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53

抑制剂 & 化合物

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Cat. No. Product Name Target Signaling Pathways
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。
T9022 AZD9977

AZD 9977

Glucocorticoid Receptor Endocrinology/Hormones
AZD9977 是一种选择性的,有效的,具有口服活性的盐皮质激素受体 (MR) 调节剂,可用于研究心力衰竭和慢性肾病。
T0154 Nebivolol hydrochloride

R 065824 hydrochloride,盐酸奈必洛尔,Nebivolol HCl,R-65824

Apoptosis; Adrenergic Receptor Apoptosis; GPCR/G Protein; Neuroscience
Nebivolol hydrochloride (R 065824 hydrochloride) 是一种β1-肾上腺素受体选择性抑制剂,IC50为0.8 nM。
T1410 Torsemide

AC-4464,JDL-464,托拉塞米,Torasemide

Na-K-Cl cotransporter Membrane transporter/Ion channel
Torsemide (AC-4464) 是具有口服活性的亨氏环利尿剂,也具有抗醛固酮和血管舒张活性。它可用于研究心力衰竭、肾脏疾病、肝硬化。
T1615 Irbesartan

厄贝沙坦,SR-47436,BMS-186295

Apoptosis; RAAS Apoptosis; Endocrinology/Hormones
Irbesartan (SR-47436) 是一种 1 型血管紧张素 II 受体拮抗剂,IC50为1.3 nM。
T80678 (S)-AK-242

(-)-Resatorvid,(S)-Resatorvid,AK-242 (S enantiomer),(-)-AK-242

Others Others
(S)-AK-242 ((S)-Resatorvid) 是一种细胞因子抑制剂,可用于治疗心脏病、自身免疫性疾病、炎症性疾病。
T20843 Aplodan

Nergize,Creatinolfosfate,磷酸肌肉醇,creatinol-O-phosphate,Creatinolfosfate, Creatinol Phosphate

Others Others
Aplodan (creatinol-O-phosphate) 表现出抗缺血和抗心律失常的能力以及对细胞膜的保护作用。 Aplodan 可用于缺血性心脏病或伴有持续性室性早搏的缺血性心脏病的研究。
T29687 Afacifenacin

Afacifenacin fumarate,SMP-986,NS 986,NS-986,SMP 986,NS986,SMP986

AChR Neuroscience
Afacifenacin (SMP-986) fumarate 是一种 M3 毒蕈碱受体选择性拮抗剂,可用于研究缺血性心脏病,尿失禁和膀胱炎和其他疾病。
T28437 Pomisartan

BIBR-363,BIBR 363,BIBR363

RAAS Endocrinology/Hormones
Pomisartan (BIBR-363) 是一种小分子血管紧张素 1 型受体(AT1R)拮抗剂,可用于治疗心血管疾病,研究心脏衰竭和高血压。
T61028 Mitiperstat

AZD4831

Glutathione Peroxidase Metabolism
Mitiperstat 是一种强效的骨髓过氧化物酶(MPO)抑制剂。Mitiperstat 对预防如心力衰竭和冠状动脉疾病类的心血管疾病有很好的效果。
T4287 Succinobucol

Probucol monosuccinate,AGI-1067

Antioxidant; Reactive Oxygen Species Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction
Succinobucol (Probucol monosuccinate) 是酚类抗氧化剂,具有抗炎、抗血小板聚集活性。
T0080 Trapidil

唑嘧胺,乐可安,Rocornal,Trapymine,Avantrin,Trapymin,AR-12008

PDGFR; PDE Angiogenesis; Metabolism; Tyrosine Kinase/Adaptors
Trapidil (Avantrin) 是一种抗血小板药物,是一种血管扩张剂,有特异性血小板衍生生长因子。
T10364 Arbutamine

GP 21213

Adrenergic Receptor GPCR/G Protein; Neuroscience
Arbutamine (GP 21213) 是一种新型非选择性β-肾上腺素受体激动剂,具有α-1-拟交感神经活性。Arbutamine 促进心脏应激,增加心率、心脏收缩力。Arbutamine 可用于研究心脏应激和冠状动脉疾病。
T7674 Thrombin Receptor Activator for Peptide

Protease-activated Receptor GPCR/G Protein
Thrombin Receptor Activator for Peptide 也称为凝血因子 II 受体 (1-5) 或蛋白酶激活受体 1 (1-5),用于研究冠心病 (CHD)。
T6581 Methyclothiazide

