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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9190 |
NAG-thiazoline
GlcNAc-thiazoline,N-乙酰 - 葡糖胺基噻唑啉 |
Others | Others |
NAG-thiazoline (GlcNAc-thiazoline) 是一种 O-GlcNAcase 抑制剂,Ki 值为 180 nM。它对 V. campbellii 有效,MIC 值为 0.5 µM。 | |||
T72482 |
Dazostinag disodium
|
STING | Immunology/Inflammation |
Dazostinag disodium (TAK-676) 是一种新型干扰素基因刺激剂 (STING) 激动剂,也是一种免疫系统调节剂,具有抗肿瘤活性,可激活树突状细胞、自然杀伤细胞和 T 细胞。 | |||
T68053 |
Denagliptin
GW823093 |
DPP-4 | Proteases/Proteasome |
Denagliptin是一种小分子二肽基肽酶IV(DPP-4)抑制剂,可用于治疗内分泌于代谢疾病,可用于研究2型糖尿病。 | |||
T1782 |
Canagliflozin
卡格列净,JNJ 24831754ZAE,JNJ 28431754AAA,TA 7284,JNJ 28431754 |
SGLT | GPCR/G Protein |
Canagliflozin (JNJ 28431754AAA) 是SGLT2的选择性抑制剂,在表达 mSGLT2,rSGLT2 和 hSGLT2 的 CHO 细胞上,IC50分别为 2 nM,3.7 nM 和 4.4 nM。 | |||
T6390 |
Anagrelide hydrochloride
BMY 26538-01,盐酸阿那格雷,Anagrelide HCl,Agrylin,BL4162A |
PDE | Metabolism |
Anagrelide hydrochloride (BL4162A) 能够有效治疗血小板增多症。 | |||
T7133 |
Anagliptin
SK-0403,阿拉格列汀 |
Proteasome; DPP-4 | Proteases/Proteasome; Ubiquitination |
Anagliptin (SK-0403) 是一种选择性的二肽酰肽酶 4 抑制剂,IC50=3.8 nM,对 DPP-8/9 的选择性相对较弱,IC50分别为 68 和 60 nM。 | |||
T0160 |
Anagrelide
Anagrelida,Xagrid,Anagrelidum,阿那格雷 |
PDE | Metabolism |
Anagrelide (Xagrid) 是III 型磷酸二酯酶(PDEIII)抑制剂 (IC50=36 nM),是咪唑喹唑啉衍生物。它能够抑制血小板生成,以及抗血栓形成作用,可用作血小板聚集抑制剂。 | |||
T16009L |
Managlinat dialanetil
MB06322,MB 6322,CS-917 |
Phosphatase | Metabolism |
Managlinat dialanetil (MB06322) 是一种可口服且具有有效性的 fructose 1,6-bisphosphatase (FBPase) 抑制剂,具有降糖活性,可用于研究 2 型糖尿病。 | |||
T67795 |
Camonagrel
|
||
Camonagrel 是一种化合物,对Prostaglandin E2具有抑制作用。 | |||
T0191 |
Linagliptin
BI 1356,利格列汀,利拉利汀 |
Ferroptosis; Proteasome; DPP-4; Autophagy | Apoptosis; Autophagy; Proteases/Proteasome; Ubiquitination |
Linagliptin (BI 1356) 是一种有效的、可口服的、基于二氢嘌呤二酮的二肽基肽酶 4 抑制剂,具有降血糖活性。 | |||
T67852 |
Linagliptin Methyldimer
|
Proteasome | Proteases/Proteasome; Ubiquitination |
Linagliptin Methyldimer 是一种强效的二肽基肽酶 IV 抑制剂,IC50=6 pM。 | |||
T1782L |
Canagliflozin hemihydrate
JNJ28431754,TA 7284,TA7284,TA-7284,JNJ 28431754,JNJ-28431754 |
SGLT | GPCR/G Protein |
Canagliflozin hemihydrate (TA 7284) (JNJ28431754 hemihydrate) 是一种选择性的 SGLT2 抑制剂,作用于表达 mSGLT2,rSGLT2 和 hSGLT2 的 CHO 细胞,IC50 分别为 2 nM,3.7 nM 和 4.4 nM。 | |||
T124826 | N-Methylhernagine | ||
N-Methylhernagine 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T124826,CAS号为 4668-25-1。 | |||
T39489 |
Ulevostinag
Ulevostinag,MK-1454 |
||
Ulevostinag (MK-1454) is a STING agonist. | |||
T20949 |
NAGKi
NAGK-i,NAGK i,3-O-Methyl-N-acetyl-D-glucosamine |
||
NAGKi is an inhibitor of N-acetylmannosamine kinase (NAMK) and N-acetylglucosamine kinase (NAGK). | |||
T10669 |
Canagliflozin-d4
Canagliflozin D4 |
