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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T2253 |
TCS PIM-1 1
3-氰基-4-苯基-6-(3-溴-6-羟基苯基)-2(1H)-吡啶酮,SC 204330 |
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
TCS PIM-1 1 (SC 204330) 是一种特异性有效的 ATP 竞争性 Pim-1 激酶抑制剂,IC50为 50 nM,对 MEK1/MEK2 和 Pim-2 表现出良好的特异性,IC50值大于 20000 nM。 | |||
T2659 |
GW2580
GW 2580,SC-203877 |
c-Fms | Tyrosine Kinase/Adaptors |
GW2580 (SC-203877) 是一种口服有效的、选择性的 c-Fms 激酶抑制剂,体外实验中在 0.06 μM 时可完全抑制人 cFMS 激酶。它是 ATP 与 cFMS 激酶结合的竞争性抑制剂,能够抑制集落刺激因子 1 信号传导。 | |||
T8478 |
SC-43
|
Apoptosis; Phosphatase; STAT | Apoptosis; JAK/STAT signaling; Metabolism; Stem Cells |
SC-43 是一种具有口服活性的SHP-1 (PTPN6)激动剂。它是Sorafenib 的衍生物,可抑制STAT3的磷酸化并诱导细胞凋亡,具有抗纤维化和抗癌作用。 | |||
T2257 |
AdipoRon
SC-396658,2-(4-苯甲酰苯氧基)-N-[1-(苯基甲基)-4-哌啶基]乙酰胺 |
Adiponectin receptor | GPCR/G Protein |
AdipoRon (SC-396658) 是可口服的脂联素受体激动剂,能够与AdipoR1(Kd:1.8 μM)及AdipoR2(Kd:3.1 μM)结合。 | |||
T2234 |
TCS JNK 5a
N-(3-氰基-4,5,6,7-四氢苯并[b]噻吩-2-基)-1-萘甲酰胺,SC202671,SC 202671,N-(3-Cyano-4,5,6,7-tetrahydrobenzo[b]thienyl-2-yl)-1-naphthalenecarboxamide,JNK Inhibitor IX,SC-202671 |
Apoptosis; JNK | Apoptosis; MAPK |
TCS JNK 5a (SC202671) 是一种 JNK2和 JNK3的有效抑制剂,pIC50分别为 6.5和 6.7。 | |||
T2274 |
SC79
SC 79,2-氨基-6-氯-alpha-氰基-3-(乙氧羰基)-4H-1-苯并吡喃-4-乙酸乙酯 |
Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
SC79 是一个 AKT 激动剂,具有特异性和血脑屏障渗透性。SC79 可以特异性结合 AKT 的 PH 结构域,激活胞质中 AKT,并抑制 AKT 膜转位。SC79 具有神经保护活性。 | |||
T12856 |
SC-26196
ALPHA,ALPHA-二苯基-4-[(3-吡啶亚甲基)氨基]-1-吡嗪戊腈 |
Others | Others |
SC-26196 是一种 Delta6 去饱和酶 (D6D, FADS2) 抑制剂 (在大鼠肝微粒体中,IC50=0.2 µM),具有口服活性,具有抗炎作用。 | |||
T23333 |
SC-58125
SC 58125,1-[(4-甲基磺酰基)苯基]-3-三氟甲基-5-(4-氟苯基)吡唑 |
COX | Immunology/Inflammation; Neuroscience |
SC-58125 是一种选择性的环氧合酶2 (COX-2)的抑制剂,IC50值为 0.04 μM。它在体内外均表现出抗肿瘤活性,还可抑制炎症部位的水肿并具有缓解疼痛作用。 | |||
T22424 |
1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea
|
Apoptosis; STAT | Apoptosis; JAK/STAT signaling; Stem Cells |
SC-1 是一种 Sorafenib 的衍生物,可抑制 STAT3磷酸化,通过依赖 SHP-1 的 STAT3失活诱导细胞凋亡,具有抗癌作用。 | |||
T18678 |
SC-VC-PAB-DM1
|
Others | Others |
SC-VC-PAB-DM1 is a drug-linker conjugate utilized in Antibody-Drug Conjugates (ADC), featuring DM1 (Mertansine, a tubulin inhibitor) linked through the SC-VC-PAB[1] ADC linker to deliver potent antitumor activity. | |||
T70476 | SML-10-70-1 | ||
SML-10-70-1 is a Novel Active Site Inhibitor of Oncogenic K-Ras G12C. | |||
T0697 |
Aspartame
阿斯巴甜,SC-18862 |
Others; Taste receptor | Metabolism; Others |
Aspartame (SC-18862) 是一种二肽的甲酯,由苯丙氨酸 (50%),天门冬氨酸 (40%) 和甲醇 (10%) 组成。它可用作合成的非营养性甜味剂。 | |||
T8505 |
SC-236
4-(5-(4-氯苯基)-3-(三氟甲基)-1H-,Sc 236 |
Apoptosis; COX; PPAR | Apoptosis; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Neuroscience |
SC-236 (Sc 236) 是一种具有口服活性的COX-2特异性抑制剂和PPARγ激动剂。它可通过 c-Jun 氨基端抑制激活蛋白-1活性,在小鼠模型中通过抑制 ERK 的磷酸化发挥抗炎作用。 | |||
T4101 |
SC-560
SC560 |
COX | Immunology/Inflammation; Neuroscience |
SC-560 是一种选择性 COX-1抑制剂,IC50值为 9 nM。 | |||
T23331 |
SC 51089
SC 51089 free base |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
SC 51089 是一种选择性的前列腺素受体 PGE2 拮抗剂,对前列腺素受体亚型具有选择性,具有抗伤害活性,可改善亨廷顿病 R6/1 小鼠模型中的运动缺陷并挽救记忆力下降。 | |||
T4100 |
AS8351
NSC51355,AS-8351,AS 8351 |
Histone Demethylase | Chromatin/Epigenetic |
AS8351 (NSC51355) 是一种组蛋白去甲基化酶抑制剂,可以诱导人胎儿肺成纤维细胞重编程为功能性心肌细胞。 | |||
T0219 |
Valdecoxib