Duretic,Enduron,甲氯噻嗪,Aquatensen

Others; Carbonic Anhydrase Metabolism; Others
Methyclothiazide (Aquatensen) 是一种具有口服活性的利尿剂,也是一种降压剂。它能够拮抗体外的电压依赖性钙通道的 (VDCC) 活性,也可以抑制内源性血管收缩刺激导致的血管反应。
T69760 TT-10

TAZ-K

YAP Stem Cells
TT-10 (TAZ-K) 作为YES相关蛋白(YAP)-转录增强因子结构域(TEAD)活性的激活剂,适用于心肌细胞丢失伴随心脏病研究。
T2226 Pergolide mesylate

甲磺酸培高利特,Pergolide mesylate salt,LY127809,Pergolide methanesulfonate

Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor GPCR/G Protein; Neuroscience
Pergolide mesylate salt(LY127809) 是一种有效的,具有口服活性的多巴胺 D1和 D2受体激动剂,是一种 Ergoline 衍生物,可用于帕金森氏病和高泌乳素血症的研究。
T0988 Trimetazidine dihydrochloride

盐酸曲美他嗪,Yoshimilon,Kyurinett,Vastarel F

Autophagy; Fatty Acid Synthase Autophagy; Metabolism
Trimetazidine dihydrochloride (Vastarel F) 是细胞保护性抗缺血剂,也用作缺血性心脏病或心绞痛的血管扩张剂,具有抗氧化,抗炎,抗伤害和胃保护作用。它可通过抑制脂肪酸代谢提高心肌葡萄糖利用率。
T0056 Oxeladin citrate

Others Others
Oxeladin citrate 是止咳剂,能够对各种病因引发咳嗽进行有效研究。
T14390L (2R,3S)-Azelaprag

Apelin receptor GPCR/G Protein
(2R,3S)-N-(4-(2,6-dimethoxyphenyl)-5-(5-methylpyridin-3-yl)-4H-1,2,4-triazol-3-yl)-3-(5-methylpyrimidin-2-yl)butane-2-sulfonamide 是一种Apelin 受体激动剂,对Apelin 受体的EC50为0.012 µM。(2R,3S)-N-(4-(2,6-dimethoxyphenyl)-5-(5-methylpyridin-3-yl)-4H-1,2,4-triazol-3-yl)-3-(5-methylpyrimidin-2-yl)butane-2-sulfonamide 可用于治疗心力衰竭、动脉粥样硬化、肥胖、糖尿病、肌萎缩侧索硬化、冠心病、高血压、中风和心肌梗塞等疾病。
T13697 FR 58664

Others Others
FR 58664 is a drug to treat heart failure disease.
T1605L Enalapril sodium

(-)-Enalapril sodium

Enalapril sodium is used to treat high blood pressure, diabetic kidney disease, and heart failure and can be generally used with a diuretic such as furosemide for heart failure.
T32782 Lipopeptin A

Lipopeptin A is a lipoprotein subclass that is a risk factor for atherosclerotic diseases such as coronary heart disease and stroke.
T34107 Polythiazide

P2525,NSC-108161,NSC 108161,P-2525,NSC108161

Polythiazide (NSC-108161, P-2525) is used to treat fluid retention (edema) caused by a variety of causes, including congestive heart failure, severe liver disease (cirrhosis), kidney disease, or steroid or hormonal medication.
T74031 Cardiolipin (Heart, Bovine) (sodium)

Cardiolipin (Heart, Bovine) sodium,一种线粒体专有磷脂,展现出在神经系统疾病研究中的应用潜力。
T26279 Tiracizine HCl

AWD-19-166,AWD19166,Bonnecor,AWD 19 166,Tiracizine Hydrochloride

Tiracizine HCl 是一种新的I 类抗心律失常药物,对缺血性心脏病患者进行了研究,结果表明该药物可降低心肌收缩功能。
T10812 Cicloprolol hydrochloride

Adrenergic Receptor GPCR/G Protein; Neuroscience
Cicloprolol hydrochloride 是一种新型有效且具有选择性的 β1-肾上腺素能受体 (β 1-adrenoceptor) 拮抗剂,具有部分激动剂活性,可用于研究冠心病。
T62351 Lotrafiban

