+1 858-523-8231
Login | Register
menu
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
932-53-6,MFCD00006457
Catalog No.:AA00GSBM

932-53-6 | 6-Azathymine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$29.00   $20.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00GSBM
Chemical Name:
6-Azathymine
CAS Number:
932-53-6
Molecular Formula:
C4H5N3O2
Molecular Weight:
127.1014
MDL Number:
MFCD00006457
SMILES:
Cc1n[nH]c(=O)[nH]c1=O
Properties
Properties
 
BP:
235.85°C (rough estimate)  
Form:
Solid  
MP:
210-212°C  
Refractive Index:
1.5000 (estimate)  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
196  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-0.3  

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1956,vol.78,p.1938,1939

[1]JournalofOrganicChemistry,1958,vol.23,p.1951

2-3-(3-nitro-phenyl)-1-ureido-triazenyl-propionicacidethylester 
  932-53-6 

[1]JournaloftheAmericanChemicalSociety,1907,vol.29,p.884

[1]Chemistryandbiodiversity,2012,vol.9,p.536-556

[2]SpisyVydavanePrirodovedeckouFakultouMassarykovyUniversity,1958,p.269,273-275    Chem.Abstr.,1959,p.11399

[3]CollectionofCzechoslovakChemicalCommunications,1958,vol.23,p.1588,1589Anm.,1590

[4]GazzettaChimicaItaliana,1953,vol.83,p.133,137

[5]SpisyVydavanePrirodovedeckouFakultouMassarykovyUniversity,1958,p.269,273-275    Chem.Abstr.,1959,p.11399

[1]JournaloftheAmericanChemicalSociety,1958,vol.80,p.1138,1139,1140

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: Synthesis and biological evaluation of L- and D-configuration 1,3-dioxolane 5-azacytosine and 6-azathymine nucleosides.

Journal: Bioorganic & medicinal chemistry letters 20000918

Title: N Tamaki, et al. Purification, Characterization and Inhibition of D-3-aminoisobutyrate Aminotransferase From the Rat Liver. Eur J Biochem. 1990 Apr 20;189(1):39-45.

Title: W H PRUSOFF, et al. Effect of the Deoxyriboside of 6-azathymine (Azathymidine) on the Biosynthesis of Deoxyribonucleic Acid by Bone Marrow and Neoplastic Cells (In Vitro). Biochim Biophys Acta. 1956 Apr;20(1):209-14.

Title: R A GAITO, et al. Studies on the Metabolism of Thymine and 6-azathymine. Biochem Pharmacol. Apr-May 1962;11:323-36.

Title: B. Gabrielsen, et al. In vitro and in vivo antiviral (RNA) evaluation of orotidine 51-monophosphatedecarboxylase inhibitors and analogues including 6-azauridine-51-(ethylmethoxyalaninyl)phosphate (a 51-monophosphate prodrug). Antiviral Chemistry & Chemotherapy (1994) 5(4), 209-220.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
Submit
SDS
Related Products of 932-53-6
24753-63-7

24753-63-7

 52236-30-3

52236-30-3
Building Blocks
More >
Tags:932-53-6 Molecular Formula|932-53-6 MDL|932-53-6 SMILES|932-53-6 6-Azathymine
Catalog No.: AA00GSBM
932-53-6,MFCD00006457
932-53-6 | 6-Azathymine
Pack Size： 250mg
Purity： 95%
in stock
$29.00 $20.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00GSBM
Chemical Name: 6-Azathymine
CAS Number: 932-53-6
Molecular Formula: C4H5N3O2
Molecular Weight: 127.1014
MDL Number: MFCD00006457
SMILES: Cc1n[nH]c(=O)[nH]c1=O
Properties
BP: 235.85°C (rough estimate)  
Form: Solid  
MP: 210-212°C  
Refractive Index: 1.5000 (estimate)  
Storage: Keep in dry area;2-8℃;  
Complexity: 196  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -0.3  
Downstream Synthesis Route
932-53-6    452-88-0 

