SGC-GAK-1

SGC-GAK-1 Structure
CAS No.
2226517-76-4
Chemical Name:
SGC-GAK-1
Synonyms
SGC-GAK-1;GAK INHIBITOR 1;SGCGAK1,Inhibitor,SGC GAK 1,inhibit;6-Bromo-N-(3,4,5-trimethoxyphenyl)-4-quinolinamine;6-Bromo-N-(3,4,5-trimethoxyphenyl)quinolin-4-amine;4-Quinolinamine, 6-bromo-N-(3,4,5-trimethoxyphenyl)-
CBNumber:
CB74742442
Molecular Formula:
C18H17BrN2O3
Molecular Weight:
389.24
MOL File:
2226517-76-4.mol
Modify Date:
2023/6/30 15:45:59

SGC-GAK-1 Properties

Boiling point 484.9±45.0 °C(Predicted)
Density 1.436±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility Soluble in DMSO (up to at least 25 mg/ml) or in Ethanol (up to 10 mg/ml)
pka 6.43±0.49(Predicted)
form powder
color white to beige
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 2 months.

SAFETY

Risk and Safety Statements

HS Code  2933499090

SGC-GAK-1 price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) SML2202 SGC-GAK-1 ≥98% (HPLC) 2226517-76-4 5MG ₹10684.28 2022-06-14 Buy
Sigma-Aldrich(India) SML2202 SGC-GAK-1 ≥98% (HPLC) 2226517-76-4 25MG ₹43061.85 2022-06-14 Buy
Product number Packaging Price Buy
SML2202 5MG ₹10684.28 Buy
SML2202 25MG ₹43061.85 Buy

SGC-GAK-1 Chemical Properties,Uses,Production

Uses

SGC GAK 1 is a high affinity cyclin G associated kinase (GAK) inhibitor (Kd = 1.9 nM). Exhibited >30-fold selectivity for GAK versus a panel of other kinases. Inhibits GAK in live cell assays (IC50 = 110 nM).

Biochem/physiol Actions

SGC-GAK-1 (CA93) is an ATP-competitive cyclin G-associated kinase (GAK) inhibitor (Ki = 3.1 nM by ATP site fluorescent tracer displacement assay; KD = 4.5 nM by ITC) that effectively inhibits Dengue viral entry and packaging in cultures (IC50 = 920 nM) without detectable cytotoxicity. SGC-GAK-1 exhibits much reduced affinity toward only 4 other kinases among a panel of ~400 (KD = 1.9 nM/GAK vs. 110 nM/RIPK2, 190 nM/ADCK3, 520 nM/NLK, 980 nM/AVCR1 by ligand competitive binding assay; IC50 = 110 nM/GAK vs. 360 nM/RIPK2 by cellular target engagement assay). SGC-GAK-1N (CA71) is a structure analog and the recommended negative control (GAK KD = 7.1 μM by ligand competitive binding assay; GAK & RIPK2 IC50 >50 μM by cellular target engagement assay). For characterization details of SGC-GAK-1, please visit the SGC-GAK-1 probe summary on the Structural Genomics Consortium (SGC) website.SGC-GAK-1N is the negative control for the active probe, SGC-GAK-1. SGC-GAK-1N is available from Sigma. To learn more about and purchase SGC-GAK-1N, click here.To learn about other SGC chemical probes, visit sigma.com/sgc

SGC-GAK-1 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 41)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
ATK CHEMICAL COMPANY LIMITED +undefined-21-51877795 China 32760 60 Inquiry
BOC Sciences +1-631-485-4226 United States 19553 58 Inquiry
SHANGHAI T&W PHARMACEUTICAL CO., LTD. +86-021-61551413 +8618813727289 China 5738 58 Inquiry
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InvivoChem +1-708-310-1919 +1-13798911105 United States 6393 58 Inquiry
LEAP CHEM CO., LTD. +86-852-30606658 China 24738 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 United States 19973 58 Inquiry
Aladdin Scientific +1-+1(833)-552-7181 United States 57511 58 Inquiry
Amadis Chemical Company Limited 571-89925085 China 131980 58 Inquiry
SGC-GAK-1 GAK INHIBITOR 1 6-Bromo-N-(3,4,5-trimethoxyphenyl)-4-quinolinamine 4-Quinolinamine, 6-bromo-N-(3,4,5-trimethoxyphenyl)- 6-Bromo-N-(3,4,5-trimethoxyphenyl)quinolin-4-amine SGCGAK1,Inhibitor,SGC GAK 1,inhibit 2226517-76-4 API