Lotrafiban 是一种口服具有活力的血小板膜糖蛋白 IIb/IIIa 阻滞剂,能够用于治疗冠心病和脑血管疾病的治疗。
TP1320 Angiogenin (108-122) TFA (112173-49-6 free base)

Angiogenin (108-122) TFA

Angiogenin (108-122) TFA is an angiogenin peptide.Angiogenin (108-122) acts as a therapeutic agent for the prophylaxis and/or treatment of cancer, an infectious disease, a fibrotic disease, an inflammatory disease, a neurodegenerative disease, an autoimmu
TP1362 Angiogenin (108-122)

Angiogenin 108-122

Angiogenin (108-122) is an angiogenin peptide. Angiogenin (108-122) acts as a therapeutic agent for the prophylaxis and/or treatment of cancer, an infectious disease, a fibrotic disease, an inflammatory disease, a neurodegenerative disease, an autoimmune
T21485 Perindopril

Perindopril (S-9490) 是一种长效血管紧张素转换酶(ACE)抑制剂,用于治疗高血压、心力衰竭或稳定性冠状动脉疾病。
T38908 MK-8262

MK-8262, an orally active and potent cholesteryl ester transfer protein (CETP) inhibitor (IC 50 = 53 nM, log D = 5.3), is a bistrifluoromethyl analogue that shows promise in research related to high-density lipoprotein (HDL) and low-density lipoprotein (LDL) with potential implications for coronary heart disease (CHD).
T79084 BET bromodomain inhibitor 3

Epigenetic Reader Domain Chromatin/Epigenetic
BET bromodomain inhibitor 3为BET溴区结构域抑制剂,对BrdT抑制作用显示Ki值高于40 µM,适用于避孕、癌症和心脏病相关研究。
T39587 APJ receptor agonist 4

APJ Receptor Agonist 4 is a potent, orally active apelin receptor (APJ) agonist, demonstrating an EC50 of 0.06 nM and a Ki of 0.07 nM. It exhibits excellent pharmacokinetic profiles in rodent heart failure (HF) models and has shown an acceptable safety profile in preclinical toxicology studies. This compound effectively improves cardiac function, making it valuable for research into HF disease.
T7496 Thrombin Receptor Activator for Peptide 5 (TRAP-5)

Thrombin Receptor Activator for Peptide

Protease-activated Receptor GPCR/G Protein
Thrombin Receptor Activator for Peptide 5 (TRAP-5) 也称为凝血因子 II 受体 (1-5) 或蛋白酶激活受体 1 (1-5),用于研究冠心病 (CHD)。
T62909 SGC agonist 2

SGC agonist 2 是一种有效的可溶性鸟苷酸环化酶 (SGC) 激动剂。其中可溶性鸟苷酸环化酶是 NO-sGC-cGMP 信号通路中的关键信号转导酶。SGC agonist 2 具有潜力进行心血管疾病 (心力衰竭、心绞痛、肺动脉高压、心肌梗塞) 和纤维化疾病 (肾纤维化、系统性硬化症) 的研究。
T33673 Niludipine

Niludipina,BAY-a 7168,Bay a 7168,Niludipinum

Nirudipine is a double (2-propoxyethyl) analogist of nifedipine and a calcium channel blocker, which is also a safe anti-angina Ca2+ antagonist with a broad range of efficacy for all types of angina. At the same time, Niludipine is a highly effective drug
T63035 Izilendustat hydrochloride

Izilendustat (hydrochloride) 是一种脯氨酰羟化酶 (prolyl hydroxylase) 的有效抑制剂,能够稳定缺氧诱导因子-1 α (HIF-1α) 和缺氧诱导因子-2 (HIF-2)。Izilendustat (hydrochloride) 具有潜力进行 HIF-1α 相关疾病的研究(包括外周血管疾病(PVD)、心力衰竭、冠状动脉疾病(CAD)、缺血、贫血、结肠炎和其他炎症性肠病)。
T37439 C18 Globotriaosylceramide (d18:1/18:0)

C18 globotriaosylceramide is an endogenous sphingolipid found in mammalian cell membranes that is synthesized from lactosylceramide . It inhibits aggregation of human neutrophils induced by phorbol 12-myristate 13-acetate (PMA; 10008014) when used at a concentration of 1 μM. C18 globotriaosylceramide acts as a receptor for Shiga toxin in B cell-derived Raji cells and THP-1 monocytes. It accumulates in the brain, heart, kidney, liver, lung, and spleen in a mouse model of Fabry disease, a lysosoma...
T69600 Spermidine-d6

