ChemicalBook > CAS DataBase List > 360 A iodide

360 A iodide

Product Name
360 A iodide
CAS No.
737763-37-0
Chemical Name
360 A iodide
Synonyms
360 A iodide;360A (iodide);3,3'-[2,6-Pyridinediylbis(carbonylimino)]bis[1-methylquinolinium] diiodide
CBNumber
CB32666580
Molecular Formula
C27H23IN5O2+
Formula Weight
576.42
MOL File
737763-37-0.mol
More
Less

360 A iodide Property

storage temp. 
Store at -20°C
solubility 
insoluble in H2O; insoluble in EtOH; insoluble in DMSO
form 
Solid
color 
Light yellow to yellow
More
Less

Hazard and Precautionary Statements (GHS)

More
Less

N-Bromosuccinimide Price

ApexBio Technology
Product number
A3120
Product name
360Aiodide
Packaging
5mg
Price
$230
Updated
2021/12/16
ChemScene
Product number
CS-1560
Product name
360Aiodide
Purity
≥98.0%
Packaging
5mg
Price
$240
Updated
2021/12/16
ApexBio Technology
Product number
A3120
Product name
360Aiodide
Packaging
10mg
Price
$350
Updated
2021/12/16
ChemScene
Product number
CS-1560
Product name
360Aiodide
Purity
≥98.0%
Packaging
10mg
Price
$384
Updated
2021/12/16
ApexBio Technology
Product number
A3120
Product name
360Aiodide
Packaging
25mg
Price
$650
Updated
2021/12/16
More
Less

360 A iodide Chemical Properties,Usage,Production

Biological Activity

360a is a 2,6-pyridine-dicarboxamide derivative displaying strong affinity and selectivity for g-quadruplex structures and selective telomerase inhibition in vitro assays. 360a is a g-quadruplex ligand, which can influence the consequence of g-quadruplex formation and/or stabilization.

in vitro

we found a s-phase accumulation in atm-proficient, but not in atm-deficient ebv-lymphocytes treated with 360a before induction of cell death. however, atm status did not modify cell cycle distribution in 360a-treated sv40-fibroblasts and hela cells compared to dmso treated controls [1]. dna-pkcs-dependent nhej was responsible for sister telomere fusions as a direct consequence of g-quadruplex formation and/or stabilization induced by 360a on parental telomere g strands. nhej and hr activation at telomeres altered mitotic progression in treated cells [2]. this compound was shown to display a potent affinity and selectivity for telomeric g-quadruplex dna over duplex dna and to induce delayed growth inhibition in ht1080 tumor cell line [3].

360 A iodide Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

360 A iodide Suppliers

MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4861
Advantage
58
AdooQ BioScience, LLC
Tel
+1 (866) 930-6790
Fax
+1 (866) 333-9607
Email
info@adooq.com
Country
United States
ProdList
2782
Advantage
58
Musechem
Tel
+1-800-259-7612
Fax
+1-800-259-7612
Email
info@musechem.com
Country
United States
ProdList
4660
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32165
Advantage
58
TargetMol Chemicals Inc.
Tel
+8613564774135
Email
zijue.cai@tsbiochem.com
Country
United States
ProdList
19885
Advantage
58
TargetMol Chemicals Inc.
Tel
Email
support@targetmol.com
Country
United States
ProdList
38632
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
52925
Advantage
58
ApexBio Technology
Tel
--
Fax
--
Email
sales@apexbt.com
Country
United States
ProdList
6251
Advantage
58
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58

737763-37-0, 360 A iodideRelated Search:


  • 360 A iodide
  • 360A (iodide)
  • 3,3'-[2,6-Pyridinediylbis(carbonylimino)]bis[1-methylquinolinium] diiodide
  • 737763-37-0
  • C27H23I2N5O2
  • C27H23N5O22I