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Cat. No. | Product Name | ||
---|---|---|---|
L3800 | NF-κB 通路分子库 | 729 compounds | |
729 个 NF-κB 信号通路相关的小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L8500 | HIF-1化合物库 | 1336 compounds | |
1336 个HIF-1相关小分子的独特集合,可用于缺血性疾病、癌症等相关领域的药物开发和药理研究; | |||
L1310 | 细胞骨架化合物库 | 759 compounds | |
759 种细胞骨架相关的化合物,可以用于高通量和高内涵筛选; | |||
L2600 | 神经信号分子库 | 2540 compounds | |
2540 种CNS 相关的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L3700 | JAK-STAT 化合物库 | 252 compounds | |
252 个 JAK/STAT 靶点相关的小分子化合物的独特集合,用于高通量、高内涵筛选; | |||
L2200 | 酪氨酸激酶分子库 | 1016 compounds | |
1016 种酪氨酸激酶抑制剂的独特集合,可用于高通量筛选和高内涵筛选; | |||
L1580 | GPCR库Plus | 338 compounds | |
338 种GPCR 靶向、结构新颖的化合物; | |||
L1600 | 激酶抑制剂库 | 2720 compounds | |
2720 种激酶抑制剂/调节剂的独特集合,用于特定靶向激酶,可用于高通量筛选和高内涵筛选; | |||
L1500 | GPCR靶点分子库 | 1940 compounds | |
1940 种与 G 蛋白及其耦联受体相关的生物活性小分子化合物,所有小分子都具有良好的生物和药理活性,部分是 FDA 批准的上市药物; | |||
L4100 | TGF-β/Smad靶点化合物库 | 184 compounds | |
184 个 TGF-β/Smad 靶点相关的小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L7700 | 神经再生化合物库 | 524 compounds | |
524 种神经再生相关化合物的独特集合,可用于高通量筛选和高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T23355 |
Signal Enhancer Hikari
|
Others | Others |
Signal enhancer for use in western blotting, dot blotting and ELISA | |||
TP2291 |
signal transducer and activator of transcription 6 fragment
|
Others | Others |
The signal transducer and activator of transcription 6 fragments is a peptide with the sequence H2N-Ser-Tyr-Trp-Ser-Asp-Arg-Leu-Ile-Ile-OH, MW= 1152.3. | |||
T83727 |
Tat-NTS Peptide TFA
Tat-Nuclear Translocation Signal Peptide |
||
Tat-NTS肽是一种能穿透细胞的肽,由HIV-1 Tat蛋白的转导域与对应于脂联素A1重复III域残基228-237的10个氨基酸肽链接而成,扮演核转运信号(NTS)的角色。它通过阻断脂联素A1与进口素β之间的蛋白质-蛋白质相互作用,阻止脂联素A1在初级鼠海马神经元中的核内转运。Tat-NTS抑制初级鼠海马神经元在葡萄糖-氧剥夺及再灌注诱导的细胞凋亡。在体内,Tat-NTS(10 mg/kg)有效减少了由中脑动脉闭塞(MCAO)引起的缺血-再灌注损伤模型小鼠的梗塞体积和神经元凋亡,并缩短了在Morris水迷宫测试中达到平台的时间。 | |||
T5358 |
Longdaysin
|
ERK; Casein Kinase; CDK | Cell Cycle/Checkpoint; MAPK; Metabolism; Stem Cells |
Longdaysin 是一种 CK1α 和 CK1δ 的抑制剂,IC50为5.6和8.8 µM。它还抑制ERK2,IC50值为52 µM。它是Wnt/β-catenin 信号通路的抑制剂,通过阻断CK1δ/ε依赖性 Wnt 信号通路发挥抗肿瘤作用。 | |||
T10479 |
BAY885
|
ERK | MAPK |
BAY885 是选择性 ERK5抑制剂,IC50为 35 nM。 | |||
T6066 |
SCH772984
|
ERK; MEK | MAPK |
SCH772984 是高选择性和 ATP 竞争性ERK 抑制剂,对 ERK1 和 ERK2 的IC50分别为 4 和 1 nM。它在含有 BRAF 或 RAS 突变的 MAPK 抑制剂初治和 MAPK 抑制剂耐药细胞中具有抗肿瘤活性。 | |||
T5535 |
ERK5-IN-2
|
ERK | MAPK |
ERK5-IN-2 是具有口服活性,亚微摩尔效力,选择性ERK5抑制剂,对ERK5和ERK5 MEF2D 的IC50s 分别是 0.82 和 3 μM。它抑制肿瘤异种移植生长和碱性成纤维细胞生长因子驱动的基质胶塞血管生成。 | |||
TQ0005 |
KO-947
|
ERK | MAPK |
KO-947是选择性ERK1/2激酶抑制剂,具有潜在的抗肿瘤作用。 | |||
T14894 |
CC-90003
|
ERK | MAPK |
CC-90003 是不可逆选择性ERK 1/2抑制剂,具有抗肿瘤活性。 | |||
T14360 |
AX-15836
|
ERK | MAPK |
AX-15836是一种选择性 ERK5抑制剂,IC50值为8 nM。 | |||
T1956 |
FR 180204
FR180204 |
Apoptosis; ERK | Apoptosis; MAPK |
FR 180204 是一种 ATP 竞争性的选择性ERK 抑制剂,对ERK1和ERK2的Ki 值分别为 0.31 μM 和 0.14 μM,IC50值分别为0.51 μM 和0.33 μM。 | |||
T4091 |
Temuterkib
LY3214996 |
ERK | MAPK |
Temuterkib (LY3214996) 是高效选择性的ERK1和ERK2抑制剂,IC50为 5 nM,具有潜在的抗肿瘤活性。 | |||
T6818 |
DEL-22379
DEL22379 |
Apoptosis; ERK | Apoptosis; MAPK |
DEL-22379 是一种水溶性 ERK 二聚化抑制剂,IC50约为 0.5 μM。 | |||
T5184 |
ERK5-IN-1
|
ERK | MAPK |
ERK5-IN-1 是 ERK5抑制剂,IC50为 87 nM。它也抑制 LRRK2[G2019S],IC50为 26 nM。 | |||
T6511 |
Ravoxertinib
GDC-0994 |
ERK | MAPK |
Ravoxertinib (GDC-0994) 是可口服的ERK 激酶抑制剂,抑制ERK1和ERK2的IC50分别为 6.1 和 3.1 nM。 | |||
T10429 |
Tizaterkib
AZD-0364 |
ERK | MAPK |
Tizaterkib (AZD-0364) 是一种选择性ERK2抑制剂,IC50为 0.6 nM。 | |||
T41287 |
N-3-Oxo-octanoyl-L-homoserine lactone
|
Others | Others |
N-3-Oxo-octanoyl-L-homoserine lactone 是一种群体感应信号分子,是农杆菌自诱导剂。 | |||
T36674 |
DMU-212
|
Apoptosis; ERK | Apoptosis; MAPK |
DMU-212 是具有口服活性的白藜芦醇的甲基化衍生物,表现出抗分裂、抗增殖、抗氧化和促进细胞凋亡的活性。它通过诱导凋亡和激活ERK1/2蛋白阻止有丝分裂。 | |||
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。 | |||
T11224 |
Rineterkib
ERK-IN-1 |
ERK; Raf | MAPK |
Rineterkib (ERK-IN-1) 是口服有效的RAF 和ERK1/2的抑制剂,与 KRAS-突变型非小细胞肺癌、BRAF-突变型非小细胞肺癌、KRAS-突变型胰腺癌、KRAS -突变型结肠癌和 KRAS-突变型卵巢癌尤为相关。 | |||
T6948 |
Pluripotin
SC1 |
ERK; Raf; S6 Kinase | MAPK; PI3K/Akt/mTOR signaling |
Pluripotin (SC1) 是ERK1和RasGAP 的双重抑制剂,KD 分别为 98 和 212 nM。它还抑制RSK1、RSK2、RSK3和RSK4,IC50分别为 0.5、2.5、3.3 和 10.0 μM。 | |||
T12069 |
MK-8353
SCH900353 |
ERK | MAPK |
MK-8353 (SCH900353) 是口服有效的ERK1/2选择性抑制剂,IC50分别为 23.0 nM 和 8.8 nM。它显示出抗肿瘤活性。 | |||
T1843 |
XMD8-92
|
ERK; BMI-1; Epigenetic Reader Domain | Cell Cycle/Checkpoint; Chromatin/Epigenetic; DNA Damage/DNA Repair; MAPK |
XMD8-92 是 ERK5 (BMK1)/BRD4的有效抑制剂,Kd 分别为80和190 nM。它抑制 DCAMKL2、PLK4 和 TNK1的 Kd 分别为190、600和890nm,具有抗癌活性。 | |||
T21295 |
BIX02189
BIX 02189 |
ERK; MEK | MAPK |
BIX02189 是一种有效的选择性 MEK5 和 ERK5 抑制剂,IC50分别为 1.5 和 59 nM。 | |||
T2029 |
Bohemine
|
ERK; CDK | Cell Cycle/Checkpoint; MAPK |
Bohemine 是一种合成的选择性CDK 抑制剂,是嘌呤类似物,具有抗癌活性。它对Cdk2/cyclin E、Cdk2/cyclin A 和Cdk9/cyclin T1的IC50分别为 4.6 μM、83 μM 和 2.7 μM。 | |||
T7506 |
Yoda 1
|
Piezo Channel | Membrane transporter/Ion channel |
Yoda 1 是Piezo1激动剂,能够激活纯化的 Piezo1 通道。 | |||
T4496 |
LM22B-10
LM22B10 |
ERK; Trk receptor; Akt | Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors |
LM22B-10 是TrkB/TrkC 神经营养因子受体激活剂,诱导体内外TrkB、TrkC、AKT 和ERK 的活化。 | |||
T1842 |
XMD17-109
