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)
- GC14976Lenalidomide (CC-5013)CAS: 191732-72-6纯度: >99.50%
Lenalidomide (CC-5013)是thalidomide的4-氨基-谷氨酰类似物,具有更强的效力,且不具有thalidomide相关的镇静和神经病变等神经系统副作用。
- GC14987GSK-3 Inhibitor IX (BIO)CAS: 667463-62-9纯度: >99.50%
GSK-3 Inhibitor IX (BIO)是一种强效、选择性和可逆的糖原合成酶激酶-3(GSK-3)抑制剂,对GSK-3α/β的IC 50 值为5nM。
- GC15013VilazodoneCAS: 163521-12-8纯度: >99.00%
Vilazodone (EMD 68843; SB 659746A) 是一种强效、选择性和口服活性的血清素再摄取抑制剂 (SSRI) 和部分 5-HT1A 受体激动剂。
- GC15015(±)-Bay K 8644CAS: 71145-03-4纯度: >98.00%
(±)-Bay K 8644是一种二氢吡啶类化合物,作为特异性的L型钙离子通道激动剂,其EC 50 值为17.3nM
- GC15020Tetracycline HydrochlorideCAS: 64-75-5纯度: >98.50% / >98.00%
A selective antibiotic used in cell culture systems
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC14975 | Loteprednol etabonate | 82034-46-6 | >99.50% | |
A glucocorticoid receptor agonist | ||||
| GC14976 | Lenalidomide (CC-5013) | 191732-72-6 | >99.50% | |
Lenalidomide (CC-5013)是thalidomide的4-氨基-谷氨酰类似物,具有更强的效力,且不具有thalidomide相关的镇静和神经病变等神经系统副作用。 | ||||
| GC14977 | Minoxidil | 38304-91-5 | >99.00% | |
An anti-hypertensive vasodilator | ||||
| GC14983 | GW0742 | 317318-84-6 | >98.00% | |
A selective agonist of PPARδ | ||||
| GC14984 | Diphenylpyraline HCl | 132-18-3 | >99.00% | |
A histamine H 1 receptor antagonist | ||||
| GC14987 | GSK-3 Inhibitor IX (BIO) | 667463-62-9 | >99.50% | |
GSK-3 Inhibitor IX (BIO)是一种强效、选择性和可逆的糖原合成酶激酶-3(GSK-3)抑制剂,对GSK-3α/β的IC 50 值为5nM。 | ||||
| GC14988 | Naphazoline HCl | 550-99-2 | >98.50% | |
A vasoconstrictor | ||||
| GC14991 | ML133 HCl | 1222781-70-5 | >98.00% | |
A K ir 2 channel inhibitor | ||||
| GC14996 | Elvitegravir (GS-9137) | 697761-98-1 | >99.50% | |
An inhibitor of HIV-1 integrase | ||||
| GC14998 | Rocilinostat (ACY-1215) | 1316214-52-4 | >98.00% | |
A selective inhibitor of HDAC6 | ||||
| GC15002 | Sodium Phenylbutyrate | 1716-12-7 | >99.50% | |
Sodium Phenylbutyrate是一种组蛋白去乙酰化酶(HDAC)抑制剂。 | ||||
| GC15008 | Phenylbutazone | 50-33-9 | >99.50% | |
An NSAID and COX inhibitor | ||||
| GC15013 | Vilazodone | 163521-12-8 | >99.00% | |
Vilazodone (EMD 68843; SB 659746A) 是一种强效、选择性和口服活性的血清素再摄取抑制剂 (SSRI) 和部分 5-HT1A 受体激动剂。 | ||||
| GC15014 | A-867744 | 1000279-69-5 | >99.50% | |
A positive allosteric modulator of α7 nAChRs | ||||
| GC15015 | (±)-Bay K 8644 | 71145-03-4 | >98.00% | |
(±)-Bay K 8644是一种二氢吡啶类化合物,作为特异性的L型钙离子通道激动剂,其EC 50 值为17.3nM | ||||
| GC15020 | Tetracycline Hydrochloride | 64-75-5 | >98.50% / >98.00% | |
A selective antibiotic used in cell culture systems | ||||
| GC15022 | Vandetanib (ZD6474) | 443913-73-3 | >99.50% | |
A multi-kinase inhibitor | ||||
| GC15023 | Telmisattan | 144701-48-4 | >99.50% | |
Selective angiotensin II receptor antagonist | ||||
| GC15025 | Fluvoxamine maleate | 61718-82-9 | >99.50% | |
A selective serotonin reuptake inhibitor | ||||
| GC15026 | AN-2690 | 174671-46-6 | >98.00% | |
A broad spectrum antifungal agent | ||||
| GC15028 | JNK-IN-7 | 1408064-71-0 | >98.00% | |
A non-selective JNK inhibitor | ||||
| GC15029 | Glycopyrrolate | 596-51-0 | >99.00% | |
A muscarinic acetylcholine receptor antagonist | ||||
| GC15031 | Rapamycin (Sirolimus) | 53123-88-9 | >98.00% / >99.50% | |
Rapamycin曾经被用作抗真菌抗生素。 | ||||
| GC15034 | SB-334867 free base | 792173-99-0 | >99.50% / >98.00% | |
An orexin 1 receptor antagonist | ||||
