Home Sulfos Isoquinoline,5-(1-piperazinylsulfonyl)-

Isoquinoline,5-(1-piperazinylsulfonyl)-

CAS No.:
84468-24-6
Catalog Number:
AG004W1X
Molecular Formula:
C13H15N3O2S
Molecular Weight:
277.3421
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5mg
99%
1 week
United States
$157
- +
10mg
99%
1 week
United States
$223
- +
25mg
99%
1 week
United States
$423
- +
50mg
99%
1 week
United States
$723
- +
100mg
99%
1 week
United States
$1307
- +
Product Description
Catalog Number:
AG004W1X
Chemical Name:
Isoquinoline,5-(1-piperazinylsulfonyl)-
CAS Number:
84468-24-6
Molecular Formula:
C13H15N3O2S
Molecular Weight:
277.3421
MDL Number:
MFCD00209852
IUPAC Name:
5-piperazin-1-ylsulfonylisoquinoline
InChI:
InChI=1S/C13H15N3O2S/c17-19(18,16-8-6-14-7-9-16)13-3-1-2-11-10-15-5-4-12(11)13/h1-5,10,14H,6-9H2
InChI Key:
UPTYCYWTFGTCCG-UHFFFAOYSA-N
SMILES:
O=S(=O)(c1cccc2c1ccnc2)N1CCNCC1
Properties
Complexity:
401  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
277.088g/mol
Formal Charge:
0
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
277.342g/mol
Monoisotopic Mass:
277.088g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
70.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.6  
Literature
Title Journal
Evaluation of broad spectrum protein kinase inhibitors to probe the architecture of the malarial cyclin dependent protein kinase Pfmrk. Bioorganic & medicinal chemistry letters 20070901
Acridone derivatives are selective inhibitors of HIV-1 replication in chronically infected cells. Antiviral research 19991001
Isoquinolinesulphonamide derivatives inhibit transcriptional elongation of human immunodeficiency virus type 1 RNA in a promyelocytic model of latency. Antiviral chemistry & chemotherapy 19990901
P-TEFb kinase is required for HIV Tat transcriptional activation in vivo and in vitro. Genes & development 19971015
Synthesis and biological activities of flavonoid derivatives as A3 adenosine receptor antagonists. Journal of medicinal chemistry 19960607
Properties