XMD17 109,ERK5-IN-1 |
ERK | MAPK |
XMD17-109 (ERK5-IN-1) 是一种特异性的ERK-5抑制剂,在 HEK293 细胞系中的EC50为 4.2 μM。 | |||
T2623 |
PD98059
PD 98059 |
ERK; Aryl Hydrocarbon Receptor; MEK; Autophagy | Autophagy; Immunology/Inflammation; MAPK |
PD98059 是一种 MEK 抑制剂,抑制 MEK1 和 MEK2 (IC50=2/50 μM),具有非 ATP 竞争性。PD98059 也是一种 AHR 的配体而起拮抗作用。PD98059 可以抑制细胞自噬。 | |||
T9141 |
ERK-IN-3
ASN007 free base |
ERK | MAPK |
ERK-IN-3 (ASN007 free base) 是一种有效的口服活性 ERK 抑制剂,以低 IC50 值抑制 ERK1/2,可用于研究由 RAS 突变驱动的癌症。 | |||
T5364 |
TBHQ
tert-Butylhydroquinone,特丁基对苯二酚,叔丁基氢醌 |
Apoptosis; ERK; Others; Ferroptosis; Nrf2; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; MAPK; Others |
TBHQ (tert-Butylhydroquinone) 是一种抗氧化剂,可通过对氧化还原敏感的转录因子 Nrf2 诱导抗氧化反应。它也是一种ERK 激活剂,逆转 Dehydrocorydaline 对黑素瘤细胞增殖的抑制作用。 | |||
T7123 |
AMG-47a
|
VEGFR; p38 MAPK; JAK; Src | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; MAPK; Stem Cells; Tyrosine Kinase/Adaptors |
AMG-47a 是具有口服活性的 Lck 抑制剂,IC50值为 0.2 nM。它具有抗炎作用,对 VEGF2、p38α、p38α、Jak3、MLR 和 IL-2的 IC50值分别为 1、3、72、30 和 21 nM。 | |||
T3166 |
VX-11e
Vertex-11e,VTX-11e,TCS ERK 11e |
ERK; GSK-3; FLT; CDK; Aurora Kinase | Angiogenesis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; MAPK; PI3K/Akt/mTOR signaling; Stem Cells; Tyrosine Kinase/Adaptors |
VX-11e (TCS ERK 11e) 是可口服的ERK 高效选择性抑制剂,Ki 值小于 2 nM。 | |||
T8472 |
ERK1/2 inhibitor 2
ASTX-029,ASTX029 |
ERK | MAPK |
ERK1/2 inhibitor 2 (ASTX029) 是一种选择性和可口服的细胞外信号调节激酶 1 和 2 (ERK 1/2) 抑制剂,具有潜在的抗肿瘤活性。 | |||
T9988 |
Wnt/β-catenin agonist 3
|
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
Wnt/β-catenin agonist 3是一种Wnt/beta-catenin 信号通路激动剂。 | |||
T7005 |
Ulixertinib
BVD-523,VRT752271,优立替尼 |
ERK | MAPK |
Ulixertinib (VRT752271) 是一种有效且可逆的 ERK1/ERK2 抑制剂,可抑制 ERK2 和下游蛋白 RSK 的磷酸化,对 ERK2 的IC50值小于 0.3 nM。 | |||
T27242 |
EF24
EF 24,EF-24,3,5-Bis[(2-fluorophenyl)Methylene]-4-piperidinone |
ERK; MEK; Caspase | Apoptosis; MAPK; Proteases/Proteasome |
EF24 (3,5-Bis[(2-fluorophenyl)Methylene]-4-piperidinone) 是姜黄素类似物,口服生物利用度高,抗肿瘤作用强。它可增强活化的 Caspase3 及 Caspase9 的水平,并抑制 MEK1 及 ERK 的磷酸化形式的表达。它可以抑制口腔鳞状细胞癌细胞的 MAPK/ERK 信号通路,从而发挥抗肿瘤作用。 | |||
T0097 |
MRT67307
MRT67307 HCl |
IκB/IKK; Autophagy | Autophagy; NF-κB |
MRT67307 是一种IKKε和TBK-1的双抑制剂,IC50分别为 160 和 19 nM。它抑制细胞自噬,也可抑制ULK1和ULK2,IC50分别为 45 和 38 nM。 | |||
T1144L |
Lidocaine Hydrochloride hydrate
|
EGFR; Sodium Channel | Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors |
Lidocaine Hydrochloride hydrate 是一种酰胺类局部麻醉剂,具有抗炎作用。 | |||
T4092 |
AG126
Tyrphostin AG126,AG 126 |
ERK; COX | Immunology/Inflammation; MAPK; Neuroscience |
AG126 (Tyrphostin AG126) 是一种酪氨酸激酶抑制剂,可阻止丝裂原活化蛋白激酶 p42MAPK(ERK2) 的激活。 | |||
T2171 |
SEW2871
SEW2871 |
S1P Receptor; LPL Receptor | GPCR/G Protein |
SEW 2871 是一种可口服的高选择性 S1P1激动剂,EC50为 13.8 nM。它减少血液中的淋巴细胞数量,可用于糖尿病、阿尔茨海默氏病、肝纤维化和炎症相关研究。它激活 ERK、Akt 和 Rac 信号通路,并诱导 S1P1 内在化和再循环。 | |||
T9776 |
TRPM4 inhibitor 8
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
TRPM4 inhibitor 8 是瞬态受体电位 melastatin 4 (TRPM4) 的抑制剂,它有助于活力、迁移、细胞周期转变和粘附。 | |||
T0468 |
Lidocaine
Lignocaine,Alphacaine,Xylocaine,利多卡因 |
Apoptosis; ERK; NF-κB; MEK; Sodium Channel; Histamine Receptor | Apoptosis; GPCR/G Protein; Immunology/Inflammation; MAPK; Membrane transporter/Ion channel; Neuroscience; NF-κB |
Lidocaine (Alphacaine) 是一种酰胺衍生物,抑制涉及复杂电压和依赖性的钠通道,可用于研究室性心律失常。它通过调节 miR-145 表达和进一步抑制 MEK/ERK 和 NF-κB 信号通路来减少胃癌细胞的生长,迁移和侵袭。 | |||
T2036 |
6-OAU
GTPL5846 |
GPR | Endocrinology/Hormones; GPCR/G Protein |
6-OAU (GTPL5846) 是 GPR84 的替代激动剂,在 Gqi5 嵌合体存在的情况下,在 HEK293 细胞中激活人 GPR84,在 PI 测定中 EC50 为 105 nM。 | |||
T0304 |
Methylthiouracil
甲基硫脲嘧啶,甲硫氧嘧啶,NSC-193526,NSC-9378,MTU |
ERK; Antiviral; TNF; NF-κB; Interleukin | Apoptosis; Immunology/Inflammation; MAPK; NF-κB |
Methylthiouracil (NSC-193526) 是一种抗甲状腺剂。它抑制TNF-α和IL-6的产生以及NF-κB 和ERK1/2的活化。 | |||
T1144 |
Lidocaine hydrochloride
Lidocaine HCL,盐酸利多卡因,Lignocaine hydrochloride,Xyloneural,Lidothesin |
Apoptosis; ERK; NF-κB; MEK; Sodium Channel | Apoptosis; MAPK; Membrane transporter/Ion channel; NF-κB |
Lidocaine hydrochloride (Lignocaine hydrochloride) 抑制涉及复杂电压和依赖性的钠通道。它通过调节 miR-145 表达和进一步抑制 MEK/ERK 和 NF-κB 信号通路来减少胃癌细胞的生长,迁移和侵袭。Lidocaine 是一种酰胺衍生物,是一种研究室性心律失常的药物和有效的肿瘤抑制剂。 | |||
T6993 |
Tauroursodeoxycholate sodium
牛磺熊脱氧胆酸钠,Sodium tauroursodeoxycholate,Tauroursodeoxycholic acid sodium salt,TUDC,牛磺熊去氧胆酸钠,Sodium Tauroursodeoxycholate (TUDC) |
Apoptosis; ERK; Caspase | Apoptosis; MAPK; Proteases/Proteasome |
Tauroursodeoxycholate sodium (TUDC) 是一种内质网应激抑制剂。Tauroursodeoxycholate sodium (TUDC) 抑制ERK,显著降低凋亡分子表达,如caspase-3和caspase-12。 | |||
T7799 |
BMP signaling agonist sb4
SB 4 |
TGF-beta/Smad | Stem Cells |
BMP signaling agonist sb4 (SB 4) 是苯并恶唑骨形态发生蛋白 4 (BMP4) 信号激动剂(EC50:74 nM),能够稳定细胞内 p-SMAD-1/5/9 ,激活 BMP 信号。它还能激活典型 BMP 信号通路中的 BMP4 靶基因 (DNA 结合抑制剂,Id1和Id3)。 | |||
T82063 |
Integrin signaling inhibitor, mP13
|
||
Integrinsignaling inhibitor, mP13 是抑制整合素信号传导,阻止内向外和外向内信号传递,涉及纤维蛋白原结合、血小板粘附及凝块收缩的化合物。 | |||
T14220 |
Amine-PEG3-Biotin
|
Others | Others |
Amine-PEG3-Biotin 可用作信号放大标记。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T38373 |
2-heptyl-3-hydroxy-4(1H)-Quinolone
2-heptyl-3-hydroxy-4(1H)-Quinolone,PQS,Pseudomonas Quinolone Signal |