Spermidine-d6 is intended for use as an internal standard for the quantification of spermidine by GC- or LC-MS. Spermidine is an endogenous polyamine. It is formed from putrescine by spermidine synthase. Spermidine (25 µM) inhibits the activity of the human inward-rectifying potassium channel Kir2.3 in a patch-clamp assay. It induces autophagy in HeLa cells when used at a concentration of 100 µM and increases the lifespan of D. melanogaster, yeast, and C. elegans. Spermidine (30 mM in the drinki...
T70990 ADMA-d6

NG,NG-dimethyl-L-arginine-d6 (ADMA-d6) (hydrochloride) is intended for use as an internal standard for the quantification of NG,NG-dimethyl-L-arginine by GC- or LC-MS. ADMA is an endogenous inhibitor of nitric oxide synthase (NOS). It is formed from arginine by protein arginine methyltransferases (PRMTs) and degraded by dimethylarginine dimethylaminohydrolases (DDAHs) and alanine-glyoxylate aminotransferase 2 (AGXT2). ADMA levels are increased concomitant with an increase in blood pressure in Da...
T63153 APJ receptor agonist 5

APJ receptor agonist 5 (compound 3) 是一种有效的、口服具有活力的 apelin 受体 (APJ) 激动剂 (EC50: 0.4 nM)。APJ receptor agonist 5 在啮齿动物心力衰竭 (HF) 模型中具有出色的药代动力学特征,在临床前毒理学研究中也具有可接受的安全性。APJ receptor agonist 5 能够改善心脏功能,可用于 HF 疾病的研究。
T64102 hCAI/II-IN-5

hCAI/II-IN-5 是 hCA I 和 hCA II (人碳酸酐酶同工酶 I 和 II) 的有效抑制剂,他们的IC50值分别为 37.88 和 45.23 nM。 hCAI/II-IN-5 也能够抑制 α-Glycosidase (IC50: 48.98 nM) 和 AChE (IC50: 420.14 nM)。hCAI/II-IN-5 能够用于研究糖尿病、心力衰竭、阿尔茨海默病、溃疡、癫痫等多种疾病。
T80973 TNF-α-IN-8

TNF-α-IN-8 (compound I-42) 作为一种TNF-α抑制剂,属于异吲哚-亚胺类化合物,适用于肿瘤、心脏病、骨质疏松、炎症、过敏及自身免疫性疾病的研究。作为点击化学试剂,其Azide基团能与含Alkyne的分子配对,通过铜催化的叠氮-炔环加成反应(CuAAc)产生反应,也可与含DBCO或BCN基团的分子进行菌株促进的炔-叠氮环加成反应(SPAAC)。
T70070 Cisapride tartrate

Cisapride tartrate is chemically related to metoclopramide, but unlike metoclopramide, it does not cross the blood-brain barrier or have antidopaminergic effects. Cisapride is a serotonin-4 (5-HT4) receptor agonist. Cisapride was indicated for the symptomatic treatment of adult patients with nocturnal heartburn due to gastroesophageal reflux disease. The Food and Drug Administration (FDA) in America stopped the marketing of cisapride as of 14th July 2000. They had received at least 341 reports o...
T63941 α-Glycosidase-IN-1

α-Glycosidase-IN-1 (compound MZ7) 是 α-GLY(α- 糖苷酶) 的有效抑制剂 (IC50: 44.72 nM, Ki: 44.74 nM)。α-Glycosidase-IN-1 也能够抑制人碳酸酐酶同工酶 I 和 II (hCA I 和hCA II)以及乙酰胆碱酯酶 (AChE),其IC50值分别为 104.87、100.04 和 654.87 nM。α-Glycosidase-IN-1 能够用于研究糖尿病、阿尔茨海默病、溃疡、心力衰竭、癫痫等多种疾病。
T81609 omega-3 Arachidonic acid ethyl ester

