+1 858-523-8231
Login | Register
menu
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
1015073-42-3,MFCD28386293
Catalog No.:AA01EOQ4

1015073-42-3 | PSI-7409

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
>98.00%
3 weeks  
$717.00   $502.00
- +
5mg
>98.00%
3 weeks  
$1,577.00   $1,104.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA01EOQ4
Chemical Name:
PSI-7409
CAS Number:
1015073-42-3
Molecular Formula:
C10H16FN2O14P3
Molecular Weight:
500.1587
MDL Number:
MFCD28386293
SMILES:
O[C@@H]1[C@@H](COP(=O)(OP(=O)(OP(=O)(O)O)O)O)O[C@H]([C@]1(C)F)n1ccc(=O)[nH]c1=O
Properties
Computed Properties
 
Complexity:
891  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
30  
Hydrogen Bond Acceptor Count:
15  
Hydrogen Bond Donor Count:
6  
Isotope Atom Count:
0  
Rotatable Bond Count:
8  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-4.9  

Literature

Title: PSI-7851, a pronucleotide of beta-D-2'-deoxy-2'-fluoro-2'-C-methyluridine monophosphate, is a potent and pan-genotype inhibitor of hepatitis C virus replication.

Journal: Antimicrobial agents and chemotherapy 20100801

Title: Characterization of the metabolic activation of hepatitis C virus nucleoside inhibitor beta-D-2'-Deoxy-2'-fluoro-2'-C-methylcytidine (PSI-6130) and identification of a novel active 5'-triphosphate species.

Journal: The Journal of biological chemistry 20071012

Title: Lam AM, et al. PSI-7851, a pronucleotide of beta-D-2'-deoxy-2'-fluoro-2'-C-methyluridine monophosphate, is a potent and pan-genotype inhibitor of hepatitis C virus replication. Antimicrob Agents Chemother. 2010 Aug;54(8):3187-96.

Title: Murakami E, et al. Mechanism of activation of PSI-7851 and its diastereoisomer PSI-7977.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
Submit
SDS
Related Products of 1015073-42-3
116295-90-0

116295-90-0

 19817-92-6

19817-92-6

 285978-18-9

285978-18-9

 84445-38-5

84445-38-5

 110988-86-8

110988-86-8

 211427-08-6

211427-08-6
Building Blocks
More >
Historical Records
139528-85-1

139528-85-1

 67035-22-7

67035-22-7

 1488879-96-4

1488879-96-4

 869340-71-6

869340-71-6

 2068065-03-0

2068065-03-0
Tags:1015073-42-3 Molecular Formula|1015073-42-3 MDL|1015073-42-3 SMILES|1015073-42-3 PSI-7409
Catalog No.: AA01EOQ4
1015073-42-3,MFCD28386293
1015073-42-3 | PSI-7409
Pack Size： 1mg
Purity： >98.00%
3 weeks
$717.00 $502.00
Pack Size： 5mg
Purity： >98.00%
3 weeks
$1,577.00 $1,104.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA01EOQ4
Chemical Name: PSI-7409
CAS Number: 1015073-42-3
Molecular Formula: C10H16FN2O14P3
Molecular Weight: 500.1587
MDL Number: MFCD28386293
SMILES: O[C@@H]1[C@@H](COP(=O)(OP(=O)(OP(=O)(O)O)O)O)O[C@H]([C@]1(C)F)n1ccc(=O)[nH]c1=O
Properties
Complexity: 891  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 4  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 30  
Hydrogen Bond Acceptor Count: 15  
Hydrogen Bond Donor Count: 6  
Isotope Atom Count: 0  
Rotatable Bond Count: 8  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -4.9  
Literature fold

Title: PSI-7851, a pronucleotide of beta-D-2'-deoxy-2'-fluoro-2'-C-methyluridine monophosphate, is a potent and pan-genotype inhibitor of hepatitis C virus replication.

Journal: Antimicrobial agents and chemotherapy20100801

Title: Characterization of the metabolic activation of hepatitis C virus nucleoside inhibitor beta-D-2'-Deoxy-2'-fluoro-2'-C-methylcytidine (PSI-6130) and identification of a novel active 5'-triphosphate species.

Journal: The Journal of biological chemistry20071012

Title: Lam AM, et al. PSI-7851, a pronucleotide of beta-D-2'-deoxy-2'-fluoro-2'-C-methyluridine monophosphate, is a potent and pan-genotype inhibitor of hepatitis C virus replication. Antimicrob Agents Chemother. 2010 Aug;54(8):3187-96.

Title: Murakami E, et al. Mechanism of activation of PSI-7851 and its diastereoisomer PSI-7977.

Related Products of of 1015073-42-3
116295-90-0
116295-90-0
19817-92-6
19817-92-6
285978-18-9
285978-18-9
84445-38-5
84445-38-5
110988-86-8
110988-86-8
211427-08-6
211427-08-6
Building Blocks More >
5537-19-9
5537-19-9
1-(4-methoxyphenyl)-2-(1-pyrrolidinyl)-1-pentanone,monohydrochloride
AA01EOZ3
208445-06-1
208445-06-1
8-bromo-guanosinecyclic3',5'-[(R)-(hydrogenphosphorothioate)],monosodiumsalt
AA01EP9Z | MFCD04037242
1435727-11-9
1435727-11-9
(5α,6β)-17-(cyclopropylmethyl)-4,5-epoxy-d3-morphinan-3,6,14-triol
AA01EPHR
330819-85-7
330819-85-7
6,7-dihydro-2-(methylthio)-5H-cyclopenta[4,5]thieno[2,3-d]pyrimidin-4-amine
AA01EPMG | MFCD00698485
226956-06-5
226956-06-5
cyclo(D-alanyl-D-tryptophyl-4-aminobutanoyl-D-alanyl-D-valyl-L-phenylalanyl-D-valyl)
AA01EPTO
95497-55-5
95497-55-5
9Z,11E,13Z-octadecatrienoicacid,methylester
AA01EQ3V | MFCD05864135
2055050-87-6
2055050-87-6
8-chloro-2,5-dihydro-2-(3-methoxyphenyl)-3H-pyrazolo[4,3-c]quinolin-3-one
AA01EQ9S | MFCD31922710
1030471-16-9
1030471-16-9
1-Ethoxy-4-trifluoromethoxybenzene
AA01EQJY | MFCD09998156
124337-35-5
124337-35-5
1-(1H-Pyrrol-1-ylmethyl)-1H-1,2,3-benzotriazole
AA01ER4Q | MFCD00957699
1365937-57-0
1365937-57-0
(S)-N-Methyl-1,1,1-trifluoro-2-propylamine
AA01ETCM | MFCD21602134
Historical Records
139528-85-1
139528-85-1
67035-22-7
67035-22-7
1488879-96-4
1488879-96-4
869340-71-6
869340-71-6
2068065-03-0
2068065-03-0
Submit
© 2017 AA BLOCKS, INC. All rights reserved.