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)
- GC17682CalcipotriolCAS: 112965-21-6纯度: >98.00% / >99.00%
卡泊三醇(Calcipotriol)是一种合成的维生素D3 类似物,对维生素D受体具有高亲和力。
- GC17697Calhex 231 hydrochlorideCAS: 652973-93-8纯度: >99.00%
Calhex 231 hydrochloride是一种钙感应受体（CaSR）的负变构调节剂，能够阻断Ca 2+ 诱导的肌醇磷酸酯积累，其在HEK293细胞中的IC 50 值为0.39μM。Calhex 231 hydrochloride常被用于血管相关疾病的研究。
- GC17700R 568 hydrochlorideCAS: 177172-49-5纯度: >99.50% / >98.00%
R 568 hydrochloride是一种能改变钙敏感受体（CaSR）结构构象，立体选择性地提高其对细胞外Ca 2+ 敏感性的拟钙剂。
- GC17733Ketotifen FumarateCAS: 34580-14-8纯度: >99.50%
A histamine H 1 receptor antagonist and mast cell stabilizer
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC17647 | AG-18 | 118409-57-7 | >98.50% | |
An inhibitor of EGF receptor kinase | ||||
| GC17648 | Dinaciclib(SCH727965) | 779353-01-4 | >98.00% | |
A CDK inhibitor | ||||
| GC17657 | Hoechst 34580 | 23555-00-2 | - | |
Hoechst 34580是一种DNA染料，最大激发波长为368nm，最大发射波长为437nm。 | ||||
| GC17662 | NSI-189 | 1270138-40-3 | - | |
An Analytical Reference Standard | ||||
| GC17676 | Nafamostat | 81525-10-2 | - | |
Nafamostat是一种合成的丝氨酸蛋白酶抑制剂。 | ||||
| GC17682 | Calcipotriol | 112965-21-6 | >98.00% / >99.00% | |
卡泊三醇(Calcipotriol)是一种合成的维生素D3 类似物,对维生素D受体具有高亲和力。 | ||||
| GC17686 | AVE 0991 sodium salt | 306288-04-0 | >98.00% | |
A Mas receptor agonist | ||||
| GC17689 | CMX001 | 444805-28-1 | >99.00% | |
CMX001 是一种亲脂性核苷酸类似物，由 3-(hexdecyloxy)propan-1-ol 与西多福韦 (CDV) 共价连接而成，用于治疗天花。 | ||||
| GC17697 | Calhex 231 hydrochloride | 652973-93-8 | >99.00% | |
Calhex 231 hydrochloride是一种钙感应受体（CaSR）的负变构调节剂，能够阻断Ca 2+ 诱导的肌醇磷酸酯积累，其在HEK293细胞中的IC 50 值为0.39μM。Calhex 231 hydrochloride常被用于血管相关疾病的研究。 | ||||
| GC17698 | SJB2-043 | 63388-44-3 | >99.00% | |
An inhibitor of the USP1-UAF1 complex and SARS-CoV-2 PL pro | ||||
| GC17700 | R 568 hydrochloride | 177172-49-5 | >99.50% / >98.00% | |
R 568 hydrochloride是一种能改变钙敏感受体（CaSR）结构构象，立体选择性地提高其对细胞外Ca 2+ 敏感性的拟钙剂。 | ||||
| GC17701 | Clemizole hydrochloride | 1163-36-6 | >99.50% | |
An antihistamine and TRPC5 channel blocker | ||||
| GC17703 | TMP269 | 1314890-29-3 | >98.00% | |
A selective class IIa HDAC inhibitor | ||||
| GC17707 | Bismuth Subsalicylate | 14882-18-9 | - | |
Bismuth Subsalicylate 是一种有效的、具有口服活性的抗酸剂和止泻剂。 | ||||
| GC17708 | IWP-L6 | 1427782-89-5 | >99.50% | |
A potent inhibitor of Porcupine | ||||
| GC17710 | A-317491 | 475205-49-3 | >99.00% | |
A-317491是一种高亲和力、选择性的P2X3和P2X2/3受体激活拮抗剂，其对大鼠P2X3和P2X2/3的K i 值分别为22nM和92nM。 | ||||
| GC17723 | 4-IBP | 155798-08-6 | >98.00% | |
A σ1 receptor ligand | ||||
| GC17728 | Cefoselis | 122841-10-5 | - | |
A cephalosporin antibiotic | ||||
| GC17731 | Betaxolol HCl | 63659-19-8 | >98.50% | |
A selective β 1 -adrenergic receptor antagonist | ||||
| GC17733 | Ketotifen Fumarate | 34580-14-8 | >99.50% | |
A histamine H 1 receptor antagonist and mast cell stabilizer | ||||
| GC17737 | PD 169316 | 152121-53-4 | >98.00% | |
A specific p38 MAPK inhibitor | ||||
| GC17741 | Vanoxerine dihydrochloride | 67469-78-7 | >98.00% | |
An inhibitor of dopamine uptake | ||||
| GC17748 | Dorzolamide HCl | 130693-82-2 | >99.50% | |
A carbonic anhydrase inhibitor | ||||
| GC17753 | AH 7614 | 6326-06-3 | >98.00% | |
A selective FFAR4 antagonist | ||||