Others | Others |
2-heptyl-3-hydroxy-4(1H)-Quinolone (Pseudomonas Quinolone Signal) 是一种铜绿假单胞菌为应对细胞密度增加而产生的一种法定人数感应信号分子。 它增加了铜绿假单胞菌中lasB 基因的表达,增加代谢物焦蓝蛋白和凝集素PA-IL 的分泌,以及增加铜绿假单胞菌种群的生物膜生产。当使用浓度为40 μM 时,它还会降低铜绿假单胞菌生长介质中的铁含量,并在硫酸铁溶液中充当一种铁螯合剂。 | |||
TN2346 |
Mogrol
|
ERK; AMPK; STAT | Chromatin/Epigenetic; JAK/STAT signaling; MAPK; PI3K/Akt/mTOR signaling; Stem Cells |
Mogrol 是罗汉果中的一种天然产物,通过抑制 ERK1/2 和 STAT3 通路,减少 CREB 激活和激活 AMPK 信号传导发挥作用。 | |||
T6S0655 |
Corynoxeine
|
ERK | MAPK |
Corynoxeine 是从钩藤中分离的一种天然产物,是 PDGF-BB 诱导血管平滑肌细胞 (VSMCs) 增殖过程中的 ERK1/ERK2抑制剂。 | |||
TN1417 |
Azadirachtin
|
Apoptosis; Antifection | Apoptosis; Microbiology/Virology |
Azadirachtin 是一种有前途的植物源杀虫剂,能够诱导昆虫 Sf9、SL-1 和 BTI-Tn-5B1-4 细胞凋亡。它广泛用于害虫防治。 | |||
T3856 |
Tenuifoliside A
|
ERK; Others | MAPK; Others |
Tenuifoliside A 是从远志分离得到的一种天然产物,具有抗凋亡、抗抑郁、抗炎和神经保护活性。 | |||
T3857 |
magnolin
木兰脂素,(+)-Magnolin,木兰苷 |
ERK | MAPK |
Magnolin 是辛夷的一种主要成分,靶向作用于ERK1和ERK2,IC50值分别为 87 和 16.5 nM,可抑制Ras/ERKs/RSK2信号通路。它在体内外降低肾脏氧化应激,抑制 caspase-3 活性,并增加 Bcl-2 表达,具有抗炎和抗氧化作用。 | |||
T3844 |
Deltonin
三角叶薯蓣皂苷 |
ERK; Others; Akt; Endogenous Metabolite | Cytoskeletal Signaling; MAPK; Metabolism; Others; PI3K/Akt/mTOR signaling |
Deltonin 是从盾叶薯蓣中得到的一种甾体皂苷,抑制ERK1/2和AKT 的活化,具有抗肿瘤活性。 | |||
TN3967 |
Epieriocalyxin A
|
ERK; BCL; ROS; Caspase; DNA/RNA Synthesis; JNK | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; MAPK; Proteases/Proteasome |
Epieriocalyxin A 可以抑制 Caco-2 结肠癌细胞的生长。它可能是未来结肠癌治疗的潜在药物。 | |||
T6947 |
Piperlongumine
PPLGM,荜茇酰胺,Piplartine |
Apoptosis; ERK; Ferroptosis; Reactive Oxygen Species; ROS; Antibacterial; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; MAPK; Metabolism; Microbiology/Virology; NF-κB |
Piperlongumine (Piplartine) 属于生物碱类天然产物,具有抗肿瘤、抗炎、抗氧化、抗血管生成等生物活性。Piperlongumine 可以增强 ROS 水平,诱导肿瘤细胞凋亡。 | |||
TL0016 |
Sulforaphene
油菜 |
Apoptosis; ERK; EGFR; NF-κB | Angiogenesis; Apoptosis; JAK/STAT signaling; MAPK; NF-κB; Tyrosine Kinase/Adaptors |
Sulforaphene 是从萝卜种子中分离出来的天然产物,对鹿茸幼苗的 ED50 约为 2 x 10 -4 M。它通过抑制 EGFR、p-ERK1/2、NF-κB 和其他信号促进癌细胞凋亡并抑制迁移。 | |||
TN1410 |
Asperulosidic acid
ASPA,车叶草苷酸 |
ERK; NF-κB | MAPK; NF-κB |
Asperulosidic acid (ASPA) 是从白花蛇舌草药中提取的一种环烯醚萜苷,具有抗肿瘤、抗氧化和抗炎作用。它通过抑制 NF-κB 和丝裂原活化蛋白激酶信号通路抑制炎性细胞因子释放发挥抗炎作用。 | |||
T7921 |
β-Cyclocitral
beta-Cyclocitral,β-环柠檬醛 |
Others | Others |
β-Cyclocitral 是 β-胡萝卜素的挥发性氧化衍生物,是微囊藻特有的掠食性动物防御信号。它是一种强大的驱虫剂。它是主要的挥发性萜类化合物之一,可以上调防御基因的表达,从而增强过量光照 (EL) 的适应性。 | |||
TMS2181 |
trans-Zeatin
(E)-Zeatin,玉米素 |
ERK; MEK; Endogenous Metabolite | MAPK; Metabolism |
trans-Zeatin ((E)-Zeatin) 是植物细胞分裂素,可抑制紫外线诱导的MEK/ERK 的活化,在细胞生长、分化和分裂中起着重要的作用。 | |||
T6S0619 |
Pachymic acid
3-O-Acetyltumulosic acid,茯苓酸 |
ERK; Akt | Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling |
Pachymic acid (3-O-Acetyltumulosic acid) 是来自茯苓的一种三萜,可抑制Akt 和ERK 信号传导途径。 | |||
T3876 |
Loureirin B
龙血素B,龙血素 B |
PAI-1; ERK; Potassium Channel; JNK | MAPK; Membrane transporter/Ion channel; Metabolism |
Loureirin B 是从剑叶龙血树中分离到的一种黄酮,是 PAI-1抑制剂,IC50值为 26.10 μM。它抑制 KATP,以及 ERK 和 JNK 的磷酸化,具有抗糖尿病的功效。 | |||
TN1721 |
Gypenoside L
|
ERK; p38 MAPK; Calcium Channel; NF-κB; ROS | Immunology/Inflammation; MAPK; Membrane transporter/Ion channel; Metabolism; NF-κB |
Gypenoside L 是存在于绞股蓝中的一种皂苷,可增加 SA-β-半乳糖苷酶活性,促进衰老相关分泌细胞因子的产生。它还可以激活p38和ERK MAPK 通路和NF-κB 通路以诱导衰老,具有抗肿瘤和抗炎活性。 | |||
T5727 |
CAFESTOL
咖啡醇,咖啡油醇 |
ERK; NF-κB; COX; PGE Synthase | Immunology/Inflammation; MAPK; Neuroscience; NF-κB |
Cafestol 是咖啡特有的一种二萜,可靶向 AP-1 抑制ERK,有化学预防、抗肿瘤、保肝、抗氧化和抗炎作用。它通过抑制NF-kB 活化途径强烈的抑制 PGE2的产生,还抑制 LGE 激活的 RAW264.7 细胞中的PGE2产生和环氧合酶(COX-2)的 mRNA 表达。 | |||
T5S0761 |
Nitidine chloride
|
Apoptosis; ERK; FAK; p38 MAPK; NF-κB; Topoisomerase; STAT; Parasite | Angiogenesis; Apoptosis; Cytoskeletal Signaling; DNA Damage/DNA Repair; JAK/STAT signaling; MAPK; Microbiology/Virology; NF-κB; Stem Cells; Tyrosine Kinase/Adaptors |
Nitidine chloride 是从Zanthoxylum nitidum (Roxb) DC 中分离得到的,具有抗疟疾活性。它通过多个靶点通路,起抗癌作用,抑制STAT3、DNA 拓扑异构酶1和2A、ERK 和c-Src/FAK 相关信号通路。它通过MAPK 和NF-kB 途径抑制Lps 诱导的炎性细胞因子的产生。 | |||
T3001 |
Honokiol
和厚朴酚,NSC 293100 |
ERK; HCV Protease; MEK; Akt; Autophagy | Autophagy; Cytoskeletal Signaling; MAPK; Microbiology/Virology; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Honokiol (NSC-293100) 是厚朴提取物的活性成分,靶向多种信号分子,具有抗氧化,抗炎,抗血管生成和抗癌活性。它可抑制 Akt 的激活并增强 ERK1/ERK2 的磷酸化。 | |||
T2973 |
Astragaloside IV
AST-IV,黄芪甲苷IV,AS-IV,黄芪皂苷 IV |
MMP; ERK; Estrogen/progestogen Receptor; JNK | Endocrinology/Hormones; MAPK; Proteases/Proteasome |
Astragaloside IV (AS-IV) 是从黄芪中分离得到的一种皂苷,抑制ERK1/2和JNK 激活,在乳腺癌细胞 MDA-MB-231 中,下调(MMP)-2和(MMP)-9的信号通路。 | |||
T19458 |
N-Hydroxypipecolic acid
1-Hydroxy-2-piperidinecarboxylic acid,NHP |
Others | Others |
N-Hydroxypipecolic acid (NHP) 是植物代谢产物和系统性获得性抗性调节剂,可与免疫信号水杨酸协调建立系统性获得性抗性,诱导系统获得性耐药对细菌和卵菌感染。它在植物叶片中系统地积累,以应对病原菌的侵袭。 | |||
T13265 |
Urolithin B
尿石素B,3-羟基-6H-苯并[C]苯并吡喃-6-酮 |
ERK; NF-κB; Akt; Endogenous Metabolite; JNK; AMPK | Chromatin/Epigenetic; Cytoskeletal Signaling; MAPK; Metabolism; NF-κB; PI3K/Akt/mTOR signaling |
Urolithin B 是一种 ellagitannins 的肠道微生物代谢产物,具有抗炎和抗氧化作用。它也是骨骼肌质量的调节因子,通过减少 IκBα 的磷酸化和降解来抑制 NF-κB 活性,并抑制 JNK、ERK 和 Akt 的磷酸化,并增强 AMPK 的磷酸化。 | |||
T17143 |
Toyocamycin
丰加霉素,Vengicide |
