87
54
12
3
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP2315 |
glatiramer Acetate
|
Others | Others |
Glatiramer acetate 是髓鞘碱性蛋白的合成类似物和免疫调节剂,可用于多发性硬化症的研究。它能够诱导 T 辅助细胞 2 的特异性抑制细胞迁移到大脑并导致原位旁观者抑制。它能够于 MHC 分子强而杂乱的结合,因此与各种髓鞘抗原竞争,使其呈现给 T 细胞。 | |||
T6761 |
Ossirene
AS101 |
IL Receptor; Caspase; Interleukin | Apoptosis; Immunology/Inflammation; Proteases/Proteasome |
Ossirene (AS101) 是一种免疫调节抑制剂,是一种新型 IL-1beta 转化酶抑制剂,可用于自身免疫性疾病和某些恶性肿瘤。它通过抑制IL-10消除 STAT3 的磷酸化,有效抑制Caspase-1。 | |||
T22922 |
Lenalidomide hemihydrate
|
TNF; Ligand for E3 Ligase; Molecular Glues | Apoptosis; PROTAC |
Lenalidomide hemihydrate 是 Thalidomide 的衍生物,也是具有口服活性免疫调节剂,以分子胶的方式作用。它是泛素 E3 连接酶 cereblon 的配体,通过 CRBN-CRL4 泛素连接酶对两种淋巴转录因子 IKZF1 和 IKZF3 进行选择性泛素化和降解。 | |||
T0222 |
Proparacaine hydrochloride
盐酸丙美卡因,Proparacaine HCl,Proxymetacaine Hydrochloride |
Apoptosis; Sodium Channel | Apoptosis; Membrane transporter/Ion channel |
Proparacaine hydrochloride (Proparacaine HCl) 是 Lidocaine 的衍生物,具有糖皮质激素样活性和免疫调节作用。 | |||
T16240 |
N,N'-Diacetyl-L-cystine
(Ac-Cys-OH)2,DiNAC |
Others | Others |
N,N'-Diacetyl-L-cystine (DiNAC) 是一种具有免疫调节特性的 N-乙酰基半胱氨酸的二硫二聚体。它在高脂血症兔中也具有抗动脉粥样硬化的作用。它是啮齿类动物中接触敏感/迟发型超敏反应的有效口服活性调节剂。 | |||
T6445 |
Cilomilast
SB-207499,西洛司特,Ariflo |
PDE | Metabolism |
Cilomilast (SB-207499) 是选择性的、口服具有活性的磷酸二酯酶 4 抑制剂。 它对 PDE4 的选择性高于 PDE1,PDE2,PDE3 和 PDE5 (IC50=74,65,>100,83 µM)。它具有抗炎和免疫调节功能,可用于研究哮喘和慢性阻塞性肺疾病。 | |||
T8799 |
(E/Z)-IT-603
IT603 |
Others; NF-κB | NF-κB; Others |
(E/Z)-IT-603 是一种c-Rel 抑制剂,其IC50=3 μM。它是 E-IT-603 和 Z-IT-603的混合物。它具有抗癌作用。它有望作为调节剂调节移植物抗宿主病和恶性病中的 T 细胞反应。 | |||
T1642 |
Lenalidomide
来那度胺,CC-5013 |
Apoptosis; TNF; Ligand for E3 Ligase; Molecular Glues | Apoptosis; PROTAC |
Lenalidomide (CC-5013) 是 Thalidomide 的衍生物,也是具有口服活性免疫调节剂,以分子胶的方式作用。它是泛素 E3 连接酶 cereblon (CRBN) 的配体,可通过 CRBN-CRL4 泛素连接酶对两种淋巴转录因子 IKZF1 和 IKZF3 进行选择性泛素化和降解。 | |||
T3549 |
Avadomide
CC 122 |
Apoptosis; E1/E2/E3 Enzyme; Ligand for E3 Ligase | Apoptosis; PROTAC; Ubiquitination |
Avadomide (CC 122) 是口服有效的cereblon 调节剂,可以调节 cereblon E3 连接酶活性,诱导弥漫性大 B 细胞淋巴瘤细胞凋亡,具有抗肿瘤和免疫调节活性。 | |||
T2601 |
Vidofludimus
SC12267,4sc-101 |
Dehydrogenase; DNA/RNA Synthesis; Interleukin | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism |
Vidofludimus (SC12267) 是一种新型的二氢乳清酸脱氢酶 (DHODH) 小分子抑制剂,可在不影响淋巴细胞增殖的条件下抑制IL-17的分泌。 | |||
T0459 |
Sulindac
Arthrocine,MK-231,舒林酸,Clinoril,Sulindac sulfoxide |
COX; Autophagy | Autophagy; Immunology/Inflammation; Neuroscience |
Sulindac (Sulindac sulfoxide) 是一种非甾体类抗炎剂,可抑制COX-2的活性,也可抑制 COX-2 的过表达。它是一种亚磺酰基茚衍生物前药,具有潜在的抗肿瘤活性。 | |||
T9083 |
TC11
CLT-003,1H-Isoindole-1,3(2H)-dione, 5-amino-2-[2,6-bis(1-methylethyl)phenyl]-TC11 |
BCL; Caspase; CDK | Apoptosis; Cell Cycle/Checkpoint; Proteases/Proteasome |
TC11 (1H-Isoindole-1,3(2H)-dione, 5-amino-2-[2,6-bis(1-methylethyl)phenyl]-TC11) 是一种有效的肿瘤细胞增殖抑制剂,并通过激活 caspase-3、8 和 9 诱导细胞凋亡。在长时间有丝分裂阻滞期间,它诱导 MCL1降解导致凋亡。它作为苯酞酰亚胺衍生物在结构上与免疫调节药物相关。 | |||
T4543 |
Telithromycin
HMR3647,泰利霉素,Ketek,RU66647 |
Antibacterial; Antibiotic | Microbiology/Virology |
Telithromycin (HMR3647) 是一种社区获得性肺炎抗生素。 | |||
T0013 |
Mecarbinate
优多降,Dimecarbine,Dimecarbin,美卡比酯 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Mecarbinate 是一种吲哚衍生物,具有抗 HCV 活性和免疫调节作用。 | |||
T25146 |
Bestim
|
Others | Others |
Bestim 是一种合成的免疫调节二肽。 | |||
T20025 |
Imipramine
HSDB 3100,Melipramine,HSDB3100,Dimipressin,HSDB-3100 |
Apoptosis | Apoptosis |
Imipramine (Dimipressin) 是一种具有口服活性的 Fascin1 抑制剂,具有抗抑郁和抗肿瘤活性。Imipramine 抑制 5-羟色胺转运体 (IC50:32 nM),诱导细胞凋亡,诱导 U-87MG 胶质瘤细胞自噬。Imipramine 具有神经保护和免疫调节活性,抑制TNBC细胞的侵袭和迁移,可用于研究乳腺癌和癫痫。 | |||
T1159 |
Leflunomide
SU101,RS-34821,HWA486,来氟米特 |
Others; Dehydrogenase; AhR | Immunology/Inflammation; Metabolism; Others |
Leflunomide (HWA486) 是嘧啶合成抑制剂,能够抑制二氢乳清酸脱氢酶,具有抗风湿的活性。 | |||
T25702 |
Levovirin
