ChemicalBook > CAS DataBase List > SGX-523

SGX-523

Product Name
SGX-523
CAS No.
1022150-57-7
Chemical Name
SGX-523
Synonyms
X-523;CS-331;SGX-523;α-Neurokinin;SGX-523, >=98%;SGX 523(SGX-523);SGX-523 USP/EP/BP;SGX-523;SGX523; SGX 523;6-[[6-(1-Methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]thio]quinoline;6-[[6-(1-methylpyrazol-4-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]sulfanyl]quinoline
CBNumber
CB42501000
Molecular Formula
C18H13N7S
Formula Weight
359.41
MOL File
1022150-57-7.mol
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SGX-523 Property

Density 
1.485
storage temp. 
Store at -20°C
solubility 
≥17.95 mg/mL in DMSO
form 
solid
pka
3.94±0.10(Predicted)
color 
Light yellow to yellow
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
448106
Product name
Met Kinase Inhibitor VI, SGX523 - CAS 1022150-57-7 - Calbiochem
Packaging
5MG
Price
$201
Updated
2024/03/01
Cayman Chemical
Product number
18093
Product name
SGX523
Purity
≥98%
Packaging
1mg
Price
$44
Updated
2024/03/01
Cayman Chemical
Product number
18093
Product name
SGX523
Purity
≥98%
Packaging
5mg
Price
$161
Updated
2024/03/01
Cayman Chemical
Product number
18093
Product name
SGX523
Purity
≥98%
Packaging
10mg
Price
$278
Updated
2024/03/01
Cayman Chemical
Product number
18093
Product name
SGX523
Purity
≥98%
Packaging
25mg
Price
$533
Updated
2024/03/01
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SGX-523 Chemical Properties,Usage,Production

Uses

SGX523 is a novel, ATP-competitive kinase inhibitor.

Definition

ChEBI: A member of the class of triazolopyridazines that is 6-(1-methylpyrazol-4-yl)[1,2,4]triazolo[4,3-b]pyridazine-3-thiol in which the thiol hydrogen is replaced by a quinolin-6-yl group.

Biological Activity

sgx-523 is a novel, potent, atp-competitive, and highly-selective hepatocyte growth factor receptor (met) inhibitor with ic50 value of 4 nm [1].sgx523 inhibits met autophosphorylation in gastric cancer cell line gtl16 and human lung carcinoma cell line a549, with ic50 of 40 nm and 12 nm, respectively [1]. additionally, tumor regression was observed in gastic cancer cell line gtl16 and human gbm cell line u87mg derived mouse xenograft models that are treated with sgx-523 by oral gavage [1].sgx523 has been shown to inhibit the phosphorylateion of mek, mapk, akt in brain cancer cell lines including u87, u373, daoy, as well as glioma stem cells 1228. the inhibition of mek in brain cancer cells and stem cells led to cell proliferation, g1/s cell cycle progression, cell migration, and cell invasion [2].

storage

Store at +4°C

References

[1] buchanan sg1, hendle j, lee ps, smith cr, bounaud py, jessen ka, tang cm, huser nh, felce jd, froning kj, peterman mc, aubol be, gessert sf,sauder jm, schwinn kd, russell m, rooney ia, adams j, leon bc, do th, blaney jm, sprengeler pa, thompson da, smyth l, pelletier la, atwell s, holme k,wasserman sr, emtage s, burley sk, reich sh. sgx523 is an exquisitely selective, atp-competitive inhibitor of the met receptor tyrosine kinase with antitumor activity in vivo. mol cancer ther. 2009 dec;8(12):3181-90.
[2] guessous f1, zhang y, dipierro c, marcinkiewicz l, sarkaria j, schiff d, buchanan s, abounader r.an orally bioavailable c-met kinase inhibitor potently inhibits brain tumor malignancy and growth. anticancer agents med chem. 2010 jan;10(1):28-35.

SGX-523 Preparation Products And Raw materials

Raw materials

Preparation Products

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SGX-523 Suppliers

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View Lastest Price from SGX-523 manufacturers

Career Henan Chemical Co
Product
SGX-523 1022150-57-7
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100kgs
Release date
2019-12-17

1022150-57-7, SGX-523Related Search:


  • SGX-523
  • 6-[[6-(1-Methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]thio]quinoline
  • SGX 523(SGX-523)
  • Quinoline,6-[[6-(1-Methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]thio]-
  • 6-[[6-(1-Methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]thio]quinoline SGX 523
  • SGX-523, >=98%
  • 6-[[6-(1-methylpyrazol-4-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]sulfanyl]quinoline
  • SGX-523;SGX523; SGX 523
  • CS-331
  • X-523
  • SGX-523 USP/EP/BP
  • α-Neurokinin
  • 1022150-57-7
  • 1022190-57-7
  • C18H13N7S
  • Inhibitors
  • API