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

Identification	Physical Data	Spectra
Route of Synthesis (ROS)	Safety and Hazards	Other Data

Product Name	Purine-Nucleoside Phosphorylase (PNP)
IUPAC Name	1,5-dihydropyrazolo[3,4-d]pyrimidin-4-one
Molecular Structure
CAS Registry Number	9030-21-1
EINECS Number	232-857-3
MDL Number	MFCD00131739
Synonyms	allopurinol 315-30-0 1H-Pyrazolo[3,4-d]pyrimidin-4-ol Zyloprim Lopurin Zyloric Suspendol Atisuril Bleminol Caplenal Takanarumin Uripurinol Embarin Foligan Milurit Progout Urosin Anoprolin Cellidrin Epidropal Ailural Allopur Allural Alositol Bloxanth Cosuric Hamarin Ledopur Lysuron Uricemil Uriprim Xanturat Aloral Anzief Apurin Apurol Geapur Gotax Remid Urbol Urolit Urtias 4-Hydroxypyrazolo[3,4-d]pyrimidine Ketobun-A Apulonga Dabrosin Dabroson Ketanrift Miniplanor Nektrohan Adenock Allozym Aluline Gichtex Monarch Riball 1H-Pyrazolo[3,4-d]pyrimidin-4(5H)-one Allopurinolum 4-HPP Hexanuret Epuric Allo-Puren Allopurinol(I) Dura Al 1H-Pyrazolo(3,4-d)pyrimidin-4-ol 4-Hydroxypyrazolopyrimidine Alopurinol 180749-06-8 4-Hydroxy-1H-pyrazolo(3,4-d)pyrimidine 73334-58-4 4-Hydroxy-3,4-pyrazolopyrimidine Urtias 100 1H-pyrazolo[3,4-d]pyrimidin-4(7H)-one 180749-08-0 4-Hydroxypyrazolo(3,4-d)pyrimidine Sigapurol Aloprim Uritas NSC-1390 Alopurinol [INN-Spanish] 2H-Pyrazolo[3,4-d]pyrimidin-4-ol Allopurinolum [INN-Latin] 4-Hydroxypyrazolyl(3,4-d)pyrimidine 1H-pyrazolo[3,4-d]pyrimidin-4(2H)-one 4H-Pyrazolo(3,4-d)pyrimidin-4-one 4′-Hydroxypyrazolol(3,4-d)pyrimidine BW 56-158 AL-100 1,5-Dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one 1,5-Dihydro-4H-pyrazolo(3,4-d)pyrimidin-4-one BW-56-158 180749-09-1 Zyloprim (TN) 1,5-Dihydro-4H-pyrazolo(3,4-d)pyrimidine-4-one 916980-04-6 B. W. 56-158 CHEBI:40279 4H-Pyrazolo(3,4-d)pyrimidin-4-one, 1,5-dihydro- 4H-Pyrazolo[3,4-d]pyrimidin-4-one, 1,5-dihydro- 1,5-Dihydropyrazolo[3,4-d]pyrimidin-4-one 1H,4H,7H-pyrazolo[3,4-d]pyrimidin-4-one 63CZ7GJN5I MFCD00599413 NSC-101655 MLS000069453 180749-07-9 184789-03-5 9002-17-9 DTXSID4022573 NSC1390 1H,2H,4H-pyrazolo[3,4-d]pyrimidin-4-one NSC101655 4H-Pyrazolo[3,4-d]pyrimidin-4-one, 1,2-dihydro- SMR000059083 4-Hydroxy-1H-pyrazolo[3,4-d]pyrimidine DTXCID502573 1H-Pyrazolo[3,4-d]pyrimidin-4-ol (9CI) 4H-Pyrazolo[3,4-d]pyrimidin-4-one, 1,7-dihydro- (9CI) Xanthine oxidase DUZALLO COMPONENT ALLOPURINOL Hexanurat NCGC00015094-02 NCGC00094580-04 4H-Pyrazolo[3,4-d]pyrimidin-4-one, 2,5-dihydro- (9CI) 4H-Pyrazolo[3,4-d]pyrimidin-4-one, 2,7-dihydro- (9CI) BW-56158 1H,4H,5H-pyrazolo[3,4-d]pyrimidin-4-one 1,5-Dihydro-pyrazolo[3,4-d]pyrimidin-4-one ALLOPURINOL (MART.) ALLOPURINOL [MART.] ALLOPURINOL (USP-RS) ALLOPURINOL [USP-RS] BW 56158 ALLOPURINOL (EP IMPURITY) ALLOPURINOL [EP IMPURITY] 4H-Pyrazolo[3, 1,5-dihydro- Ailurial ALLOPURINOL (EP MONOGRAPH) ALLOPURINOL [EP MONOGRAPH] WLN: T56 BMN GN INJ FQ ALLOPURINOL (USP MONOGRAPH) ALLOPURINOL [USP MONOGRAPH] 4-Hydroxypyrazolyl[3,4-d]pyrimidine 4′-Hydroxypyrazolol[3,4-d]pyrimidine NSC 1390 CAS-315-30-0 CCRIS 626 NSC 101655 HSDB 3004 SR-05000001983 EINECS 206-250-9 UNII-63CZ7GJN5I allopurinolo Zurinol Uricto ATH008 4-Hydroxypyrazol[3,4-D]pyrimidine Prestwick_511 Xanthomax-100 Xanthomax-300 Aluline 100 Aluline 300 Hamarin 100 