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ALADDIN SCIENTIFIC
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ALADDIN SCIENTIFIC
Supplier:
ALADDIN SCIENTIFIC
Description:
Triapine ≥98% (by HPLC)
Supplier:
ALADDIN SCIENTIFIC
Description:
H-D-4-Pal-OH·2HCl ≥98%
Supplier:
ALADDIN SCIENTIFIC
Description:
Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.Product Introduction:A cell-permeable pyrimidinyl compound that displays anti-inflammatory properties. Acts as a potent, reversible, and ATP-competitive inhibitor of c-Jun N-terminal kinase (JNK, IC50 = 150, 220, and 70 nM for hJNK1, hJNK2, and hJNK3, respectively) with a 10- to 100-fold greater selectivity over a panel of 25 other commonly studied kinases (IC50 typically in the range of 1-10 µM or no effect at 10 µM). Its in vivo efficacy has been demonstrated in gerbils, mice, and rats via oral, i.v., or i.p. administration. Biochemical mechanism:Cell permeable: yesProduct competes with ATP.Primary TargethJNK 1, hJNK 2, hJNK 3Reversible: yesTarget IC50: 150, 220, and 70 nM for hJNK1, hJNK2, and hJNK3, respectively
Supplier:
ALADDIN SCIENTIFIC
Description:
Product Introduction:Aminopurvalanol A is a potent, selective, and cell permeable inhibitor of Cyclins/Cdk complexes. Aminopurvalanol A preferentially targets the G2/M-phase transition inhibiting cancer cell differentiation. Aminopurvalanol A causes the inhibition of sperm fertilizing ability via the inhibition of physiological capacitation-dependent actin polymerization.
Supplier:
ALADDIN SCIENTIFIC
Description:
2-(3-Aminooxetan-3-yl)ethan-1-ol hemioxalate ≥97%
Catalog Number:
(ALA151770-1G)
Supplier:
ALADDIN SCIENTIFIC
Description:
5-Amino-6-chloro-2,3-dicyanopyrazine ≥98%
Supplier:
ALADDIN SCIENTIFIC
Description:
Key building block for the efficient synthesis of carbazole alkaloids mukonine and mukonidine via oxidative annulation.
Supplier:
ALADDIN SCIENTIFIC
Description:
6-Amino-2H-1,4-benzoxazin-3(4H)-one 97
Supplier:
ALADDIN SCIENTIFIC
Description:
7-Amino-1-tetralone ≥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:
2-Ethoxypyridin-4-amine ≥95%
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ALADDIN SCIENTIFIC
Description:
3-Aminopiperidin-2-one hydrochloride ≥95%
Supplier:
ALADDIN SCIENTIFIC
Description:
5-Allyl-3-methoxysalicylaldehyde ≥98%
Catalog Number:
(ALA283288-5G)
Supplier:
ALADDIN SCIENTIFIC
Description:
Aluminium sulfide ≥99%
Supplier:
ALADDIN SCIENTIFIC
Description:
Application:2-Amino-5-chlorobenzamide react with 2-Azido-benzoyl chloride to get 2-Azido-5'-chloro-2'-carboxamidobenzanilide.
Supplier:
ALADDIN SCIENTIFIC
Description:
ɑ,ɑ'-Dianilino-p-xylene ≥98%
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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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