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)
- GC17391Physostigmine hemisulfateCAS: 64-47-1纯度: >99.00% / >99.50%
毒扁豆碱半硫酸盐 (Eserine hemisulfate) 是一种可逆的乙酰胆碱酯酶 (AChE) 抑制剂。
- GC17392PB 28 dihydrochlorideCAS: 172907-03-8纯度: >99.50%
A σ receptor ligand with anticancer and antiviral activities
- GC17412Deferasirox Fe3+ chelateCAS: 554435-83-5纯度: >98.00%
Deferasirox Fe3+ Chelate 是从专利 WO2003053986 中提取的铁螯合剂。
- GC17426Cobimetinib (racemate)CAS: 934662-91-6纯度: >99.50%
Cobimetinib（消旋体）（GDC-0973 消旋体；XL518 消旋体）是 Cobimetinib 的消旋体。 Cobimetinib 是一种有效的选择性 MEK 抑制剂。
- GC17427Geneticin, G-418 SulfateCAS: 108321-42-2纯度: {{1-12}>98.00%}
Geneticin，G-418硫酸盐是一类氨基糖苷类抗生素，其结构与新霉素卡那霉素相似。
- GC17452LDK378 dihydrochlorideCAS: 1380575-43-8纯度: >99.50%
LDK378 dihydrochloride (LDK378 dihydrochloride) 是一种选择性、口服生物利用度和 ATP 竞争性的 ALK 酪氨酸激酶抑制剂，IC50 为 200 pM。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC17385 | KML 29 | 1380424-42-9 | >98.50% | |
An inhibitor of MAGL | ||||
| GC17386 | YK-4-279 | 1037184-44-3 | >98.00% | |
YK-4-279 阻断 RNA Helicase A (RHA) 与 EWS-FLI1（致癌蛋白）的结合。 YK-4-279 诱导细胞凋亡并对各种癌细胞显示出抗增殖活性。 YK-4-279 有一个手性中心，它可以分成两种对映体。 YK-4-279可用于癌症研究。 | ||||
| GC17389 | Gatifloxacin hydrochloride | 121577-32-0 | >98.00% | |
A fluoroquinolone antibiotic | ||||
| GC17390 | Vorinostat (SAHA, MK0683) | 149647-78-9 | >98.00% / >99.00% | |
An HDAC inhibitor | ||||
| GC17391 | Physostigmine hemisulfate | 64-47-1 | >99.00% / >99.50% | |
毒扁豆碱半硫酸盐 (Eserine hemisulfate) 是一种可逆的乙酰胆碱酯酶 (AChE) 抑制剂。 | ||||
| GC17392 | PB 28 dihydrochloride | 172907-03-8 | >99.50% | |
A σ receptor ligand with anticancer and antiviral activities | ||||
| GC17396 | Tulathromycin A | 217500-96-4 | >99.00% | |
A macrolide antibiotic | ||||
| GC17405 | Chetomin | 1403-36-7 | >95.00% | |
Chetomin是一种来源于 Chaetomium 属真菌的天然生物碱，具有显著的抗癌和抗炎作用。 | ||||
| GC17412 | Deferasirox Fe3+ chelate | 554435-83-5 | >98.00% | |
Deferasirox Fe3+ Chelate 是从专利 WO2003053986 中提取的铁螯合剂。 | ||||
| GC17414 | Palosuran | 540769-28-6 | >99.00% | |
A urotensin II receptor antagonist | ||||
| GC17421 | Vicriviroc maleate | 599179-03-0 | >99.50% | |
A CCR5 antagonist | ||||
| GC17426 | Cobimetinib (racemate) | 934662-91-6 | >99.50% | |
Cobimetinib（消旋体）（GDC-0973 消旋体；XL518 消旋体）是 Cobimetinib 的消旋体。 Cobimetinib 是一种有效的选择性 MEK 抑制剂。 | ||||
| GC17427 | Geneticin, G-418 Sulfate | 108321-42-2 | {{1-12}>98.00%} | |
Geneticin，G-418硫酸盐是一类氨基糖苷类抗生素，其结构与新霉素卡那霉素相似。 | ||||
| GC17430 | 2-Deoxy-D-glucose | 154-17-6 | >98.00% | |
2-Deoxy-D-glucose (2DG)，是一种葡萄糖类似物，作为竞争性糖酵解抑制剂。 | ||||
| GC17439 | Ledipasvir | 1256388-51-8 | >99.50% | |
An HCV NS5A inhibitor | ||||
| GC17440 | Epothilone D | 189453-10-9 | >99.50% | |
A microtubule-stabilizing agent | ||||
| GC17443 | Metformin HCl | 1115-70-4 | >98.00% | |
A biguanide with diverse biological activities | ||||
| GC17444 | TFLLR-NH2 | 197794-83-5 | - | |
A peptide agonist of PAR1 | ||||
| GC17452 | LDK378 dihydrochloride | 1380575-43-8 | >99.50% | |
LDK378 dihydrochloride (LDK378 dihydrochloride) 是一种选择性、口服生物利用度和 ATP 竞争性的 ALK 酪氨酸激酶抑制剂，IC50 为 200 pM。 | ||||
| GC17455 | TAK-632 | 1228591-30-7 | >98.00% | |
A selective pan-Raf inhibitor | ||||
| GC17456 | NMDA (N-Methyl-D-aspartic acid) | 6384-92-5 | >98.00% | |
An excitatory neurotransmitter | ||||
| GC17457 | FRATide | 251087-38-4 | - | |
GSK-3 inhibitor | ||||
| GC17458 | Sulfamerazine sodium salt | 127-58-2 | - | |
A sulfonamide antibiotic | ||||
| GC17464 | Prasugrel | 150322-43-3 | >98.00% | |
A prodrug form of R-99224 | ||||