h-ntpdase-in-4

h-NTPDase-IN-4 is a pan-inhibitor of NTPDase, which can inhibit h-NTPDase1, 1h-NTPDase2, h-NTPDase3, h-NTPDase8. The IC50 values were 3.58 μM, 10.21 μM, 0.13 μM and 13.57 μM, respectively.

h-NTPDase-IN-3 is an h-NTPDase inhibitor that inhibits h-NTPDase1, h-NTPDase2, h-NTPDase3 and h-NTPDase8.

h-NTPDase-IN-2 is a broad-spectrum NTPDase inhibitor that inhibits multiple h-NTPDas isoforms.

H-Phg(4-Cl)-OH is an amino acid derivative with extensive applications in life science research.

H-Phe(4-NO2)-OH.H2O is an amino acid derivative and has a wide range of applications in life science related research.

H-D-Phe(4-CN)-OH is an important organic compound utilized in life sciences research, catalog number T65897 and CAS number 263396-44-7.

(2S,4R)-H-L-Pro(4-N3)-OH is a click chemistry reagent containing an azido group. It is used in various biochemical research applications.

(2R,4R)-H-D-Pro(4-N3)-OH (hydrochloride) is a click chemistry reagent featuring an azide group that enables it to undergo copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules containing alkyne groups. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition reactions (SPAAC) with molecules that have DBCO or BCN groups.

H-DL-Phe(4-NO2)-OH is a valuable organic compound used in life sciences research, identified by catalog number T67312 and CAS number 2922-40-9.

H-D-4-Pal-OH.2HCl, an amino acid derivative, has a wide range of applications in life science research.

H-4-Nitro-Phe-OEt . HCl is an alanine derivative.

(2S,4S)-H-L-Pro(4-N3)-OH is a click chemistry reagent featuring an azide group. Click chemistry holds immense potential for creating bonds between nucleic acids, lipids, proteins, and other molecules, and is utilized across various research domains due to its high yield, specificity, and simplicity.

H-Phe(4-NO2)-OMe.HCl is an amino acid derivative and has a wide range of applications in life science related research.

H-D-Phg(4-Cl)-OH has diverse applications in life science-related research.

h-NTPDase-IN-1 (Compound 3i) is an inhibitor of human NTPDase with IC50 values of 2.88 μM for h-NTPDase1 and 0.72 μM for h-NTPDase3, indicating potential utility for thrombosis, inflammation, diabetes, and cancer research [1].

H-D-Phe(4-NO2)-OH is a useful organic compound for research related to life sciences and the catalog number is T64975.

H-Phe(4-Ac)-OH, with catalog number T66400 and CAS number 122555-04-8, is a valuable organic compound for life sciences research.

h-NTPDase-IN-5 (compound 3b) serves as a pan-inhibitor of NTPDase, exhibiting inhibitory concentration 50 (IC50) values of 1.10 μM [h-NTPDase1], 44.73 μM [h-NTPDase2], 26.14 μM [h-NTPDase3], and 0.32 μM [h-NTPDase8].

(2R,4S)-H-D-Pro(4-N3)-OH is a click chemistry reagent characterized by its azide group. This compound can participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules that contain alkyne groups. Additionally, it undergoes strain-promoted alkyne-azide cycloaddition reactions (SPAAC) with molecules featuring DBCO or BCN groups.

H-L-Phe(4-NH-Poc)-OH (hydrochloride) is a chemical reagent utilized in the modification of phenylalanine or tyrosine analogues in protein and peptide biosynthesis. It contains an alkyne group, facilitating its role in copper-catalyzed azide-alkyne cycloaddition (CuAAC) with molecules that have azide groups. Commonly abbreviated as Poc or Pryoc, this compound acts as both a conventional click conjugation alkyne component and can be combined with tetrazine linkers in copper-free Diels-Alder type click reactions. Additionally, H-L-Phe(4-NH-Poc)-OH serves as a specialized protective group for amines, hydroxyl, and ester groups. Stable under neat trifluoroacetic acid (TFA), degradation occurs at room temperature using TFA:DCM with Co2(CO)8. Deprotection involving other transition metals such as palladium has also been reported.

H-L-Lys(4-N3-Z)-OH hydrochloride is a click chemistry reagent that features a lysine-modified azide moiety, serving as a bioorthogonal ligation handle. It functions both as an infrared probe and a photo-affinity reagent [1] [2]. This compound contains an azide group integral to these applications.