ChemicalBook > CAS DataBase List > BAY 11-7085

BAY 11-7085

Product Name
BAY 11-7085
CAS No.
196309-76-9
Chemical Name
BAY 11-7085
Synonyms
CS-1876;BAY 117083;BAY 11-7085;BAY117085;BAY11-7085;BAY 11-7085 USP/EP/BP;BAY 11-7085;BAY-11-7085;BAY 11-7083;BAY 11-7085 - CAS 196309-76-9 - Calbiochem;(E)-3-(T-BUTYLPHENYLSULFONYL)-2-PROPENENITRILE;(E)-3-(4-tert-butylphenylsulfonyl)acrylonitrile;(E)3-[(4-T-BUTYLPHENYL)SULFONYL]-2-PROPENENITRILE
CBNumber
CB0675833
Molecular Formula
C13H15NO2S
Formula Weight
249.33
MOL File
196309-76-9.mol
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BAY 11-7085 Property

Melting point:
80-82℃
Boiling point:
407.1±45.0 °C(Predicted)
Density 
1.144
Flash point:
200℃
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO: >25 mg/mL, soluble
form 
solid
color 
white
Sensitive 
Light Sensitive
InChIKey
VHKZGNPOHPFPER-ONNFQVAWSA-N
CAS DataBase Reference
196309-76-9
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Safety

WGK Germany 
3
RTECS 
UD1312500
HS Code 
29309090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
B5681
Product name
Bay 11-7085
Purity
≥98% (HPLC), solid
Packaging
10mg
Price
$163
Updated
2024/03/01
TCI Chemical
Product number
B4845
Product name
BAY 11-7085
Purity
>97.0%(N)
Packaging
10mg
Price
$90
Updated
2024/03/01
TCI Chemical
Product number
B4845
Product name
BAY 11-7085
Purity
>97.0%(N)
Packaging
100mg
Price
$535
Updated
2024/03/01
Alfa Aesar
Product number
J67222
Product name
BAY 11-7085, 99%
Packaging
10mg
Price
$169
Updated
2023/06/20
Cayman Chemical
Product number
14795
Product name
BAY 11-7085
Purity
≥98%
Packaging
5mg
Price
$57
Updated
2024/03/01
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BAY 11-7085 Chemical Properties,Usage,Production

Uses

In the classical pathway of NF-κB activation, phosphorylation of the inhibitor of NF-κB (IκBα) releases the inhibitor from NF-κB, allowing IκBα degradation and NF-κB activation and nuclear import. BAY-11-7085 is an irreversible inhibitor of IκBα phosphorylation, preventing activation of NF-κB by cytokines and lipopolysaccharide (IC50 = 10 μM). It blocks gene expression that is regulated through the classical pathway of NF-κB activation and in this way blocks apoptosis, cell adhesion, and inflammation. BAY-11-7085 is also used to study IκBα actions that are independent of NF-κB signaling.

Uses

Bay 11-7085 has been used as:

  • nuclear factor-κB inhibitor in Panc-1 cells, macrophages
  • inhibitory κB kinase IKK inhibitor in human astrocytoma cells U87MGs
  • phospho-p65 inhibitor human monocyte cell line THP-1

Definition

ChEBI: BAY11-7085 is a sulfone that is benzene substituted by [(E)-2-cyanoethenyl]sulfonyl and tert-butyl groups at position 1 and 4, respectively. It is an irreversible inhibitor of IkappaB-alpha phosphorylation in cells (IC50 = 10 muM) and prevents the activation of NF-kappaB. It has a role as an anti-inflammatory agent, a ferroptosis inducer, a NF-kappaB inhibitor, an apoptosis inducer, an autophagy inducer, an antibacterial agent, an EC 2.7.11.10 (IkappaB kinase) inhibitor and an antineoplastic agent. It is a nitrile, a sulfone and a member of benzenes.

Biological Activity

Irreversible inhibitor of TNF- α -stimulated I κ B α phosphorylation (IC 50 ~ 10 μ M); leads to decreased NF- κ B and subsequent decreased expression of adhesion molecules. Also reversibly activates MAP kinases and stimulates apoptosis. Anti-inflammatory in vivo .