[1]JournaloftheAmericanChemicalSociety,1956,vol.78,p.1938,1939

2704-30-5    932-53-6 

[1]JournalofOrganicChemistry,1958,vol.23,p.1951

2-3-(3-nitro-phenyl)-1-ureido-triazenyl-propionicacidethylester 
  932-53-6 

[1]JournaloftheAmericanChemicalSociety,1907,vol.29,p.884

615-76-9    932-53-6 

[1]Chemistryandbiodiversity,2012,vol.9,p.536-556

[2]SpisyVydavanePrirodovedeckouFakultouMassarykovyUniversity,1958,p.269,273-275    Chem.Abstr.,1959,p.11399

[3]CollectionofCzechoslovakChemicalCommunications,1958,vol.23,p.1588,1589Anm.,1590

[4]GazzettaChimicaItaliana,1953,vol.83,p.133,137

[5]SpisyVydavanePrirodovedeckouFakultouMassarykovyUniversity,1958,p.269,273-275    Chem.Abstr.,1959,p.11399

932-53-6    50-89-5    13410-30-5 

[1]JournaloftheAmericanChemicalSociety,1958,vol.80,p.1138,1139,1140

Literature fold

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters20101101

Title: Synthesis and biological evaluation of L- and D-configuration 1,3-dioxolane 5-azacytosine and 6-azathymine nucleosides.

Journal: Bioorganic & medicinal chemistry letters20000918

Title: N Tamaki, et al. Purification, Characterization and Inhibition of D-3-aminoisobutyrate Aminotransferase From the Rat Liver. Eur J Biochem. 1990 Apr 20;189(1):39-45.

Title: W H PRUSOFF, et al. Effect of the Deoxyriboside of 6-azathymine (Azathymidine) on the Biosynthesis of Deoxyribonucleic Acid by Bone Marrow and Neoplastic Cells (In Vitro). Biochim Biophys Acta. 1956 Apr;20(1):209-14.

Title: R A GAITO, et al. Studies on the Metabolism of Thymine and 6-azathymine. Biochem Pharmacol. Apr-May 1962;11:323-36.

Title: B. Gabrielsen, et al. In vitro and in vivo antiviral (RNA) evaluation of orotidine 51-monophosphatedecarboxylase inhibitors and analogues including 6-azauridine-51-(ethylmethoxyalaninyl)phosphate (a 51-monophosphate prodrug). Antiviral Chemistry & Chemotherapy (1994) 5(4), 209-220.

Related Products of of 932-53-6
24753-63-7
24753-63-7
52236-30-3
52236-30-3
Building Blocks More >
925890-13-7
925890-13-7
1,2,3-Trifluoro-5-methoxy-4-nitrobenzene
AA00GSJI | MFCD09025341
909858-38-4
909858-38-4
3-(1-Methyl-1h-pyrrol-2-yl)-1h-pyrazole-5-carboxylic acid
AA00GSQN | MFCD06010512
90723-11-8
90723-11-8
N1-(tert-Butyl)-N2-isopropylethane-1,2-diamine
AA00GSZG | MFCD07370039
914458-42-7
914458-42-7
JWH 309
AA00GT8J | MFCD30718356
889954-12-5
889954-12-5
(4'-(1,3-Dioxolan-2-yl)-[1,1'-biphenyl]-4-yl)methanol
AA00GTCF | MFCD07699388
878797-09-2
878797-09-2
Fmoc-Tyr(tBu)-Ser(psiMe,Mepro)-OH
AA00GTK5 | MFCD11974986
92322-05-9
92322-05-9
[1-(2-Phenylethyl)piperidin-3-yl]methanol
AA00GTO4 | MFCD01452809
92664-05-6
92664-05-6
Potassium 1-cyano-3-ethoxy-2,3-dioxopropan-1-ide
AA00GTT6 | MFCD28016957
890087-21-5
890087-21-5
LUF 6000
AA00GU19 | MFCD25541739
898230-59-6
898230-59-6
Morinidazole R-Enantiomer
AA00GU6D | MFCD29472250
Submit
© 2017 AA BLOCKS, INC. All rights reserved.