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ALADDIN SCIENTIFIC
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ALADDIN SCIENTIFIC
Catalog Number:
(ALA126970-5MG)
Supplier:
ALADDIN SCIENTIFIC
Description:
17-AAG (Tanespimycin) is a potent HSP90 inhibitor with IC50 of 5 nM, having a 100-fold higher binding affinity for HSP90 derived from tumour cells than HSP90 from normal cells.A potent Hsp90 inhibitor for tumor cells
Supplier:
ALADDIN SCIENTIFIC
Description:
4-Aminocyclohexanecarboxylic acid (mixture of cis and trans isomers) ≥95%
Supplier:
ALADDIN SCIENTIFIC
Description:
Azetidin-3-amine dihydrochloride ≥97%
Catalog Number:
(ALA264876-25G)
Supplier:
ALADDIN SCIENTIFIC
Description:
Ammonium thiosulfate is a non-toxic inorganic compound that is majorly used as a fertilizer and can be used as an alternative to cyanide based leaching. It has a hygroscopic nature and is soluble in water. It can be produced by the reaction of ammonia, water, and sulfur dioxide. It can be used as a photographic fixing salt.Ammonium thiosulfide can be used as a source of sulfur for the formation of cadmium sulfide thin films for electronic applications.It can also be used in the treatment of copper-gold ores for the recovery of gold.
Supplier:
ALADDIN SCIENTIFIC
Description:
2-Aminopentane ≥97% (by GC)
Supplier:
ALADDIN SCIENTIFIC
Description:
Methyl α-bromoisobutyrate was used in Reformatsky reaction to prepare 1,4-disubstituted 3,3-dimethylazetidin-2-ones.Atom Transfer Radical Polymerization (ATRP) initiator that will generate a polymer with a methyl end group
Supplier:
ALADDIN SCIENTIFIC
Description:
A 83-01 is a potent inhibitor of TGF-β type I receptor ALK5 kinase, type I nodal receptor ALK4 and type I nodal receptor ALK7, with IC50s of 12 nM, 45 nM and 7.5 nM against the transcription induced by ALK5, ALK4 and ALK7, respectively。
Supplier:
ALADDIN SCIENTIFIC
Description:
Allyl phenyl sulfone ≥95% (by GC)
Supplier:
ALADDIN SCIENTIFIC
Description:
7-Aza-spiro[3.5]nonane hydrochloride ≥97%
Supplier:
ALADDIN SCIENTIFIC
Description:
Acrylate functionalized polyethylene glycol (PEG Acrylate) is a reactive PEG derivative that can be used to modify proteins, peptides and other materials via available acrylic groups. It is also a polymerizable PEG that can form biocompatible hydrogel. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces.
Catalog Number:
(ALA151770-1G)
Supplier:
ALADDIN SCIENTIFIC
Description:
5-Amino-6-chloro-2,3-dicyanopyrazine ≥98%
Supplier:
ALADDIN SCIENTIFIC
Description:
4-Bromo-2-(trifluoromethyl)aniline has been used in the preparation of 2,5-dibromo-(trifluoromethyl)benzene and 5-bromo-2-iodo-(trifluoromethyl)benzene.
Supplier:
ALADDIN SCIENTIFIC
Description:
Product Introduction:3-Aminobenzophenone forms cyclodextrin (α and β) based nanostructures through the supramolecular self assembly.  Application3-Aminobenzophenone has been used in the synthesis of racemic benzophenone ureas, chiral photoaffinity labeling probes.
Supplier:
ALADDIN SCIENTIFIC
Description:
4-Bromo-3-methylisoxazol-5-amine 97
Catalog Number:
(ALA163303500MG)
Supplier:
ALADDIN SCIENTIFIC
Description:
Azide/azido functionalized polyethylene glycol (N3-PEG-X) is a bifunctional PEG derivative that can be used to modify proteins, peptides and other materials. Azide group can react with alkyne in aqueous solution catalyzed by copper. It can also be reduced into amine group easily while another functional group can be react with other molecules or functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces.
Supplier:
ALADDIN SCIENTIFIC
Description:
Reactant for: Preparation of a diol and carbamate chemistry library for common functional groups Regioselective synthesis of alkenes via semihydrogenation and semihydrogenation-oxidation of dienes Alkene addition of frustrated Lewis pairs Olefination of N-sulfonyl imines for stereoselective synthesis of vinyl arenes Wittig olefination of aldehydes for preparation of conjugated dienes Tandem Michael addition / ylide olefination reactions for the synthesis of highly functionalized cyclohexadienes
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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