伐地考昔,代他考昔,SC 65872 |
COX | Immunology/Inflammation; Neuroscience |
Valdecoxib (SC 65872) 是可口服的高选择性 COX-2抑制剂,对 COX-2 和 COX-1 的 IC50值分别为 5 nM 和 140 μM,可用于治疗骨关节炎、类风湿性关节炎以及痛经和经期症状。 | |||
T28697 |
SC-2001
SC2001 |
||
SC-2001 is a MCL-1 inhibitor. SC-2001 inhibits STAT3 phosphorylation through enhancing SHP-1 expression and induces apoptosis in human breast cancer cells. SC-2001 overcomes STAT3-mediated sorafenib resistance through RFX-1/SHP-1 activation in hepatocellu | |||
T18679 |
SC-VC-PAB-MMAE
|
Others | Others |
SC-VC-PAB-MMAE is a potent antitumor drug-linker conjugate for antibody-drug conjugates (ADCs), comprising the anti-mitotic agent monomethyl auristatin E (MMAE, a tubulin inhibitor) connected through the cleavable linker SC-VC-PAB[1]. | |||
T78547 |
2-Phenyl-2-(2-pyridyl)acetonitrile
α-Phenyl-2-pyridineacetonitrile |
Drug Metabolite | Metabolism |
2-Phenyl-2-(2-pyridyl)acetonitrile 是 SC 15396 在大鼠肝脏匀浆上清中的主要代谢产物,后者为一种胃分泌抑制剂,作用于抗胃泌素受体。 | |||
T77163 | Pexelizumab | ||
Pexelizumab (h5G1.1-SC)为一种针对C5补体成分的人源化单克隆抗体。该化合物可抑制凋亡(apoptosis)和白细胞浸润,常用于研究脑缺血再灌注损伤和心肌梗死。 | |||
T75285 | Metronidazole hydrochloride | ||
Metronidazole hydrochloride (SC 326421) 是一种有口服活性的硝基咪唑抗生素,适用于厌氧微生物感染的研究。该化合物能穿越血脑屏障,长期服用可能引发炎症和骨骼肌收缩问题。 | |||
T36374 |
Naloxegol (NKTR-118)
|
||
Naloxegol (NKTR-118; AZ-13337019) is an opioid-receptor antagonist[1]. [1]. Yoon SC, et al. Naloxegol in opioid-induced constipation: a new paradigm in the treatment of a common problem. Patient Prefer Adherence. 2017 Jul 24;11:1265-1271. | |||
T75766 |
GP(33-41) TFA
|
||
GP(33-41) TFA 是一种由 9 个氨基酸残基组成的多肽,它是淋巴细胞性脉络丛脑膜炎病毒 GP1 抗原决定基中的序列。GP(33-41) TFA 能够上调 RMA-S (Db Kb) 细胞表面 H-2Db 分子,SC50值为 344 nM。 | |||
T36822 |
Benzovindiflupyr
|
||
Benzovindiflupyr is a fungicide.1It inhibits mitochondrial complex II, also known as succinate dehydrogenase (SDH; IC50= 5.2 nM), and mycelial growth ofS. sclerotiorum(EC50= 0.011 μg/ml). Benzovindiflupyr (60 μg/ml) completely protects eggplant leaves fromS. sclerotioruminfection. Formulations containing benzovindiflupyr have been used to control various fungal diseases in agriculture. 1.Gao, Y., He, L., Zhu, J., et al.The relationship between features enabling SDHI fungicide binding to the Sc-S... | |||
T36996 |
MSA-2 dimer
|
||
MSA-2 dimer is a selective, orally active non-nucleotide STING agonist (Kd=145 μM) with long-term antitumor and immunogenic activity. MSA-2 dimer is bound to STING as a non-covalent dimer exhibiting higher permeability than cyclic dinucleotide[1]. MSA-2 dimer (60 mg/kg; p.o.; 50 days) inhibits tumor growth and prolongs overall survival[1]. MSA-2 dimer (40 mg/kg; s.c.; 25 days) induces complete tumor regression[1].MSA-2 dimer (60 mg/kg; p.o.; 4 hours) increases proinflammatory cytokine (IFN-β) le... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN6754 |
1-Nonadecanol
|
Others | Others |
1-Nonadecanol 是一种 Heracleum thomsonii 的超临界二氧化碳精油的成分,也是 Neotinea ustulata 的重要香气化合物。 | |||
T4943 |
Monoolein
1-Oleoyl-rac-glycerol,甘油单油酸酯 |
Others; Endogenous Metabolite | Metabolism; Others |
Monoolein (1-Oleoyl-rac-glycerol) 是内源性代谢产物的一种。 | |||
T4973 |
Paraxanthine
1,7-二甲基黄嘌呤,1,7-DIMETHYLXANTHINE |
Endogenous Metabolite | Metabolism |
Paraxanthine (1,7-dimethylxanthine) 是一种 caffeine 的代谢物,能够刺激Ryanodine 受体通道来抑制多巴胺能细胞的死亡。 |