Purine-Nucle­o­side Phos­pho­ry­lase (PNP) CAS 9030-21-1

• Iden­ti­fi­ca­tion
• Prop­er­ties
• Safe­ty Data
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Iden­ti­fi­ca­tion

CAS Number

9030-21-1

Name

urine-Nucle­­o­­side Phos­pho­ry­lase (PNP)

Syn­onyms

3,4-Pyridinediamine, 6-chloro- [ACD/​Index Name]
4,5-Diamino-2-chloropyridine
6-Chlor-3,4-pyridindiamin [Ger­man] [ACD/IUPAC Name]
6-Chloro-3,4-pyridinediamine [ACD/IUPAC Name]
6-Chloro-3,4-pyridinediamine [French] [ACD/IUPAC Name]
6-chloropyridine-3,4-diamine
89182-17-2 [RN]
[89182-17-2] [RN]
1H-Indole-2-car­balde­hyde [ACD/IUPAC Name]
2-Chloro-4,5-diaminopyridine
2-Chloro-4,5-diaminopyridine, 6-Chloro-3,4-diaminopyridine
2-Chloro-4,5-diaminopyridine ; 6-Chloro-3,4-diaminopyridine
2-chloropyridine-4,5-diamine
3,4-Diamino-6-chloropyridine
3,4-Pyridinediamine,6-chloro-
5-(2-Chloro-phenyl)-oxazole-4-carboxylic acid methyl ester
6-chloro-3 4-pyridine­di­amine
6-Chloro-3,4-diaminepyridine
6-Chloro-3,4-diaminopyridine
6-Chloro-pyridine-3,4-diamine
89204-91-1 [RN]
9030-21-1 [RN]
BD23009
BR-36763
Indole-2-car­box­alde­hyde
MFCD04037269 [MDL num­ber]
PS-5607
SS-0409

SMILES

c1c(c(cnc1Cl)N)N

Std­InChI

InChI=1S/C5H6ClN3/c6-5-1-3(7)4(8)2-9-5/h1-2H,8H2,(H2,7,9)

Std­InChIKey

OQRXBX­­NATI­HDQO-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C₅H₆ClN₃

Mol­e­c­u­lar Weight

143.574

EINECS

232-857-3

MDL Number

MFCD00131739

Prop­er­ties

Appear­ance

White amor­phous powder

Struc­ture

Safe­ty Data

Sym­bol

Sig­nal Word

Warn­ing

Haz­ard statements

WGK Germany

3

MSDS Download

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our 

Iden­ti­fi­ca­tion Methods

HNMR, HPLC

ACTIV­I­TY (U/​mg solid)

＞40

SPE­CIF­IC ACTIV­I­TY (U/​mg)

≥200

ACCEL­ER­AT­ED STA­BIL­I­TY (37°C, 7days)

≥90%

SOL­U­BIL­I­TY

Clear

Shelf Life

2 years

Stor­age

Store at -20°C for long time, sealed and away from light.

Known Appli­ca­tion

Purine-Nucle­­o­­side Phos­pho­ry­lase (PNP) CAS 9030-21-1 a type of enzyme, is pri­mar­i­ly involved in the metab­o­lism of purine nucleotides. Its main func­tion is to cat­alyze the trans­fer of a phos­phate group between two adenylic acid (adeny­late) mol­e­cules, form­ing an adenylic acid and an adeno­sine diphos­phate (ADP) mol­e­cule. And Purine-Nucle­­o­­side Phos­pho­ry­lase (PNP) func­tions in var­i­ous cel­lu­lar process­es, includ­ing ener­gy trans­fer, purine metab­o­lism, and sig­nal trans­duc­tion. These func­tions are essen­tial for main­tain­ing nor­mal cel­lu­lar phys­i­ol­o­gy and adapt­ing to changes in the cel­lu­lar environment.

Gen­er­al View of Documents

Links

This prod­uct is devel­oped by our R&D com­pa­ny Ulcho Bio­chem­i­cal Lim­it­ed (http://​www​.ulcho​.com/).

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