49
10
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T35664 |
Tetracosactide acetate
|
Others | Others |
Tetracosactide acetate 是一种合成的多肽,可刺激肾上腺释放皮质类固醇 ,如皮质醇。Tetracosactide acetate 在溃疡性结肠炎和克罗恩病、青少年和成人类风湿性关节炎和骨关节病方面有研究的价值。 | |||
T22344 |
Icatibant Acetate
|
Bradykinin Receptor | GPCR/G Protein |
Icatibant acetate 是一种特异性缓激肽 B2 受体拮抗剂,其 IC50=1.07 nM,Ki=0.798 nM。 | |||
T20615 |
Olsalazine
奥沙拉嗪,Dipentium,Salicylic acid |
Others | Others |
Olsalazine (Dipentium) 是一种抗炎药,用于治疗炎症性肠病。它也是一种新型的 DNA 去甲基化剂。 | |||
T22368 |
Metyrosine
甲酪氨酸,α-Methyltyrosine |
COX | Immunology/Inflammation; Neuroscience |
Metyrosine (α-Methyltyrosine) 是一种选择性酪氨酸羟化酶抑制剂,可显著抑制高 COX-2 活性和有效控制血压,具有抗炎和抗溃疡作用。 | |||
T9377 |
ASK1-IN-2
|
Apoptosis; ASK; MAPK | Apoptosis; MAPK |
ASK1-IN-2 是一种口服有活性的凋亡信号调节激酶 1 抑制剂(IC50:32.8 nM)。它可用于研究溃疡性结肠炎。 | |||
T4084 |
Sibofimloc
VRT-1353385,Antibiotic-202,Antibiotic 202 |
Antibacterial; Antibiotic | Microbiology/Virology |
Sibofimloc (Antibiotic-202) 是一种肠道限制性的,具有口服活性的 FimH 粘附抑制剂,有抗细菌感染活性,被开发用于治疗炎症性肠病的研究。 | |||
T4602 |
Hydrocortisone hemisuccinate
Hydrocortisone 21-he,氢化可的松琥珀酸酯,hydrocortisone 21-hemisuccinate*free acid,Hydrocortisone 21-hemisuccinate |
Glucocorticoid Receptor; Others; Interleukin | Endocrinology/Hormones; Immunology/Inflammation; Others |
Hydrocortisone hemisuccinate (hydrocortisone 21-hemisuccinate*free acid) 是糖皮质激素, 是口服有活性的甾体抗炎剂。它能够降低IL-6(IC50:6.7 μM)、IL-3(IC50:21.4 μM)的生物活性,可用于研究溃疡性结肠炎。 | |||
T3147 |
Pyrrolidinedithiocarbamate ammonium
PDTC,Pyrrolidinedithiocarbamate,吡咯烷二硫代氨基甲酸铵,APDC,1-Pyrrolidinedithiocarboxylic acid ammonium salt,Ammonium pyrrolidinedithiocarbamate,吡咯烷二硫代甲酸铵 |
NF-κB | NF-κB |
Pyrrolidinedithiocarbamate ammonium (1-Pyrrolidinedithiocarboxylic acid ammonium salt) 是一种选择性的、能透过血脑屏障的NF-κB 抑制剂。 | |||
T9914 |
Vedolizumab
|
Integrin | Cytoskeletal Signaling |
Vedolizumab 是一种人源化单克隆抗体,靶向α4β7整联蛋白,用于溃疡性结肠炎和克罗恩病的相关研究。 | |||
T35898 |
Izencitinib
|
||
Izencitinib (TD-1473) is an orally active, gut-restricted JAK inhibitor with non-selective properties. It is primarily employed in the investigation of ulcerative colitis [1]. | |||
T3620 |
Solcitinib
索西替尼,GLPG-0778,GSK-2586184 |
JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
Solcitinib (GLPG-0778) 是一种可口服的,选择性的竞争性JAK1抑制剂,IC50值为 9.8 nM,可用于银屑病的研究。它对其选择性是对 JAK2、JAK3 和 TYK2 的 11、55 和 23 倍。 | |||
T1544 |
Olsalazine disodium
Dipentum,奥沙拉秦钠,Olsalazine Sodium |
Others; COX; Antibacterial; Antibiotic | Immunology/Inflammation; Microbiology/Virology; Neuroscience; Others |
Olsalazine disodium (Dipentum) 是抗炎化合物,可作用于溃疡性结肠炎和炎症性肠病。 | |||
T77582 |
Anti-inflammatory agent 51
|
NF-κB | NF-κB |
Anti-inflammatory agent 51 是一种具有抗炎活性和潜在抗肿瘤活性的酰胺/磺酰胺衍生物,对 NF-κB 激活有抑制作用,可用于研究急性肺损伤和溃疡性结肠炎。 | |||
