ChemicalBook > CAS DataBase List > TPCA-1

TPCA-1

Product Name
TPCA-1
CAS No.
507475-17-4
Chemical Name
TPCA-1
Synonyms
TPCA-1;CS-991;GW683965;GW683965A;TPCA-1(TPCA 1);TPCA-1 USP/EP/BP;TPCA-1 (GW-683965;TPCA-1 IKK-2 Inhibitor IV;IKK-2 Inhibitor IV - CAS 507475-17-4 - Calbiochem;5-(4-Fluorophenyl)-2-ureidothiophene-3-carboxamide
CBNumber
CB41073580
Molecular Formula
C12H10FN3O2S
Formula Weight
279.29
MOL File
507475-17-4.mol
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TPCA-1 Property

Melting point:
>217°C (dec.)
Boiling point:
442.6±45.0 °C(Predicted)
Density 
1.490
storage temp. 
2-8°C
solubility 
DMSO: soluble5mg/mL, clear
form 
powder
pka
13.12±0.50(Predicted)
color 
white to light brown
Stability:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
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Safety

Hazard Codes 
Xn
Risk Statements 
22-36
Safety Statements 
26
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H319Causes serious eye irritation

Precautionary statements

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

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
T1452
Product name
TPCA-1
Purity
≥95% (HPLC)
Packaging
1mg
Price
$174
Updated
2024/03/01
Sigma-Aldrich
Product number
401481
Product name
IKK-2 Inhibitor IV - CAS 507475-17-4 - Calbiochem
Packaging
500μg
Price
$144
Updated
2024/03/01
Cayman Chemical
Product number
15115
Product name
TPCA-1
Purity
≥98%
Packaging
500μg
Price
$68
Updated
2024/03/01
Cayman Chemical
Product number
15115
Product name
TPCA-1
Purity
≥98%
Packaging
1mg
Price
$95
Updated
2024/03/01
Sigma-Aldrich
Product number
T1452
Product name
TPCA-1
Purity
≥95% (HPLC)
Packaging
5mg
Price
$697
Updated
2024/03/01
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TPCA-1 Chemical Properties,Usage,Production

Description

TPCA-1 (507475-17-4) selective inhibitor of IκB kinase 2 (IKK2) (IC50 = 17.9 nM).1 Inhibits production of pro-inflammatory cytokines in arthritis and other animal models of inflammation.1,2 Also attenuates NLRP3 inflammasome activation in THP-1 myeloid cells, and suppresses IL1β-induced proliferation, migration, and invasion of HeLa cells.3,4 Continuous exposure to TPCA-1 promotes expansion of hematopoietic stem/progenitor cells (HSPCs) via improved glycolysis and limited ROS production.5

Uses

TPCA-1 is a direct dual inhibitor for both IKKβ (IKK-2) and STAT3. It inhibits STAT3 phosphorylation, DNA binding, and transactivation in vivo. Synergistic treatment of TPCA-1 with tyrosine kinase inhibitors (TKIs) can potentially be a more effective method for treating cancers.

Definition

ChEBI: 2-(carbamoylamino)-5-(4-fluorophenyl)-3-thiophenecarboxamide is a member of thiophenes and an aromatic amide.

Biological Activity

Potent, selective inhibitor of I κ B kinase-2 (IKK-2) (IC 50 = 17.9 nM) that displays > 22-fold selectivity over IKK-1 and > 550-fold selectivity over other kinases and enzymes. Inhibits production of pro-inflammatory cytokines in vitro and in vivo and inhibits NF- κ B nuclear localisation. Reduces the severity and onset of collagen-induced arthritis; anti-inflammatory.

Biochem/physiol Actions

TPCA-1 is a potent and selective inhibitor of human IκB kinase-2 (IKK-2) with IC50 = 17.9 nM for IKK-2 compared to 400nm for IKK-1. It has been used to study inhibition of IKK-2 to prevent inflammatory mediator release in animal models of arthritis and airway inflammation.

in vitro

determination of the activity of tpca-1 against ten selected kinases, cox-1 and cox-2, showed the compound to be ~550-fold selective for ikk-2 versus ten of these enzymes. tpca-1 inhibits lipopolysaccharide-induced human monocyte production of tnf-α, il-6, and il-8 with an ic50 of 170 to 320 nm [1].

in vivo

prophylactic administration of tpca-1 at 3, 10, or 20 mg/kg resulted in a dose dependent reduction in the severity of murine collagen-induced arthritis. the significantly reduced disease severity and delay of disease onset resulting from administration of tpca-1 at 10 mg/kg were comparable to the effects of the antirheumatic drug, etanercept [1].

storage

Store at -20°C

References

Podolin et al. (2005), Attenuation of murine collagen-induced arthritis by a novel, selective small molecule inhibitor of IkappaB Kinase 2, TPCA-1 (2-[(aminocarbonyl)amino]-5-(4-fluorophenyl)-3-thiophenecarboxamide), occurs via reduction of proinflammatory cytokines and antigen-induced T cell Proliferation; Pharmacol. Exp. Ther., 312 373 Wang et al. (2021), TPCA-1 negatively regulates inflammation mediated by NF-kB pathway in mouse chronic periodontitis model; Oral Microbiol., 36 192 Unterreiner et al. (2021), Pharmacological inhibition of IKKb dampens NLRP3 inflammasome activation after priming in the human myeloid cell line THP-1; Biophys. Res. Commun., 545 177 Tao et al. (2021), IL-1b promotes cervical cancer though activating NF-κB/CCL-2; J. Exp. Pathol., 14 426 Sun et al. (2021), Continuous NF-κB pathway inhibition promotes expansion of human phenotypical hematopoietic stem/progenitor cells through metabolism regulation; Cell Res., 399 112468

TPCA-1 Preparation Products And Raw materials

Raw materials

Preparation Products

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TPCA-1 Suppliers

3B Pharmachem (Wuhan) International Co.,Ltd.
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View Lastest Price from TPCA-1 manufacturers

Career Henan Chemical Co
Product
TPCA-1 507475-17-4
Price
US $1.00/g
Min. Order
100g
Purity
99%
Supply Ability
G/KG/T
Release date
2019-12-20

507475-17-4, TPCA-1Related Search:


  • TPCA-1
  • 2-[(Aminocarbonyl)amino]-5-(4-fluorophenyl)-3-thiophenecarboxamide
  • 5-(4-Fluorophenyl)-2-ureidothiophene-3-carboxamide
  • TPCA-1(TPCA 1)
  • 3-ThiophenecarboxaMide, 2-[(aMinocarbonyl)aMino]-5-(4-fluorophenyl)-
  • 5-(4-Fluorophenyl)-2-ureidothiophene-3-carboxamide TPCA-1
  • TPCA-1 IKK-2 Inhibitor IV
  • GW683965
  • GW683965A
  • CS-991
  • IKK-2 Inhibitor IV - CAS 507475-17-4 - Calbiochem
  • TPCA-1 USP/EP/BP
  • TPCA-1 (GW-683965
  • 2-(carbamoylamino)-5-(4-fluorophenyl)thiophene-3-carboxamide
  • TPCA-1,Inhibitor,STAT,TPCA 1,Apoptosis,IKK,I kappa B kinase,IκB kinase,inhibit
  • 507475-17-4
  • NF-kB