16 products were found matching "SYN-1021-M100"!

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AV-412
AV-412

Item number: SYN-1012-M100

Soluble in DMSO or ethanol. AV-412 is a potent dual inhibitor of EGFR and ErbB2 tyrosine kinases, including the mutant EGFR(L858R,T790M), which is clinically resistant to the EGFR-specific kinase inhibitors erlotinib and gefitinib. In enzyme assays assay the compound inhibited the EGFR variants and ErbB2 in the...
Keywords: MP-412, AV412
Application: EGFR / ErbB2 inhibitor
CAS 451492-95-8
MW: 507 D
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GSK-2606414
GSK-2606414

Item number: SYN-1201-M100

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
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R406
R406

Item number: SYN-1121-M001

Soluble in DMSO or ethanol. R406 is a strong Syk inhibitor with an IC(50) of 41nM. It inhibits Syk but not Lyn. It shows 5-fold less potency to Flt3. Target: Syk , Kinase Group: PTK , Substrate: Tyrosine
Keywords: R-406
Application: Syk inhibitor
CAS 841290-80-0
MW: 470,5 D
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BX-912
BX-912

Item number: SYN-1027-M100

Soluble in DMSO or ethanol. BX912 is a PDK1 (3-Phosphoinositide-dependent Kinase-1) inhibitor, with an IC(50) of 26nM. Target: PDK1 , Kinase Group: AGC , Substrate: Serine-Threonine
Keywords: BX912
Application: PDPK1 inhibitor
CAS 702674-56-4
MW: 471,4 D
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BMS-5
BMS-5

Item number: SYN-1024-M100

Soluble in DMSO. Kinases, such as LIM kinase 1 (LIMK1) and LIM kinase 2 (LIMK2), have been identified as participating in signal pathways affecting actin dynamics by deactivating cofilin. Over expression of LMK1 has been found in invasive breast and prostate cancer cell lines and suppression of LIMK 2 expression has...
Keywords: BMS5
Application: LIMK1 / LIMK2 inhibitor
CAS 1338247-35-0
MW: 431,3 D
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CC-401 hydrochloride
CC-401 hydrochloride

Item number: SYN-1028-M100

Soluble in DMSO. CC-401 is a competitive inhibitor of the ATP binding site in the active, phosphorylated, form of JNK. This prevents JNK from phosphorylating its various target molecules, including the amino terminus of c-Jun. It is a potent inhibitor of all three forms of JNK (Ki of 25-50 nM), and has at least...
Keywords: CC401
Application: JNK inhibitor
CAS 1438391-30-0
MW: 424,9 D
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GDC-0941
GDC-0941

Item number: SYN-1041-M100

Soluble in DMSO. Slightly soluble (<1mg/ml) in ethanol. GDC-0941 is a potent class I PI3 kinase (PI3K) inhibitor. It selectively binds to PI3K isoforms in an ATP-competitive manner. It has an IC(50) of 3nM, and shows slight selectivity toward p110beta (11-fold) and p110gamma (25-fold). Target: PI3K , Kinase Group:...
Keywords: GDC0941
Application: PI3K inhibitor
CAS 957054-30-7
MW: 513,6 D
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SNS-314
SNS-314

Item number: SYN-1081-M100

Soluble in DMSO or ethanol. Aurora kinases constitute a family of serine-threonine kinases that are strongly associated with cancer. Aurora A and B are essential in mitosis. Perturbation of their activity leads to multiple defects in mitosis including aberrant centrosome duplication, misalignment of chromosomes,...
Keywords: SNS314
Application: Aurora inhibitor
CAS 1057249-41-8
MW: 430,9 D
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ABT-737
ABT-737

Item number: SYN-1001-M100

Soluble in DMSO. Slightly soluble (<1mg/ml) in ethanol. ABT-737 is a small-molecule inhibitor of the anti-apoptotic proteins Bcl-2, Bcl-X(L) and Bcl-w, with an affinity two to three orders of magnitude more potent than previously reported compounds. Mechanistic studies reveal that ABT-737 does not directly initiate...
Keywords: ABT737
Application: Bcl-2 / Bcl-X(L) / Bcl-w inhibitor
CAS 852808-04-9
MW: 813,4 D
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AT9283
AT9283

Item number: SYN-1011-M100

Soluble in DMSO or ethanol. Aurora kinases play a key role in the regulation of mitosis and in recent years have become attractive targets for the treatment of cancer. AT9283 is a powerful inhibitor of Aurora A and B kinases as well as several other important kinases including JAK2 and Abl (T315I). AT9283 has also...
Keywords: AT-9283
Application: Aurora inhibitor
CAS 896466-04-9
MW: 381,4 D
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PD-173955
PD-173955

Item number: SYN-1061-M100

PD173955 is an ATP-competitive, dual Src/Abl kinase inhibitor. It is a potent inhibitor of Bcr-Abl with an IC(50) of 1-2nM in kinase inhibition assays. In cellular growth assays it inhibits Bcr-Abl-dependent substrate tyrosine phosphorylation. PD173955 also inhibits Src kinase activity in vitro with an IC(50) of...
Keywords: PD173955, PD-173,955
Application: BCR-Abl inhibitor
CAS 260415-63-2
MW: 443,4 D
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BI-D1870
BI-D1870

Item number: SYN-1020-M100

Soluble in DMSO. Slightly soluble (<1mg/ml) in ethanol. BI-D1870 is a small molecule, specific inhibitor of p90 RSK (ribosomal S6 kinase) isoforms RSK1, RSK2, RSK3 and RSK4, both in vitro and in vivo, with IC(50)s are 31nM, 24nM, 18nM, 15nM, respectively. It shows a 10- to 100-fold selectivity for RSK over MST2,...
Keywords: BID1870
Application: RPS6KA inhibitor
CAS 501437-28-1
MW: 391,4 D
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