Apoptosis; Others; IRE1; Antibiotic; Antifungal | Apoptosis; Cell Cycle/Checkpoint; Microbiology/Virology; Others |
Toyocamycin (Vengicide) 是放线菌类产生的腺苷类似物,为 X 盒结合蛋白 1 (XBP1) 抑制剂,抑制 IRE1α 诱导的 ATP 依赖性 XBP1 mRNA 的断裂,IC50值为 80 nM。它还诱导凋亡。 | |||
TN2354 |
Methylnissolin
3-Hydroxy-9,10-dimethoxyptercarpan,黄芪紫檀烷,黄芪紫檀烷苷,3-羟基-9,10-二甲氧基紫檀烷 |
ERK; PDGFR | Angiogenesis; MAPK; Tyrosine Kinase/Adaptors |
Methylnissolin 是从黄芪中分离的一种天然产物,可抑制血小板衍生生长因子 (PDGF)-BB 诱导的细胞增殖,IC50为 10 μM。。它通过抑制ERK1/2MAP 激酶级联反应抑制 PDGF-BB 诱导的血管平滑肌细胞增殖。它还抑制 PDGF-BB 诱导的细胞外信号调节激酶 1/2 (ERIC1/2) 丝裂原活化蛋白 (MAP) 激酶的磷酸化,具有抗菌和抗癌作用。 | |||
T6S0117 |
Avicularin
Fenicularin,扁蓄苷 |
ERK | MAPK |
Avicularin (Fenicularin) 具有抗过敏、抗炎、保肝、抗氧化、抗肿瘤等活性。它能通过调节 NF-κB(p65)、COX-2 和 PPAR-γ 的活性来改善人类肝细胞癌。在 LPS 刺激的 RAW 264.7 巨噬细胞中,它通过抑制 ERK 信号通路产生抗炎活性。 | |||
T2532 |
Tauroursodeoxycholate
Taurolite,牛磺熊去氧胆酸,Tauroursodeoxycholic Acid,UR 906,Ursodeoxycholyltaurine,TUDCA |
Apoptosis; ERK; P450; Caspase; Endogenous Metabolite | Apoptosis; MAPK; Metabolism; Proteases/Proteasome |
Tauroursodeoxycholate (UR 906) 是一种天然的高度亲水性的三级胆汁酸。Tauroursodeoxycholate 可用于原发性胆汁性肝硬化 (PBC)、胰岛素抵抗、淀粉样变性、囊性纤维化、胆汁淤滞和肌萎缩性侧索硬化症的研究。 | |||
TCS2170 |
2,5-Dihydroxyacetophenone
Quinacetophenone,2-Acetylhydroquinone,2-5-dihydroxyacetophenone,2 ',5'-二羟基苯乙酮,Acetylhydroquinone,2,5-二羟基苯乙酮,DHAP |
ERK; NF-κB; Tyrosinase | MAPK; NF-κB; Proteases/Proteasome |
2,5-Dihydroxyacetophenone (Quinacetophenone) 是从熟地黄中分离出的一种天然产物,通过阻断 ERK1/2和 NF-κB 信号通路,抑制活化巨噬细胞中炎症介质的产生。 | |||
T3364 |
Veratramine
NSC17821,黎芦碱,NSC23880,藜芦胺 |
Sodium Channel | Membrane transporter/Ion channel |
Veratramine (NSC-23880) 是一种信号转导抑制剂,可作用于肿瘤。 | |||
T3406 |
Kuromanin chloride
Glucocyanidin chloride,Chrysontemin,矢车菊素-3-O-葡萄糖苷,Chrysontemin chloride,Cyanidin 3-O-glucoside chloride |
NF-κB | NF-κB |
Kuromanin chloride (Chrysontemin chloride) 是从桑叶中获得,能够提高血糖浓度、维持脂质代谢平衡,表现出降低肥胖的作用。 | |||
T2896 |
Alantolactone
土木香内酯,helenin,Eupatal,Helenine,(+)-Alantolactone,Alant camphor,土木香脑,Inula camphor |
Apoptosis; STAT; TGF-beta/Smad | Apoptosis; JAK/STAT signaling; Stem Cells |
Alantolactone (Inula camphor) 是一种STAT3的选择性抑制剂,可诱导癌症相关的凋亡,具有抗肿瘤活性。 | |||
T7457 |
5-Methyl-2'-deoxycytidine
5-Methyldeoxycytidine,5-甲基-2'-脱氧胞苷,5MedCyd |
DNA Methyltransferase; Endogenous Metabolite | Chromatin/Epigenetic; Metabolism |
5-Methyl-2'-deoxycytidine (5MedCyd) 是嘧啶核苷,当掺入到单链 DNA 中时,可以顺式作用以从头发出信号。 | |||
T4969 |
Guanosine 5'-triphosphate trisodium salt
鸟苷-5'-三磷酸三钠盐,GTP Trisodium salt,5'-GTP trisodium salt |
Endogenous Metabolite | Metabolism |
Guanosine 5'-triphosphate trisodium salt (5'-GTP trisodium salt) 为G蛋白(G proteins)信号转导过程中的活化剂。 | |||
T3908 |
10-Gingerol
10-姜酚 |
Apoptosis | Apoptosis |
10-Gingerol 是一种姜根脂的主要刺激性成分,具有抗炎、抗氧化和抗增殖作用,能够抑制 MDA-MB-231 肿瘤细胞的增殖(IC50:12.1 μM)。 | |||
T3892 |
Isoacteoside
异麦角甾苷,Isoverbascoside |
NF-κB | NF-κB |
Isoacteoside 具有抗炎作用,通过作用于 caspase-1、丝裂原活化蛋白激酶(c-Jun N-末端激酶、p38、细胞外信号调节蛋白激酶)和核因子-kappa B 途径介导。 | |||
TN1134 |
Euscaphic acid
|
Apoptosis; LDL; PI3K; DNA/RNA Synthesis; NO Synthase; Prostaglandin Receptor | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; Metabolism; PI3K/Akt/mTOR signaling |
Euscaphic acid 是来源于枣的一种三萜,是DNA 聚合酶抑制剂,可诱导细胞凋亡。它抑制小牛 DNA 聚合酶 α 和大鼠 DNA 聚合酶 β 的IC50值分别为 61 和 108 μM。 | |||
T6S1141 |
Ganoderic acid A
灵芝酸 A,灵芝酸A |
Apoptosis; NF-κB; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Metabolism; NF-κB |
Ganoderic acid A 能够抑制 JAK-STAT3信号通路,也能抑制细胞增殖,存活率和 ROS。 它对人骨肉瘤 HOS 和MG-63细胞具有增殖抑制、凋亡和侵袭抑制作用。 | |||
T5769 |
Stachydrine
Methyl hygrate betaine,水苏碱,L-stachydrine,Proline betaine,N,N-Dimethyl-L-proline |
NF-κB; Endogenous Metabolite | Metabolism; NF-κB |
Stachydrine (N,N-Dimethyl-L-proline) 是中国草本植物益母草的主要成分,具有促进血液循环和消除血瘀的功效。Stachydrine (N,N-Dimethyl-L-proline) 能够抑制NF-κB 信号通路。 | |||
T34698 |
Spongosine
2-Methoxy adenosine |
Others | Others |
Spongosine (2-Methoxy adenosine) 是一种重要的细胞间信号递质,具有多种生物活性,包括抗炎活性、镇痛和血管舒张特性。Spongosine 是从海洋生物中分离出来的天然产物,于1950年首次从海洋海绵隐毛隐(Cryptotethia crypta)中分离出来。 | |||
T2133 |
Adenosine monophosphate
5'-Adenylic acid,5'-腺嘌呤核苷酸,AMP,Adenosine 5'-monophosphate |
Endogenous Metabolite; AMPK | Chromatin/Epigenetic; Metabolism; PI3K/Akt/mTOR signaling |
Adenosine monophosphate (AMP) 是一种嘌呤核糖核苷5'-单磷酸腺苷,是信号转导和调节能量稳态的关键细胞代谢物。它具有EC 3.1.3.11(果糖-二磷酸酶)抑制剂、EC 3.1.3.1(碱性磷酸酶)抑制剂和腺苷A1受体激动剂的作用。 | |||
TN1911 |
Marein
马里苷,马里甙 |
transporter; Akt; HDAC; AMPK | Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Metabolism; PI3K/Akt/mTOR signaling |
Marein 能通过CaMKK/AMPK/GLUT1促进葡萄糖摄取,IRS/Akt/GSK-3β增加糖原合成,并通过Akt/FoxO1减少糖异生,从而改善 HepG2 细胞中高葡萄糖诱导的胰岛素抵抗。它对甲基乙二醛诱导的 PC12 细胞损伤具有神经保护作用,还有抗氧化、降压、降血脂和抗糖尿病作用。 | |||
T20879 |
Tacrolimus monohydrate
FK-506,FR 900506,Prograf,FR900506,Tacrolimus hydrate,LCP-Tacro,他克莫司一水合物,FK 506 |
Phosphatase; Others; Antibacterial; Antibiotic; Autophagy | Autophagy; Metabolism; Microbiology/Virology; Others |
Tacrolimus monohydrate (LCP-Tacro) 是大环内酯类化合物,它与 FK506 结合蛋白 (FKBP) 结合形成复合物并抑制钙调神经磷酸酶,从而抑制 T 淋巴细胞信号转导和 IL-2 转录。具有强免疫抑制特性。 | |||
T4672 |
Brevilin A
|
Apoptosis; Anti-infection; JAK; STAT; Autophagy | Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; JAK/STAT signaling; Microbiology/Virology; Stem Cells |