ICN-17261,ICN 17261,ICN17261,L-Ribavirin |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Levovirin (L-Ribavirin) 是利巴韦林的L-对映异构体,是一种鸟苷核苷类似物,具有免疫调节活性,可用于研究丙型肝炎病毒感染。 | |||
T15437 |
GSK3145095
|
RIP kinase | Apoptosis; NF-κB |
GSK3145095 是一种口服有效的 RIPK1 抑制剂,IC50 为 5 nM,具有潜在的免疫调节活性和抗肿瘤活性。 | |||
T13180 |
TOK-8801
|
Others | Others |
TOK-8801 是一种合成的二氢咪唑噻唑羧酰胺,具有免疫调节活性,通过去除 T 细胞消除抗体产生的刺激作用。 | |||
T61107 |
Tilomisole
Wy 18251 |
Others | Others |
Tilomisole (Wy 18251) 是一种可口服的苯并咪唑噻唑,具有抗炎活性和免疫调节活性。Tilomisole 可用于研究癌症和炎症。 | |||
T1813 |
VGX-1027
VGX1027,VGX 1027,GIT 27 |
IL Receptor; TNF; Interleukin | Apoptosis; Immunology/Inflammation |
VGX-1027 (GIT 27) 是一种口服有效的异恶唑化合物,靶向巨噬细胞,减少促炎性介质 TNF-α、IL-1β和 IL-10 的产生,具有免疫调节特性。它通过限制细胞因子介导的免疫炎症而具有抗糖尿病作用。 | |||
T12644L |
(S)-Thalidomide
(S)-(-)-Thalidomide |
Apoptosis | Apoptosis |
(S)-Thalidomide ((S)-(-)-Thalidomide) 是 Thalidomide 的 S 型异构体,具有免疫调节,抗炎,抗癌,抗血管生成活性和促凋亡活性,可用于研究麻风结节性红斑和骨髓瘤。 | |||
T9942 |
WAY-639418
|
HIV Protease; CCR | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
WAY-639418 具有潜在的抗炎和抗 HIV 活性,可用于研究 CCR5 介导的炎症和免疫调节性疾病。 | |||
T14078 |
AB928
|
Adenosine Receptor | GPCR/G Protein; Neuroscience |
AB928 是可口服的选择性腺苷受体(A2aR/A2bR)双拮抗剂,可减轻腺苷介导的免疫抑制,具有免疫调节和抗肿瘤活性。 | |||
T37076 |
Zabedosertib
BAY 1834845 |
IRAK | Immunology/Inflammation; NF-κB |
Zabedosertib (BAY 1834845) 是一种 IRAK4 抑制剂,具有免疫调节潜能。最新研究表明,Zabedosertib 可预防急性呼吸窘迫综合征 | |||
T16809 |
Rupintrivir
AG-7088,AG7088,Rupintrivirvr |
Virus Protease; Antiviral | Immunology/Inflammation; Microbiology/Virology |
Rupintrivirvr (AG7088) 是一种选择性鼻病毒 (HRV) 3C 半胱氨酸蛋白酶的拟肽抑制剂,具有抗病毒活性和免疫调节活性。Rupintrivirvr 抑制 EV71 和 EV-D68 复制,可用于研究病毒感染。 | |||
T1532 |
Pidotimod
|
Others; Antibacterial | Microbiology/Virology; Others |
Pidotimod 是一种具有免疫调节特性的合成二肽。它增加巨噬细胞活性和体液免疫功能。它可研究慢性支气管炎、慢性阻塞性肺疾病 、支气管扩张、慢性特发性荨麻疹等。 | |||
T9906 |
Ipilimumab
|
Others | Others |
Ipilimumab 是全人类单克隆抗体 IgG1κ,能够抗 CTLA-4。其中CTLA-4是一种由活化的 T 细胞产生的免疫抑制分子。 | |||
T27034 |
CL075
3M002,CL-075 |
NF-κB; TLR; MyD88 | Immunology/Inflammation; NF-κB |
CL075 (3M002) 是一种选择性TLR8 激动剂。CL075具有免疫调节活性,通过触发 MyD88 依赖性信号通路,激活 NF-κB 和 IRF7 引发炎症性细胞因子和 I 型干扰素 (IFN) 的产生。 | |||
T10389 |
Aspartyl-alanyl-diketopiperazine
DA-DKP |
Interleukin | Immunology/Inflammation |
Aspartyl-alanyl-diketopiperazine (DA-DKP) 是一种由人血白蛋白的 N 端裂解和环化产生的免疫调节分子,通过与 T 淋巴细胞无反应相关的分子途径调节炎症免疫反应。 | |||
T13219 |
TTA-Q6
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
TTA-Q6 是一种选择性 T 型 Ca2+ 通道拮抗剂,具有潜在的抗肿瘤和免疫调节活性,可抑制肿瘤细胞摄取细胞外钙离子,诱导细胞内钙缺乏和内质网(ER)应激,用于治疗神经系统疾病。 | |||
T68182L |
3-Hydroxykynurenamine Dihydrochloride
3-OH-Kynurenamine HCl,3-Hydroxykynurenamine HCl(99362-47-7 Free base) |
Others | Others |
3-Hydroxykynurenamine HCl (3-OH-Kynurenamine HCl) 是一种免疫调节生物胺,是氨基酸分解代谢的中间体,可诱导氧化损伤和促进细胞死亡。 | |||
T8932 |
GSK046
iBET-BD2 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
GSK046 (iBET-BD2) 是一种选择性和具有口服活性的 BET 蛋白 BD2溴结构域的抑制剂,对 BRD2 BD2、BRD3 BD2、BRD4 BD2 和 BRDT BD2的 IC50值为 264、98、49 和 214 nM,具有免疫调节活性。 | |||
T0213 |
Thalidomide
Thalomid,沙利度胺,Sedoval |
Apoptosis; TNF; Autophagy; Ligand for E3 Ligase; Molecular Glues | Apoptosis; Autophagy; PROTAC |
Thalidomide (Thalomid) 能够抑制 cereblon,即 cullin-4 E3 泛素连接酶复合物 CUL4-RBX1-DDB1 的一部分,Kd 值约为 250 nM,具有免疫调节、抗炎、抗肿瘤作用。它可以作为分子胶来增强底物。 | |||
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 。 | |||
T8550 |
NDMC101
|
Others; NF-κB; Proteasome | NF-κB; Others; Proteases/Proteasome; Ubiquitination |
NDMC101 是有效的破骨细胞形成抑制剂,通过下调 NFATc1 调控基因表达抑制破骨细胞分化。它与 DPP4底物相似,通过抑制DPP4抑制早期 T 细胞激活。它能够用于骨疾病的研究,如类风湿关节炎、滑膜炎等。 | |||
T21632 |
Myoseverin
|
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
Myoseverina 是多核肌管可逆分裂成单核片段的诱导剂,影响多种生长因子、免疫调节、细胞外基质重塑和应激反应基因的表达,与伤口愈合和组织再生相关通路的激活一致。 | |||
T76941 |
Carotuximab
DE-122,TRC105 |
TGF-beta/Smad; Immunology/Inflammation related | Immunology/Inflammation; Stem Cells |