(all-Z)-8,11,14,17-Eicosatetraenoic acid ethyl ester,ω-3 Arachidonic acid ethyl ester

omega-3 Arachidonic Acid ethyl ester 是一种少见的多不饱和脂肪酸,饮食来源稀少。ω-3脂肪酸对婴幼儿生长发育极为重要,能够帮助预防心脏病、血栓、高血压及炎症和自身免疫性疾病。该化合物在人血小板膜中通过抑制花生四烯酰辅酶A合成酶发挥作用,Ki值达到14 μM;同时在小牛脑提取物中也表现出抑制作用,IC50大约5 μM。omega-3 Arachidonic Acid ethyl ester 作为游离酸的亲脂性更强的形式,具备独特的生物活性。
T79358 PF-07247685

Endogenous Metabolite Metabolism
PF-07247685是一种BCKDC激酶(BDK)抑制剂,具有较强的活性(EC50=2.2 nM)。该化合物能有效稳定BDK与BCKDH E2核心亚基之间的相互作用,并阻断E1亚基的磷酸化过程。BCKDH的活性受到BDK介导的磷酸化调控,从而控制支链氨基酸(BCAA)降解的关键步骤。BCAA的代谢失调与心力衰竭(HF)、2型糖尿病(T2DM)、非酒精性脂肪肝病(NAFLD)及肥胖等多种疾病相关联,尤其在心脏代谢疾病中表现明显。PF-07247685在小鼠模型中对心脏代谢终点产生改善效果,并提升了葡萄糖耐量。
T35604 Osteocalcin (1-49) (human) (trifluoroacetate salt)

Osteocalcin (1-49) is a non-collagenous peptide that is secreted by osteoblasts and odontoblasts and comprises 1-2% of the total protein in bone. Secretion of osteocalcin (1-49) is stimulated by 1,25-dihydroxy vitamin D and plasma levels increase in diseases that induce dysregulated bone turnover such as osteoporosis, Paget's disease, and primary hyperparathyroidism. Osteocalcin (1-49) is positively correlated with insulin sensitivity and negatively correlated with high blood glucose levels in w...
T79357 PF-07238025

Endogenous Metabolite Metabolism
PF-07238025是一种BCKDC激酶(BDK)抑制剂,具有EC50值为19 nM。它通过稳定BDK和BCKDH复合体中的E2亚基相互作用,阻碍E1亚基的磷酸化过程,从而抑制了BCKDH的活性。由于BDK的磷酸化作用是控制支链氨基酸(BCAA)降解过程中的限速步骤,PF-07238025的作用与包括心力衰竭(HF)、2型糖尿病(T2DM)、非酒精性脂肪肝病(NAFLD)及肥胖在内的多种代谢性疾病的发病机制相关。研究显示PF-07238025能在小鼠体内改善心脏代谢指标并提升葡萄糖耐量。

