl,Savella,Dalcipran |
Serotonin Transporter; Norepinephrine | Neuroscience |
Milnacipran hydrochloride (Savella) 是一种5-羟色胺-去甲肾上腺素重吸收抑制剂(SNRI),可用于纤维肌痛的研究。 | |||
T64317 |
ZZL-7
|
Serotonin Transporter | Neuroscience |
ZZL-7是一种起效快的抗抑郁药。ZZL-7破坏中缝背核(DRN)神经元一氧化氮合酶(nNOS)和血清素转运蛋白(SERT)之间的相互作用。ZZL-7可以很容易地穿过血脑屏障。ZZL-7在重度抑郁症(MDD)中具有研究价值。 | |||
T10075L2 |
2-Methyl-5-HT hydrochloride
2-Methyl-5-hydroxytryptamine hydrochloride |
5-HT Receptor | GPCR/G Protein; Neuroscience |
2-Methyl-5-HT hydrochloride (2-Methyl-5-hydroxytryptamine) is a potent and selective 5-HT3 receptor agonist with anti-depressive-like effects. | |||
T27939 |
LY2940094 tartrate
LY2940094,LY 2940094,LY-2940094 tartrate,LY-2940094 |
Others | Others |
LY-2940094, a nociceptin receptor antagonist, is used potentially for the treatment of major depressive disorder and alcoholism. | |||
T0338 |
Minaprine
Cantor,Minaprine dihydrochloride,米那卜林,米那卜林 二盐酸盐,Minaprina,Minaprinum |
MAO; Dopamine Receptor; 5-HT Receptor; AChR; AChE; Monoamine Oxidase | GPCR/G Protein; Metabolism; Neuroscience |
Minaprine 是一种单胺氧化酶 MAO-A 可逆性抑制剂,对乙酰胆碱酯酶有微弱抑制,是一种抗抑郁类化合物。 | |||
T30147 |
AS 701
AS-701,AS701 |
Others | Others |
AS-701 is a Li+ selective ionophore in the therapy of manic-depressive illness. | |||
T69364 |
Elzasonan
|
Others | Others |
Elzasonan is a selective 5-hydroxytryptamine 1B receptor antagonist used to treat patients with major depressive disorder and obsessive compulsive disorder. | |||
T10075L |
2-Methyl-5-HT maleate
2-Methylserotonin maleate,2-Methyl-5-hydroxytryptamine maleate,2-Me-HT maleate |
5-HT Receptor | GPCR/G Protein; Neuroscience |
2-Methyl-5-HT maleate (2-Methyl-5-hydroxytryptamine maleate) is a potent and selective 5-HT3 receptor agonist, which is shown to display anti-depressive-like effects[1]. | |||
T40778 |
Tyrosylleucine TFA
Tyr-Leu TFA |
||
Tyrosylleucine (Tyr-Leu, YL) TFA is a dipeptide compound with potent antidepressant-like activity. This orally active compound demonstrates effective modulation of depressive symptoms. | |||
T69063 |
Orvepitant
|
Others | Others |
Orvepitant is a potent and selective NK1 antagonist, which may be potentially useful for patients with major depressive disorder (MDD), anxiety and insomnia. | |||
T27331 |
Flerobuterol HCl
CRL-40996,CRL40996,CRL 40996,Flerobuterol hydrochloride |
Others | Others |
Flerobuterol is a β adrenergic receptor agonist potentially for the treatment of major depressive disorder. Flerobuterol enhances serotonergic neurotransmission. Flerobuterol acutely increases 5-HT synthesis, in part, through an elevation of brain Trp ava | |||
T61544 |
Edivoxetine hydrochloride
|
Others | Others |
Edivoxetine hydrochloride is a highly effective and specialized compound used primarily as a norepinephrine reuptake inhibitor (NERI), indicated for the treatment of depressive disorder and attention-deficit/hyperactivity disorder. | |||
T11008 |
Desmethylnortriptyline
|
Others | Others |
Desmethylnortriptyline is a metabolite of nortriptyline. Nortriptyline is a tricyclic antidepressant. It is the main active metabolite of amitriptyline and is used to relieve depressive symptoms. | |||
T71587 |
Fluoxetine succinate ester