T22963 |
McN-A 343
|
AChR | Neuroscience |
McN-A 343作为选择性M1 muscarinic激动剂, 以其刺激交感神经节中muscarinic传导的能力而闻名。在溃疡性结肠炎的实验模型中,它已被发现能有效减轻炎症和氧化应激。 | |||
T70084 |
Dersalazine
Dersalazine Free Base |
IL Receptor; Platelet aggregation | Immunology/Inflammation; Others |
Dersalazine (Dersalazine Free Base) 是血小板活化因子抑制剂,通过下调 IL-17表达,在不同啮齿动物型结肠炎中发挥肠道抗炎活性,对溃疡性结肠炎患者具有潜在疗效。 | |||
T6923 |
Ozanimod
奥扎莫德,RPC-1063 |
S1P Receptor; LPL Receptor | GPCR/G Protein |
Ozanimod (RPC-1063) 是一种选择性S1P1和S1P5受体激动剂,在[35S]-GTPγS 结合实验中,EC50分别为 410 pM 和 11 nM。它可研究治疗克罗恩病、溃疡性结肠炎、多发性硬化症和复发性多发性硬化症的试验。 | |||
T10208 |
A-69412
N-1-(Fur-3-ylethyl)-N-hydroxyurea |
Lipoxygenase | Metabolism |
A-69412 (N-1-(Fur-3-ylethyl)-N-hydroxyurea) 是一种特异性的 5-脂氧合酶 (5-LO) 的可逆抑制剂。 A-69412 能用于哮喘和溃疡性结肠炎,以及其他炎症和过敏症状的研究。 | |||
T77404 |
Tesnatilimab
IPH-23XX,JNJ-64304500,JNJ 4500 |
Others | Others |
Tesnatilimab 是一种有效的人源化 IgG4 单克隆抗体,可与免疫激活受体 NKG2D 结合。Tesnatilimab 具有潜在的免疫调节和抗炎活性,可用于研究活动性溃疡性结肠炎 。 | |||
T76741 |
Eldelumab
BMS-936557,MDX-1100 |
CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation |
Eldelumab (BMS-936557) 是一种人源化抗 IP-10 IgG 1型单克隆抗体,对 CXCL10 具有抑制作用。Eldelumab 具有抗炎活性,可与 CXCL10 结合,可用于研究类风湿性关节炎。 | |||
T67942 |
Antimicrobial agent-21
|
MAPK | MAPK |
Antimicrobial agent-21是一种有效的丝裂原活化蛋白激酶抑制剂 ,具有抗菌、抗炎和抗肿瘤活性,可用来治疗白内障,溃疡性结肠炎,脑膜炎和川崎氏病帕金森氏症。 | |||
T64334 |
Glycolithocholic acid, sodium salt
|
Others | Others |
Glycolithocholic acid, sodium salt 是 Glycolithocholic acid 的钠盐。Glycolithocholic acid 是一种甘氨酸结合的次级胆汁酸。Glycolithocholic acid 可用于诊断溃疡性结肠炎 (UC),非酒精性脂肪性肝炎 (NASH0) 和原发性硬化性胆管炎 (PSC)。 | |||
T77666 |
MoTPS1-IN-1
|
Antifungal | Microbiology/Virology |
MoTPS1-IN-1(Compound j11),一种MoTPS1抑制剂,可作为抗真菌剂。该化合物通过与MoTPS1的Glu396相互作用发挥抑制作用,进而抑制M. oryzae的致病性。 | |||
T60657 | (R)-STU104 | TNF; MAPK | Apoptosis; MAPK |
(R)-STU104 是一种新型 TAK1-MKK3 蛋白-蛋白相互作用 (PPI)抑制剂,抑制 TNF-α,通过与 MKK3 结合并破坏TAK1磷酸化MKK3来抑制TAK1/MKK3/p38/MnK1/MK2/elF4E信号通路。(R)-STU104 是治疗溃疡性结肠炎的候选化合物。 | |||
T5095 |
Oxazolone
4-乙氧基亚甲基-2-苯基-2-唑啉-5-酮,4-Ethoxymethylene-2-phenyl-2-oxazolin-5-one |
Others | Others |
Oxazolone 已被用作半抗原化剂,可在成年斑马鱼肠道组织中诱导炎症反应,并可用作两种形式的炎症性肠病(如克罗恩病和溃疡性结肠炎)的基因表达研究模型。 | |||
T4615 |
Balsalazide sodium hydrate
巴柳氮钠水合物,Balsalazide disodium dihydrate,巴柳氮钠,Balsalazide disodium salt dihydrate,Balsalazide disodium |
STAT; Interleukin | Immunology/Inflammation; JAK/STAT signaling; Stem Cells |
Balsalazide sodium hydrate (Balsalazide disodium) 可通过调节IL-6/STAT3通路起抑癌作用,可用于治疗炎症性肠病。 | |||
T0346L |
Camylofin Hydrochloride
Camylofin HCl,Acamylophenine hydrochloride,Acamylophenine HCl,Belosin,Avocan |
||
Camylofin HCl is an antispasmodic used in labor treatment and is also used to deliver drug therapy for ulcerative colinitis. | |||
