PD 180970

Modify Date: 2024-01-02 18:16:27

PD 180970 Structure
PD 180970 structure
Common Name PD 180970
CAS Number 287204-45-9 Molecular Weight 429.27400
Density N/A Boiling Point N/A
Molecular Formula C21H15Cl2FN4O Melting Point N/A
MSDS Chinese USA Flash Point N/A
Symbol GHS06
GHS06
Signal Word Danger

 Use of PD 180970


PD180970 is a highly potent and ATP-competitive p210Bcr-Abl kinase inhibitor, with an IC50 of 5 nM for inhibiting the autophosphorylation of p210Bcr-Abl. PD180970 also inhibits Src and KIT kinase with IC50s of 0.8 nM and 50 nM, respectively. PD180970 indcues apoptosis of K562 leukemic cells, and can be used for chronic myelogenous leukemia research[1][2][3].

 Names

Name 6-(2,6-dichlorophenyl)-2-(4-fluoro-3-methylanilino)-8-methylpyrido[2,3-d]pyrimidin-7-one
Synonym More Synonyms

 PD 180970 Biological Activity

Description PD180970 is a highly potent and ATP-competitive p210Bcr-Abl kinase inhibitor, with an IC50 of 5 nM for inhibiting the autophosphorylation of p210Bcr-Abl. PD180970 also inhibits Src and KIT kinase with IC50s of 0.8 nM and 50 nM, respectively. PD180970 indcues apoptosis of K562 leukemic cells, and can be used for chronic myelogenous leukemia research[1][2][3].
Related Catalog
Target

Bcr-Abl:5 nM (IC50, p210Bcr-Abl kinase)

Src:0.8 nM (IC50)

KIT:50 nM (IC50)

In Vitro PD180970 (0.5 μM; 24-96 hours) treatment causes cell death K562 cells[1]. PD180970 (0.5 μM; 24-48 hours) treatment induces apoptosis of K562 cells. The result shows increase in annexin V-PI double-positive cells[1]. PD180970 inhibits tyrosine phosphorylation of p210Bcr-Abl, Gab2, and CrkL in K562 cells with IC50 values of 170 nM, 80 nM, and 80 nM, respectively. In vitro, PD180970 potently inhibits autophosphorylation of p210Bcr-Abl (IC50 of 5 nM) and the kinase activity of purified recombinant Abl tyrosine kinase (IC50 of 2.2 nM)[1]. The blocking Bcr-Abl kinase activity using PD180970 in the human K562 CML cell line resulted in inhibition of Stat5 DNA-binding activity with an IC50 of 5 nM[2]. Cell Viability Assay[1] Cell Line: K562 cells Concentration: 0.5 μM Incubation Time: 24 hours, 48 hours, 72 hours, 96 hours Result: Resulted in cell death. Apoptosis Analysis[1] Cell Line: K562 cells Concentration: 0.5 μM Incubation Time: 24 hours, 48 hours Result: Increased annexin V-positive/PI-negative cells.
In Vivo PD180970 (5 mg/kg; intraperitonial injection; daily; for 7 days) mitigates MPTP-induced neuronal loss in mice. PD180970 has the neuroprotective ability in a preclinical mouse model of Parkinson's disease (PD)[4]. Animal Model: Male C57BL/6J mice (3-4 months old) injected with MPTP[4] Dosage: 5 mg/kg Administration: Intraperitonial injection; daily; for 7 days Result: Decreased number of activated microglia on activation by MPTP in mice brains. And showed significant reduction in intensity of Iba1 expression in activated microglia.
References

[1]. J F Dorsey, et al. The pyrido[2,3-d]pyrimidine derivative PD180970 inhibits p210Bcr-Abl tyrosine kinase and induces apoptosis of K562 leukemic cells. Cancer Res. 2000 Jun 15;60(12):3127-31.

[2]. Mei Huang, et al. Inhibition of Bcr-Abl kinase activity by PD180970 blocks constitutive activation of Stat5 and growth of CML cells. Oncogene. 2002 Dec 12;21(57):8804-16.

[3]. Amie S Corbin, et al. Sensitivity of oncogenic KIT mutants to the kinase inhibitors MLN518 and PD180970. Blood. 2004 Dec 1;104(12):3754-7.

[4]. Suresh Sn, et al. Small molecule modulator of aggrephagy regulates neuroinflammation to curb pathogenesis of neurodegeneration. EBioMedicine. 2019 Dec;50:260-273.

 Chemical & Physical Properties

Molecular Formula C21H15Cl2FN4O
Molecular Weight 429.27400
Exact Mass 428.06100
PSA 63.04000
LogP 4.91530

 Safety Information

Symbol GHS06
GHS06
Signal Word Danger
Hazard Statements H301-H413
Precautionary Statements P301 + P310
Hazard Codes Xi
RIDADR UN 2811 6.1 / PGIII

 Synonyms

2hzi
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  • DC Chemicals Limited
  • China
  • Product Name: PD180970
  • Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/500mg
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao


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