Carotuximab(DE-122)是一种新型内胆苷抗体,具有强大的抗血管生成活性和抗炎活性。Carotuximab 可阻断内皮糖蛋白 (CD105) 及其下游 Smad 信号通路。Carotuximab 具有免疫调节和抗肿瘤作用,可预防高胆固醇血症和高血糖诱导的人内皮功能障碍。 | |||
T3614 |
Inosine pranobex
Groprinosin,Isoprinosine,异丙肌苷,Immunovir,Delimmun |
IL Receptor; HIV Protease | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
Inosine pranobex (Delimmun) 是一种免疫增强剂,它是一种广谱抗病毒剂,用于 HIV 感染。 | |||
T14922 |
Cefodizime
|
Antibacterial; Antibiotic | Microbiology/Virology |
Cefodizime 是一种新型头孢菌素抗生素,具有广泛的生物活性。Cefodizime 对肾脏没有毒性且具有良好的耐受性和免疫调节活性,具有抗菌活性,可用于研究呼吸系统和泌尿系统的严重感染。 | |||
T77401 |
Bavituximab
Anti-PS MAb 3G4 |
Others | Others |
Bavituximab (Anti-Human Phosphatidylserine Recombinant Antibody) 是一种针对磷脂酰丝氨酸 (PS) 的单克隆抗体,具有血管靶向和免疫调节特性,能够重新激活抗肿瘤免疫来抑制肿瘤生长。Bavituximab 具有抗癌活性,常联合Paclitaxel 和 Carboplatin 来研究非小细胞肺癌。 | |||
T11412 |
IPN60090
GLS1-IN-1 |
Others; transporter | Metabolism; Others |
IPN60090是一种新型、强效、口服生物利用度高的 肾型谷氨酰胺酶(GLS1)特异性抑制剂,对GLS1的IC50值为31 nM。IPN60090 具有潜在的抗癌和免疫刺激/免疫调节活性,可选择性地靶向、结合并抑制人谷氨酰胺酶,可用于研究 GLS1 介导的疾病。 | |||
T11449L |
Golotimod
Gamma-D-glutamyl-L-tryptophan,SCV 07 |
Antibiotic | Microbiology/Virology |
Golotimod (SCV 07) 是一种具有抗菌活性的二肽,具有免疫调节活性,能显著提高抗结核治疗的疗效,诱导胸腺和脾脏细胞增殖,调节巨噬细胞功能,抑制 STAT3 信号传导。Golotimod 可用于研究复发性生殖器单纯疱疹病毒 2 (HSV-2)感染和口腔黏膜炎。 | |||
T77499 |
MSU-42011
|
NOS; Retinoid Receptor; NO Synthase; PERK; Lipid | Apoptosis; Immunology/Inflammation; Metabolism |
MSU-42011 是一种具有口服活性的类视黄醇 X 受体 (RXR) 激动剂。MSU-42011 有效抑制iNOS,低SREBP 诱导和激活RXR 以及 p-ERK 蛋白水平的表达。MSU-42011在kras 驱动的肺癌小鼠模型中表现出抗肿瘤活性。MSU-42011可有效治疗临床前Krasdriven 肺癌且具有免疫调节活性。 | |||
T7310 |
Paquinimod
帕奎莫德,ABR 25757 |
Others | Others |
Paquinimod (ABR 25757) 是一种特异性的 S100A8/S100A9 抑制剂,具有口服活性。Paquinimod 具有免疫调节活性,可以用于治疗系统性红斑狼疮。 | |||
T26753 |
BC12-4
|
Others | Others |
BC12-4 is a novel potent inhibitor of IL-2 secretion, it has potent immunomodulatory activity. | |||
T26121 |
Rooperol
|
Others | Others |
Rooperol is a norlignan derivative with numerous biological activities including immunomodulatory, antitumor, antibacterial, anticonvulsant, and antioxidant activities. It is a novel p38α inhibitor. | |||
T26101 |
RM 06
RM06,RM-06 |
Others | Others |
RM 06 is an immunomodulatory agent containing a peptidyl-hypoxanthine structure. | |||
T34697 |
Splenopentin
Thymopoietin III pentapeptide (32-36),Splenin pentapeptide (32-36),Arg-lys-glu-val-tyr |
Others | Others |
Splenopentin (SP-5) is a synthetic immunomodulatory peptide that can reproduce the biological activity of TP and SP, respectively. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMS1743 |
Salvigenin
|
MAO; Autophagy; ROS Kinase | Autophagy; Metabolism; Neuroscience; Tyrosine Kinase/Adaptors |
Salvigenin 是从鼠尾草中发现的一种多酚类天然产物,具有神经保护、抗肿瘤、免疫调节和细胞毒作用。 | |||
T2598 |
Thymopentin
TP5,胸腺五肽 |
Estrogen/progestogen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Thymopentin (TP5) 是主要由胸腺皮质和髓质上皮细胞分泌的生物特性肽。它能促使自人类胚胎干细胞产生 T 细胞群。它是有效免疫调节剂,具有很短的血浆半衰期(30 秒)。 | |||
T8716 |
physalin F
酸浆苦味素F,酸浆苦素 F |
Apoptosis | Apoptosis |
Physalin F 是一种分泌型甾体,诱导人外周血单个核细胞凋亡,降低人 T 淋巴细胞 1 型病毒感染后的自发增殖和细胞因子的产生,具有强烈抗炎和免疫调节作用。 | |||
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。 | |||
T13808 |
p-Coumaric Acid Ethyl Ester
对香豆酸乙酯,Ethyl (E)-p-hydroxycinnamate,Ethyl trans-4-hydroxycinnamate |
Others; Drug Metabolite | Metabolism; Others |
p-Coumaric Acid Ethyl Ester (Ethyl (E)-p-hydroxycinnamate) 是 p-Coumaric acid 的乙酯形式。p-Coumaric Acid 是一种免疫抑制剂, 能够用于自身免疫性炎性疾病 (如类风湿关节炎) 的研究。 | |||
T2833 |
Dehydrocostus Lactone
Epiligulyl oxide,去氢木香内酯,(-)-Dehydrocostus lactone,去氢木香烃内酯 |
IκB/IKK | NF-κB |
Dehydrocostus Lactone ((-)-Dehydrocostus lactone) 是一种倍半萜内酯,从云木香中分离得到。 | |||
T3672 |
Nomilin
|
MAPK | MAPK |
Nomilin 是一种柠檬苦素类化合物,从柑桔类提取物中获得,是抗肥胖症和降糖药。 | |||
T0492 |
Dimethyl fumarate
富马酸二甲酯,DMF |
