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CE3F4

Product Name
CE3F4
CAS No.
143703-25-7
Chemical Name
CE3F4
Synonyms
CE3F4;CE3F4 >=98% (HPLC);CE3F4, 10 mM in DMSO;inhibit,Inhibitor,CE3F4,CE-3F4;5,7-Dibromo-6-fluoro-3,4-dihydro-2-methyl-1(2H)-quinolinecarboxaldehyde;5,7-dibromo-6-fluoro-2-methyl-1,2,3,4-tetrahydroquinoline-1-carbaldehyde;1(2H)-Quinolinecarboxaldehyde, 5,7-dibromo-6-fluoro-3,4-dihydro-2-methyl-
CBNumber
CB33152589
Molecular Formula
C11H10Br2FNO
Formula Weight
351.01
MOL File
143703-25-7.mol
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CE3F4 Property

storage temp. 
Store at -20°C
solubility 
Soluble in DMSO > 10 mM
form 
Powder
color 
White to off-white
InChI
InChI=1S/C11H10Br2FNO/c1-6-2-3-7-9(15(6)5-16)4-8(12)11(14)10(7)13/h4-6H,2-3H2,1H3
InChIKey
ZZLQPWXVZCPUGC-UHFFFAOYSA-N
SMILES
N1(C=O)C2=C(C(Br)=C(F)C(Br)=C2)CCC1C
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Safety

WGK Germany 
WGK 3
Storage Class
11 - Combustible Solids
Hazard Classifications
Acute Tox. 4 Oral
Aquatic Chronic 2
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P330Rinse mouth.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML2041
Product name
CE3F4
Purity
≥98% (HPLC)
Packaging
5 mg
Price
$85.8
Updated
2026/03/19
Sigma-Aldrich
Product number
SML2041
Product name
CE3F4
Purity
≥98% (HPLC)
Packaging
25 mg
Price
$347
Updated
2026/03/19
Cayman Chemical
Product number
17767
Product name
CE3F4
Purity
≥98%
Packaging
5mg
Price
$78
Updated
2024/03/01
Cayman Chemical
Product number
17767
Product name
CE3F4
Purity
≥98%
Packaging
10mg
Price
$146
Updated
2024/03/01
Cayman Chemical
Product number
17767
Product name
CE3F4
Purity
≥98%
Packaging
50mg
Price
$614
Updated
2024/03/01
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CE3F4 Chemical Properties,Usage,Production

Uses

CE3F4 has been used as a selective exchange protein directly activated by cAMP isoform 1 (Epac1) inhibitor in cell proliferation assay to study the influence of Epac type I on cell proliferation of C6 cells (a model of glioma).

Biological Activity

CE3F4 is a tetrahydroquinoline derivative th at blocks agonist-stimulated Epac1 (exchange protein directly activated by cAMP isoform 1) guanine nucleotide exchange activity toward its effector Rap1 (IC50 = 23 μM; Epac agonist = 2 μM 8-CPT-2μ-O-Me-cAMP) by targeting agonist-bound Epac1 in an agonist-uncompetitive manner without affecting the GDP exchange on Rap1, Rap1-Epac1 interaction, or PKA type I/II activity (CβRIβ & CαRIIβ). CE3F4 (20 μM) effectively inhbits cellular Rap1 activation upon 10 μM Sp-8-pCPT-2μ-O-Me-cAMPS (Epac1-transfected HEK293 and r at neonatal cardiac myocytes) or 10 μM β-adrenergic receptor agonist isoprenaline stimulation (β1AR & Epac1 dually transfected HEK293). The isolated CE3F4 R enantiomer is reported to display 10-fold Epac1 selectivity over Epac2, and is 10-times more potent than the CE3F S enantiomer against Epac1.', 'Epac1 is a downstream effector of the cyclic adenosine monophosphate (cAMP) pathway.

in vivo

CE3F4 (1-3 mg/kg; through a catheter in the internal jugular vein) inhibits atrial fibrillation (AF) and CE3F4 (3 mg/kg; i.v.) inhibits ventricular arrhythmias[4].
CE3F4 (10 mg/kg; i.v.) improves cardiac function after myocardial infarction in mice[5].

Animal Model:Wild-type (WT) mice (induced AF after 20min of CE3F4 administration)[4]
Dosage:3 mg/kg and 1mg/kg
Administration:Through a catheter in the internal jugular vein
Result:Shortened the duration of the pacing-induced AF at 3mg/kg.
Animal Model:Casq2-KO mice (premature ventricular contraction induced by isoproterenol injection 20min after CE3F4 administration)[4]
Dosage:3 mg/kg
Administration:I.v.
Result:Reduced the incidence of sympathetic activation-induced ventricular arrhythmias.

storage

Store at -20°C

CE3F4 Preparation Products And Raw materials

Raw materials

Preparation Products

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CE3F4 Suppliers

Shanghai Lollane Biological Technology Co.,Ltd.
Tel
021-52996696,15000506266 15000506266
Fax
+86-21-52996696
Country
China
ProdList
4817
Advantage
55
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9803
Advantage
58
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
86249
Advantage
60
ShangHai Biochempartner Co.,Ltd
Tel
177-54423994 17754423994
Fax
QQ:2853530913
Email
2853530910@QQ.com
Country
China
ProdList
8000
Advantage
62
TargetMol Chemicals Inc.
Tel
+1-781-999-5354; +17819995354
Email
marketing@targetmol.com
Country
United States
ProdList
32467
Advantage
58
Career Henan Chemica Co
Tel
+86-0371-86658258 +8613203830695
Fax
0371-86658258
Email
laboratory@coreychem.com
Country
China
ProdList
30227
Advantage
58
Changzhou Chenhong Biotechnology Co., Ltd.
Tel
+86-0519-85788828 +86-13775037613
Email
sales@chemrenpharm.com
Country
China
ProdList
4032
Advantage
58
Suzhou youruike Chemical Pharmaceutical Technology Co., Ltd
Tel
15317229551
Fax
QQ:3607245178
Email
15151849396@163.com
Country
China
ProdList
999
Advantage
58
ShangHai ChuanQian Chemcial Technique Centre
Tel
15869524721
Email
3525679403@qq.com
Country
China
ProdList
4986
Advantage
58
MedBioPharmaceutical Technology Inc
Tel
021-69568360 18916172912
Email
order@med-bio.cn
Country
China
ProdList
8140
Advantage
58

143703-25-7, CE3F4Related Search:


  • CE3F4
  • 5,7-Dibromo-6-fluoro-3,4-dihydro-2-methyl-1(2H)-quinolinecarboxaldehyde
  • 1(2H)-Quinolinecarboxaldehyde, 5,7-dibromo-6-fluoro-3,4-dihydro-2-methyl-
  • CE3F4 >=98% (HPLC)
  • inhibit,Inhibitor,CE3F4,CE-3F4
  • 5,7-dibromo-6-fluoro-2-methyl-1,2,3,4-tetrahydroquinoline-1-carbaldehyde
  • CE3F4, 10 mM in DMSO
  • 143703-25-7
  • C11H10Br2FNO