Others | Others |
Canagliflozin D4 is a deuterium-labeled Canagliflozin. Canagliflozin is an SGLT2 inhibitor. | |||
T71081 | Nagstatin | ||
Nagstatin is an inhibitor of N-acetyl-beta-D-glucosaminidase and is produced by Streptomyces amakusaensis MG846-fF3. | |||
T75293 | Anagrelide hydrochloride monohydrate | ||
Anagrelide hydrochloride monohydrate 是一种咪唑并喹唑啉制剂。Anagrelide hydrochloride monohydrate 可降低血液中血小板的水平,防止血栓形成。Anagrelide hydrochloride monohydrate 可用于研究原发性血小板增多症 (ET) 和与真性红细胞增多症 (PV) 相关的血小板增多症。 | |||
T39682 |
Gunagratinib
ICP-192 |
||
Gunagratinib (ICP-192) is a potent and selective, orally active pan-FGFR (fibroblast growth factor receptors) inhibitor with low toxicity, exhibiting irreversible covalent binding to effectively inhibit FGFR activities. It is particularly suitable for cancer research purposes. | |||
T75405 | GlcNAc kinase (EcNagK) | ||
GlcNAc kinase (EcNagK) (N-Acetylglucosamine kinase) 为GlcNAc代谢过程中的关键酶。通过将ATP的γ-磷酰基转移到GlcNAc的C-6位羟基,生成GlcNAc-6-P。 | |||
T24898 |
Trifenagrel
BW-325U,BW 325U,BW325U |
||
Trifenagrel is an antithrombotic. It has been found to produce less gastric irritation and fecal blood loss in humans. | |||
T131025 | Anagallosaponin IX | ||
Anagallosaponin IX 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T131025。 | |||
T32058 |
Henagliflozin
SHR3824,SHR 3824,SHR-3824 |
||
Henagliflozin (SHR3824) is an effective, oral, and selective SGLT2 inhibitor that effectively inhibits human SGLT2 in vitro, but has very weak inhibitory effects on human SGLT1. | |||
T12605 |
Quinagolide hydrochloride
盐酸喹高利特,CV205-502 hydrochloride |
Others | Others |
Quinagolide hydrochloride is a selective agonist of dopamine D2 receptor. | |||
T16009 |
(Rac)-Managlinat dialanetil
CS-917,(Rac)-MB06322,MB06322,(Rac)-CS-917 |
Others; DHFR | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Others |
(Rac)-Managlinat dialanetil ((Rac)-MB06322) 是 Managlinat dialanetil 的外消旋体,Managlinat dialanetil 是一种可口服且具有有效性的 fructose 1,6-bisphosphatase (FBPase) 抑制剂,可用于研究 2 型糖尿病。 | |||
T75086 | Dazostinag | ||
Dazostinag (TAK-676 free base) 为干扰素基因刺激剂 (STING) 蛋白的激动剂,展现出抗肿瘤活性。它能作为有效载荷 (payload) 用于合成抗体偶联活性分子 (ADC) 的构建。 | |||
T37695 |
NMNNAGDKWSAFLKEQSTLAQMYPLQEIQNLTVKLQLQALQQ
|
||
NMNNAGDKWSAFLKEQSTLAQMYPLQEIQNLTVKLQLQALQQ, an ACE2-related peptide, serves as a valuable research tool for comprehending ACE2 functions. | |||
T28397 |
Phenaglycodol
Atadiol,Felixin,Puasital,Sedapsin,Acalmid |
||
Chlordimeform Hydrochloride is an acaricide. | |||
T25270 | Conagenin | ||
Conagenin is a small molecular immunomodulator isolated by Streptomyces roseosporus. | |||
T76263 |
Beinaglutide
|
||