Reactive Oxygen Species; HIV Protease; Nrf2; Endogenous Metabolite; Autophagy | Autophagy; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome |
Dimethyl fumarate (DMF) 是具有口服活性且可透过血脑屏障的Nrf2激活剂,可诱导抗氧化剂基因表达上调。它是一种富马酸盐衍生物,可作抗炎和免疫调节剂,可研究多发性硬化症。 | |||
T3408 |
Syringin
Lilacin,Syringoside,eleutheroside-b,Methoxyconiferine,紫丁香苷 |
NOS; Autophagy | Autophagy; Immunology/Inflammation |
Syringin (eleutheroside-b) 是欧丁香中的一种苯丙素类天然产物,通过抑制自噬来防止压力超载引起的心肌肥厚,具有抗肿瘤、抗增殖、抗骨质疏松、免疫调节和血小板聚集抑制作用。 | |||
T5771 |
Hypocrellin A
|
Antibacterial; PKC; Parasite | Chromatin/Epigenetic; Cytoskeletal Signaling; Microbiology/Virology |
Hypocrellin A 是一种天然的PKC 抑制剂,具有光诱导的抗肿瘤、抗真菌和抗病毒活性,还对 MHC 限制性抗原呈递发挥免疫调节作用。 | |||
T3S0807 |
Berbamine
|
CaMK; NF-κB; Autophagy | Autophagy; Neuroscience; NF-κB |
Berbamine 是从黄柏中提取的一种天然产物,是钙通道阻滞剂,具有抗肿瘤、免疫调节和心血管作用。 | |||
T7054 |
N-Benzoyl-(2R,3S)-3-phenylisoserine
N-苯甲酰基-(2R,3S)-3-苯基异丝氨酸,taxol side chain |
Antiviral | Immunology/Inflammation |
N-Benzoyl-(2R,3S)-3-phenylisoserine (taxol side chain) 是一种制备用于研究结合位点位置的强效抗癌药物紫杉醇的中间体。 它显示出细胞毒性、抗病毒和免疫调节活性。 | |||
T1082 |
Benzyl isothiocyanate
Benzoylthiocarbimide,苄基异硫氰酸酯,异硫氰酸苯甲酯,Isothiocyanic Acid Benzoyl Ester |
Apoptosis; Antibacterial; Antibiotic | Apoptosis; Microbiology/Virology |
Benzyl isothiocyanate (Benzoylthiocarbimide) 是一种具有杀菌活性的天然异硫氰酸酯,最初存在于十字花科蔬菜中。 它显示出免疫调节、抗寄生虫、抗生素、抗氧化、抗动脉粥样硬化、抗血管生成、抗转移、抗癌化疗和化学预防活性。 | |||
T2788 |
Baccatin III
巴卡亭 Ⅲ,浆果赤霉素III,Baccatin Ⅲ |
Others | Others |
Baccatin III (Baccatin Ⅲ) 是一种分离自太平洋紫杉树和其近缘种中的天然产物,能够减少 MDSCs 积累并抑制其功能,延缓肿瘤发展进程。 | |||
T19882 |
Bryonolic acid
UNII-J7YR6A878I,20-epi-Bryonolic acid |
Apoptosis; Antioxidant; Calcium Channel | Apoptosis; Membrane transporter/Ion channel; Metabolism; oxidation-reduction |
Bryonolic acid (20-epi-Bryonolic acid) 是一种从 Sandoricum indicum 提取的三萜类化合物,具有免疫调节、抗炎,抗氧化和抗癌等活性,通过抑制Ca2+内流和调节Ca2+-CaMKII-CREB信号通路中的基因表达来避免PC12细胞免受NMDA诱导的细胞凋亡反应。 | |||
T73602 |
Phosphorylcholine
Phosphocholine |
Endogenous Metabolite | Metabolism |
Phosphorylcholine 广泛存在于生物界,是存在于真核生物膜中的磷脂,也存在于与真核生物相关联的共生菌或致病菌中。Phosphorylcholine 具有免疫调节特性,可用于研究动脉粥样硬化。 | |||
T4A2462 |
Telocinobufagin
Telobufotoxin,远华蟾蜍精,Telocinobufogenin |
Others | Others |
Telocinobufagin (Telobufotoxin) 是一种从蟾酥中分离提取获得的组份。 | |||
T5712 |
zerumbone
花薑酮,球姜酮 |
Antioxidant; HSV | Microbiology/Virology; oxidation-reduction |
Zerumbone 是从Zingiber zerumbetSmith 的根茎中分离的一种单环倍半萜烯,可有效抑制Epstein-Barr 病毒的激活,IC50为 0.14 mM,具有抗癌、抗炎、抗氧化和抗增殖的作用。 | |||
T0610 |
Piceatannol
白皮杉醇,trans-Piceatannol,Astringenin |
Apoptosis; Serine/threonin kinase; PKA; Syk; PKC; Autophagy | Angiogenesis; Apoptosis; Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism; Tyrosine Kinase/Adaptors |
Piceatannol (Astringenin) 是一种Syk 抑制剂,可降低由 TNF 诱导的 iNOS 表达,可研究急性肺损伤。它是存在于各种水果和蔬菜中天然存在的多酚二苯乙烯,可诱导细胞自噬和凋亡,具有抗癌和抗炎特性。 | |||
T3028 |
Tripterin
Celastrol,Tripterine,雷公藤红素 |
Apoptosis; Mitophagy; Proteasome; Autophagy | Apoptosis; Autophagy; Proteases/Proteasome; Ubiquitination |
Tripterin (Celastrol) 属于天然产物,是一种蛋白酶体抑制剂,抑制 20S 蛋白酶体的胰凝乳蛋白酶样活性 (IC50=2.5 μM)。Tripterin 具有抗炎、抗感染和免疫调节的作用。 | |||
TN1088 |
3,5,6,7,8,3',4'-Heptemthoxyflavone
3,3',4',5,6,7,8-heptamethoxyflavone,3,5,6,7,8,3',4'-七甲氧基黄酮 |
Others | Others |
3,5,6,7,8,3',4'-Heptemthoxyflavone 是来自蜜柑皮中的黄酮,具有抗肿瘤起始活性和抗神经炎症作用。它能通过 cAMP/ERK/CREB 信号诱导脑源性神经营养因子表达,降低 C6 细胞磷酸二酯酶活性。它能抑制胶原酶的活性,增加人真皮成纤维细胞新生细胞中 I 型前胶原含量。 | |||
T2768 |
Saikosaponin A
柴胡皂苷A,柴胡皂苷 A |
NF-κB; Antibacterial; Liver X Receptor | Metabolism; Microbiology/Virology; NF-κB |
Saikosaponin A 是银柴胡中的主要活性成分,有抗炎活性,可上调 LXRα的表达。 | |||
T1257 |
Bestatin
Ubenimex,乌苯美司 |
Others; Aminopeptidase; Antibacterial; Antibiotic; LTR | Immunology/Inflammation; Metabolism; Microbiology/Virology; Others |
Bestatin (Ubenimex) 是 CD13 (Aminopeptidase N)/APN 和 leukotriene A4 hydrolase 抑制剂,可用于癌症研究。 | |||
T64744 |
Ovalbumins
|