Hamarin 300 Zyloric-300 Allopurinol [USAN:USP:INN:BAN:JAN] Allopurinol (Zyloprim) Spectrum_000026 ALLOPURINOL [MI] Opera_ID_1680 Spectrum2_000098 Spectrum3_000289 Spectrum4_000135 Spectrum5_000768 ALLOPURINOL [INN] ALLOPURINOL [JAN] Lopac-A-8003 1,4-d]pyrimidin-4-one ALLOPURINOL [HSDB] ALLOPURINOL [USAN] A 8003 cid_2094 SCHEMBL4627 CHEMBL1467 NCIOpen2_001825 Lopac0_000102 ALLOPURINOL [WHO-DD] ALLOPURINOL [WHO-IP] BSPBio_001798 KBioGR_000550 KBioSS_000386 MLS001148183 US9138393, Allopurinol US9144538, Allopurinol DivK1c_000685 SPECTRUM1500108 SPBio_000056 ALLOPURINOLUM [WHO-IP] 4′-HPP GTPL6795 SCHEMBL1128219 Allopurinol (JP17/USP/INN) BDBM35440 HMS502C07 KBio1_000685 KBio2_000386 KBio2_002954 KBio2_005522 KBio3_001298 ALLOPURINOL [ORANGE BOOK] M04AA01 NINDS_000685 BDBM181133 HMS1920A15 HMS2091G15 HMS2234M09 HMS3259K13 HMS3260E06 HMS3371I11 HMS3651O13 HMS3714L22 Pharmakon1600-01500108 AMY18272 BCP26973 HY-B0219 STR05189 Tox21_110082 Tox21_200922 Tox21_500102 4-Hydroxy-pyrazolo[3,4-d]pyrimidin AC-019 BDBM50016784 BDBM50140241 CCG-38916 NSC755858 s1630 SC1118 SC2251 AKOS000267490 AKOS000269759 AKOS024255717 Tox21_110082_1 Allopurinol, xanthine oxidase inhibitor CCG-204197 CCG-221406 CCG-266128 DB00437 LP00102 NC00492 NSC-755858 SB10164 SDCCGSBI-0050090.P005 IDI1_000685 NCGC00015094-01 NCGC00015094-03 NCGC00015094-04 NCGC00015094-05 NCGC00015094-06 NCGC00015094-07 NCGC00015094-08 NCGC00015094-18 NCGC00015094-22 NCGC00091134-01 NCGC00091134-02 NCGC00091134-03 NCGC00094580-01 NCGC00094580-02 NCGC00094580-05 NCGC00188948-01 NCGC00258476-01 NCGC00260787-01 TS-00028 SBI-0050090.P004 1H-PYRAZOLO(3,4-D)PYRIMDIN-4-OL 2H-Pyrazolo[3,4-d]pyrimidin-4-ol (9CI) A0907 EU-0100102 NS00000618 SW199406-4 1,5-dihydropyrazolo[3,4-d]-pyrimidin-4-one EN300-34144 VU0611037-1 BIM-0061756.0001 D00224 F18007 AB00173448-03 AB00173448-04 AB00173448_05 AB01274719-01 AB01274719_02 1,5-Dihydro-4H-pyrazolo(3,4-d)pryimidin-4-one AB-323/25048497 Allopurinol (4-Hydroxypyrazolo[3,4-d]pyrimidine) Q412486 SR-01000075595 4H-pyrazolo[3,4-d]pyrimidin-4-one, 1,7-dihydro- J-504736 SR-01000075595-1 SR-05000001983-1 SR-05000001983-2 W-106892 F2173-0394 F3329-0375
Molecular Formula	C5H4N4O
Molecular Weight	136.11
InChI	InChI=1S/C5H4N4O/c10-5-3-1-8-9-4(3)6-2-7-5/h1-2H,(H2,6,7,8,9,10)
InChI Key	CUYKNJBYIJFOFCNXPDARWKPPY-UHFFFAOYSA-N
Isomeric SMILES	C1=NNC2=C1C(=O)NC=N2

Appearance

White amorphous powder

Pictogram(s)
Signal	Danger
GHS Hazard Statements	H301 (53.15%): Toxic if swallowed [Danger Acute toxicity, oral] H317 (94.41%): May cause an allergic skin reaction [Warning Sensitization, Skin]
Precautionary Statement Codes	P261, P264, P270, P272, P280, P301+P316, P302+P352, P321, P330, P333+P317, P362+P364, P405, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.)

HS Code
Storage	Store at -20°C for long time, sealed and away from light.
Shelf Life	2 years
Market Price

Use Pattern

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.


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Purine-Nucleoside Phosphorylase (PNP) CAS#: 9030-21-1; ChemWhat Code: 1417519

Identification

Physical Data

Spectra

Route of Synthesis (ROS)

Safety and Hazards

Other Data

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