ChemicalBook >> CAS DataBase List >>360 A iodide

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+
Molecular Weight:
576.42
MDL Number:
MOL File:
737763-37-0.mol
Last updated:2024-07-02 08:55:06

360 A iodide Properties

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

360 A iodide price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ApexBio Technology A3120 360Aiodide 737763-37-0 5mg $230 2021-12-16 Buy
ChemScene CS-1560 360Aiodide ≥98.0% 737763-37-0 5mg $240 2021-12-16 Buy
ApexBio Technology A3120 360Aiodide 737763-37-0 10mg $350 2021-12-16 Buy
ChemScene CS-1560 360Aiodide ≥98.0% 737763-37-0 10mg $384 2021-12-16 Buy
ApexBio Technology A3120 360Aiodide 737763-37-0 25mg $650 2021-12-16 Buy
Product number Packaging Price Buy
A3120 5mg $230 Buy
CS-1560 5mg $240 Buy
A3120 10mg $350 Buy
CS-1560 10mg $384 Buy
A3120 25mg $650 Buy

360 A iodide Chemical Properties,Uses,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

Global( 34)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32760 60
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Aladdin Scientific
+1-+1(833)-552-7181 sales@aladdinsci.com United States 52927 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131980 58
Chembest Research Laboratories Limited 021-20908456 sales@BioChemBest.com China 6008 61
Haoyuan Chemexpress Co., Ltd. 021-58950125 info@chemexpress.com China 7553 61
MedChemexpress LLC 021-58955995 sales@medchemexpress.cn United States 4863 58
AdooQ BioScience, LLC +1 (866) 930-6790 info@adooq.com United States 2784 58
Guangzhou QiYun Biotechnology Co., Ltd. 020-61288194 61288195 505721671@qq.com China 3868 58
Musechem +1-800-259-7612 info@musechem.com United States 4662 60

360 A iodide Spectrum

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