Other Signal Transduction
Signal Transduction
Cellular responses are triggered by proteins, drugs, or pathogens binding to specific receptors. Receptor mediated signaling is a cascade of enzymatic reactions that amplifies the signal. The agonists and antagonists modulating receptor functionality are essential tools for research and medical practice. read more
Products Related to Other Signal Transduction(131)
- GC49692Tofacitinib-d3 (citrate)Purity: >99.00%
An internal standard for the quantification of tofacitinib
- GC49890β-Glycerophosphate-d5 (sodium salt hydrate)Purity: >99.00%
An internal standard for the quantification of β-glycerophosphate
- GC4991213C20,15N10-Cyclic di-GMP (sodium salt)Purity: >98.00%
An internal standard for the quantification of cyclic di-GMP
- GC52002EmavusertibCAS: 1801344-14-8Purity: >99.00%
Emavusertib (CA-4948) es un potente inhibidor de IRAK4/FLT3 con actividad antitumoral.
- GC52274Y-33075 (hydrochloride)CAS: 471843-75-1Purity: >98.00%
Y-33075 (hydrochloride) es un potente inhibidor de la quinasa asociada a Rho ROCK, con un IC 50 de 3.6nM.
- GC90529Myelin Basic Protein Peptide (mouse, bovine) (trifluoroacetate salt)Purity: >95.00%
Un sustrato péptido para PKC
- GC90893Rp-Adenosine-5'-O-(1-thiodiphosphate) (sodium salt)CAS: 2005478-89-5Purity: >95.00%
Un isómero de ADP-α-S
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC49403 | Benzarone | 1477-19-6 | >98.00% | |
La benzarona (Fragivix) es un potente inhibidor del transportador de Ácido Úrico humano 1 (hURAT1), con una IC50 de 2,8 μM en el ovocito. | ||||
| GC49433 | Capsiate | 205687-01-0 | >85.00% | |
El capsiato, como un anÁlogo de la capsaicina extraÍdo de una variedad no picante de pimiento rojo dulce CH-19, es un agonista activo por vÍa oral de TRPV1. | ||||
| GC49494 | 4-Aminobenzylphosphonic Acid | 5424-27-1 | >95.00% | |
An alkaline phosphatase inhibitor | ||||
| GC49556 | Cl-Necrostatin-1 | 862377-51-3 | >95.00% | |
A RIPK1 inhibitor | ||||
| GC49692 | Tofacitinib-d3 (citrate) | - | >99.00% | |
An internal standard for the quantification of tofacitinib | ||||
| GC49789 | Dihydronarwedine | 21041-10-1 | >90.00% | |
An alkaloid and GSK3β inhibitor | ||||
| GC49890 | β-Glycerophosphate-d5 (sodium salt hydrate) | - | >99.00% | |
An internal standard for the quantification of β-glycerophosphate | ||||
| GC49912 | 13C20,15N10-Cyclic di-GMP (sodium salt) | - | >98.00% | |
An internal standard for the quantification of cyclic di-GMP | ||||
| GC50003 | AG 490 | 133550-30-8 | >98% | |
EGFR-kinase inhibitor. Also JAK2, JAK3 inhibitor | ||||
| GC52002 | Emavusertib | 1801344-14-8 | >99.00% | |
Emavusertib (CA-4948) es un potente inhibidor de IRAK4/FLT3 con actividad antitumoral. | ||||
| GC52115 | S-99 | 1124381-69-6 | >98.00% | |
An inhibitor of ASK1 | ||||
| GC52129 | 3-Amino-5-hydroxybenzoic Acid | 76045-71-1 | >98.00% | |
| GC52141 | 2-Chloro-N-methyl-N-(4-nitrophenyl)acetamide | 2653-16-9 | >98.00% | |
| GC52151 | PKCθ Inhibitor (hydrochloride) | 2253640-49-0 | >98.00% | |
| GC52274 | Y-33075 (hydrochloride) | 471843-75-1 | >98.00% | |
Y-33075 (hydrochloride) es un potente inhibidor de la quinasa asociada a Rho ROCK, con un IC 50 de 3.6nM. | ||||
| GC52277 | ENPP3 Inhibitor | 333413-02-8 | >95.00% | |
An ENPP3 inhibitor | ||||
| GC52322 | ENPP3 Inhibitor 4t | - | >95.00% | |
An ENPP3 inhibitor | ||||
| GC52328 | KYL (trifluoroacetate salt) | - | >95.00% | |
An EphA4 inhibitor | ||||
| GC52336 | ENPP1 Inhibitor 43 | 2631703-41-6 | >98.00% | |
An ENPP1 inhibitor | ||||
| GC52361 | AMARA Peptide (trifluoroacetate salt) | - | >95.00% | |
A peptide substrate for AMPK | ||||
| GC52362 | ENPP3 Inhibitor 4g | 2803505-78-2 | >95.00% | |
An ENPP1 and ENPP3 inhibitor | ||||
| GC90529 | Myelin Basic Protein Peptide (mouse, bovine) (trifluoroacetate salt) | - | >95.00% | |
Un sustrato péptido para PKC | ||||
| GC90886 | SZM-1209 | 2919801-86-6 | >98.00% | |
Un inhibidor de RIPK1 | ||||
| GC90893 | Rp-Adenosine-5'-O-(1-thiodiphosphate) (sodium salt) | 2005478-89-5 | >95.00% | |
Un isómero de ADP-α-S | ||||