Brevilin A 是从Centipeda minima 中分离的倍半萜内酯,具有抗癌活性。它通过线粒体途径和 PI3K/AKT/mTOR 失活诱导结肠腺癌细胞 CT26 的凋亡和自噬。它是一种选择性JAK-STAT 信号通路抑制剂,通过减弱 JAK 信号和 阻塞 STAT3 信号起作用。 | |||
T6S1597 |
Mulberroside A
桑皮苷 A,桑皮苷A |
TNF; Tyrosinase; Interleukin | Apoptosis; Immunology/Inflammation; Proteases/Proteasome |
Mulberroside A 是桑中的一种主要活性成分,可降低TNF-α、IL-1β和IL-6的表达,抑制 NALP3、caspase-1 和 NF-κB 的激活以及 ERK、JNK 和 p38 的磷酸化 。它抑制蘑菇酪氨酸酶,具有抗炎和抗细胞凋亡作用。 | |||
T5S1805 |
5,7-Dihydroxychromone
5,7-Dihydroxy-4H-Chromen-4-One,5,7-二羟基色酮,5,7-二羟基色原酮 |
Others; Virus Protease; PARP; Caspase; Nrf2 | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; Microbiology/Virology; Others; Proteases/Proteasome |
5,7-Dihydroxychromone (5,7-Dihydroxy-4H-Chromen-4-One) 是一种Cudrania tricuspidata 的提取物,通过激活 Nrf2/ARE 信号对 6-OHDA 诱导的氧化应激和细胞凋亡发挥神经保护作用。它抑制 6-OHDA 诱导的 SH-SY5Y 细胞中活化的caspase-3,caspase-9以及切割的PARP 表达。 | |||
T6S1418 |
Praeruptorin C
|
Antioxidant; Calcium Channel | Membrane transporter/Ion channel; Metabolism; oxidation-reduction |
Praeruptorin C 是白花前胡中的一种主要成分,是钙拮抗剂,pD2′值为 5.7。 | |||
TJS1779 |
Protosappanin A
原苏木素A,PTA |
NADPH-oxidase; IL Receptor; IκB/IKK; TNF; NF-κB; TLR; ROS; COX; HIV Protease; JAK; NO Synthase; STAT | Angiogenesis; Apoptosis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Microbiology/Virology; Neuroscience; NF-κB; Proteases/Proteasome; Stem Cells |
Protosappanin A (PTA) 是从苏木中分离得到的免疫抑制成分和主要联苯化合物,通过下调 JAK2和 STAT3的磷酸化,抑制 JAK2/STAT3依赖的炎症通路。 | |||
T6S1917 |
Schisandrol B
Gomisin A,TJN-101,Besigomsin,五味子醇乙,Gamma-Schisandrin,戈米辛A,Schizandrol B,Wuweizi alcohol-B |
P450; Reactive Oxygen Species; Autophagy | Autophagy; Immunology/Inflammation; Metabolism; NF-κB |
Schisandrol B (Besigomsin) 是华中五味子的主要活性成分,具有保肝、抗炎、抗糖尿病和抗氧化的作用。它抑制活性氧的产生,也抑制 P-糖蛋白和CYP3A 的活性。 | |||
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。 | |||
T4S2063 |
Tetrahydrocoptisine
人血草碱,STYLOPINE |
ERK; p38 MAPK; NF-κB | MAPK; NF-κB |
Tetrahydrocoptisine (STYLOPINE) 具有抑制炎症的有效作用。它通过抑制 NF-κB 信号通路对 LPS 诱导的 ALI 具有保护作用,这可能涉及抑制肺部炎症过程。它具有胃保护活性,归因于减少 NO 产生和调节促炎细胞因子,抑制中性粒细胞积累和 NF-κB 表达。它是一种活性抗炎成分,通过下调 NF-κB 活化、磷酸化 ERK1/2 和磷酸化-p38MAPK 信号通路抑制 TNF-α、IL-6 和 NO 的产生。 | |||
T6S1572 |
Sauchinone
|
ERK; p38 MAPK; NF-κB | MAPK; NF-κB |
Sauchinone 是一种从Saururus chinensis 中获得的非对映异构的木脂素。它通过抑制I-κBα磷酸化和p65核易位来抑制 LPS 诱导的 iNOS,TNF-α 和 COX-2 表达。它具有抗炎和抗氧化活性。 | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-05841 |
SIRP alpha Protein, Cynomolgus, Recombinant (His)
signal-regulatory protein α,signal-regulat... |
Cynomolgus | HEK293 Cells |
SIRP alpha Protein, Cynomolgus, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 38.93 kDa and the accession number is XP_015313153.1. | |||
TMPY-05153 |
TROP-2 Protein, Cynomolgus, Rhesus, Recombinant (His)
tumor-associated calcium signal transducer 2 |
Cynomolgus,Rhesus | HEK293 Cells |
TROP-2 Protein, Cynomolgus, Rhesus, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 28.7 kDa and the accession number is XP_001114599.1. | |||
TMPY-01853 |
SIRP gamma Protein, Human, Recombinant (His)
bA77C3.1,signal-regulatory protein gamma,SIRP γ/SIR... |
Human | HEK293 Cells |
SIRP gamma Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 38.5 kDa and the accession number is Q9P1W8-1. | |||
TMPY-01076 |
gp130/IL6ST Protein, Human, Recombinant (His & hFc)
interleukin 6 signal transducer,IL-6RB,CD130,CDW130... |
Human | HEK293 Cells |
gp130/IL6ST Protein, Human, Recombinant (His & hFc) is expressed in HEK293 mammalian cells with His and hFc tag. The predicted molecular weight is 96 kDa and the accession number is P40189-1. | |||
TMPY-01832 |
gp130/IL6ST Protein, Mouse, Recombinant (His)
CD130,D13Ertd699e,interleukin 6 signal transducer,g... |
Mouse | HEK293 Cells |
gp130/IL6ST Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 68 kDa and the accession number is Q00560. | |||
TMPY-02632 |
SIRP alpha Protein, Mouse, Recombinant (His)
SHP-1,CD172a,SIRP,SHPS-1,SIRP α,Ptpns1,signal-regul... |
Mouse | HEK293 Cells |
SIRP alpha Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 39.4 kDa and the accession number is BAA20376.1. | |||
TMPY-06051 |
SIRP alpha Protein, Human, Recombinant (hFc)
signal-regulatory protein alpha,SIRP alpha,PTPNS1,P... |
Human | HEK293 Cells |
SIRP alpha Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 64 kDa and the accession number is P78324-1. | |||
TMPY-01573 |
SIRP alpha Protein, Human, Recombinant (G75A, His)
PTPNS1,signal-regulatory protein alpha,SIRP,MYD-1,C... |
Human | HEK293 Cells |
SIRP alpha Protein, Human, Recombinant (G75A, His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 39 kDa and the accession number is P78324-1. | |||
TMPY-06052 |
SIRP alpha V2 Protein, Human, Recombinant (His)
SIRP α,P84,PTPNS1,signal-regulatory protein α,s... |
Human | HEK293 Cells |
SIRP alpha V2 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 38.6 kDa and the accession number is AAH38510.1. | |||
TMPY-02667 |
TROP-2 Protein, Mouse, Recombinant (His)
Ly97,TROP2,tumor-associated calcium signal transduc... |
Mouse | HEK293 Cells |
TROP-2 Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 29.4 kDa and the accession number is Q8BGV3. | |||
TMPY-06624 |
STAT3 Protein, Human, Recombinant (His)
