Comparison

cIAP1 Ligand-Linker Conjugates 15 (hydrochloride) European Partner

Item no. HY-128813A-1g
Manufacturer MedChem Express
CASRN 1225383-36-7
Amount 1 g
Quantity options 1 g 2 g
Category
Type Molecules
Specific against other
Citations [1]Itoh Y, et al. Protein knockdown using methyl bestatin-ligand hybrid molecules: design and synthesis of inducers of ubiquitination-mediated degradation of cellular retinoic acid-binding proteins. J Am Chem Soc. 2010 Apr 28;132(16):5820-6.
Smiles NCCOCCOCCOC([C@H](CC(C)C)NC([C@@H](O)[C@@H](CC1=CC=CC=C1)NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)=O)=O.Cl
ECLASS 10.1 32169090
ECLASS 11.0 32169090
UNSPSC 12000000
Alias E3 ligase Ligand-Linker Conjugates 34 (hydrochloride)
Shipping Condition Room temperature
Available
Manufacturer - Type
Reference compound
Manufacturer - Applications
Cancer-programmed cell death
Manufacturer - Targets
E3 Ligase Ligand-Linker Conjugates
Shipping Temperature
Room temperature
Molecular Weight
698.25
Product Description
cIAP1 Ligand-Linker Conjugates 15 hydrochloride incorporates an IAP ligand for the E3 ubiquitin ligase, and a PROTAC linker. cIAP1 Ligand-Linker Conjugates 15 hydrochloride can be used to design SNIPERs[1].
Manufacturer - Research Area
Cancer
Solubility
10 mM in DMSO
Manufacturer - Pathway
PROTAC
Isoform
cIAP1
Clinical information
No Development Reported

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 1 g
Available: In stock
available

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