Biochem/physiol Actions

Bay 11-7085 inactivates peroxisome proliferator-activated receptors γ (PPAR-γ) and increases the microtubule-associated proteins 1A/1B light chain 3B (LC3B), a marker of autophagy resulting in apoptosis in human synovial fibroblasts. It promotes apoptosis in pancreatic carcinoma and may serve as radiotherapy-sensitizing drug. BAY 11-7085 decreases B-cell lymphoma 2 (Bcl-2) by inhibiting pI-κBα (inhibitor of nuclear factor κ B kinase subunit α

storage

Store at +4°C

References

[1]nasu k1, nishida m, ueda t, yuge a, takai n, narahara h. application of the nuclear factor-kappab inhibitor bay 11-7085 for the treatment of endometriosis: an in vitro study. am j physiol endocrinol metab. 2007 jul;293(1):e16-23

BAY 11-7085 Preparation Products And Raw materials

Raw materials

Preparation Products

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BAY 11-7085 Suppliers

Shanghai Boyle Chemical Co., Ltd.
Tel
Fax
86-21-57758967
Email
sales@boylechem.com
Country
China
ProdList
2923
Advantage
55
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15848
Advantage
69
Chembest Research Laboratories Limited
Tel
021-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6011
Advantage
61
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
Tetranov Biopharm
Tel
13526569071
Email
sales@leadmedpharm.com
Country
China
ProdList
7891
Advantage
64
Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
sales@meilune.com
Country
China
ProdList
4648
Advantage
58
TOKYO CHEMICAL INDUSTRY CO., LTD.
Tel
03-36680489
Fax
03-3668-0520
Email
Sales-JP@TCIchemicals.com
Country
Japan
ProdList
28398
Advantage
80
TCI Europe
Tel
320-37350700
Fax
+32 (0)37350701
Email
sales@tcieurope.eu
Country
Europe
ProdList
23680
Advantage
75
TCI AMERICA
Tel
800-4238616
Fax
+1-888-520-1075 / +1-503-283-1987
Email
sales@tciamerica.com
Country
Americas
ProdList
23662
Advantage
75
Shanghai Jiyi Biological Technology Co., LTD
Tel
021-54135696 18516235431
Fax
50815371
Email
shgegenetech@163.com
Country
China
ProdList
986
Advantage
55
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View Lastest Price from BAY 11-7085 manufacturers

Career Henan Chemical Co
Product
BAY 11-7085 196309-76-9
Price
US $1.00/g
Min. Order
1g
Purity
99%
Supply Ability
200kg
Release date
2019-12-30

196309-76-9, BAY 11-7085Related Search:


  • BAY 117083 (2E)-3-[[4-(1,1-Dimethylethyl)phenyl]sulfonyl]-2-propenenitrile
  • (2E)-3-[[4-(1,1-DIMETHYLETHYL)PHENYL]SULFONYL]-2-PROPENENITRILE
  • BAY 11-7085 - CAS 196309-76-9 - Calbiochem
  • CS-1876
  • BAY117085;BAY11-7085
  • BAY 11-7085;BAY-11-7085;BAY 11-7083
  • (E)-3-(T-BUTYLPHENYLSULFONYL)-2-PROPENENITRILE
  • (E)3-[(4-T-BUTYLPHENYL)SULFONYL]-2-PROPENENITRILE
  • BAY 11-7085
  • (E)-3-(4-tert-butylphenylsulfonyl)acrylonitrile
  • BAY 117083
  • (2E)-3-[[4-(1,1-Dimethylethyl)phenyl]sulfonyl]-2-propenenitrile BAY 11-7085
  • (E)-3-(4-tert-butylphenyl)sulfonylprop-2-enenitrile
  • 2-Propenenitrile, 3-[[4-(1,1-dimethylethyl)phenyl]sulfonyl]-, (2E)-
  • BAY 11-7085 USP/EP/BP
  • 196309-76-9
  • C13H15O2NS
  • Gene Regulation and Expression
  • Gene Regulation
  • BioChemical
  • Cell Biology
  • Cell Signaling and Neuroscience
  • Inhibitors
  • Cytokine signaling