Beinaglutide 是一种重组人 GLP-1(rhGLP-1) 多肽,与人 GLP-1(7-36) 具有几乎 100% 的同源性。Beinaglutide 在血糖控制、抑制食物摄入和胃排空和促进体重减轻方面表现出依赖于剂量的作用。Beinaglutide 具有研究超重/肥胖和非酒精性脂肪性肝炎 (NASH) 的潜力。 | |||
T62213 |
Anagliptin hydrochloride
|
||
Anagliptin (SK-0403) hydrochloride 是一种有效的、高度选择性的、口服具有活力的二肽酰肽酶 4 (DPP-4) 抑制剂 (IC50: 3.8 nM),对 DPP-8 (IC50: 68 nM) 和 DDP-9 (IC50: 60 nM) 的选择性相对较弱。 | |||
T31378 |
Denagliptin tosylate
GSK-823093,GSK 823093,GW-823093,GW 823093,GSK823093,GW823093 |
||
Denagliptin (GW823093 or GSK-823093) is a dipeptidyl peptidase IV (DPP-IV) inhibitor. | |||
T32758 |
Linagliptin mixture with metformin
Jentadueto Xr,Linagliptin / metformin,Jentadueto |
||
Linagliptin mixture with metformin is used for the treatment of type 2 diabetes. | |||
T68483 | Quinagolide Free Base | ||
Quinagolide Free Base is a non-ergot dopamine D(2)-agonist. | |||
T81708 |
Nagrestipen
|
||
Nagrestipen 是一种人巨噬细胞炎症蛋白-1α 变体,也称为 ECI 301,主要用于癌症、肿瘤、转移、放射肿瘤学以及肿瘤转移研究试验,具有显著的抗肿瘤活性。 | |||
TF0019 |
2,6-Dimethyl-4-Heptyl-β-D-Maltopyranoside, Anagrade
|
||
2,6-Dimethyl-4-Heptyl-β-D-Maltopyranoside, Anagrade 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 TF0019,CAS号为 869638-31-3。 | |||
T28971 |
Tianagliflozin
|
||
Tianagliflozin, a sodium/glucose cotransporter 2 (SGLT-2) inhibitor, is used potentially for the treatment of type 2 diabetes. | |||
T0755 |
Carglumic Acid
Carbaglu,N-Carbamylglutamate,N-Carbamyl-L-glutamic acid,氨甲酰谷氨酸,Carbamylglutamic acid,Carbamino-L-glutamic acid,Ureidoglutaric acid |
Others | Others |
Carglumic Acid (Ureidoglutaric acid) 是一种 N-乙酰谷氨酸 (NAG) 的功能类似物和氨甲酰磷酸合成酶 1(CPS1)的活化剂,可用于与 N-乙酰谷氨酸合成酶 (NAGS) 缺陷相关的急性和慢性高氨血症的研究。 | |||
T29090 | Valibose | ||
Valibose An α-glucosidase inhibitor. Valibose ameliorated metabolic disturbance of glucose and lipids. valibose markedly reduced level of serum BUN and NAG, and decreased the weight index of kidney. | |||
T38225 |
N-Arachidonoyl-3-hydroxy-γ-Aminobutyric Acid
|
||
Several different arachidonoyl amino acids, including N-arachidonoyl-3-hydroxy-γ-aminobutyric acid (NAG-3H-ABA), have been isolated and characterized from bovine brain. The glycine congener was further characterized and found to suppress formalin-induced pain in rats. NAG-3H-ABA was also found in rat brain by LC-MS techniques, but has not been fully characterized to date. Most arachidonoyl amino acids are poor ligands for the CB1 receptor. | |||
T73993 |
Fazirsiran
|
||
Fazirsiran (ARO-AAT) 是第二代 RNA 干扰 (RNAi) 活性分子。Fazirsiran 由胆固醇偶联的 RNAi 触发器 (chol-RNAi) 组成,通过 RNAi 选择性降解 AAT mRNA,以及与 N-乙酰半乳糖胺 (NAG) 偶联的蜂毒肽衍生肽配制成赋形剂 EX1,促进肝细胞内 chol RNAi 的内体逃逸。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4514 |
N-Acetyl-D-Glucosamine
N-乙酰-D-氨基葡萄糖,NAG,N-Acetyl-2-amino-2-deoxyglucose,Marine Sweet,N-Acetyl-2-amino-2-deoxy-D-glucose,N-乙酰氨基葡萄糖,GlcNAc |