|
Others | Others |
Fluoxetine succinate ester is an antidepressant of the selective serotonin reuptake inhibitor (SSRI) class. It is used for the treatment of major depressive disorder, obsessive–compulsive disorder, bulimia nervosa, panic disorder, and premenstrual dysphoric disorder. | |||
T71389 |
Fluoxetine oxalate
|
Others | Others |
Fluoxetine oxalate is an antidepressant of the selective serotonin reuptake inhibitor (SSRI) class. It is used for the treatment of major depressive disorder, obsessive–compulsive disorder, bulimia nervosa, panic disorder, and premenstrual dysphoric disorder. | |||
T82075 |
Imipramine pamoate
|
Others | Others |
Imipramine pamoate为抗抑郁化合物,具有抗抑郁作用。 | |||
T68973 |
EVT-101 free base
|
Others | Others |
EVT-101, also known as ENS-101, is an experimental medication which originated from Roche and is under development by Evotec AG for the treatment of major depressive disorder. It acts as a selective NMDA receptor subunit 2B (NR2B) antagonist. | |||
T61625 |
GABAA receptor agonist 2
|
Others | Others |
GABAA receptor agonist 2 (compound 4c) is a highly potent GABAA receptor agonist which exhibits anti-depressive properties in classical mouse models of depression, such as the FST and TST. By binding to the GABA binding site on the GABAA receptor, GABAA receptor agonist 2 produces GABAergic effects. Notably, Compound 4c holds promise for depression research [1]. | |||
T16406 |
Orvepitant maleate
GW823296 maleate |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Orvepitant maleate is an effective, selective, and well-tolerated neurokinin-1 receptor (NK-1) antagonist (pKi: 10.2 for human neurokinin-1 receptor). Orvepitant maleate has the potential for depressive disorder and chronic refractory cough (CRC) treatmen | |||
T68579 |
Fluvoxamine acid
|
Others | Others |
Fluvoxamine acid is a medication which functions as a selective serotonin reuptake inhibitor (SSRI) and σ1 receptor agonist. Fluvoxamine is used primarily for the treatment of obsessive-compulsive disorder (OCD), and is also used to treat major depressive disorder (MDD), and anxiety disorders such as panic disorder and post-traumatic stress disorder (PTSD). | |||
T79229 |
ETAP
|
Monoamine Oxidase | Neuroscience |
ETAP为一种既抑制MAO-A也抑制MAO-B的化合物,展现出抗抑郁样活性,可应用于重度抑郁症的研究领域。 | |||
T71537 |
Tofenacin hydrochloride
|
Others | Others |
Tofenacin hydrochloride is an antidepressant drug with a tricyclic-like structure. It acts as a serotonin-norepinephrine reuptake inhibitor, and based on its close relation to orphenadrine, may also possess anticholinergic and antihistamine properties. Tofenacin is also the major active metabolite of orphenadrine and likely plays a role in its beneficial effects against depressive symptoms seen in Parkinson's disease patients. | |||
T70487 |
Tofenacin (free base)
|
Others | Others |
Tofenacin (free base) is an antidepressant drug with a tricyclic-like structure. It acts as a serotonin-norepinephrine reuptake inhibitor, and based on its close relation to orphenadrine, may also possess anticholinergic and antihistamine properties. Tofenacin is also the major active metabolite of orphenadrine and likely plays a role in its beneficial effects against depressive symptoms seen in Parkinson's disease patients. | |||
