Adooq Bioscience
KRN 633 is a cell-permeable, reversible, ATP-competitive VEGFR kinase inhibitor that inhibits PDGFR-?? and c-Kit at higher concentrations only (IC50 = 0.97 ??M and 4.33 ??M, respectively) and inactive towards 17 other kinases (IC50 ??? 10 ??M).
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KRN 633 100mg
100mg
| Purity Not Available
Adooq Bioscience
KRN 633 is a cell-permeable, reversible, ATP-competitive VEGFR kinase inhibitor that inhibits PDGFR-?? and c-Kit at higher concentrations only (IC50 = 0.97 ??M and 4.33 ??M, respectively) and inactive towards 17 other kinases (IC50 ??? 10 ??M).
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KRN 633 10mg
10mg
| Purity Not Available
Adooq Bioscience
KRN 633 is a cell-permeable, reversible, ATP-competitive VEGFR kinase inhibitor that inhibits PDGFR-?? and c-Kit at higher concentrations only (IC50 = 0.97 ??M and 4.33 ??M, respectively) and inactive towards 17 other kinases (IC50 ??? 10 ??M).
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Adooq Bioscience
Kinetin 100mg
100mg
| Purity Not Available
Adooq Bioscience
Ki8751 50mg
50mg
| Purity Not Available
Adooq Bioscience
Ki8751 is a cell-permeable quinolyloxyphenyl-urea compound that acts as a Flk-1 (VEGFR-2)-selective inhibitior in both cell-based and cell-free assays.
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Ki8751 5mg
5mg
| Purity Not Available
Adooq Bioscience
Ki8751 is a cell-permeable quinolyloxyphenyl-urea compound that acts as a Flk-1 (VEGFR-2)-selective inhibitior in both cell-based and cell-free assays.
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Adooq Bioscience
JNJ-7706621 is a novel cell cycle inhibitor that showed potent inhibition of several cyclin-dependent kinases (CDK) and Aurora kinases.
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Adooq Bioscience
JNJ-7706621 is a novel cell cycle inhibitor that showed potent inhibition of several cyclin-dependent kinases (CDK) and Aurora kinases.
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Adooq Bioscience
c-Met inhibitor JNJ-38877605 selectively binds to c-Met, thereby inhibiting c-Met phosphorylation and disrupting c-Met signal transduction pathways.
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