Endogenous Metabolite | Metabolism |
Ovalbumins 是蛋清中的主要蛋白质。Ovalbumins 具有多种生物活性,如降压、抗菌、抗癌、抗氧化和免疫调节活性。Ovalbumins 是雌激素或孕酮处理的输卵管中合成的丰富的蛋白质。Ovalbumins 通常用作研究激素控制该组织中基因表达的标志物。 | |||
T1611 |
Isotretinoin
13-cis-Retinoic acid,异维A酸 |
Retinoid Receptor; Endogenous Metabolite; Autophagy | Autophagy; Metabolism |
Isotretinoin (13-cis-Retinoic acid) 是一种天然存在的维甲酸,具有潜在的抗肿瘤活性。 它结合并激活核视黄酸受体 (RAR), 活化的 RARs 作为促进细胞分化和凋亡的转录因子。它是一种类维生素A 和维生素A 衍生物,用于治疗严重的痤疮和某些形式的皮肤、头颈癌。 | |||
T3123 |
Allicin
|
ERK; IL Receptor; Others; IκB/IKK; p38 MAPK; TNF; ROS; Caspase; Antifection | Apoptosis; Immunology/Inflammation; MAPK; Microbiology/Virology; NF-κB; Others; Proteases/Proteasome |
Allicin 具有抗氧化、杀菌、抗癌、抗炎活性,对肠上皮细胞具有抑制性免疫调节作用。 Allicin 能显着抑制胰岛素诱导的血管平滑肌细胞的增殖和迁移,这可能与抑制 ERK 信号通路的激活有关。 Allicin 有利于降低高胆固醇血症大鼠的血液胆固醇、甘油三酯水平和收缩压,它可能有益于影响动脉粥样硬化的两个危险因素——高脂血症和高血压。 | |||
T4S2326 |
Cornuside
7-Galloylsecologanol,7-O-Galloylsecologanol,山茱萸新苷,Comuside |
ERK; p38 MAPK; NF-κB; JNK | MAPK; NF-κB |
Cornuside (Comuside) 是从山茱萸的果实中分离出的环烯醚萜苷,可用于炎症疾病的研究和促进血液循环。 它通过下调 MAPK 和 NF-κB 信号通路抑制肥大细胞介导的过敏反应,用于炎性过敏性疾病中的潜能。 | |||
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。 | |||
T2S0843 |
Negletein
黄芩素-7-甲醚,7-O-Methylbaicalein,Baicalein-7-methylether |
IL Receptor; TNF; NOS; Interleukin | Apoptosis; Immunology/Inflammation |
Negletein (7-O-Methylbaicalein) 一种神经保护剂,可增强神经生长因子的作用并诱导 PC12 细胞中的神经突生长。它通过抑制TNF-α和IL-1β表现出抗炎活性,其 IC50值分别为 16.4 和 10.8 μM。它还具有抗菌、抗缺氧和抗阿尔茨海默病活性。 | |||
T2961 |
Notoginsenoside R1
Sanqi glucoside R1,Sanchinoside R1,三七皂苷R1 |
Apoptosis; ERK; Beta Amyloid | Apoptosis; MAPK; Neuroscience |
Notoginsenoside R1 (Sanchinoside R1) 属于皂苷类天然产物,是三七的主要活性单体。Notoginsenoside R1 具有心血管保护、神经保护、肝脏保护、抗肿瘤、免疫调节等活性。 | |||
TMA2008 |
3-Hydroxy-1,5-diphenyl-1-pentanone
|
||
(+)-3-Hydroxy-1,5-diphenyl-1-pentanone exhibits both immunomodulatory and anti-tumor activity. | |||
TN3537 |
Braylin
|
IL Receptor; TNF; NF-κB | Apoptosis; Immunology/Inflammation; NF-κB |
Braylin has anti-inflammatory, antinociceptive and immunomodulatory effects, which possibly act through the glucocorticoid receptor activation and by inhibition of the transcriptional activity of NF-κB. Braylin is also a phosphodiesterase-4 inhibitor, it could represent an ideal prototype of glucocorticoid receptor ligand, able to induce synergic immunomodulatory effects. | |||
TN6510 |
Cordifolioside A
|
||
Cordifolioside A possesses immunomodulatory activity, it has a potential in vivo radioprotective effect as well as in vitro cytoprotective activity. | |||
TN5653 |
Cnidioside B methyl ester
|
||
Cnidioside B exerts little immunomodulatory effect in RAW 264.7 cells. | |||
TN4951 |
Sarracine
|
Others | Others |
Sarracine and neosarracine show immunomodulatory activities. | |||
T12789 |
S-1-Propenyl-L-cysteine
|
Others | Others |
S-1-Propenyl-L-cysteine, a stereoisomer of S-allyl-l-cysteine, exhibits immunomodulatory effects and has been shown to decrease blood pressure in hypertensive animal models. | |||
TN4506 |
(+)-Matairesinol
|
Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
(+)-Matairesinol exhibits immunomodulatory activity; it also shows inhibition of the discoloration of yellowtail dark muscle. | |||
TN2911 |
3,9-Dihydroeucomin
|
IL Receptor | Immunology/Inflammation |
(+/-)-3,9-Dihydroeucomin has immunomodulatory effects, it shows inhibitory effects on PBMC proliferation activated by PHA with the IC(50) value of 19.4 microM. | |||
TN1549 |
Damnacanthal
丹宁卡 |
IL Receptor; Akt; Syk | Angiogenesis; Cytoskeletal Signaling; Immunology/Inflammation; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors |
Damnacanthal possesses anti-cancer, immunomodulatory, antinociceptive and anti-inflammatory actions, it can treat or prevent hepatocellular carcinoma through its inhibitory effects on the HGF/c-Met axis. | |||