T40849 |
C20 Ceramide
N-Arachidoyl-D-sphingosine |
Endogenous Metabolite | Metabolism |
C20 Ceramide (N-Arachidoyl-D-sphingosine) 是一种存在于大脑中的 20:0 神经酰胺,可穿越血脑屏障激活小胶质细胞,诱导抑郁样行为。 | |||
T61008 |
(±)-Duloxetine hydrochloride
|
Others | Others |
(±)-Duloxetine ((Rac)-Duloxetine) hydrochloride 是 Duloxetine hydrochloride 的外消旋物。Duloxetine hydrochloride 可用于研究糖尿病性神经性疼痛、纤维肌痛和重度抑郁症,它是 5-羟色胺去甲肾上腺素再摄取的抑制剂。 | |||
T73779 |
5β-Androstan-3β-ol-17-one
|
Others | Others |
5β-Androstan-3β-ol-17-one(3β-Etiocholanolone;5β-Epiandrosterone),为5β还原型类固醇,主要是脱氢表雄酮(DHEA)的关键代谢物之一。在C57BL/KsJ基因型糖尿病(db/db)小鼠中,该化合物显示出显著的降糖效果,并且具有对神经元的抑制活性。 | |||
T72824 |
RAGE/SERT-IN-1
|
Others | Others |
RAGE/SERT-IN-1 是一种 RAGE 和 SERT 抑制剂,口服活性良好,IC50 分别为 8.26 μM 和 31.09 nM。它对 Aβ25-35 诱发的神经元损伤具有显著神经保护效果,并可缓解小鼠抑郁症状。RAGE/SERT-IN-1 适用于阿尔茨海默病与抑郁症并发症的研究。 | |||
T83948 |
Sakura 6
|
Others | Others |
Sakura 6是一种合成的5-HT转运体(SERT)结合肽,促进SERT与神经元型一氧化氮合酶的相互作用,降低SERT活性和细胞表面的SERT,增加自我抑制,减少突触5-HT释放并降低背侧绕束核的放电。在抑郁症小鼠模型中诱导急性抑郁表型。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3933 |
Jatrorrhizine
Yatrorizine,neprotin,药根碱 |
MAO; 5-HT Receptor; Antibacterial; AChE | GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience |
Jatrorrhizine (neprotin) 是一种从黄连中分离得到的生物碱,具有抗菌、抗氧化、抗疟原虫和神经保护活性。它通过抑制 uptake-2 transporter 的活性减少血清素和去甲肾上腺素的摄取。它是一种有口服活性的乙酰胆碱酯酶制剂。 | |||
T4912 |
Jatrorrhizine chloride
盐酸药根碱,Yatrorhizine chloride,Neprotine chloride |
Others; 5-HT Receptor; OCT; Antibacterial; AChE | GPCR/G Protein; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Others |
Jatrorrhizine chloride (Neprotine chloride) 是从黄连中分离得到的生物碱,具有神经保护、抗菌、抗氧化和抗疟原虫活性。它通过抑制摄取2转运蛋白的活性减少血清素和去甲肾上腺素的摄取。它是具有口服活性的乙酰胆碱酯酶抑制剂。 | |||
TWS0704 |
N-Methylnuciferine
|
Others | Others |
N-Methylnuciferine 是一种从Lotus Plumule提取的生物碱,可改善脂多糖诱导的抑郁样行为。 | |||
TN1383 |
Timosaponin B III
Anemarsaponin BIII,知母皂苷B3,知母皂苷BIII |
Others; Platelet aggregation | Others |
Timosaponin B III (Anemarsaponin BIII) 是一种具有生物活性的甾体皂苷,从知母中分离出来。Timosaponin B III 具有抗炎、抗血小板聚集和抗抑郁作用。 | |||
T0611 |
Vanillylmandelic acid
4-Hydroxy-3-methoxymandelic acid,3-甲氧基-4-羟基扁桃酸 |
Others; Antioxidant | Others; oxidation-reduction |
Vanillylmandelic acid 是儿茶酚胺、肾上腺素和去甲肾上腺素代谢的最终产物,具有抗氧化活性,常用于帮助诊断嗜铬细胞瘤,以及其升高与抑郁症状有关。 | |||
T2563 |
Acetyl-L-carnitine hydrochloride
Acetyl L-carnitine hydrochloride,O-Acetylcarnitine,乙酰-L-肉(毒)碱盐酸盐,O-acetyl-L-carnitine,O-Acetyl-L-carnitine hydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
Acetyl-L-carnitine hydrochloride (Acetyl L-carnitine hydrochloride) 是一种由内源性左旋肉碱的乙酰化形式的盐酸盐组成的营养补充剂,具有潜在的神经保护、认知增强、抗抑郁和免疫调节活性。还可缓解化疗、糖尿病或其他疾病引起的周围神经病变。此外,乙酰左旋肉碱可能通过增加T淋巴细胞成熟来调节免疫反应,并可能下调促炎细胞因子对病毒(如SARS-CoV-2)的反应。它还可能破坏ACE2信号通路并抑制活性氧(ROS)的产生。 | |||
T3011 |
2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid
Kynurenine,Dl-Kynurenine,Kynurenin,3-Anthraniloylalanine,犬尿氨酸 |
Others; Endogenous Metabolite | Metabolism; Others |
2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid 是一种酮类和氨基酸衍生物,具有多种生物功能,包括血管舒张、免疫调节和神经调节活性。2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid 是烟酸的前体。2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid 的异常产生与神经系统疾病相关的认知缺陷和抑郁症状有关。2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid 在某些类型的癌细胞中过度表达,可能被用作评估癌症风险的生物标志物。 | |||
