ALADDIN SCIENTIFIC
Supplier:
ALADDIN SCIENTIFIC
Description:
2-Amino-3-chloro-5-nitropyridine ≥97%
Supplier:
ALADDIN SCIENTIFIC
Description:
Reactant: Evaulated as a small molecule inhibitor of CD4-gp120 binding Reagent Involved in solvothermal preparation of germanium oxide hydroxide 3D net zeotype Involved in zeolite synthesis Coupling agent for adhesive systems
Supplier:
ALADDIN SCIENTIFIC
Description:
Biflavonoid with anti-inflammatory, anti-viral and cancer chemopreventive activity. It inhibits vascularization of tumors by blocking the activity of angiogenic VEGFs. Blocks the induction of COX-2 and up-regulates PPAR-γ. It is a negative modulator of the GABAA receptor at the benzodiazepine binding site.
Supplier:
ALADDIN SCIENTIFIC
Description:
(S)-3-Amino-4-oxo-4-(((R)-1-oxo-1-((2,2,4,4-tetramethylthietan-3-yl)amino)propan-2-yl)amino)butanoic acid ≥95%
Supplier:
ALADDIN SCIENTIFIC
Description:
Reactant for synthesis of: TRPV1 antagonists CHK1 inhibitors p38a MAP kinase inhibitors Carbamoylphosphonates Macrolactams via c
Supplier:
ALADDIN SCIENTIFIC
Description:
2-Amino-4,5-dimethylthiophene-3-carbonitrile ≥98%
Supplier:
ALADDIN SCIENTIFIC
Description:
Nanocs' metal chelate PEG conjugates were made to chelate metal ions for biomedical applications. Pegylated metal chelators have strong afinity with many metal ions and they are water soluble. Conjugates were provided in lyophilized powder form.
Catalog Number:
(ALA163108500MG)
Supplier:
ALADDIN SCIENTIFIC
Description:
4 arm PEG derivatives have multiple reactive groups that can be used to modify proteins, peptides and other materials via their 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:
5-Aminovaleric acid hydrochloride ≥98%
Supplier:
ALADDIN SCIENTIFIC
Description:
Ethyl 1-(aminomethyl)cyclopropanecarboxylate ≥95%
Supplier:
ALADDIN SCIENTIFIC
Description:
4-(Aminomethyl)-N,N-diethylaniline ≥97%
Supplier:
ALADDIN SCIENTIFIC
Description:
6-Bromo-2-naphthylamine ≥98%
Supplier:
ALADDIN SCIENTIFIC
Description:
Avanafil is a highly selective PDE5 inhibitor with IC50 of 5.2 nM, >121-fold selectivity over other PDEs.
Supplier:
ALADDIN SCIENTIFIC
Description:
1-(2-Amino-5-bromophenyl)ethanone ≥98%
Supplier:
ALADDIN SCIENTIFIC
Description:
AZD5363 potently inhibits all isoforms of Akt(Akt1/Akt2/Akt3) with IC50 of 3 nM/8 nM/8 nM in cell-free assays, similar to P70S6K/PKA and lower activity towards ROCK1/2.
Supplier:
ALADDIN SCIENTIFIC
Description:
1-Allylhydantoin ≥98%
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