TN4811 |
Plumieride
|
||
Plumieride has plant growth inhibiting properties, it shows strong fungitoxicity against some dermatophytes causing dermatomycosis to animals and human beings. Plumieride also has antioxidant , and immunomodulatory activities. | |||
TN6524 |
Irilone
|
||
Irilone has immunomodulatory, and α-amylase inhibitory activities, it exhibits the selective inhibition toward CYP3 A4 rather than other major human CYPs. Irilone exhibited prominent antioxidant activities with the IC50 value of 10.46μM. Irilone potentiat | |||
TN1778 |
Isoformononetin
异刺芒柄花素,黄豆苷元杂质 |
IL Receptor; Antifection | Immunology/Inflammation; Microbiology/Virology |
Isoformononetin shows fungitoxic activity against Cladosporium sphaerospermum; it also has immunomodulatory activity, it inhibits the differentiation of Th17 cells and B-cell lymphopoesis to promote osteogenesis in estrogen-deficient bone loss conditions. | |||
TN5880 |
Mesuol
|
||
Mesuol has antioxidant activity, it shows very high scavenging activity against DPPH radical; it also has immunomodulatory activity, can potentiate percentage neutrophil adhesion in neutrophil adhesion test in rats and phagocytosis in carbon clearance assay. Mesuol can suppress HIV-1 replication in Jurkat T cells, it inhibits TNFα-induced HIV-1-LTR transcriptional activity by targeting the nuclear factor-κB (NF-κB) pathway. | |||
T80939 |
Triptoquinone H
|
Others | Others |
Triptoquinone H是从雷公藤中提取的天然产物,显示出显著的细胞毒性、免疫调节作用和抗炎活性,适用于癌症和炎症疾病的研究。 | |||
T80019 |
17-Hydroxyneomatrine
|
Others | Others |
17-Hydroxyneomatrine 是一种从苦参 (Sophora flavescens) 提取的化合物,有效抑制人宫颈癌Hela细胞生长,并展现抗菌、抗过敏、抗肿瘤、抗心律失常、消肿、利尿、免疫调节等多种生物活性。 | |||
T75661 |
Thymopentin acetate
|
Others | Others |
Thymopentin acetate为胸腺皮质及髓质上皮细胞主要分泌的生物活性肽,是一有效免疫调节剂,具有极短的血浆半衰期(30秒),能促进自人类胚胎干细胞生成T细胞群。 | |||
T75691 |
Amaroswerin
|
Others | Others |
Amaroswerin为从獐牙菜提取的硫环烯醚萜苷,显示出抗炎、抗糖尿病、抗病毒、抗胆碱能及免疫调节生物活性。在RAW264.7细胞模型中,Amaroswerin能够抑制NO的释放,其IC50值达到5.42 μg/mL。 | |||
TN3395 |
Alpinone 3-acetate
|
IFNAR | Immunology/Inflammation |
Alpinone 3-acetate 具有抗炎作用,可抑制12-O-tetradecanophenol 13-acetate 所致小鼠耳部水肿模型的炎症反应。Alpinone 3-acetate 是Alpinone 衍生物 。Alpinone 是一种具有活性的天然化合物,来源于向日葵,具有免疫调节和抗病毒活性 。 | |||
TN2775 |
2-Methoxystypandrone
|
MMP; BCL; IκB/IKK; GSK-3; TNF; NOS; NF-κB; Wnt/beta-catenin; COX; JAK; STAT | Angiogenesis; Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells |
2-Methoxystypandrone displays an immunomodulatory effect in a cellular model, it blocks inflammatory responses by impairing NF-κB signaling to limit the inflammation and oxidative stress for preservation of BBB integrity. 2-Methoxystypandrone concomitant | |||
TN2169 |
Saikogenin D
柴胡皂甙元 D,皂苷元 D |
IL Receptor; Calcium Channel; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism |
Saikogenin D possesses a dual effect: an inhibition of A23187-induced PGE2 production without a direct inhibition of cyclooxygenase activity; and an elevation of [Ca2+]i that is attributed to Ca2+ release from intracellular stores. Saikogenin D has immuno | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-00766 |
LZ-8 Protein, Ganoderma lucidum, Recombinant (His & Myc)
Immunomodulatory protein Ling Zhi-8 |
Ganoderma lucidum | E. coli |
LZ-8 Protein, Ganoderma lucidum, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 19.8 kDa and the accession number is P14945. | |||
TMPK-00172 |
B7-H4 Protein, Human, Recombinant (His & Avi)
B7H4,B7x,VTCN1,PRO1291,B7S1,B7h.5,FLJ22418,B7-H4 |
Human | HEK293 Cells |
B7-H4, also known as B7x and B7S1, is a 50-80 kDa glycosylated member of the B7 family of immunomodulatory proteins.B7-H4 is up-regulated in several carcinomas in correlation with tumor progression and metastasis. A soluble form of B7-H4 is elevated in the serum of ovarian cancer, renal cell carcinoma, and rheumatoid arthritis patients, also in correlation with advanced disease status . | |||
