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)
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- 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)
- GC13815Vinflunine TartrateCAS: 1201898-17-0
Etanercept is an inhibitor of the inflammatory factor TNF-α and is mainly used for the clinical treatment of rheumatoid arthritis .
- GC14080Apogossypolone (ApoG2)CAS: 886578-07-0
Apogossypolone (ApoG2) (ApoG2) 是一种具有口服活性的 Bcl-2 家族蛋白抑制剂,对 Bcl-2、Mcl-1 和 Bcl-XL 的 Ki 值分别为 35、25 和 660 nM。
- GC15261Guanosine-2'(3')-monophosphate disodium saltCAS: 6027-83-4
A mixture of the 2' and 3'-isomers of GMP
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC13688 | Naltrindole hydrochloride | 111469-81-9 | - | |
A potent, selective δ-opioid receptor antagonist | ||||
| GC13738 | SKLB1002 | 1225451-84-2 | - | |
A VEGFR2 inhibitor | ||||
| GC13744 | AZ505 | 1035227-43-0 | >99.50% | |
An inhibitor of SMYD2 | ||||
| GC13815 | Vinflunine Tartrate | 1201898-17-0 | - | |
Etanercept is an inhibitor of the inflammatory factor TNF-α and is mainly used for the clinical treatment of rheumatoid arthritis . | ||||
| GC13868 | GNE-9605 | 1536200-31-3 | >99.50% | |
A potent LRRK2 inhibitor | ||||
| GC13901 | AS-252424 | 900515-16-4 | >99.00% | |
A potent, selective inhibitor of PI3-kinase γ | ||||
| GC13910 | Salvinorin A | 83729-01-5 | >95.00% | |
An Analytical Reference Material | ||||
| GC14080 | Apogossypolone (ApoG2) | 886578-07-0 | - | |
Apogossypolone (ApoG2) (ApoG2) 是一种具有口服活性的 Bcl-2 家族蛋白抑制剂,对 Bcl-2、Mcl-1 和 Bcl-XL 的 Ki 值分别为 35、25 和 660 nM。 | ||||
| GC14310 | NVP-ADW742 | 475488-23-4 | >99.00% | |
An IGF-1R inhibitor | ||||
| GC14318 | CAY10505 | 1218777-13-9 | >99.50% | |
Inhibitor of PI3Kγ | ||||
| GC14525 | ML 190 | 1355244-02-8 | - | |
ML 190 是一种选择性 κ 阿片受体 (KOR) 拮抗剂,IC50 分别为 120 nM 和 EC50 分别为 129 nM 。 | ||||
| GC14613 | Aldicarb | 116-06-3 | - | |
cholinesterase inhibitor | ||||
| GC14739 | GR 89696 fumarate | 126766-32-3 | - | |
κ-opioid agonist | ||||
| GC14774 | DSLET | 75644-90-5 | - | |
δ Opioid receptor agonist | ||||
| GC14868 | Milrinone | 78415-72-2 | >99.50% | |
An inhibitor of PDE3 | ||||
| GC14886 | PETCM | 10129-56-3 | - | |
PETCM 是 caspase-3 的激活剂,并以细胞色素 c (细胞 c) 依赖性方式发挥作用。 PETCM 促进 Apaf-1 寡聚化并诱导 HeLa 细胞中的细胞凋亡。 | ||||
| GC14979 | N-MPPP Hydrochloride | 207452-97-9 | - | |
High affinity κ agonist | ||||
| GC15035 | PM00104 | 308359-57-1 | - | |
Potent antimyeloma agent | ||||
| GC15062 | Ki16198 | 355025-13-7 | >98.50% | |
Ki16198 是一种有效且具有口服活性的 LPA 受体拮抗剂,即 Ki16425 的甲酯。 Ki16198 抑制 LPA1 和 LPA3 诱导的磷酸肌醇产生,Ki 值分别为 0.34 μM 和 0.93 μM。 Ki16198 对体内胰腺癌的肿瘤发生和转移有效。 | ||||
| GC15078 | Dynorphin B | 83335-41-5 | - | |
An endogenous κ 1b -opioid receptor agonist | ||||
| GC15179 | Ketorolac | 74103-06-3 | - | |
An NSAID and COX inhibitor | ||||
| GC15261 | Guanosine-2'(3')-monophosphate disodium salt | 6027-83-4 | - | |
A mixture of the 2' and 3'-isomers of GMP | ||||
| GC15313 | BRL 52537 hydrochloride | 112282-24-3 | - | |
κ/μ opioid receptor agonist,potent and selective | ||||
| GC15480 | Marinopyrrole A | 1227962-62-0 | >99.50% | |
An alkaloid with antibacterial activity | ||||