T15211 | Elucaine | Others | Others |
Elucaine is an antagonist of the muscarinic acetylcholine receptor. It has anti-ulcerative activity. | |||
T27150 |
Dersalazine sodium
UR12746,Dersalazine,UR 12746S (sodium salt),UR-12746S (sodium salt),UR-12746 |
||
Dersalazine, a PAF antagonist and TNFα inhibitor, is used potentially for the treatment of ulcerative colitis. It showed anti-inflammatory effect in reactivated colitis in rats, as evidenced by a significant reduction in MPO activity. | |||
T29013 |
HE 3286
Triolex,HE-3286,HE3286 |
||
Triolex, an NF-kB inhibitor, is used potentially for the treatment of rheumatoid arthritis, ulcerative colitis. | |||
T27142 |
Delmitide
Rationally Designed Peptide-58,RDP-1258,RDP5,Allotrap-1258,RDP1258,RDP-5 |
||
Delmitide, a TNF-alpha production inhibitor, is used potentially for the treatment of Crohn's disease and ulcerative colitis. | |||
T34126 | Prednisolone sodium metazoate | ||
Prednisolone sodium metazoate is used in the treatment of Inflammatory Bowel Disease, Ulcerative Colitis, and GI Disorders. | |||
T27077 |
CPUY192018 Disodium
CPUY-192018,CPUY192018,CPUY192018disodium,CPUY192018 Na2,CPUY192018-disodium |
||
CPUY192018 Disodium is a potent inhibitor of the Keap1-Nrf2 PPI. The inhibition of the Keap1-Nrf2 PPI may be beneficial as a treatment for ulcerative colitis. | |||
T68891 | Rivanicline galactarate | ||
Rivanicline galactarate is a Nicotinic Receptor Agonist that may be useful in the treatment of Ulcerative Colitis. | |||
T76906 | Anrukinzumab | ||
Anrukinzumab (IMA-638),一种针对人IL-13的人源化单克隆抗体,展示了在食蟹猕猴肺部炎症模型中显著的疗效。Anrukinzumab 目前被用于溃疡性结肠炎(UC)和哮喘的研究中。 | |||
T62363 |
Salazopyridazine
|
||
Salazopyridazine 是一种抗菌剂,可以抑制溃疡性结肠炎。Salazopyridazine 能够用于研究风湿病。 | |||
T76839 | Visilizumab | ||
Visilizumab (Anti-HumanCD3ERecombinant Antibody) 是一种人源化低 Fc 受体结合抗 CD3单克隆 IgG2抗体。Visilizumab 可用于溃疡性结肠炎和克罗恩病的研究。 | |||
T77088 | Mirikizumab | ||
Mirikizumab (LY3074828),一种靶向白介素23的p19亚基的人源化IgG4单克隆抗体,适用于溃疡性结肠炎的研究。 | |||
T82231 | hCES2-IN-1 | ||
hCES2-IN-1(Compound 24)是一种选择性的hCES2可逆抑制剂,其IC50值为6.72 μM。该化合物能够减少活细胞中hCES2的表达量,并且能有效抵抗由Irinotecan引起的迟发性腹泻以及DSS诱发的溃疡性结肠炎。 | |||
T63284 |
PAD-IN-2
|
||
PAD-IN-2 是 pad4 的有效抑制剂,IC50 值 <1 μM,能够用于研究自身免疫性疾病和癌症,如类风湿性关节炎、血管炎、系统性红斑狼疮、皮肤红斑狼疮、囊性纤维化、溃疡性结肠炎、哮喘、多发性硬化和牛皮癣。 | |||
T72406 | Tofacitinib Prodrug-1 | ||
Tofacitinib Prodrug-1 是减轻托法替尼 (Tofacitinib) 全身性不良反应的口服有效前药。Tofacitinib Prodrug-1 能在小鼠模型有效减轻恶唑酮诱导的结肠炎,具有低毒性,是治疗溃疡性结肠炎的潜在候选药物。 | |||
T77082 | Melredableukin alfa | ||
Melredableukin alfa (RO-7049665)是一种由人IgG1-κ通过多肽连接子与人突变白细胞介素2(IL2 mutin)融合形成的融合蛋白。它适用于乙型肝炎和溃疡性结肠炎的研究。 | |||
T78508 |
Delmitide acetate
RDP-58 acetate |