ADMIO,signal transducer and activator of transcript... |
Human | E. coli |
STAT3 Protein, Human, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 65.31 kDa and the accession number is P40763-1. | |||
TMPY-02603 |
STAT6 Protein, Human, Recombinant (His)
STAT6C,IL-4-STAT,STAT6B,signal transducer and activ... |
Human | Baculovirus Insect Cells |
Signal transducer and activator of transcription 6 (STAT6) is a transcription factor that is activated by interleukin-4 (IL-4)-induced tyrosine phosphorylation and mediates most of the IL-4-induced gene expression. STAT6 plays a central role in exerting interleukin-4 (IL-4) mediated biological responses and is found to induce the expression of BCL2L1/BCL-XL, which is responsible for the anti-apoptotic activity of IL4. Transcriptional activation by STAT6 requires the interaction with coactivators... | |||
TMPY-01262 |
TROP-2 Protein, Human, Recombinant (His)
TROP2,M1S1,GA733-1,TROP-2,GA7331,tumor-associated calcium |
Human | HEK293 Cells |
TROP-2 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 29.4 kDa and the accession number is P09758. | |||
TMPY-05745 |
SIRP alpha Protein, Rat, Recombinant (hFc)
signal-regulatory protein α,signal-regulat... |
Rat | HEK293 Cells |
SIRP alpha Protein, Rat, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 64.25 kDa and the accession number is BAA20368.1. | |||
TMPY-01995 |
gp130/IL6ST Protein, Rat, Recombinant (His & mFc)
interleukin 6 signal transducer |
Rat | HEK293 Cells |
gp130/IL6ST Protein, Rat, Recombinant (His & mFc) is expressed in HEK293 mammalian cells with His, mFc tag. The predicted molecular weight is 94.3 kDa and the accession number is H9BFG4. | |||
TMPY-03743 |
gp130/IL6ST Protein, Rhesus, Recombinant (His)
interleukin 6 signal transducer |
Rhesus | HEK293 Cells |
gp130/IL6ST Protein, Rhesus, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 69.2 kDa and the accession number is A0A8J8YAN3. | |||
TMPY-03687 |
gp130/IL6ST Protein, Rhesus, Recombinant (hFc)
interleukin 6 signal transducer |
Rhesus | HEK293 Cells |
gp130/IL6ST Protein, Rhesus, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 102.6 kDa and the accession number is A0A8J8YAN3. | |||
TMPY-03543 |
SIRP gamma Protein, Cynomolgus, Recombinant (His)
signal-regulatory protein γ,signal-regulat... |
Cynomolgus | HEK293 Cells |
SIRP gamma Protein, Cynomolgus, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 38.1 kDa. | |||
TMPY-00374 |
SSTR1 Protein, Human, Recombinant (hFc)
TRAPA,signal sequence receptor, α,signal s... |
Human | HEK293 Cells |
SSTR1 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 47.8 kDa and the accession number is P43307-1. | |||
TMPY-03666 |
SIRP alpha Protein, Rat, Recombinant (His)
signal-regulatory protein alpha,signal-reg... |
Rat | HEK293 Cells |
SIRP alpha Protein, Rat, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 47.10 kDa and the accession number is P97710. | |||
TMPY-02148 |
gp130/IL6ST Protein, Rat, Recombinant (His)
interleukin 6 signal transducer |
Rat | HEK293 Cells |
gp130/IL6ST Protein, Rat, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 68.2 kDa and the accession number is H9BFG4. | |||
TMPY-03669 |
SIRP gamma Protein, Cynomolgus, Recombinant (hFc)
signal-regulatory protein γ,signal-regulat... |
Cynomolgus | HEK293 Cells |
SIRP gamma Protein, Cynomolgus, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 41.10 kDa and the accession number is G7PGS5. | |||
TMPH-02111 |
SRP72 Protein, Human, Recombinant (GST)
SRP72,Signal recognition particle 72 kDa protein, |
Human | E. coli |
Signal-recognition-particle assembly has a crucial role in targeting secretory proteins to the rough endoplasmic reticulum membrane. Binds the 7S RNA only in presence of SRP68. This ribonucleoprotein complex might interact directly with the docking protein in the ER membrane and possibly participate in the elongation arrest function. SRP72 Protein, Human, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 101.1 kDa and the accession numb... | |||
TMPY-05152 |
TROP-2 Protein, Rat, Recombinant (His)
tumor-associated calcium signal transducer 2 |
Rat | HEK293 Cells |
TROP-2 Protein, Rat, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 29.5 kDa and the accession number is A0A0G2JSJ1. | |||
TMPJ-01160 |
SIRP beta 2 Protein, Human, Recombinant (hFc)
Signal-Regulatory Protein β-2,PTPN1L,SIRP-beta-2, |
Human | HEK293 Cells |
Signal-regulatory protein beta-2(SIRP-beta-2), is a monomeric single pass type I membrane glycoprotein, belongs to the SIRP/SHPS (CD172) family of the immunoglobulin (Ig) superfamily. The SIRP family are paired receptors that have similar extracellular domains but differing C-terminal domains and functions. A positively charged residue within the transmembrane domain, in analogy to SIRP-beta-1, is implicated to mediate interaction with the adaptor DAP12 protein, which contains immunoreceptor tyr... | |||
TMPY-03977 |
DAP10 Protein, Human, Recombinant (mFc)
PIK3AP,DAP10,hematopoietic cell signal transducer,K... |
Human | HEK293 Cells |
