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)
- GC122582,3-DCPE hydrochlorideCAS: 418788-90-6
2,3-DCPE 是一种促凋亡化合物，对癌细胞\u003cem\u003e相对于\u003c/em\u003e正常人细胞具有选择性
- GC12534ICI 199,441 hydrochlorideCAS: 115199-84-3纯度: >97.00%
ICI 199,441 hydrochloride 是一种有效的选择性 κ-阿片受体激动剂。
- GC13645nor-Binaltorphimine dihydrochlorideCAS: 113158-34-2纯度: >98.00%
nor-Binaltorphimine dihydrochloride是一种有效的选择性κ阿片受体（KOR）拮抗剂。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC12141 | RO4987655 | 874101-00-5 | >99.00% | |
A MEK inhibitor | ||||
| GC12143 | Deltorphin I | 122752-15-2 | - | |
Deltorphin I 是一种 δ-阿片受体激动剂，具有高亲和力和选择性。 | ||||
| GC12258 | 2,3-DCPE hydrochloride | 418788-90-6 | - | |
2,3-DCPE 是一种促凋亡化合物，对癌细胞\u003cem\u003e相对于\u003c/em\u003e正常人细胞具有选择性 | ||||
| GC12372 | SC-514 | 354812-17-2 | >99.50% | |
Selective inhibitor of IKK2 | ||||
| GC12534 | ICI 199,441 hydrochloride | 115199-84-3 | >97.00% | |
ICI 199,441 hydrochloride 是一种有效的选择性 κ-阿片受体激动剂。 | ||||
| GC12548 | UNC 0631 | 1320288-19-4 | >99.00% | |
An inhibitor of G9a/GLP methyltransferases | ||||
| GC12659 | Begacestat | 769169-27-9 | >99.50% | |
An inhibitor of γ-secretase | ||||
| GC12663 | N-Benzylnaltrindole hydrochloride | 1206487-81-1 | - | |
δ2 opioid receptor antagonist | ||||
| GC12688 | (+)-U-50488 hydrochloride | 114528-81-3 | - | |
An Analytical Reference Material | ||||
| GC12701 | NSC 207895 (XI-006) | 58131-57-0 | >98.00% | |
An inhibitor of MDMX | ||||
| GC12724 | Phenoxybenzamine HCl | 63-92-3 | >98.00% | |
An α-AR antagonist | ||||
| GC12810 | SR 11302 | 160162-42-5 | >98.00% / >95.00% | |
SR 11302是一种类视黄醇类AP-1选择性转录因子抑制剂，能够阻断AP-1活性，而不激活视黄醇反应元件（RARE）转录。 | ||||
| GC13097 | ICI 204,448 hydrochloride | 121264-04-8 | - | |
κ opioid receptor agonist | ||||
| GC13103 | AZ505 ditrifluoroacetate | 1035227-44-1 | >99.50% | |
An inhibitor of SMYD2 | ||||
| GC13189 | Cyprodime hydrochloride | 118111-54-9 | - | |
μ-opioid receptor antagonist | ||||
| GC13393 | Epinephrine Bitartrate | 51-42-3 | - | |
肾上腺素能受体激动剂 | ||||
| GC13471 | kb-NB77-78 | 1350622-33-1 | >99.50% | |
An inactive analog of CID755673 | ||||
| GC13498 | BM-1074 | 1391108-10-3 | - | |
BM-1074 是一种有效且特异性的 Bcl-2/Bcl-xL 抑制剂，对 Bcl-2 和 Bcl-xL 的 Ki 值 < 1 nM，IC50 值分别为 1.8 nM 和 6.9 nM。 BM-1074 诱导细胞凋亡，并对四种小细胞肺癌细胞系（H146、H1963、H187 和 H1417）具有抗增殖活性，IC50 值为 1-2 nM。 | ||||
| GC13529 | CC-401 | 395104-30-0 | - | |
A potent, specific pan-JNK inhibitor | ||||
| GC13546 | Dynorphin A | 80448-90-4 | >98.50% | |
Dynorphin A是一种内源性阿片肽，可激活孤儿受体XOR1-K + 通道，EC 50 值为45nM。 | ||||
| GC13581 | SB 205607 dihydrobromide | 148545-09-9 | - | |
non-peptide δ1 opioid receptor agonist | ||||
| GC13612 | PIK-294 | 900185-02-6 | >99.50% | |
A potent inhibitor of p110δ | ||||
| GC13645 | nor-Binaltorphimine dihydrochloride | 113158-34-2 | >98.00% | |
nor-Binaltorphimine dihydrochloride是一种有效的选择性κ阿片受体（KOR）拮抗剂。 | ||||
| GC13687 | NSC 66811 | 6964-62-1 | >98.00% | |
A potent inhibitor of Mdm2-p53 interaction | ||||