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)
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- JAK/STAT Signaling(13)
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- GPCR/G protein(3)
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- 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)
- GC14624Galanthamine HBrCAS: 1953-04-4
An alkaloid with AChE inhibitory and nAChR potentiating activities
- GC14677FPH2 (BRD-9424)CAS: 957485-64-2纯度: >99.00%
A small molecule inducer of hepatocyte proliferation
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC14572 | KY 02111 | 1118807-13-8 | >99.50% | |
Induces stem cell differentiation | ||||
| GC14576 | Terbinafine HCl | 78628-80-5 | >99.50% | |
A broad-spectrum antifungal agent | ||||
| GC14577 | Sulfacetamide Sodium | 127-56-0 | >99.50% | |
A sulfonamide antibiotic | ||||
| GC14580 | SB705498 | 501951-42-4 | >99.50% | |
SB705498是一种口服生物可利用的、竞争性的辣椒素介导的 TRPV1 受体拮抗剂(人类、大鼠和豚鼠的pKis分别为7.6、7.5和7.3)。SB705498能够快速、可逆地抑制辣椒素、酸或热介导的人类TRPV1激活。 | ||||
| GC14581 | JNJ-1661010 | 681136-29-8 | >98.50% | |
A selective FAAH inhibitor | ||||
| GC14590 | AR-42 (OSU-HDAC42) | 935881-37-1 | - | |
HDAC inhibitor,novel and potent | ||||
| GC14592 | KW 2449 | 1000669-72-6 | >99.50% | |
A multi-kinase inhibitor | ||||
| GC14602 | Avibactam | 1192500-31-4 | - | |
A β-lactamase inhibitor | ||||
| GC14606 | Regorafenib hydrochloride | 835621-07-3 | >99.50% | |
A multi-kinase inhibitor | ||||
| GC14615 | KPT-9274 | 1643913-93-2 | - | |
Orally acitve allosteric inhibitor of PAK4 | ||||
| GC14624 | Galanthamine HBr | 1953-04-4 | - | |
An alkaloid with AChE inhibitory and nAChR potentiating activities | ||||
| GC14632 | Sulfadiazine | 68-35-9 | >99.50% | |
A sulfonamide antibiotic | ||||
| GC14633 | HPGDS inhibitor 1 | 1033836-12-2 | >99.00% | |
An inhibitor H-PGDS | ||||
| GC14636 | KW-2478 | 819812-04-9 | >98.50% | |
An Hsp90 inhibitor | ||||
| GC14643 | AZD8330 | 869357-68-6 | >99.00% | |
A MEK1/2 inhibitor | ||||
| GC14651 | Reversine | 656820-32-5 | >98.00% | |
Reversine是一种靶向Aurora A激酶、Aurora B激酶和MPS1(Monopolar Spindle 1)激酶的非特异性、具有口服活性的小分子抑制剂。Reversine常用于细胞分化和多种癌症的研究。 | ||||
| GC14660 | SU 5402 | 215543-92-3 | >98.00% | |
SU 5402是一种多靶点受体酪氨酸激酶抑制剂,对血管内皮生长因子受体2(VEGF-R2)和成纤维细胞生长因子受体1(FGF-R1)酪氨酸激酶活性的IC 50 分别为20nM和30nM。 | ||||
| GC14667 | Dexamethasone (DHAP) | 50-02-2 | - | |
Glucocorticoidan;anti-inflammatory | ||||
| GC14668 | BAMB-4 | 891025-25-5 | >99.50% | |
BAMB-4 (ITPKA-IN-C14) 是一种特异性且可透过膜的 ITPKA 抑制剂。 BAMB-4 具有很高的稳定性和膜通透性,并能对抗 1,4,5-三磷酸肌醇 (ITPKA) 的 1,4,5-三磷酸肌醇 (InsP3) 激酶活性,IC50 值为 20微米。 BAMB-4可用于肺癌转移的研究。 | ||||
| GC14670 | Aztreonam | 78110-38-0 | >98.00% | |
A β-lactam antibiotic | ||||
| GC14671 | JANEX-1 | 202475-60-3 | >98.00% | |
A selective JAK3 inhibitor | ||||
| GC14672 | RP 001 hydrochloride | 1781880-34-9 | >98.00% | |
A potent S1P 1 receptor agonist | ||||
| GC14673 | Safinamide Mesylate | 202825-46-5 | >98.00% | |
An inhibitor of MAO-B | ||||
| GC14677 | FPH2 (BRD-9424) | 957485-64-2 | >99.00% | |
A small molecule inducer of hepatocyte proliferation | ||||