TN6028 |
Gardneramine
|
||
Gardneramine has a mild central depressive effect. Gardneramine and hirsutine show a local anesthetic action, they also can inhibit the ganglionic transmission of the dog urinary bladder and that the blockade of the nicotinic receptor plays a main role. | |||
T7475 |
S-Adenosyl-L-methionine
AdoMet,Ademetionine,SAMe,S-Adenosyl methionine,S-腺苷-L-蛋氨酸 |
Others; Endogenous Metabolite | Metabolism; Others |
S-Adenosyl-L-methionine (Ademetionine) 是一种具有有效的抗抑郁和减轻疼痛作用的膳食补充剂,是通过蛋氨酸腺苷转移酶的作用由蛋氨酸和 ATP 内源性生产的,是一种重要的口服具有活力的甲基供体,能够用于肝病和骨关节炎的研究。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-02924 |
RGS1 Protein, Human, Recombinant (His)
1R20,IER1,BL34,HEL-S-87,regulator of G-protein signaling 1,I... |
Human | E. coli |
RGS1 (regulator of G-protein signaling 1) has been associated with multiple autoimmune disorders including type I diabetes. RGS1 desensitizes the chemokine receptors CCR7 and CXCR4 that are critical to the localization of T and B cells in lymphoid organs. RGS1 expression may be a prognostic marker for risk stratification and a promising target for the development of a new Multiple myeloma (MM) therapy. The markers in the RGS1 gene might be in linkage disequilibrium with a protective allele that ... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TMIH-0582 |
Trazodone-d8 hydrochloride
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Trazodone-d8 hydrochloride 是 Trazodone hydrochloride 的氘代化合物。Trazodone hydrochloride 的 CAS 号为 25332-39-2。Trazodone hydrochloride 是5 羟色胺受体拮抗剂和重吸收抑制剂,用作抗抑郁药,可治疗失眠和焦虑。 | |||
T11113 |
Duloxetine D3 hydrochloride
(S)-Duloxetine D3 hydrochloride,LY248686 D3 hydrochloride |
Others | Others |
Duloxetine D3 hydrochloride is a serotonin-norepinephrine reuptake inhibitor (SNRI) with a Ki of 4.6 nM, used for treatment of major depressive disorder and generalized anxiety disorder (GAD).Duloxetine D3 hydrochloride ((S)-Duloxetine D3 hydrochloride) i | |||
TMIJ-0300 |
Duloxetine-d7
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Duloxetine-d7 是 Duloxetine 的氘代化合物。Duloxetine 的 CAS 号为 116539-59-4。Duloxetine 是一种 5 羟色胺-去甲肾上腺素重吸收 (serotonin-norepinephrine reuptake) 抑制剂,Ki=4.6 nM,可作用于广泛性焦虑症的研究。 | |||
T70174 |
Pirlindole-d4 HCl
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Pirlindole-d4 is intended for use as an internal standard for the quantification of pirlindole by GC- or LC-MS. Pirlindole is a selective and reversible monoamine oxidase A (MAO-A) inhibitor. It is selective for MAO-A over MAO-B. In rats, it reverses the depressive-like effects induced by chronic mild stress (CMS), increases proliferation of hippocampal neural progenitor cells, and reverses dendritic atrophy in granule neurons. Pirlindole is also an inhibitor of enterovirus-D68 and coxsackieviru... | |||
TMID-0190 |
Milnacipran-d10 Hydrochloride
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Milnacipran-d10 Hydrochloride 是 Milnacipran Hydrochloride 的氘代化合物。Milnacipran Hydrochloride 的 CAS 号为 101152-94-7。Milnacipran hydrochloride 是一种5-羟色胺-去甲肾上腺素重吸收抑制剂(SNRI),可用于纤维肌痛的研究。 |