HCST (Hematopoietic Cell Signal Transducer, also known as DAP1) is a Protein Coding gene. HCST belongs to the DAP10 family. It is a transmembrane signaling adaptor that contains a YxxM motif in its cytoplasmic domain. The encoded protein may form part of the immune recognition receptor complex with the C-type lectin-like receptor NKG2D. HCST may be part of the immune recognition receptor complex. This receptor plays a major role in triggering cytotoxicity against target cells expressing cell sur... | |||
TMPJ-01003 |
STAT5B Protein, Human, Recombinant (His)
Signal Transducer and Activator of Transcription 5B... |
Human | E. coli |
Signal Transducer and Activator of Transcription 5b (STAT5B) is a member of the STAT family of transcription factors. They are responsible for an array of cellular activities including regulating growth, survival, differentiation, motility, and the immune response. STAT5B mediates the signal transduction triggered by various cell ligands, such as IL2, IL4, CSF1, and different growth hormones. It has been shown to be involved in diverse biological processes, such as TCR signaling, apoptosis, adul... | |||
TMPJ-00248 |
SIRP gamma Protein, Human, Recombinant (hFc)
SIRP-Gamma,SIRP-β-2,SIRP-Beta-2,Signal-Regulatory P... |
Human | HEK293 Cells |
Signal-Regulatory Protein Gamma (SIRPG) is a member of the signal-regulatory protein (SIRP) family and also belongs to the immunoglobulin superfamily. SIRPG is detected in the liver, and at very low levels in the brain, heart, lung, pancreas, kidney, placenta, and skeletal muscle. SIRPG is an immunoglobulin-like cell surface receptor. On binding with CD47, SIRPG mediates cell-cell adhesion. Engagement on T-cells by CD47 on antigen-presenting cells results in enhanced antigen-specific T-cell prol... | |||
TMPY-02581 |
STAT4 Protein, Human, Recombinant (His)
signal transducer and activator of transcription 4,... |
Human | Baculovirus Insect Cells |
High expression of STAT4 in gastric cancer predicted a better clinical outcome. STAT4 might be a useful biomarker to identify patients at high risk of recurrence after gastrectomy. Genetic variants in the transcription factor STAT4 are associated with increased susceptibility to systemic lupus erythematosus (SLE) and a more severe disease phenotype. | |||
TMPH-00733 |
SPase I Protein, E. coli, Recombinant (His & SUMO)
Leader peptidase I,Signal peptidase I,lepB |
E. coli | E. coli |
N/A. SPase I Protein, E. coli, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 43.7 kDa and the accession number is P00803. | |||
TMPU-00004 |
STAT5A Protein, Human, Recombinant (His)
MGF,Signal transducer and activator of transcriptio... |
Human | E. coli |
Signal transducer and activator of transcription 5A is a protein that in humans is encoded by the STAT5A gene. Many studies have indicated a key role of STAT5a in leukemia, breast, colon, head and neck, and prostate cancer. Until recently, the unique characteristics and function of STAT5a in these cancers have not been delineated from STAT5b, and more research into their differential behavior is warranted. Because of its integral role in immune cell development, STAT5a may contribute to tumor de... | |||
TMPY-00387 |
gp130/IL6ST Protein, Human, Recombinant (hFc)
GP130,CD130,interleukin 6 signal transducer,IL-6RB,... |
Human | HEK293 Cells |
gp130/IL6ST Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 94.4 kDa and the accession number is AAA59155.1. | |||
TMPY-06745 |
gp130/IL6ST Protein, Human, Recombinant (mFc)
interleukin 6 signal transducer,CD130,CDW130,IL-6RB... |
Human | HEK293 Cells |
gp130/IL6ST Protein, Human, Recombinant (mFc) is expressed in HEK293 mammalian cells with mFc tag. The predicted molecular weight is 94.11 kDa and the accession number is AAA59155.1. | |||
TMPY-06039 |
gp130/IL6ST Protein, Human, Recombinant (aa 1-618, DDDDK)
GP130,CD130,interleukin 6 signal transducer,CDW130,... |
Human | HEK293 Cells |
gp130/IL6ST Protein, Human, Recombinant (aa 1-618, DDDDK) is expressed in HEK293 mammalian cells. The predicted molecular weight is 68.4 kDa and the accession number is P40189-1. | |||
TMPH-02110 |
SEC11C Protein, Human, Recombinant (His & SUMO)
Microsomal signal peptidase 21 kDa subunit,SEC11-li... |
Human | E. coli |
Component of the microsomal signal peptidase complex which removes signal peptides from nascent proteins as they are translocated into the lumen of the endoplasmic reticulum. | |||
TMPH-02826 |
PEX5 Protein, Mouse, Recombinant (His & Myc)
PTS1-BP,Peroxisomal C-terminal targeting signal imp... |
Mouse | E. coli |
Binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import. | |||
TMPY-05263 |
SIRP alpha Protein, Human, Recombinant (mFc)
signal-regulatory protein alpha,SIRP alpha,SHPS1,MY... |
Human | HEK293 Cells |
SIRP alpha Protein, Human, Recombinant (mFc) is expressed in HEK293 mammalian cells with mFc tag. The predicted molecular weight is 63.7 kDa and the accession number is P78324-1. | |||
TMPY-05793 |
gp130/IL6ST Protein, Mouse, Recombinant (hFc)
BB405851,interleukin 6 signal transducer,D13Ertd699... |
Mouse | HEK293 Cells |
gp130/IL6ST Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 93.38 kDa and the accession number is Q00560. | |||