Endogenous Metabolite | Metabolism |
N-Acetyl-D-Glucosamine (NAG) 是葡萄糖的单糖衍生物。 | |||
TN2296 |
Vinaginsenoside R4
越南参皂苷R4 |
Others | Others |
Vinaginsenoside R4 是分离自水培人参的叶子中。它能够抑制黑色素的生物合成,并增强斑马鱼的色素沉着,对 melan-a 细胞没有任何细胞毒性作用。 | |||
T8198 |
Visnagin
|
Others | Others |
Visnagin 是一种抗氧化剂呋喃香豆素衍生物。它具有预防Cerulein 诱导的急性胰腺炎的潜力。它在血管平滑肌中具有良好的血管扩张作用。它具有抗炎作用,可用于缓解疼痛的研究。 | |||
TN2297 |
Vinaginsenoside R8
越南参皂苷R8 |
Others | Others |
Vinaginsenoside R8 is a natural product | |||
TN6267 | Tannagine | ||
Tannagine 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6267,CAS号为 123750-34-5。 | |||
T4416 |
Vinaginsenoside R3
越南参皂苷 R3 |
Others | Others |
Vinaginsenoside R3是一种天然产物,属于五加科人参属,其产品编号为 T4416,CAS号为 156012-92-9。Vinaginsenoside R3可用作对照参考。 | |||
T73856 |
Anagyrine hydrochloride
|
||
Anagyrine ((-)-Anagyrine) hydrochloride 是一种存在于Lupinus albus 中的喹啉类生物碱。Anagyrine hydrochloride 可与毒蕈碱和烟碱乙酰胆碱受体 (AChR) 结合,IC50值分别为 132 和 2096 µM。Anagyrine hydrochloride 是一种有效的nAChR 脱敏剂,Anagyrine hydrochloride 可以直接脱敏nAChR,不需要代谢。 | |||
TN4623 | Nagilactone C | Antifection | Microbiology/Virology |
Nagilactone C and phyllanthoside are novel protein synthesis inhibitors, they are specific for the eukaryotic translation apparatus, function in vivo and in vitro, and interfere with translation elongation. Nagilactone C shows high insecticidal activity against second-instar nymphs of Eocanthecona furcellata. Nagilactone C possesses potent antiproliferative activity against human fibrosarcoma and murine colon carcinoma tumor cell lines exhibiting ED50 values of 2.3 and 1.2 microg/ml, respectivel... | |||
TN1971 | Nagarine | Others | Others |
Nagarine has toxic and analgesic effects. | |||
TN3409 |
Anagyrine
|
Antifection | Microbiology/Virology |
Anagyrine, is the responsible teratogen from teratogenic lupins, can produce congenital deformities in calves typical of crooked calf disease; it also can induce red cell aplasia, vascular anomaly, and skeletal dysplasia.(-)-Anagyrine and (-)--Methylcytisine have nematicidal activities against Pine Wood Nematodes. | |||
TN5853 |
Naginata ketone
Dehydroelsholtzione |
||
Naginata ketone 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5853,CAS号为 6138-88-1。 | |||
T16264 | Nagilactone B | Others | Others |
Nagilactone B is extracted from the root bark of Podocarpus nagi and it also is a liver X receptor (LXR) agonist. | |||
TN4286 | Isodunnianol | NOS; NF-κB; ROS; AChR | Immunology/Inflammation; Neuroscience; NF-κB |
Isodunnianol exhibits anti-AChE activity with an IC50 value of 13.0 uM; it also exhibits neurite outgrowth-promoting activity at the concentration ranging from 0.1 to 10 uM in the primary cultured rat cortical neurons. Isodunnianol, dunnianol, and Macrant |