化合物

Conoidin A
Cat.No: T21687
Synonym:
Target: Parasite
AZD9977
Cat.No: T9022
Synonym: AZD 9977
Target: Glucocorticoid Receptor
Nebivolol hydrochloride
Cat.No: T0154
Synonym: R 065824 hydrochloride,盐酸奈必洛尔,Nebivolol HCl,R-65824
Target: Apoptosis, Adrenergic Receptor
Torsemide
Cat.No: T1410
Synonym: AC-4464,JDL-464,托拉塞米,Torasemide
Target: Na-K-Cl cotransporter
Irbesartan
Cat.No: T1615
Synonym: 厄贝沙坦,SR-47436,BMS-186295
Target: Apoptosis, RAAS
(S)-AK-242
Cat.No: T80678
Synonym: (-)-Resatorvid,(S)-Resatorvid,AK-242 (S enantiomer),(-)-AK-242
Target: Others
Aplodan
Cat.No: T20843
Synonym: Nergize,Creatinolfosfate,磷酸肌肉醇,creatinol-O-phosphate,Creatinolfosfate, Creatinol Phosphate
Target: Others
Afacifenacin
Cat.No: T29687
Synonym: Afacifenacin fumarate,SMP-986,NS 986,NS-986,SMP 986,NS986,SMP986
Target: AChR
Pomisartan
Cat.No: T28437
Synonym: BIBR-363,BIBR 363,BIBR363
Target: RAAS
Mitiperstat
Cat.No: T61028
Synonym: AZD4831
Target: Glutathione Peroxidase
Succinobucol
Cat.No: T4287
Synonym: Probucol monosuccinate,AGI-1067
Target: Antioxidant, Reactive Oxygen Species
Trapidil
Cat.No: T0080
Synonym: 唑嘧胺,乐可安,Rocornal,Trapymine,Avantrin,Trapymin,AR-12008
Target: PDGFR, PDE
Arbutamine
Cat.No: T10364
Synonym: GP 21213
Target: Adrenergic Receptor
Thrombin Receptor Activator for Peptide
Cat.No: T7674
Synonym:
Target: Protease-activated Receptor
Methyclothiazide
Cat.No: T6581
Synonym: Duretic,Enduron,甲氯噻嗪,Aquatensen
Target: Others, Carbonic Anhydrase
TT-10
Cat.No: T69760
Synonym: TAZ-K
Target: YAP
Pergolide mesylate
Cat.No: T2226
Synonym: 甲磺酸培高利特,Pergolide mesylate salt,LY127809,Pergolide methanesulfonate
Target: Dopamine Receptor, 5-HT Receptor, Adrenergic Receptor
Trimetazidine dihydrochloride
Cat.No: T0988
Synonym: 盐酸曲美他嗪,Yoshimilon,Kyurinett,Vastarel F
Target: Autophagy, Fatty Acid Synthase
Oxeladin citrate
Cat.No: T0056
Synonym:
Target: Others
(2R,3S)-Azelaprag
Cat.No: T14390L
Synonym:
Target: Apelin receptor
FR 58664
Cat.No: T13697
Synonym:
Target: Others
Enalapril sodium
Cat.No: T1605L
Synonym: (-)-Enalapril sodium
Target:
Lipopeptin A
Cat.No: T32782
Synonym:
Target:
Polythiazide
Cat.No: T34107
Synonym: P2525,NSC-108161,NSC 108161,P-2525,NSC108161
Target:
Cardiolipin (Heart, Bovine) (sodium)
Cat.No: T74031
Synonym:
Target:
Tiracizine HCl
Cat.No: T26279
Synonym: AWD-19-166,AWD19166,Bonnecor,AWD 19 166,Tiracizine Hydrochloride
Target:
Cicloprolol hydrochloride
Cat.No: T10812
Synonym:
Target: Adrenergic Receptor
Lotrafiban
Cat.No: T62351
Synonym:
Target:
Angiogenin (108-122) TFA (112173-49-6 free base)
Cat.No: TP1320
Synonym: Angiogenin (108-122) TFA
Target:
Angiogenin (108-122)
Cat.No: TP1362
Synonym: Angiogenin 108-122
Target:
Perindopril
Cat.No: T21485
Synonym:
Target:
MK-8262
Cat.No: T38908
Synonym:
Target:
BET bromodomain inhibitor 3
Cat.No: T79084
Synonym:
Target: Epigenetic Reader Domain
APJ receptor agonist 4
Cat.No: T39587
Synonym:
Target:
Thrombin Receptor Activator for Peptide 5 (TRAP-5)
Cat.No: T7496
Synonym: Thrombin Receptor Activator for Peptide
Target: Protease-activated Receptor
SGC agonist 2
Cat.No: T62909
Synonym:
Target:
Niludipine
Cat.No: T33673
Synonym: Niludipina,BAY-a 7168,Bay a 7168,Niludipinum
Target:
Izilendustat hydrochloride
Cat.No: T63035
Synonym:
Target:
C18 Globotriaosylceramide (d18:1/18:0)
Cat.No: T37439
Synonym:
Target:
Spermidine-d6
Cat.No: T69600
Synonym:
Target:
ADMA-d6
Cat.No: T70990
Synonym:
Target:
APJ receptor agonist 5
Cat.No: T63153
Synonym:
Target:
hCAI/II-IN-5
Cat.No: T64102
Synonym:
Target:
TNF-α-IN-8
Cat.No: T80973
Synonym:
Target:
Cisapride tartrate
Cat.No: T70070
Synonym:
Target:
α-Glycosidase-IN-1
Cat.No: T63941
Synonym:
Target:
omega-3 Arachidonic acid ethyl ester
Cat.No: T81609
Synonym: (all-Z)-8,11,14,17-Eicosatetraenoic acid ethyl ester,ω-3 Arachidonic acid ethyl ester
Target:
PF-07247685
Cat.No: T79358
Synonym:
Target: Endogenous Metabolite
Osteocalcin (1-49) (human) (trifluoroacetate salt)
Cat.No: T35604
Synonym:
Target:
PF-07238025
Cat.No: T79357
Synonym:
Target: Endogenous Metabolite
Cat. No. Product Name Target Signaling Pathways
T4903 Heptadecanoic acid

