+1 858-523-8231
Login | Register
menu
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
18422-05-4,MFCD00149360
Catalog No.:AA00384Y

18422-05-4 | 5'-Adenylic acid, hydrate (1:1)

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
95%
in stock  
$13.00   $9.00
- +
25g
95%
in stock  
$30.00   $21.00
- +
100g
95%
in stock  
$75.00   $53.00
- +
500g
95%
in stock  
$266.00 $186.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00384Y
Chemical Name:
5'-Adenylic acid, hydrate (1:1)
CAS Number:
18422-05-4
Molecular Formula:
C10H16N5O8P
Molecular Weight:
365.2365
MDL Number:
MFCD00149360
SMILES:
O[C@@H]1[C@H](O)[C@H](O[C@H]1n1cnc2c1ncnc2N)COP(=O)(O)O.O
Properties
Computed Properties
 
Complexity:
481  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
4  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
24  
Hydrogen Bond Acceptor Count:
12  
Hydrogen Bond Donor Count:
6  
Isotope Atom Count:
0  
Rotatable Bond Count:
4  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

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: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

Title: Rittiner JE, et al. AMP is an adenosine A1 receptor agonist. J Biol Chem. 2012 Feb 17;287(8):5301-9.

Title: Zhan Y, et al. Adenosine 5'-monophosphate ameliorates D-galactosamine/lipopolysaccharide-induced liver injury through an adenosine receptor-independent mechanism in mice. Cell Death Dis. 2014 Jan 9;5:e985.

Title: Ayisi NK, et al. Comparison of the antiviral effects of 5-methoxymethyldeoxyuridine-5'-monophosphate with adenine arabinoside-5'-monophosphate. Antiviral Res. 1983 Sep;3(3):161-74.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
Submit
SDS
Related Products of 18422-05-4
61-19-8

61-19-8

 102029-95-8

102029-95-8

 102029-87-8

102029-87-8

 102129-65-7

102129-65-7

 146877-92-1

146877-92-1

 1638241-89-0

1638241-89-0
Building Blocks
More >
Historical Records
198545-20-9

198545-20-9

 899214-82-5

899214-82-5

 1105239-96-0

1105239-96-0
Tags:18422-05-4 Molecular Formula|18422-05-4 MDL|18422-05-4 SMILES|18422-05-4 5'-Adenylic acid, hydrate (1:1)
Catalog No.: AA00384Y
18422-05-4,MFCD00149360
18422-05-4 | 5'-Adenylic acid, hydrate (1:1)
Pack Size： 5g
Purity： 95%
in stock
$13.00 $9.00
Pack Size： 25g
Purity： 95%
in stock
$30.00 $21.00
Pack Size： 100g
Purity： 95%
in stock
$75.00 $53.00
Pack Size： 500g
Purity： 95%
in stock
$266.00 $186.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00384Y
Chemical Name: 5'-Adenylic acid, hydrate (1:1)
CAS Number: 18422-05-4
Molecular Formula: C10H16N5O8P
Molecular Weight: 365.2365
MDL Number: MFCD00149360
SMILES: O[C@@H]1[C@H](O)[C@H](O[C@H]1n1cnc2c1ncnc2N)COP(=O)(O)O.O
Properties
Complexity: 481  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 4  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 24  
Hydrogen Bond Acceptor Count: 12  
Hydrogen Bond Donor Count: 6  
Isotope Atom Count: 0  
Rotatable Bond Count: 4  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
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: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology20060501

Title: Rittiner JE, et al. AMP is an adenosine A1 receptor agonist. J Biol Chem. 2012 Feb 17;287(8):5301-9.

Title: Zhan Y, et al. Adenosine 5'-monophosphate ameliorates D-galactosamine/lipopolysaccharide-induced liver injury through an adenosine receptor-independent mechanism in mice. Cell Death Dis. 2014 Jan 9;5:e985.

Title: Ayisi NK, et al. Comparison of the antiviral effects of 5-methoxymethyldeoxyuridine-5'-monophosphate with adenine arabinoside-5'-monophosphate. Antiviral Res. 1983 Sep;3(3):161-74.

Related Products of of 18422-05-4
61-19-8
61-19-8
102029-95-8
102029-95-8
102029-87-8
102029-87-8
102129-65-7
102129-65-7
146877-92-1
146877-92-1
1638241-89-0
1638241-89-0
Building Blocks More >
1170-02-1
1170-02-1
Ethylenediamine-n,n'-bis((2-hydroxyphenyl)acetic acid)
AA00388I | MFCD00004247
848482-93-9
848482-93-9
(S)-4-BOC-Piperazine-2-carboxylic acid
AA0038BJ | MFCD02179098
67567-55-9
67567-55-9
1-(Methoxymethyl)cyclopropanecarboxylic acid
AA0038ER | MFCD10686615
63010-72-0
63010-72-0
4-Chloro-8-fluoroquinoline
AA0038I5 | MFCD00278785
536-59-4
536-59-4
Perillyl Alcohol
AA0038L5 | MFCD00001567
40644-14-2
40644-14-2
5-Iodo-1H-benzo[d]imidazol-2(3H)-one
AA0038OE | MFCD05663527
27258-32-8
27258-32-8
1-Methyl-1h-pyrazole-3-carbaldehyde
AA0038RK | MFCD03419800
14166-28-0
14166-28-0
(3Ar,4s,7r,7as)-hexahydro-4,7-methanoisobenzofuran-1,3-dione
AA0038UY | MFCD11046554
745011-75-0
745011-75-0
Boc-d-homoserine
AA0038Y1 | MFCD12545888
736990-88-8
736990-88-8
3,5-Difluoro-4-formylbenzoic acid
AA00391L | MFCD09835188
Historical Records
198545-20-9
198545-20-9
899214-82-5
899214-82-5
1105239-96-0
1105239-96-0
Submit
© 2017 AA BLOCKS, INC. All rights reserved.