Signaling Pathways
Signaling Pathways(信号通路)
- Proteases(63)
- Apoptosis(1190)
- Chromatin/Epigenetics(17)
- Metabolism(420)
- MAPK Signaling(32)
- Tyrosine Kinase(97)
- DNA Damage/DNA Repair(62)
- PI3K/Akt/mTOR Signaling(56)
- Microbiology & Virology(68)
- Cell Cycle/Checkpoint(205)
- Ubiquitination/ Proteasome(43)
- JAK/STAT Signaling(13)
- TGF-β / Smad Signaling(30)
- Angiogenesis(85)
- GPCR/G protein(3)
- Stem Cell(27)
- Membrane Transporter/Ion Channel(273)
- Cancer Biology(514)
- Endocrinology and Hormones(168)
- Neuroscience(462)
- Obesity, Appetite Control & Diabetes(9)
- Peptide Inhibitors and Substrate(1)
- Other Signal Transduction(141)
- Immunology/Inflammation(1111)
- Cardiovascular(63)
- Vitamin D Related
- Antibody-drug Conjugate/ADC Related
- PROTAC(254)
- Ox Stress Reagents(25)
- Others(1718)
- Antiparasitics(21)
- Toxins(90)
Signaling Pathways 相关产品(35130)
- GC12661Indirubin-3'-oximeCAS: 160807-49-8纯度: >99.00%
Inhibitor of GSK3β and cyclin-dependent kinases
- GC12690MLN8237 (Alisertib)CAS: 1028486-01-2纯度: >99.00%
Alisertib (MLN8237) 作为一种在研、可口服的选择性极光 A 激酶抑制剂,通常用于治疗实体瘤和血液系统恶性肿瘤。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC12611 | Triamcinolone Acetonide | 76-25-5 | >99.50% / >98.00% | |
A synthetic corticosteroid | ||||
| GC12612 | JNJ-7706621 | 443797-96-4 | >99.50% | |
A dual inhibitor of CDKs and Aurora kinases | ||||
| GC12619 | Alvimopan dihydrate | 170098-38-1 | >98.50% | |
A μ-opioid receptor antagonist | ||||
| GC12622 | HBX 41108 | 924296-39-9 | >98.00% | |
HBX 41108是USP7的强效抑制剂,其IC 50 值为424nM。HBX 41108在体外和细胞中均能影响USP7介导的p53蛋白去泛素化。 | ||||
| GC12627 | Conivaptan HCl | 168626-94-6 | >99.50% | |
A vasopressin V 1A and V 2 receptor antagonist | ||||
| GC12628 | ITE | 448906-42-1 | >99.00% | |
ITE是一种有效的免疫抑制性内源性芳香烃受体(AhR)激动剂,与AhR结合的K i 值为3nM。 | ||||
| GC12631 | Miglustat | 72599-27-0 | - | |
Miglustat (N-Butyldeoxynojirimycin) 是一种具有口服活性的神经酰胺葡糖基转移酶抑制剂。 | ||||
| GC12632 | Cyanopindolol hemifumarate | 106469-57-2 | - | |
5-HT1A/1B antagonist and β-adrenoceptor antagonist | ||||
| GC12637 | PD 180970 | 287204-45-9 | - | |
An inhibitor of Bcr-Abl | ||||
| GC12645 | Imiquimod maleate | 896106-16-4 | >98.00% | |
A TLR7 agonist | ||||
| GC12649 | TW-37 | 877877-35-5 | >99.00% | |
An inhibitor of the Bcl-2 family proteins | ||||
| GC12651 | IRAK inhibitor 2 | 928333-30-6 | >98.50% | |
IRAK inhibitor 2 是 IL-1 受体相关激酶抑制剂。 | ||||
| GC12656 | ZM323881 | 193001-14-8 | >98.00% | |
A potent and selective VEGFR2 inhibitor | ||||
| GC12660 | AZD1208 | 1204144-28-4 | >98.00% | |
AZD1208 是一种有效、高选择性且可口服的 Pim 激酶抑制剂,对 PIM1、PIM2 和 PIM3 的 IC50 值分别为 0.4、5 和 1.9nM。 | ||||
| GC12661 | Indirubin-3'-oxime | 160807-49-8 | >99.00% | |
Inhibitor of GSK3β and cyclin-dependent kinases | ||||
| GC12666 | Cidofovir | 113852-37-2 | >99.00% | |
Cidofovir dihydrate是一种无环单磷酸核苷酸类似物,一种CMV抑制剂,具有抗病毒活性。 | ||||
| GC12680 | DR 2313 | 284028-90-6 | >98.50% | |
A PARP inhibitor | ||||
| GC12683 | Cefaclor monohydrate | 70356-03-5 | >98.00% / >99.00% | |
A cephalosporin antibiotic | ||||
| GC12684 | NCX 4040 | 287118-97-2 | - | |
NCX 4040 (NO-Aspirin) 是一种非甾体抗炎药 (NSAID),是一种一氧化氮 (NO) 释放形式的阿司匹林。 | ||||
| GC12687 | Bimatoprost | 155206-00-1 | >99.50% | |
The ocular hypotensive ingredient in Lumigan | ||||
| GC12690 | MLN8237 (Alisertib) | 1028486-01-2 | >99.00% | |
Alisertib (MLN8237) 作为一种在研、可口服的选择性极光 A 激酶抑制剂,通常用于治疗实体瘤和血液系统恶性肿瘤。 | ||||
| GC12691 | XMD17-109 | 1435488-37-1 | >98.00% | |
A selective ERK5 inhibitor | ||||
| GC12693 | JZL 195 | 1210004-12-8 | >98.00% | |
JZL 195是一种具有高效选择性、不可逆的脂肪酸酰胺水解酶(FAAH)和单酰甘油脂肪酶(MAGL)双重抑制剂,IC 50 值分别为2nM和4nM。 | ||||
| GC12698 | BAY 87-2243 | 1227158-85-1 | >99.50% | |
BAY 87-2243是一种具有高效选择性的缺氧诱导因子-1(HIF-1)抑制剂。 | ||||