TMPJ-00252 |
SIRP beta 1 Protein, Human, Recombinant (His)
CD172b,CD172 antigen-like family member B,Signal-re... |
Human | HEK293 Cells |
Signal-regulatory protein beta-1 (SIRPB1, CD172b) is a member of the signal-regulatory-protein (SIRP) family, and also belongs to the immunoglobulin superfamily. SIRP family members are receptor-type transmembrane glycoproteins known to be involved in the negative regulation of receptor tyrosine kinase-coupled signaling processes. This protein was found to interact with TYROBP/DAP12, a protein bearing immunoreceptor tyrosine-based activation motifs. This protein was also reported to participate... | |||
TMPY-05126 |
SIRP alpha Protein, Human, Recombinant (G75A, His), Biotinylated
SIRP α,SIRP alpha,MYD-1,BIT,MFR,SHPS1,CD172A,P84,SIRP,si... |
Human | HEK293 Cells |
SIRP alpha Protein, Human, Recombinant (G75A, His), Biotinylated is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 38.8 kDa and the accession number is P78324-1. | |||
TMPY-06284 |
SIRP alpha Protein, Human, Recombinant (hFc & Avi), Biotinylated
SIRP,P84,signal-regulatory protein α,BIT,SHPS1,CD17... |
Human | HEK293 Cells |
SIRP alpha Protein, Human, Recombinant (hFc & Avi), Biotinylated is expressed in HEK293 mammalian cells with hFc and Avi tag. The predicted molecular weight is 65.85 kDa and the accession number is P78324-1. | |||
TMPJ-00961 |
STAT1 Protein, Human, Recombinant
Transcription Factor ISGF-3 Components p91/p84,STAT1,Sig... |
Human | E. coli |
Signal Transducer and Activator of Transcription 1-Alpha/Beta (STAT1) contains one SH2 domain and belongs to the transcription factor STAT family. When tyrosine- and serine-phosphorylated, STAT1 can form a homodimer termed IFN-gamma-activated factor (GAF), migrate into the nucleus and bind to the IFN gamma activated sequence (GAS) to drive the expression of the target genes, inducing a cellular antiviral state. STAT1 functions as signal transducer and transcription activator that mediates cellul... | |||
TMPY-02636 |
SIRP alpha Protein, Mouse, Recombinant (hFc)
CD172a,AI835480,SIRP,signal-regulatory protein α, |
Mouse | HEK293 Cells |
SIRP alpha Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 64.9 kDa and the accession number is BAA20376.1. | |||
TMPJ-01182 |
SIRP alpha Protein, Mouse, Recombinant (MIgG2a)
SIRP,CD172 Antigen-Like Family Member A,SIRPA,MFR,Signal... |
Mouse | HEK293 Cells |
SIRPα is a type I transmembrane glycoprotein.It contains two Ig-like C1-type domains and one Ig-like V-type domain. Mouse SIRP alpha ECD shares 61%, 75%, 62%, 61%, and 59% aa sequence identity with human, rat, equine, bovine, and porcine SIRP alpha, respectively.SIRPα can express in various tissues, mainly on brain and myeloid cells, including macrophages, neutrophils, dendritic and Langerhans cells. It also can detect in neurons, smooth muscle and endothelial cells. SIRPA is an immunoglobulin-l... | |||
TMPY-06055 |
SIRP alpha V8 Protein, Human, Recombinant (mFc)
signal-regulatory protein α,signal-regulat... |
Human | HEK293 Cells |
SIRP alpha V8 Protein, Human, Recombinant (mFc) is expressed in HEK293 mammalian cells with mFc tag. The predicted molecular weight is 63.6 kDa and the accession number is AAH38510.1. | |||
TMPJ-01181 |
SIRP alpha Protein, Mouse, Recombinant (aa 32-373, hFc)
SIRPA,SHPS1,Tyrosine-Protein Phosphatase Non-Receptor Type S... |
Mouse | HEK293 Cells |
SIRP alpha Protein, Mouse, Recombinant (aa 32-373, hFc) is expressed in HEK293 mammalian cells with C-Fc tag. The predicted molecular weight is 115-125 KDa and the accession number is Q6P6I8. | |||
TMPY-06054 |
SIRP alpha V8 Protein, Human, Recombinant (His)
SIRP α,BIT,SIRP,PTPNS1,P84,SIRP α(SIRP αV8),CD172A,SIRP alph... |
Human | HEK293 Cells |
SIRP alpha V8 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 38.6 kDa and the accession number is AAH38510.1. | |||
TMPY-06053 |
SIRP alpha V2 Protein, Human, Recombinant (mFc)
MFR,CD172A,P84,PTPNS1,SIRP alpha,SIRP α(SIRP αV2),signal... |
Human | HEK293 Cells |
SIRP alpha V2 Protein, Human, Recombinant (mFc) is expressed in HEK293 mammalian cells with mFc tag. The predicted molecular weight is 63.5 kDa and the accession number is AAH38510.1. | |||
TMPY-06248 |
SIRP alpha V2 Protein, Human, Recombinant (His), Biotinylated
SIRP α(SIRP αV2),BIT,signal-regulatory protein alph... |
Human | HEK293 Cells |
SIRP alpha V2 Protein, Human, Recombinant (His), Biotinylated is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 38.6 kDa and the accession number is AAH38510.1. | |||
TMPY-02666 |
TROP-2 Protein, Mouse, Recombinant (hFc)
EGP-1,GA733-1,TROP2,tumor-associated calcium signal... |
Mouse | HEK293 Cells |
TROP-2 Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 55 kDa and the accession number is Q8BGV3. | |||
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Cat. No. | Product Name | Target | Signaling Pathways |
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TMIJ-0274 |
Sulindac-d3
|
||
Sulindac-d3 是 Sulindac 的氘代化合物。Sulindac 的 CAS 号为 38194-50-2。Sulindac 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。 |