IFNAR | Immunology/Inflammation |
Delmitide acetate (RDP58) 是一种 d-异构体十肽,具有抗炎活性和口服活性。该化合物能够抑制 TNF-α、IFN-γ 以及白细胞介素 (IL)-12 的生成,同时提高血红素加氧酶 1 的活性,可用于针对溃疡性结肠炎的研究。 | |||
T76872 | Neihulizumab | ||
Neihulizumab (ALTB-168) 是一种免疫检查点激动性抗体,可与人 CD162 (PSGL-1)结合,导致活化的 T 细胞下调。Neihulizumab 可用于类固醇难治性急性移植物抗宿主病 (SR-aGVHD)、银屑病、银屑病关节炎和溃疡性结肠炎的研究。 | |||
T72536 |
GPR84 antagonist 2
|
||
GPR84antagonist 2 是一种口服有效的,选择性的 GPR84拮抗剂(IC50=8.95 nM)。GPR84antagonist 2 在钙动员试验中显示出更强的效力,并在 GPR84激活时抑制中性粒细胞和巨噬细胞的趋化性。GPR84antagonist 2 具有研究溃疡性结肠炎的潜力。 | |||
T63423 | AFM-30a hydrochloride | ||
AFM-30a hydrochloride 是一种有效的、高度选择性的蛋白质精氨酸脱亚胺酶 2(PAD2) 抑制剂。AFM-30a hydrochloride 能够与 PAD2 结合 (EC50: 9.5 μM),也能够抑制 H3 瓜氨酸化 (EC50: 0.4 μM)。AFM-30a hydrochloride 能够用于研究某些癌症和多种自身免疫性疾病如类风湿性关节炎 (RA)、多发性硬化症、狼疮和溃疡性结肠炎。 | |||
T71293 |
Nifuroxazide-d4
|
||
Nifuroxazide-d4 is intended for use as an internal standard for the quantification of nifuroxazide by GC- or LC-MS. Nifuroxazide is a nitrofuran antibiotic. It is active against strains of the enteropathogenic bacteria C. jejuni, Salmonella, Y. enterocolitica, Shigella, and E. coli. It inhibits quorum sensing and virulence factor production in P. aeruginosa. Nifuroxazide inhibits STAT3 activity in a reporter assay and decreases viability of U266 and INA-6 myeloma cells, which have constitutive S... | |||
T38052 | CRA-2059 TFA | ||
CRA-2059 is a highly specific and selective tryptase inhibitor, with a Ki of 620 pM for recombinant human tryptase-β (rHTβ)[1][2]. Tryptase is a trypsin-like serine protease found as a major protein component in human mast cell secretory granules. CRA-2059 has the potential for inflammatory bowel disease research[1]. [1]. Tremaine WJ, et al. Treatment of mildly to moderately active ulcerative colitis with a tryptase inhibitor (APC 2059): an open-label pilot study. Aliment Pharmacol Ther. 2002;16... | |||
T38051 | CRA-2059 hydrochloride | ||
CRA-2059 hydrochloride is a highly specific and selective tryptase inhibitor, with a Ki of 620 pM for recombinant human tryptase-β (rHTβ)[1][2]. Tryptase is a trypsin-like serine protease found as a major protein component in human mast cell secretory granules. CRA-2059 hydrochloride has the potential for inflammatory bowel disease research[1]. [1]. Tremaine WJ, et al. Treatment of mildly to moderately active ulcerative colitis with a tryptase inhibitor (APC 2059): an open-label pilot study. Ali... | |||
T36660 |
Olsalazine-13C6
Olsalazine-13C6 |
||