Others; Endogenous Metabolite Metabolism; Others
Heptadecanoic acid 是奇链饱和脂肪酸,与一些疾病(如冠心病、糖尿病前期和 2 型糖尿病以及多发性硬化症)有关。
T3S0128 Hydroprotopine

氢化原阿片碱,氢化物碱

Others Others
Hydroprotopine 是一种来自Hypecoum leptocarpumand 的生物碱,能够有效的治疗冠心病及心绞痛。
T14840 Butyrylcarnitine

Endogenous Metabolite Metabolism
Butyrylcarnitine 是血浆中的代谢物,是疾病引起异常代谢的指标,可用于诊断心力衰竭和胰腺囊肿。
T10584 Bovinic acid

(9Z,11E)-Octadecadienoic acid,Rumenic acid

Endogenous Metabolite Metabolism
Bovinic acid ((9Z,11E)-Octadecadienoic acid) 是一种具有抗癌和抗动脉硬化的活性的共轭亚油酸,可用于研究老年冠心病和肥胖。
T3243 Betaine

Abromine,glycine betaine,oxyneurine,trimethylglycine,lycine,甜菜碱

Others; Endogenous Metabolite Metabolism; Others
Betaine (trimethylglycine) 是许多食物中发现的天然化合物,也是能够维持正常 DNA 甲基化模式的特性甲基供体。它广泛存在于植物,动物,微生物和丰富的膳食来源中。它能够促进各种肠道微生物抵抗渗透变化,从而改善微生物发酵特性。它也能够作为渗透物,通过防止脱水和渗透失活来维持禽类的细胞水和离子平衡,从而提高禽类对热应激的能力。
T13933 Toringin

Others Others
Toringin is a bioflavonoid isolated from the bark of Docyniopsis tschonoski, and have various biological activities and beneficial actions against cancers, coronary heart disease, among other pathologies.
T4863 DL-Homocysteine

DL-高半胱氨酸,2-Amino-4-mercaptobutyric acid

Endogenous Metabolite Metabolism
DL-Homocysteine (2-Amino-4-mercaptobutyric acid) 是弱神经毒素,能够影响犬尿酸的产生。
TN4860 Pueroside B

COX; PPAR DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Neuroscience
Pueroside B may can treat coronary heart disease, it can interact with two or more targets[peroxisome proliferator activated receptor γ (PPAR-γ), angiotensin-converting enzyme (ACE), hydroxymethylglutaryl coenzyme A receptor (HMGR), cyclooxygenase-2 (COX2
T37291 Lyso-Globotriaosylceramide (d18:1)

Lyso-Globotriaosylceramide (d18:1)

Lyso-globotriaosylceramide is a form of globotriaosylceramide that is lacking the fatty acyl group. It binds to Shiga toxin 1 (Stx1) in the presence of cholesterol and phosphatidylcholine but does not bind Stx2. It also reduces viability and aggregation of human neutrophils induced by phorbol 12-myristate 13-acetate when used at concentrations of 50 and 1 μM, respectively. Lyso-globotriaosylceramide accumulates in the brain, heart, kidney, liver, lung, and spleen in a mouse model of Fabry diseas...

天然产物

Heptadecanoic acid
Cat.No: T4903
Synonym:
Target: Others, Endogenous Metabolite
Hydroprotopine
Cat.No: T3S0128
Synonym: 氢化原阿片碱,氢化物碱
Target: Others
Butyrylcarnitine
Cat.No: T14840
Synonym:
Target: Endogenous Metabolite
Bovinic acid
Cat.No: T10584
Synonym: (9Z,11E)-Octadecadienoic acid,Rumenic acid
Target: Endogenous Metabolite
Betaine
Cat.No: T3243
Synonym: Abromine,glycine betaine,oxyneurine,trimethylglycine,lycine,甜菜碱
Target: Others, Endogenous Metabolite
Toringin
Cat.No: T13933
Synonym:
Target: Others
DL-Homocysteine
Cat.No: T4863
Synonym: DL-高半胱氨酸,2-Amino-4-mercaptobutyric acid
Target: Endogenous Metabolite
Pueroside B
Cat.No: TN4860
Synonym:
Target: COX, PPAR
Lyso-Globotriaosylceramide (d18:1)
Cat.No: T37291
Synonym: Lyso-Globotriaosylceramide (d18:1)
Target:
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