Products from SYNkinase

SYNkinase

SYNkinase, headquartered in Australia, is a primary producer of research-use-only biomedical reagents, which it markets to life-science and drug-discovery researchers affiliated with universities, research institutes and industry. SYNkinase was established in 2008 by Professor Andrew Wilks and Dr. Xian Bu. The founders of the company have been involved in pharmaceutical drug discovery for three decades and have extensive scientific, company and board experience.

More information at: www.adipogen.com/synkinase

Go to the catalogs of SYNkinase

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GSK-F1
GSK-F1

Item number: SYN-1220-M001

Solid. Soluble in DMSO. GSK-F1 is a potent PI4KA inhibitor. It has better pharmacokinetic properties in vivo than to GSK-A1 (SYN-1219). GSK-F1 does not cross the blood-brain barrier. Phosphatidylinositol 4-kinase type III? (PI4KA) is a host factor essential for hepatitis C virus replication and hence is a target for...
Keywords: 5-(2-Amino-4-oxo-3-(2-(trifluoromethyl)phenyl)-3,4-dihydroquinazolin-6-yl)-N-(2,4-difluorophenyl)-2-methoxypyridine-3-sulf...
Application: Potent PI4KA inhibitor
CAS 1402345-92-9
MW: 603,5 D
From 158.00€ *
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Regorafenib
Regorafenib

Item number: SYN-1169-M100

Soluble in DMSO or ethanol. Regorafenib (BAY 73-4506, Fluoro-Sorafenib) is a multi-target inhibitor for VEGFR1, VEGFR2, VEGFR3, PDGFR beta, Kit, RET and Raf-1 with IC(50) values of 13, 4.2, 46, 22, 7, 1.5 and 2.5nM, respectively. Target: VEGFR , Kinase Group: RTK , Substrate: Tyrosine
Keywords: BAY-73-4506
Application: VEGFR2 / RET / Raf-1 inhibitor
CAS 755037-03-7
MW: 482,8 D
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CX-5461
CX-5461

Item number: SYN-3031-M001

Slightly soluble (<1mg/ml) in DMSO or ethanol. CX-5461 is an inhibitor of rRNA synthesis, selectively inhibits Pol I-driven transcription of rRNA with IC(50) of 142nM, has no effect on Pol II, and possesses 250- to 300-fold selectivity for inhibition of rRNA transcription versus DNA replication and protein translation.
Keywords: Chantix, Champix
Application: RNA polymerase I inhibitor
CAS 1138549-36-6
MW: 513.6 D
From 119.00€ *
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(R)-BI-2536
(R)-BI-2536

Item number: SYN-1019-M001

Soluble in DMSO, Ethanol. Polo-like kinase 1 (Plk1) is a regulator of the cell cycle that has been implicated in the pathology of many cancers. BI-2536 is a potent and selective small-molecule inhibitor of mammalian Plk1. It has inhibitory activity at subnanomolar concentrations and inhibits tumor growth in multiple...
Keywords: (R)-BI2536
Application: PLK1 inhibitor
CAS 755038-02-9
MW: 521,7 D
From 106.00€ *
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TAE-684
TAE-684

Item number: SYN-1159-M001

Soluble in DMSO or ethanol. TAE684 is a potent and selective ALK inhibitor with an IC(50) of 3nM. It is 100-fold more sensitive for ALK over InsR. Target: ALK , Kinase Group: RTK , Substrate: Tyrosine
Keywords: NVP-TAE684
Application: ALK inhibitor
CAS 761439-42-3
MW: 614,2 D
From 119.00€ *
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GSK-A1
GSK-A1

Item number: SYN-1219-M001

Solid. Soluble in DMSO. GSK-A1 is a potent PI4KA inhibitor with an IC50 of about 3nM in vitro using HEK-AT1 cells. Phosphatidylinositol 4-kinase type III? (PI4KA) is a host factor essential for hepatitis C virus replication and hence is a target for drug development. RNAi studies have shown that PI4KA is a mandatory...
Keywords: 5-(2-Amino-1-(4-morpholinophenyl)-1H-benzo[d]imidazol-6-yl)-N-(2-fluorophenyl)-2-methoxypyridine-3-sulfonamide, GSKA1
Application: Potent PI4KA inhibitor
CAS 1416334-69-4
MW: 574,6 D
From 158.00€ *
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LY2801653
LY2801653

Item number: SYN-1222-M005

Solid. Soluble in DMSO. LY2801653 is an orally bioavailable multi-kinase inhibitor with potent activity against MET, MST1R and other oncoproteins. It displays anti-tumour activities in mouse xenograft models. In vitro, LY2801653 has an IC50 for inhibition of MET phosphorylation between 35.2-59.2nM. LY2801653 was...
Keywords: LY-2801653,...
Application: Multi-kinase inhibitor
CAS 1206799-15-6
MW: 552,5 D
From 106.00€ *
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Erlotinib hydrochloride
Erlotinib hydrochloride

Item number: SYN-1039-M001

Soluble in DMSO. Slightly soluble ( 1000-fold more sensitive for EGFR than for c-Src or v-Abl. Target: EGFR , Kinase Group: RTK , Substrate: Tyrosine
Keywords: OSI774, CP-358774, Tarceva, NSC718781
Application: EGFR inhibitor
CAS 183319-69-9
MW: 429,9 D
From 66.00€ *
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GW-441756
GW-441756

Item number: SYN-1044-M001

Soluble in DMSO. Slightly soluble (<1mg/ml) in ethanol. GW441756 is an orally active, potent and highly selective TrkA tyrosine kinase inhibitor (IC(50) of 2nM). It specifically blocks TrkA-induced cell death in a dose-dependent manner. Target: TrkA , Kinase Group: RTK , Substrate: Tyrosine
Keywords: GW441756
Application: TrkA inhibitor
CAS 504433-23-2
MW: 275,3 D
From 79.00€ *
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PF-4618433
PF-4618433

Item number: SYN-1163-M001

Soluble in DMSO. PF-4618433 shows improved PYK2 potency, reduced p38 activity, and superior overall selectivity relative to the prototype BIRB796. In the functional osteogenesis assays, cultures treated with increasing concentrations of PF-4618433 starting at day 1 and maintained throughout showed a dose-dependent...
Keywords: PF4618433
Application: PYK2 inhibitor
CAS 1166393-85-6
MW: 445,5 D
From 250.00€ *
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BKM-120
BKM-120

Item number: SYN-1200-M005

Soluble in DMSO or ethanol. NVP-BKM120 is a potent, selective, orally bioavailable Class I PI3Kalpha Inhibitor with IC(50) of 20nM, currently in Phase II clinical trials for the treatment of cancer. It exhibits lower potency against class III and class IV PI3Ks Target: PI3K , Kinase Group: Lipid Kinase ,...
Keywords: NVP-BKM120
Application: PI3K inhibitor
CAS 944396-07-0
MW: 410,4 D
From 79.00€ *
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GSK-2606414
GSK-2606414

Item number: SYN-1201-M001

Soluble in DMSO or ethanol. GSK2606414 is an orally available, potent, and selective PERK inhibitor with IC(50) of 0.4nM, displaying at least 100-fold selectivity over the other EIF2AKs assayed Target: PERK , Kinase Group: Other , Substrate: Serine-Threonine
Keywords: GSK-2606414
Application: EIF2AK3 / PERK inhibitor
CAS 1337531-36-8
MW: 451,4 D
From 119.00€ *
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