Olsalazine-13C6is intended for use as an internal standard for the quantification of olsalazine by GC- or LC-MS. Olsalazine is an orally bioavailable prodrug form of the anti-inflammatory agent 5-aminosalicylic acid that is cleaved by bacterial azo reductases in the gut to generate active 5-ASA.1In vitro, olsalazine increases ion transport in isolated rabbit distal ileum when applied to the luminal side (ED50= 0.3 mM) and stimulates fluid transport in rat jejunum when used at a concentration of ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2S0342 |
Armillarisin A
|
Others; Interleukin | Immunology/Inflammation; Others |
Armillarisin A 具有上调 IL-4和下调 IL-1β 的效果,对溃疡性结肠炎具有潜在的研究价值。 | |||
TN1084 |
1,3,5,8-Tetrahydroxyxanthone
Desmethylbellidifolin,去甲基雏叶龙胆酮 |
Anti-infection | Microbiology/Virology |
1,3,5,8-Tetrahydroxyxanthone (Desmethylbellidifolin) 是一种天然黄酮,从 Gentianella acuta 中提取得到。它具有镇痉作用和抗炎作用。 | |||
T2718 |
Palmatine chloride
|
Others; Indoleamine 2,3-Dioxygenase (IDO); Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Metabolism; Others |
Palmatine chloride 是口服具有活力的不可逆 IDO-1抑制剂。它能够减轻结肠损伤,预防肠道菌群失调和调节色氨酸分解代谢,并改善 DSS 诱发的结肠炎。 | |||
T5S0802 |
Palmatine
巴马汀,Berbericinine,Burasaine |
Indoleamine 2,3-Dioxygenase (IDO); AChR; AChE; Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Metabolism; Neuroscience |
Palmatine (Burasaine) 是口服具有活力的、不可逆IDO-1抑制剂。它可以减轻结肠损伤,预防肠道菌群失调和调节色氨酸分解代谢,从而改善DSS (Dextran Sulphate Sodium Salt) 诱发的结肠炎。它有用于结肠炎的研究潜力。 | |||
T31964 |
Glycolithocholic acid
Lithocholic acid glycine conjugate,甘氨石胆酸,Lithocholylglycine |
Others | Others |
Glycolithocholic acid (Lithocholic acid glycine conjugate) 属于内源性代谢产物,是甘氨酸结合的次级胆汁酸。它可用于诊断非酒精性脂肪性肝炎,溃疡性结肠炎和原发性硬化性胆管炎。 | |||
T2735 |
5-Acetylsalicylic acid
5-乙酰水杨酸(阿司匹林),5-acetyl-2-hydroxybenzoic acid |
Others | Others |
5-Acetylsalicylic acid (5-acetyl-2-hydroxybenzoic acid) 是炎症性肠病中的活性剂,具有抗炎活性。 | |||
T0036 |
18β-Glycyrrhetinic acid
Enoxolone,甘草次酸,18β-甘草次酸,Glycyrrhetin |
Dehydrogenase; Endogenous Metabolite | Metabolism |
18β-Glycyrrhetinic acid (Enoxolone) 是甘草的主要生物活性成分,具有抗炎,抗增殖和抗溃疡的特性。 | |||
T5S1177 |
Aloin B
Isobarbaloin,芦荟苷B,芦荟素B |
Others | Others |
Aloin B (Isobarbaloin) 是一种芦荟素的异构体。其中芦荟素是芦荟中的具生理活性蒽醌化合物。 | |||
T75433 | Norisoboldine hydrochloride | ||
Norisoboldine hydrochloride是一种口服活性天然芳基烃受体(AhR)激动剂,作为林参中的主要异喹啉类生物碱,适用于类风湿性关节炎和溃疡性结肠炎的研究。 | |||
T37770 |
Taurohyodeoxycholic acid
|
||
Taurohyodeoxycholic acid (THDCA) is a taurine-conjugated form of the secondary bile acid hyodeoxycholic acid .1THDCA decreases the size and weight of human gallstonesin vitro. It increases bile flow, biliary cholesterol secretion, and biliary lipid secretion in rats.2Co-administration of THDCA with taurochenodeoxycholic acid prevents TCDCA-induced hepatotoxicity, increasing bile flow as well as biliary acid and phospholipid secretion in rats.3THDCA also reduces myeloperoxidase activity, expressi... |