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2574-78-9

2574-78-9 Structure

2574-78-9 Structure
IdentificationMore
[Name]

Orazamide
[CAS]

2574-78-9
[Synonyms]

1,2,3,6-tetrahydro-2,6-dioxopyrimidine-4-carboxylic acid compound with 5-amino-1h-imidazole-4-carboxamide (1:1)
5-aminoimidazole-4-carboxamide orotate
ORAZAMIDE
4-amino-5-imidazolecarboxamideorotatedihydrate
5-Aminoimedazole-4-carboxamideorotate
5-aminoimidazole-4-carboxamideorotatedihydrate
aicamindihydrate
aicaorotatedihydrate
aicoratdihydrate
imidazole-4-carboxamide,5-amino-,compd.withoroticacid(1:1),dihydrate
orazamidedihydrate
oroticacidcompd.with5(or4)-aminoimidazole-4(or5)-carboxamide(1:1)dihy
1,2,3,6-tetrahydro-2,6-dioxopyrimidine-4-carboxylic acid, compound with 5-amino-1H-imidazole-4-carboxamide (1:1)
AICA orotate
5-AMINOIMIDAZOLE-4-CARBOXAMIDEOROTATE(ORAZAMIDE)
1,2,3,6-Tetrahydro-2,6-dioxopyrimidine-4-carboxylic acid compound with 5-amino-1H-imidazole-4-carboxamide (1:1)
5-Aminoimidazole-4-carboxamide orotate
Orazamide
[EINECS(EC#)]

219-923-7
[Molecular Formula]

C9H10N6O5
[MDL Number]

MFCD00867162
[Molecular Weight]

282.21
[MOL File]

2574-78-9.mol
Chemical PropertiesBack Directory
[Melting point ]

284-285 °C (decomp)
[CAS DataBase Reference]

2574-78-9(CAS DataBase Reference)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Imidazole-->Orotic acid-->OROTIC ACID MONOHYDRATE-->4-AMINO-5-IMIDAZOLECARBOXAMIDE
Hazard InformationBack Directory
[Originator]

Aicamine, Labaz , France ,1971
[Uses]

Orazamide is an AICA orotate. Orazamide can prevent anti-TB drug-induced liver damage by downregulating the protein expression of HMGB 1 and RAGE in liver tissue and inhibiting the secretion of inflammatory factors. Orazamide can be used in research on hepatitis and liver cirrhosis[1].
[Manufacturing Process]

14.4 grams of 4-amino-5-imidazolecarboxamide (monohydrate) and 17.4 grams of orotic acid (monohydrate) were dissolved with heating in 600 cc of water. The solution is decolorized with Norit, cooled and then filtered off. 28.8 grams of a white crystalline salt (dihydrate) is obtained with MP 284°C (decomposition).
[Therapeutic Function]

Hepatoprotectant
[References]

[1] HE L, et al. Study on the Prevention Mechanism of Anti-tuberculosis Drug-induced Liver Injury with Orazamide Based on HMGB1-RAGE Signaling Pathway[J]. China Pharmacy, 2021: 2229-2235.
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