Details of the Drug-Related molecule(s) Interaction Atlas

General Information of Drug (ID: DM7V8DZ)

Drug Name

Ribose-1-Phosphate Drug Info

Synonyms

ribose 1-phosphate; ribose-1-phosphate; alpha-D-Ribose 1-phosphate; CHEBI:16300; 1-O-phosphono-alpha-D-ribofuranose; alpha-D-ribofuranose 1-(dihydrogen phosphate); D-ribose-1-phosphate; alpha-D-ribose-1-phosphate; alpha-D-ribofuranose 1-phosphate; R1P; D-ribofuranose 1-(dihydrogen phosphate); 14075-00-4; D-ribose-1P; ribofuranose 1-phosphate; a-D-ribose 1-phosphate; D-ribofuranose 1-phosphate; alpha-D-Ribofuranose, 1-(dihydrogen phosphate); 1-phospho-alpha-D-ribofuranose; CHEMBL603367; SCHEMBL1995711; AC1L96Y2

Indication

Disease Entry	ICD 11	Status	REF
Discovery agent	N.A.	Investigative	[1]

Cross-matching ID

PubChem CID: 439236
ChEBI ID: CHEBI:16300
CAS Number: CAS 14075-00-4
TTD Drug ID: DM7V8DZ

Molecule-Related Drug Atlas

Molecule Type:

DTT

Drug Status:

Clinical Trial Drug(s)

Discontinued Drug(s)

Investigative Drug(s)

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Drug(s) Targeting Purine nucleoside phosphorylase (PNP)

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
BCX-3408	DMRSG31	Autoimmune diabetes	5A10	Phase 2	[2]
2'3'-Dideoxyinosine	DMZWNQF	N. A.	N. A.	Phase 2	[1]
Forodesine	DME2W4T	B-cell acute lymphoblastic leukaemia	2B33.3	Phase 1/2	[3]
Guanosine	DM4T5LH	N. A.	N. A.	Phase 1	[1]
Peldesine	DMHV58T	N. A.	N. A.	Phase 1	[1]
CI-972	DM9ZBO0	Rheumatoid arthritis	FA20	Discontinued in Phase 1	[4]
7-tert-butyl-2, 3-dihydro-3, 3-dimethyl substituted dihydrofuran 30 (DHDMBF30)	DMSU06X	Discovery agent	N.A.	Investigative	[5]
Hypoxanthine	DMLSABI	Discovery agent	N.A.	Investigative	[1]
8-Iodo-Guanine	DM3K1EO	Discovery agent	N.A.	Investigative	[1]
8-Azaguanine	DM7VP90	Discovery agent	N.A.	Investigative	[1]
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Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

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Drug Therapeutic Target (DTT)

DTT Name	DTT ID	UniProt ID	MOA	REF
Purine nucleoside phosphorylase (PNP)	TTMCF1Y	PNPH_HUMAN	Inhibitor	[1]

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References

1	How many drug targets are there Nat Rev Drug Discov. 2006 Dec;5(12):993-6.
2	BCX-4208 (RO5092888), a Purine Nucleoside Phosphorylase (PNP) Inhibitor, Is a Novel, Potent Orally Active Anti-T-Cell and B-Cell Agent. 50th ASH Annual Meeting and Exposition. 2008.
3	Forodesine has high antitumor activity in chronic lymphocytic leukemia and activates p53-independent mitochondrial apoptosis by induction of p73 an... Blood. 2009 Aug 20;114(8):1563-75.
4	Inhibitors of human purine nucleoside phosphorylase. Synthesis of pyrrolo[3,2-d]pyrimidines, a new class of purine nucleoside phosphorylase inhibitors as potentially T-cell selective immunosuppressive agents. Description of 2,6-diamino-3,5-dihydro-7-(3-thienylmethyl)-4H-pyrrolo[3,2-d] pyrimidin-4-one. J Med Chem. 1992 May 1;35(9):1605-9.
5	Expression of human malaria parasite purine nucleoside phosphorylase in host enzyme-deficient erythrocyte culture. Enzyme characterization and identification of novel inhibitors. J Biol Chem. 1986 Sep 5;261(25):11667-73.