Dmog Stressmarq

Lab Reagents

Human IgG antibody Laboratories manufactures the dmog stressmarq reagents distributed by Genprice. The Dmog Stressmarq reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Stressmarq Biosciences Inc.. Other Dmog products are available in stock. Specificity: Dmog Category: Stressmarq

Serum / Plasma information

SU1498 (VEGFR kinase inhibitor)
SIH-480-5MG	Stressmarq	5 mg	EUR 141
SU1498 is a potent and selective inhibitor of Flk-1, a VEGF receptor kinase, and VEGFR2.
Description: The substance SU1498 is a vegfr kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is solid which is soluble in DMSO .

SU 4312 (VEGFR, PDGFR kinase inhibitor)
SIH-481-25MG	Stressmarq	25 mg	EUR 395
SU 4312 is a potent and selective inhibitor of VEGFR and PDGFR tyrosine kinases, including VEGFR-2 (Flk-1, KDR).
Description: The substance SU 4312 is a vegfr, pdgfr kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is orange solid which is soluble in DMSO (25 mg/ml).

SU 4312 (VEGFR, PDGFR kinase inhibitor)
SIH-481-5MG	Stressmarq	5 mg	EUR 149
SU 4312 is a potent and selective inhibitor of VEGFR and PDGFR tyrosine kinases, including VEGFR-2 (Flk-1, KDR).
Description: The substance SU 4312 is a vegfr, pdgfr kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is orange solid which is soluble in DMSO (25 mg/ml).

Sunitinib malate (VEGFR, PDGFR kinase inhibitor)
SIH-482-25MG	Stressmarq	25 mg	EUR 485
Sunitinib malate is a receptor tyrosine kinase inhibitor. It has been shown to target VEGF-R1, VEGF-R2, VEGF-R3, PDGF-R?, PDGF-R?, KIT, c-KIT, FLT3, CSF-1R, Flk-1, and RET.
Description: The substance Sunitinib malate is a vegfr, pdgfr kinase inhibitor. It is synthetically produced and has a purity of ?99%. The pure substance is yellow solid which is soluble in DMSO (40 mg/ml).

Sunitinib malate (VEGFR, PDGFR kinase inhibitor)
SIH-482-5MG	Stressmarq	5 mg	EUR 165
Sunitinib malate is a receptor tyrosine kinase inhibitor. It has been shown to target VEGF-R1, VEGF-R2, VEGF-R3, PDGF-R?, PDGF-R?, KIT, c-KIT, FLT3, CSF-1R, Flk-1, and RET.
Description: The substance Sunitinib malate is a vegfr, pdgfr kinase inhibitor. It is synthetically produced and has a purity of ?99%. The pure substance is yellow solid which is soluble in DMSO (40 mg/ml).

Vandetanib (VEGFR inhibitor)
SIH-483-10MG	Stressmarq	10 mg	EUR 121
Vandetanib is a specific inhibitor of Flk-1 and Flt-4.
Description: The substance Vandetanib is a vegfr inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is yellow solid which is soluble in DMSO (30 mg/ml) or EtOH (10 mg/ml).

Vandetanib (VEGFR inhibitor)
SIH-483-50MG	Stressmarq	50 mg	EUR 289
Vandetanib is a specific inhibitor of Flk-1 and Flt-4.
Description: The substance Vandetanib is a vegfr inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is yellow solid which is soluble in DMSO (30 mg/ml) or EtOH (10 mg/ml).

Vatalanib Dihydrochloride (VEGFR inhibitor)
SIH-484-10MG	Stressmarq	10 mg	EUR 137
Vatalanib Dihydrochloride is an inhibitor of Flk, c-Kit and PDGFR-?. It has been shown to inhibit VEGFR-dependent tumor angiogenesis and EGFR- and RET-dependent tumor cell proliferation and survival.
Description: The substance Vatalanib Dihydrochloride is a vegfr inhibitor. It is synthetically produced and has a purity of ?96%. The pure substance is solid which is soluble in DMSO (30 mg/ml), ethanol (10 mg/ml) with warming; very poorly soluble in water; maximum solubility in plain water is estimated to be about 10-20 µM; buffers, serum, or other additives may increase or decrease the aqueous solubility.Also soluble in methanol, and water ( ?10 mg/ml ).