TMPK-00314 |
B7-H3 (4Ig) /B7-H3b Protein, Human, Recombinant (His & Avi)
B7-H3,PSEC0249,PRO352, 4Ig-B7-H3,B7 homolog 3,UNQ309,CD276 |
Human | HEK293 Cells |
B7-H3, a member of the B7 family of immunomodulatory molecules, is overexpressed in a wide range of solid cancers.B7-H3 binds to activated T cells via an as yet unidentified receptor. In assays using sub-optimal amount so anti-CD3 stimulation, 2Ig‑B7‑H3 enhances T cell proliferation, T cell interferon-gamma (IFN-gamma) production, and cytotoxic T cells induction. B7-H3 (4Ig) /B7-H3b Protein, Human, Recombinant (His & Avi) is expressed in HEK293 mammalian cells with C-His-Avi tag. The predicted m... | |||
TMPK-01017 |
B7-H3 Protein, Human, Recombinant (aa 29-245, hFc)
B7H3,B7-H3,B7 homolog 3,PSEC0249,CD276,PRO352, UNQ309 |
Human | HEK293 Cells |
B7-H3, a member of the B7 family of immunomodulatory molecules, is overexpressed in a wide range of solid cancers.B7-H3 binds to activated T cells via an as yet unidentified receptor. In assays using sub-optimal amount so anti-CD3 stimulation, 2Ig‑B7‑H3 enhances T cell proliferation, T cell interferon-gamma (IFN-gamma) production, and cytotoxic T cells induction. B7-H3 Protein, Human, Recombinant (aa 29-245, hFc) is expressed in HEK293 mammalian cells with C-hFc tag. The predicted molecular weig... | |||
TMPK-00889 |
IFNAR2 Protein, Human, Recombinant (aa 27-243, His)
IFN-alpha/beta R2,IFNAR2,IFNbR2,IFNABR,IFN α/β R2,IFNARB,IFN... |
Human | HEK293 Cells |
Although interferon (IFN)-α is known to exert immunomodulatory and antiproliferative effects on dendritic cells (DCs) through induction of protein-coding IFN-stimulated genes (ISGs), little is known about IFN-α-regulated miRNAs in DCs. Since several miRNAs are involved in regulating DC functions, it is important to investigate whether IFN-α's effects on DCs are mediated through miRNAs as well. IFNAR2 Protein, Human, Recombinant (aa 27-243, His) is expressed in HEK293 mammalian cells with C-His t... | |||
TMPK-01016 |
B7-H3 Protein, Human, Recombinant (hFc), FITC-Labeled
B7H3, UNQ309,PRO352,PSEC0249,B7 homolog 3,B7-H3,CD276 |
Human | HEK293 Cells |
B7-H3, a member of the B7 family of immunomodulatory molecules, is overexpressed in a wide range of solid cancers.B7-H3 binds to activated T cells via an as yet unidentified receptor. In assays using sub-optimal amount so anti-CD3 stimulation, 2Ig‑B7‑H3 enhances T cell proliferation, T cell interferon-gamma (IFN-gamma) production, and cytotoxic T cells induction. B7-H3 Protein, Human, Recombinant (hFc), FITC-Labeled is expressed in HEK293 mammalian cells with C-hFc tag. The predicted molecular w... | |||
TMPJ-01371 |
Limitin Protein, Mouse, Recombinant (His)
Ifnz,Lmtn,IFN-z,IFN-ζ,BGIF,interferon ζ,IFN-zeta,Limitin,int... |
Mouse | HEK293 Cells |
Limitin, also called IFN-ζ, is a secreted interferon (IFN)-like glycoprotein. Limitin has approximately 30% sequence homology with IFN-α, IFN-β, and IFN-ω and binds to the IFN-α/β receptors. Like IFN-α and IFN-β, limitin has antiproliferative, immunomodulatory, and antiviral properties, it is unique in lacking influence on myeloid and erythroid progenitors. Similar dose requirement between limitin and IFN-α was observed for the enhancement of cytotoxic T lymphocyte activity, the augmentation of ... | |||
TMPK-01018 |
B7-H3 Protein, Human, Recombinant (aa 29-245, His)
PRO352,B7H3, UNQ309,PSEC0249,CD276,B7-H3,B7 homolog 3 |
Human | HEK293 Cells |