Vatalanib Dihydrochloride (VEGFR inhibitor)
SIH-484-50MG	Stressmarq	50 mg	EUR 317
Vatalanib Dihydrochloride is an inhibitor of Flk, c-Kit and PDGFR-?. It has been shown to inhibit VEGFR-dependent tumor angiogenesis and EGFR- and RET-dependent tumor cell proliferation and survival.
Description: The substance Vatalanib Dihydrochloride is a vegfr inhibitor. It is synthetically produced and has a purity of ?96%. The pure substance is solid which is soluble in DMSO (30 mg/ml), ethanol (10 mg/ml) with warming; very poorly soluble in water; maximum solubility in plain water is estimated to be about 10-20 µM; buffers, serum, or other additives may increase or decrease the aqueous solubility.Also soluble in methanol, and water ( ?10 mg/ml ).

WHI P131 (JAK3 kinase inhibitor)
SIH-485-10MG	Stressmarq	10 mg	EUR 149
WHI P131 also known as Janex-1, is a reversible, potent, and specific inhibitor of JAK3. WHI P131 is cell permeable. It has been seen to inhibit glioblastoma cell adhesion and migration, as well as, thrombin-induced platelet aggregation.
Description: The substance WHI P131 is a jak3 kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to off-white solid which is soluble in DMSO (~1 mg/ml), and DMF (~1 mg/ml).

WHI P131 (JAK3 kinase inhibitor)
SIH-485-50MG	Stressmarq	50 mg	EUR 384
WHI P131 also known as Janex-1, is a reversible, potent, and specific inhibitor of JAK3. WHI P131 is cell permeable. It has been seen to inhibit glioblastoma cell adhesion and migration, as well as, thrombin-induced platelet aggregation.
Description: The substance WHI P131 is a jak3 kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to off-white solid which is soluble in DMSO (~1 mg/ml), and DMF (~1 mg/ml).

Y 27632 (ROCK kinase inhibitor)
SIH-486-1MG	Stressmarq	1 mg	EUR 149
Y 27632 is a very potent and selective ROCK1 and ROCK2 inhibitor. Y 27632 is cell permeable and is an ATP competitive inhibitor.
Description: The substance Y 27632 is a rock kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to pale yellow powder which is soluble in DMSO (25 mg/ml), methanol (25 mg/ml), acetonitrile (<1 mg/ml), dioxan (<1 mg/ml), water (very soluble.

Y 27632 (ROCK kinase inhibitor)
SIH-486-5MG	Stressmarq	5 mg	EUR 328
Y 27632 is a very potent and selective ROCK1 and ROCK2 inhibitor. Y 27632 is cell permeable and is an ATP competitive inhibitor.
Description: The substance Y 27632 is a rock kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to pale yellow powder which is soluble in DMSO (25 mg/ml), methanol (25 mg/ml), acetonitrile (<1 mg/ml), dioxan (<1 mg/ml), water (very soluble.

ZM 306416 (VEGFR kinase inhibitor)
SIH-487-25MG	Stressmarq	25 mg	EUR 395
ZM 306416 is a potent and selective VEGF receptor tyrosine kinase inhibitor. Specifically, it inhibits Flk-1 (KDR) and Flt.
Description: The substance ZM 306416 is a vegfr kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is off-white solid which is soluble in DMSO (3 mg/ml) or ethanol (1 mg/ml).

ZM 306416 (VEGFR kinase inhibitor)
SIH-487-5MG	Stressmarq	5 mg	EUR 149
ZM 306416 is a potent and selective VEGF receptor tyrosine kinase inhibitor. Specifically, it inhibits Flk-1 (KDR) and Flt.
Description: The substance ZM 306416 is a vegfr kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is off-white solid which is soluble in DMSO (3 mg/ml) or ethanol (1 mg/ml).

ZM 336372 (c-Raf kinase inhibitor)
SIH-488-25MG	Stressmarq	25 mg	EUR 574
ZM 336372 is a potent, specific and reversible inhibitor of the protein kinase c-Raf. It has also been shown to inhibit SAPK2/p38. ZM 336372 is cell permeable.
Description: The substance ZM 336372 is a c-raf kinase inhibitor. It is synthetically produced and has a purity of ?95%. The pure substance is white to off-white solid which is soluble in DMSO (200 mg/ml).

ZM 336372 (c-Raf kinase inhibitor)
SIH-488-5MG	Stressmarq	5 mg	EUR 188
ZM 336372 is a potent, specific and reversible inhibitor of the protein kinase c-Raf. It has also been shown to inhibit SAPK2/p38. ZM 336372 is cell permeable.
Description: The substance ZM 336372 is a c-raf kinase inhibitor. It is synthetically produced and has a purity of ?95%. The pure substance is white to off-white solid which is soluble in DMSO (200 mg/ml).