B7-H3, a member of the B7 family of immunomodulatory molecules, is overexpressed in a wide range of solid cancers.B7-H3 binds to activated T cells via an as yet unidentified receptor. In assays using sub-optimal amount so anti-CD3 stimulation, 2Ig‑B7‑H3 enhances T cell proliferation, T cell interferon-gamma (IFN-gamma) production, and cytotoxic T cells induction. B7-H3 Protein, Human, Recombinant (aa 29-245, His) is expressed in HEK293 mammalian cells with C-His tag. The predicted molecular weig... | |||
TMPK-00315 |
B7-H3 (4Ig) /B7-H3b Protein, Human, Recombinant (His & Avi), Biotinylated
4Ig-B7-H3,CD276,UNQ309,B7-H3,PRO352,PSEC0249,B7 homolog 3 |
Human | HEK293 Cells |
B7-H3, a member of the B7 family of immunomodulatory molecules, is overexpressed in a wide range of solid cancers.B7-H3 binds to activated T cells via an as yet unidentified receptor. In assays using sub-optimal amount so anti-CD3 stimulation, 2Ig‑B7‑H3 enhances T cell proliferation, T cell interferon-gamma (IFN-gamma) production, and cytotoxic T cells induction. B7-H3 (4Ig) /B7-H3b Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian cells with C-His-Avi tag. T... | |||
TMPK-00637 |
IFNAR2 Protein, Cynomolgus, Recombinant (aa 27-243, His)
β receptor10,IFNbR2,IFN α/β R2,IFN-R,IFNAR2,β receptor 2,IFN... |
Cynomolgus | HEK293 Cells |
Although interferon (IFN)-α is known to exert immunomodulatory and antiproliferative effects on dendritic cells (DCs) through induction of protein-coding IFN-stimulated genes (ISGs), little is known about IFN-α-regulated miRNAs in DCs. Since several miRNAs are involved in regulating DC functions, it is important to investigate whether IFN-α's effects on DCs are mediated through miRNAs as well. IFNAR2 Protein, Cynomolgus, Recombinant (aa 27-243, His) is expressed in HEK293 mammalian cells with C-... | |||
TMPJ-00076 |
IL-28B Protein, Human, Recombinant
IL-28C,IFN-λ-4,IFNL4,Interferon λ-4,IL28B,IL-28B,Interleukin... |
Human | HEK293 Cells |
Interleukin-28B, also known as Cytokine Zcyto22, Interferon lambda-3, Interferon lambda-4, IFNL3, IFNL4, ZCYTO22 and IL28B, is a secreted cytokine which belongs to the IL-28/IL-29 family. IL-28 has also been shown to play a role in the adaptive immune response. IL28B has immunomodulatory activity and up-regulates MHC class I antigen expression. IL28B displays potent antiviral activity and antitumor activity. In addition, IL28B is a ligand for the heterodimeric class II cytokine receptor composed... | |||
TMPY-06983 |
IFN gamma Protein, Human, Recombinant (E. coli)
Interferon Gamma,IFN γ,IFN gamma,IFG,IFI,干扰素,Interferon γ |
Human | E. coli |
IFN gamma, also known as IFNG, is a secreted protein that belongs to the type II interferon family. IFN gamma is produced predominantly by natural killer and natural killer T cells as part of the innate immune response, and by CD4 and CD8 cytotoxic T lymphocyte effector T cells once antigen-specific immunity develops. IFN gamma has antiviral, immunoregulatory, and anti-tumor properties. IFNG, in addition to having antiviral activity, has important immunoregulatory functions, it is a potent activ... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T13141 |
Thalidomide D4
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Others | Others |
Thalidomide D4 is a deuterium labeled Thalidomide, has immunomodulatory, anti-inflammatory and anti-angiogenic cancer properties. | |||
TMID-0237 |
Leflunomide-d4
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Leflunomide-d4 是 Leflunomide 的氘代化合物。Leflunomide 的 CAS 号为 75706-12-6。Leflunomide 是嘧啶合成抑制剂,能够抑制二氢乳清酸脱氢酶,具有抗风湿的活性。 | |||
TMIJ-0361 |
Dimethyl Fumarate-2,3-d2
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Dimethyl Fumarate-2,3-d2 是 Dimethyl Fumarate 的氘代化合物。Dimethyl Fumarate 的 CAS 号为 624-49-7。Dimethyl fumarate 是具有口服活性且可透过血脑屏障的Nrf2激活剂,可诱导抗氧化剂基因表达上调。它是一种富马酸盐衍生物,可作抗炎和免疫调节剂,可研究多发性硬化症。 |